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Volumn 37, Issue 6, 2005, Pages 881-903

The human gene map for performance and health-related fitness phenotypes: The 2004 update

Author keywords

Candidate genes; Genetic variants; Genetics; Linkage; Mitochondrial genome; Nuclear genome; Quantitative trait loci

Indexed keywords

AUTOSOME; CONTROLLED STUDY; FITNESS; GENE LOCUS; GENE MAPPING; GENE TECHNOLOGY; GENETIC VARIABILITY; HEALTH CARE ACCESS; HUMAN; MITOCHONDRIAL GENETICS; PEER REVIEW; PHENOTYPE; PHYSICAL PERFORMANCE; QUANTITATIVE TRAIT LOCUS; REVIEW; SITTING; X CHROMOSOME;

EID: 20544441894     PISSN: 01959131     EISSN: None     Source Type: Journal    
DOI: 10.1249/01.mss.0000168663.55604.1d     Document Type: Review
Times cited : (98)

References (222)
  • 1
    • 0036787666 scopus 로고    scopus 로고
    • Angiotensin-convertingenzyme genotype modulates pulmonary function and exercise capacity in treatedpatients with congestive stable heart failure
    • ABRAHAM, M. R., L. J. OLSON, and M. J. JOYNER. Angiotensin- convertingenzyme genotype modulates pulmonary function and exercise capacity in treatedpatients with congestive stable heart failure. Circulation 106:1794-1799, 2002.
    • (2002) Circulation , vol.106 , pp. 1794-1799
    • Abraham, M.R.1    Olson, L.J.2    Joyner, M.J.3
  • 2
    • 12944266975 scopus 로고    scopus 로고
    • Genetic variation in the renin-angiotensin system and athletic performance
    • ALVAREZ, R., N. TERRADOS, and R. ORTOLANO. Genetic variation in the renin-angiotensin system and athletic performance. Eur. J. Appl. Physiol. 82:117-120, 2000.
    • (2000) Eur. J. Appl. Physiol. , vol.82 , pp. 117-120
    • Alvarez, R.1    Terrados, N.2    Ortolano, R.3
  • 3
    • 0032929367 scopus 로고    scopus 로고
    • A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria
    • ANDREU, A. L., C. BRUNO, and T. C. DUNNE. A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria. Ann. Neurol. 45:127-130, 1999.
    • (1999) Ann. Neurol. , vol.45 , pp. 127-130
    • Andreu, A.L.1    Bruno, C.2    Dunne, T.C.3
  • 4
    • 0031744009 scopus 로고    scopus 로고
    • Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy
    • ANDREU, A. L., C. BRUNO, and S. SHANSKE. Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy. Neurology 51:1444-1447, 1998.
    • (1998) Neurology , vol.51 , pp. 1444-1447
    • Andreu, A.L.1    Bruno, C.2    Shanske, S.3
  • 5
    • 0033619147 scopus 로고    scopus 로고
    • Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA
    • ANDREU, A. L., M. G. HANNA, and H. REICHMANN. Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA. N. Engl. J. Med. 341:1037-1044, 1999.
    • (1999) N. Engl. J. Med. , vol.341 , pp. 1037-1044
    • Andreu, A.L.1    Hanna, M.G.2    Reichmann, H.3
  • 6
    • 0033013692 scopus 로고    scopus 로고
    • Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene
    • ANDREU, A. L., K. TANJI, and C. BRUNO. Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene. Ann. Neurol. 45:820-823, 1999.
    • (1999) Ann. Neurol. , vol.45 , pp. 820-823
    • Andreu, A.L.1    Tanji, K.2    Bruno, C.3
  • 7
  • 9
    • 0032876874 scopus 로고    scopus 로고
    • Physical activity modulates the effect of a lipoprotein lipase mutation (D9N) on plasma lipids and lipoproteins
    • BOER, J. M., J. A. KUIVENHOVEN, and E. J. FESKENS. Physical activity modulates the effect of a lipoprotein lipase mutation (D9N) on plasma lipids and lipoproteins. Clin. Genet. 56:158-163, 1999.
    • (1999) Clin. Genet. , vol.56 , pp. 158-163
    • Boer, J.M.1    Kuivenhoven, J.A.2    Feskens, E.J.3
  • 10
    • 0033954517 scopus 로고    scopus 로고
    • Genomic scan for maximal oxygen uptake and its response to training in the HERITAGE Family Study
    • BOUCHARD, C., T. RANKINEN, and Y. C. CHAGNON. Genomic scan for maximal oxygen uptake and its response to training in the HERITAGE Family Study. J. Appl. Physiol. 88:551-559, 2000.
    • (2000) J. Appl. Physiol. , vol.88 , pp. 551-559
    • Bouchard, C.1    Rankinen, T.2    Chagnon, Y.C.3
  • 11
    • 0035818285 scopus 로고    scopus 로고
    • Bradykinin B2BKR receptor polymorphism and left-ventricular growth response
    • BRULL, D., S. DHAMRAIT, and S. MYERSON. Bradykinin B2BKR receptor polymorphism and left-ventricular growth response. Lancet 358:1155-1156, 2001.
    • (2001) Lancet , vol.358 , pp. 1155-1156
    • Brull, D.1    Dhamrait, S.2    Myerson, S.3
  • 12
    • 0036146049 scopus 로고    scopus 로고
    • The effect of fibrinogen genotype on fibrinogen levels after strenuous physical exercise
    • BRULL, D. J., S. DHAMRAIT, and R. MOULDING. The effect of fibrinogen genotype on fibrinogen levels after strenuous physical exercise. Thromb. Haemost. 87:37-41, 2002.
    • (2002) Thromb. Haemost. , vol.87 , pp. 37-41
    • Brull, D.J.1    Dhamrait, S.2    Moulding, R.3
  • 13
    • 10744231062 scopus 로고    scopus 로고
    • Human CRP gene polymorphism influences CRP levels: Implications for the prediction and pathogenesis of coronary heart disease
    • BRULL, D. J., N. SERRANO, and F. ZITO. Human CRP gene polymorphism influences CRP levels: implications for the prediction and pathogenesis of coronary heart disease. Arterioscler. Thromb. Vasc. Biol. 23:2063-2069, 2003.
    • (2003) Arterioscler. Thromb. Vasc. Biol. , vol.23 , pp. 2063-2069
    • Brull, D.J.1    Serrano, N.2    Zito, F.3
  • 14
    • 0032575672 scopus 로고    scopus 로고
    • A splice junction mutation in the alpha(M) gene of phosphorylase kinase in a patient with myopathy
    • BRUNO, C., G. MANFREDI, and A. L. ANDREU. A splice junction mutation in the alpha(M) gene of phosphorylase kinase in a patient with myopathy. Biochem. Biophys. Res. Commun. 249: 648-651, 1998.
    • (1998) Biochem. Biophys. Res. Commun. , vol.249 , pp. 648-651
    • Bruno, C.1    Manfredi, G.2    Andreu, A.L.3
  • 15
    • 0141704179 scopus 로고    scopus 로고
    • Progressive exercise intolerance associated with a new muscle-restricted non-sense mutation (0142X) in the mitochondrial cytochrome b gene
    • BRUNO, C., F. M. SANTORELLI, and S. ASSERETO. Progressive exercise intolerance associated with a new muscle-restricted non-sense mutation (0142X) in the mitochondrial cytochrome b gene. Muscle Nerve 28:508-511, 2003.
    • (2003) Muscle Nerve , vol.28 , pp. 508-511
    • Bruno, C.1    Santorelli, F.M.2    Assereto, S.3
  • 16
    • 0035071837 scopus 로고    scopus 로고
    • The association between the val/ala-55 polymorphism of the uncoupling protein 2 gene and exercise efficiency
    • BUEMANN, B., B. SCHIERNING, and S. TOUBRO. The association between the val/ala-55 polymorphism of the uncoupling protein 2 gene and exercise efficiency. Int. J. Obes. Relat. Metab. Disord. 25:467-471, 2001.
    • (2001) Int. J. Obes. Relat. Metab. Disord. , vol.25 , pp. 467-471
    • Buemann, B.1    Schierning, B.2    Toubro, S.3
  • 17
    • 0028928815 scopus 로고
    • Clinical heterogeneity in two pedigrees with the 3243 bp tRNA(Leu(UUR)) mutation of mitochondrial DNA
    • CAMPOS, Y., J. BAUTISTA, and E. GUTIERREZ-RIVAS. Clinical heterogeneity in two pedigrees with the 3243 bp tRNA(Leu(UUR)) mutation of mitochondrial DNA. Acta Neurol. Scand. 91:62-65, 1995.
    • (1995) Acta Neurol. Scand. , vol.91 , pp. 62-65
    • Campos, Y.1    Bautista, J.2    Gutierrez-Rivas, E.3
  • 18
    • 0036158877 scopus 로고    scopus 로고
    • Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy
    • CAMPOS, Y., A. GARCIA, and A. LOPEZ. Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy. Muscle Nerve 25:185-188, 2002.
    • (2002) Muscle Nerve , vol.25 , pp. 185-188
    • Campos, Y.1    Garcia, A.2    Lopez, A.3
  • 19
    • 0035063158 scopus 로고    scopus 로고
    • Oenomic scan for genes affecting body composition before and after training in Caucasians from HERITAGE
    • CHAGNON, Y. C., T. RICE, and L. PERUSSE. Oenomic scan for genes affecting body composition before and after training in Caucasians from HERITAGE. J. Appl. Physiol. 90:1777-1787, 2001.
    • (2001) J. Appl. Physiol. , vol.90 , pp. 1777-1787
    • Chagnon, Y.C.1    Rice, T.2    Perusse, L.3
  • 20
    • 3543001610 scopus 로고    scopus 로고
    • The ACE gene and endurance performance during the South African Ironman Triathlons
    • COLLINS, M., S. L. XENOPHONTOS, and M. A. CARIOLOU. The ACE gene and endurance performance during the South African Ironman Triathlons. Med. Sci. Sports Exerc. 36:1314-1320, 2004.
    • (2004) Med. Sci. Sports Exerc. , vol.36 , pp. 1314-1320
    • Collins, M.1    Xenophontos, S.L.2    Cariolou, M.A.3
  • 21
    • 0034909902 scopus 로고    scopus 로고
    • Beta-enolase deficiency, a new metabolic myopathy of distal glycolysis
    • COMI, G. P., F. FORTUNATO, and S. LUCCHIARI. Beta-enolase deficiency, a new metabolic myopathy of distal glycolysis. Ann. Neurol. 50:202-207, 2001.
    • (2001) Ann. Neurol. , vol.50 , pp. 202-207
    • Comi, G.P.1    Fortunato, F.2    Lucchiari, S.3
  • 22
    • 0036525939 scopus 로고    scopus 로고
    • The 27Glu polymorphism of the beta2-adrenergic receptor gene interacts with physical activity influencing obesity risk among female subjects
    • CORBALAN, M. S. The 27Glu polymorphism of the beta2-adrenergic receptor gene interacts with physical activity influencing obesity risk among female subjects. Clin. Genet. 61:305-307, 2002.
    • (2002) Clin. Genet. , vol.61 , pp. 305-307
    • Corbalan, M.S.1
  • 23
    • 0034872780 scopus 로고    scopus 로고
    • Environmental factors modulate the effect of the APOE genetic polymorphism on plasma lipid concentrations: Ecogenetic studies in a Mediterranean Spanish population
    • CORELLA D., M. GUILLEN, and C. SAIZ. Environmental factors modulate the effect of the APOE genetic polymorphism on plasma lipid concentrations: ecogenetic studies in a Mediterranean Spanish population. Metabolism 50:936-944, 2001.
    • (2001) Metabolism , vol.50 , pp. 936-944
    • Corella, D.1    Guillen, M.2    Saiz, C.3
  • 25
    • 0842326412 scopus 로고    scopus 로고
    • Beta-adrenergic receptor blockade and the angiotensin-converting enzyme deletion polymorphism in patients with chronic heart failure
    • DE GROOTE, P., N. HELBECQUE, and N. LAMBLIN. Beta-adrenergic receptor blockade and the angiotensin-converting enzyme deletion polymorphism in patients with chronic heart failure. Eur. J. Heart Fail. 6:17-21, 2004.
    • (2004) Eur. J. Heart Fail. , vol.6 , pp. 17-21
    • De Groote, P.1    Helbecque, N.2    Lamblin, N.3
  • 27
    • 0037195196 scopus 로고    scopus 로고
    • Exercise-induced changes in insulin action are associated with ACE gene polymorphisms in older adults
    • DENGEL, D. R., M. D. BROWN, R. E. FERRELL, T. H. REYNOLDS IV, and M. A. SUPIANO. Exercise-induced changes in insulin action are associated with ACE gene polymorphisms in older adults. Physiol. Genomics 11:73-80, 2002.
    • (2002) Physiol. Genomics , vol.11 , pp. 73-80
    • Dengel, D.R.1    Brown, M.D.2    Ferrell, R.E.3    Reynolds IV, T.H.4    Supiano, M.A.5
  • 28
    • 8844231004 scopus 로고    scopus 로고
    • Interleukin-1 polymorphisms are associated with the inflammatory response in human muscle to acute resistance exercise
    • DENNIS, R. A., T. A. TRAPPE, and P. SIMPSON. Interleukin-1 polymorphisms are associated with the inflammatory response in human muscle to acute resistance exercise. J. Physiol. 560:617-626, 2004.
    • (2004) J. Physiol. , vol.560 , pp. 617-626
    • Dennis, R.A.1    Trappe, T.A.2    Simpson, P.3
  • 29
    • 0038311030 scopus 로고    scopus 로고
    • Cortical bone resorption during exercise is interleukin-6 genotype-dependent
    • DHAMRAIT, S. S., L. JAMES, and D. J. BRULL. Cortical bone resorption during exercise is interleukin-6 genotype-dependent. Eur. J. Appl. Physiol. 89:21-25, 2003.
    • (2003) Eur. J. Appl. Physiol. , vol.89 , pp. 21-25
    • Dhamrait, S.S.1    James, L.2    Brull, D.J.3
  • 31
    • 1542319160 scopus 로고    scopus 로고
    • The Arg16/Gly beta2-adrenergic receptor polymorphism is associated with altered cardiovascular responses to isometric exercise
    • EISENACH, J. H., A. M. MCGUIRE, R. M. SCHWINGLER, S. T. TURNER, and M. J. JOYNER. The Arg16/Gly beta2-adrenergic receptor polymorphism is associated with altered cardiovascular responses to isometric exercise. Physiol. Genomics 16:323-328. 2004.
    • (2004) Physiol. Genomics , vol.16 , pp. 323-328
    • Eisenach, J.H.1    McGuire, A.M.2    Schwingler, R.M.3    Turner, S.T.4    Joyner, M.J.5
  • 32
    • 10744219801 scopus 로고    scopus 로고
    • Promoter but not exon 7 polymorphism of endothelial nitric oxide synthase affects training-induced correction of endothelial dysfunction
    • ERBS, S., Y. BAITHER, and A. LINKE. Promoter but not exon 7 polymorphism of endothelial nitric oxide synthase affects training-induced correction of endothelial dysfunction. Arterioscler. Thromb. Vasc. Biol. 23:1814-1819, 2003.
    • (2003) Arterioscler. Thromb. Vasc. Biol. , vol.23 , pp. 1814-1819
    • Erbs, S.1    Baither, Y.2    Linke, A.3
  • 33
    • 0033777742 scopus 로고    scopus 로고
    • RAS genes influence exercise-induced left ventricular hypertrophy: An elite athletes study
    • FATINI, C., R. GUAZZELLI, and P. MANETTI. RAS genes influence exercise-induced left ventricular hypertrophy: an elite athletes study. Med. Sci. Sports Exerc. 32:1868-1872, 2000.
    • (2000) Med. Sci. Sports Exerc. , vol.32 , pp. 1868-1872
    • Fatini, C.1    Guazzelli, R.2    Manetti, P.3
  • 34
    • 0033795956 scopus 로고    scopus 로고
    • Angiotensin-converting enzyme genotype affects the response of human skeletal muscle to functional overload
    • FOLLAND, J., B. LEACH, and T. LITTLE. Angiotensin-converting enzyme genotype affects the response of human skeletal muscle to functional overload. Exp. Physiol. 85:575-579, 2000.
    • (2000) Exp. Physiol. , vol.85 , pp. 575-579
    • Folland, J.1    Leach, B.2    Little, T.3
  • 35
    • 0345097647 scopus 로고    scopus 로고
    • PGC-1alpha genotype modifies the association of volitional energy expenditure with [OV0312]O2max
    • FRANKS, P. W., I. BARROSO, and J. LUAN. PGC-1alpha genotype modifies the association of volitional energy expenditure with [OV0312]O2max. Med. Sci. Sports Exerc. 35:1998-2004, 2003.
    • (2003) Med. Sci. Sports Exerc. , vol.35 , pp. 1998-2004
    • Franks, P.W.1    Barroso, I.2    Luan, J.3
  • 36
    • 10744222766 scopus 로고    scopus 로고
    • Association between physical activity and blood pressure is modified by variants in the G-protein coupled receptor 10
    • FRANKS, P. W., S. BHATTACHARYYA, and J. LUAN. Association between physical activity and blood pressure is modified by variants in the G-protein coupled receptor 10. Hypertension 43:224-228, 2004.
    • (2004) Hypertension , vol.43 , pp. 224-228
    • Franks, P.W.1    Bhattacharyya, S.2    Luan, J.3
  • 37
    • 0030469161 scopus 로고    scopus 로고
    • Insertion/deletion polymorphism in the angiotensin-converting-enzyme gene and blood pressure during ergometry in normal males
    • FRIEDL, W., F. KREMPLER, F. SANDHOFER, and B. PAULWEBER. Insertion/deletion polymorphism in the angiotensin-converting-enzyme gene and blood pressure during ergometry in normal males. Clin. Genet. 50:541-544, 1996.
    • (1996) Clin. Genet. , vol.50 , pp. 541-544
    • Friedl, W.1    Krempler, F.2    Sandhofer, F.3    Paulweber, B.4
  • 38
    • 0032557927 scopus 로고    scopus 로고
    • Insertion/deletion polymorphism in the angiotensin-converting enzyme gene is associated with atrial natriuretic peptide activity after exercise
    • FRIEDL, W., J. MAIR, M. PICHLER, B. PAULWEBER, F. SANDHOFER, and B. PUSCHENDORF. Insertion/deletion polymorphism in the angiotensin-converting enzyme gene is associated with atrial natriuretic peptide activity after exercise. Clin. Chim. Acta 274: 199-211, 1998.
    • (1998) Clin. Chim. Acta , vol.274 , pp. 199-211
    • Friedl, W.1    Mair, J.2    Pichler, M.3    Paulweber, B.4    Sandhofer, F.5    Puschendorf, B.6
  • 39
    • 0033555898 scopus 로고    scopus 로고
    • Role of serotonin in the paradoxical calming effect of psychostimulants on hyperactivity
    • GAINETDINOV, R. R., W. C. WETSEL, S. R. JONES, E. D. LEVIN, M. JABER, and M. G. CARON. Role of serotonin in the paradoxical calming effect of psychostimulants on hyperactivity. Science 283:397-401, 1999.
    • (1999) Science , vol.283 , pp. 397-401
    • Gainetdinov, R.R.1    Wetsel, W.C.2    Jones, S.R.3    Levin, E.D.4    Jaber, M.5    Caron, M.G.6
  • 40
    • 0034867319 scopus 로고    scopus 로고
    • Evidence of LPL gene-exercise interaction for body fat and LPL activity: The HERITAGE Family Study
    • GARENC, C., L. PERUSSE, and J. BERCERON. Evidence of LPL gene-exercise interaction for body fat and LPL activity: the HERITAGE Family Study. J. Appl. Physiol. 91:1334-1340, 2001.
    • (2001) J. Appl. Physiol. , vol.91 , pp. 1334-1340
    • Garenc, C.1    Perusse, L.2    Berceron, J.3
  • 41
    • 3343023655 scopus 로고    scopus 로고
    • Effects of beta2-adrenergic receptor gene variants on adiposity: The HERITAGE Family Study
    • GARENC, C., L. PERUSSE, and Y. C. CHAGNON. Effects of beta2-adrenergic receptor gene variants on adiposity: the HERITAGE Family Study. Obes. Res. 11:612-618, 2003.
    • (2003) Obes. Res. , vol.11 , pp. 612-618
    • Garenc, C.1    Perusse, L.2    Chagnon, Y.C.3
  • 42
    • 0031705720 scopus 로고    scopus 로고
    • Elite endurance athletes and the ACE I allele - The role of genes in athletic performance
    • GAYACAY, G., B. YU, and B. HAMBLY. Elite endurance athletes and the ACE I allele-the role of genes in athletic performance. Hum. Genet. 103:48-50, 1998.
    • (1998) Hum. Genet. , vol.103 , pp. 48-50
    • Gayacay, G.1    Yu, B.2    Hambly, B.3
  • 43
    • 0030862171 scopus 로고    scopus 로고
    • Quadriceps and grip strength are related to vitamin D receptor genotype in elderly nonobese women
    • GEUSENS, P., C. VANDEVYVER, J. VANHOOF, J. J. CASSIMAN, S. BOONEN, and J. RAUS. Quadriceps and grip strength are related to vitamin D receptor genotype in elderly nonobese women. J. Bone Miner. Res. 12:2082-2088, 1997.
    • (1997) J. Bone Miner. Res. , vol.12 , pp. 2082-2088
    • Geusens, P.1    Vandevyver, C.2    Vanhoof, J.3    Cassiman, J.J.4    Boonen, S.5    Raus, J.6
  • 44
    • 1342283022 scopus 로고    scopus 로고
    • Selected genetic polymorphisms and plasma coagulation factor VII changes with exercise training
    • GHIU, I. A., R. E. FERRELL, O. KULAPUTANA, D. A. PHARES, and J. M. HAGBERG. Selected genetic polymorphisms and plasma coagulation factor VII changes with exercise training. J. Appl. Physiol 96:985-990, 2004.
    • (2004) J. Appl. Physiol , vol.96 , pp. 985-990
    • Ghiu, I.A.1    Ferrell, R.E.2    Kulaputana, O.3    Phares, D.A.4    Hagberg, J.M.5
  • 46
    • 0142244225 scopus 로고    scopus 로고
    • Exercise intolerance, muscle pain and lactic acidaemia associated with a 7497G>A mutation in the tRNASer(UCN) gene
    • GRAFAKOU, O., F. A. HOL, and K. OTFRIED SCHWAB. Exercise intolerance, muscle pain and lactic acidaemia associated with a 7497G>A mutation in the tRNASer(UCN) gene. J. Inherit. Metab. Dis. 26:593-600, 2003.
    • (2003) J. Inherit. Metab. Dis. , vol.26 , pp. 593-600
    • Grafakou, O.1    Hol, F.A.2    Otfried Schwab, K.3
  • 47
    • 1842422417 scopus 로고    scopus 로고
    • Genetic variation in the human vitamin D receptor is associated with muscle strength, fat mass and body weight in Swedish women
    • GRUNDBERG, E., H. BRANDSTROM, E. L. RIBOM, O. LJUNGGREN, H. MALLMIN, and A. KINDMARK. Genetic variation in the human vitamin D receptor is associated with muscle strength, fat mass and body weight in Swedish women. Eur. J. Endocrinol. 150: 323-328, 2004.
    • (2004) Eur. J. Endocrinol. , vol.150 , pp. 323-328
    • Grundberg, E.1    Brandstrom, H.2    Ribom, E.L.3    Ljunggren, O.4    Mallmin, H.5    Kindmark, A.6
  • 48
    • 0034609543 scopus 로고    scopus 로고
    • Abnormal pulmonary artery pressure response in asymptomatic carriers of primary pulmonary hypertension gene
    • GRUNIO, E., B. JANSSEN, and D. MERELES. Abnormal pulmonary artery pressure response in asymptomatic carriers of primary pulmonary hypertension gene. Circulation 102:1145-1150. 2000.
    • (2000) Circulation , vol.102 , pp. 1145-1150
    • Grunio, E.1    Janssen, B.2    Mereles, D.3
  • 49
    • 0032829329 scopus 로고    scopus 로고
    • Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) gene
    • HADJIGEORGIOU, G. M., N. KAWASHIMA, and C. BRUNO. Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) gene. Neuromuscul. Disord. 9:399-402, 1999.
    • (1999) Neuromuscul. Disord. , vol.9 , pp. 399-402
    • Hadjigeorgiou, G.M.1    Kawashima, N.2    Bruno, C.3
  • 50
    • 0032800446 scopus 로고    scopus 로고
    • Exercise training-induced blood pressure and plasma lipid improvements in hypertensives may be genotype dependent
    • HAGBERG, J. M., R. E. FERRELL, D. R. DENGEL, and K. R. WILUND. Exercise training-induced blood pressure and plasma lipid improvements in hypertensives may be genotype dependent. Hypertension 34:18-23, 1999.
    • (1999) Hypertension , vol.34 , pp. 18-23
    • Hagberg, J.M.1    Ferrell, R.E.2    Dengel, D.R.3    Wilund, K.R.4
  • 51
    • 0032865059 scopus 로고    scopus 로고
    • Apolipoprotein e genotype and exercise training-induced increases in plasma high-density lipoprotein (HDL)- and HDL2-cholesterol levels in overweight men
    • HAGBERG, J. M., R. E. FERRELL, L. I. KATZEL, D. R. DENGEL, J. D. SORKIN, and A. P. GOLDBERG. Apolipoprotein E genotype and exercise training-induced increases in plasma high-density lipoprotein (HDL)- and HDL2-cholesterol levels in overweight men. Metabolism 48:943-945, 1999.
    • (1999) Metabolism , vol.48 , pp. 943-945
    • Hagberg, J.M.1    Ferrell, R.E.2    Katzel, L.I.3    Dengel, D.R.4    Sorkin, J.D.5    Goldberg, A.P.6
  • 53
    • 0036092930 scopus 로고    scopus 로고
    • ACE insertion/deletion polymorphism and submaximal exercise hemodynamics in postmenopausal women
    • HAGBERG, J. M., S. D. MCCOLE, and M. D. BROWN. ACE insertion/deletion polymorphism and submaximal exercise hemodynamics in postmenopausal women. J. Appl. Physiol. 92:1083-1088, 2002.
    • (2002) J. Appl. Physiol. , vol.92 , pp. 1083-1088
    • Hagberg, J.M.1    McCole, S.D.2    Brown, M.D.3
  • 54
    • 0345374668 scopus 로고    scopus 로고
    • High-density lipoprotein-cholesterol, its subfractions, responses to exercise training are dependent on endothelial lipase genotype
    • HALVERSTADT, A., D. A. PHARES, R. E. FERRELL, K. R. WILUND, A. P. GOLDBERG, and J. M. HAGBERG. High-density lipoprotein-cholesterol, its subfractions, responses to exercise training are dependent on endothelial lipase genotype. Metabolism 52:1505-1511, 2003.
    • (2003) Metabolism , vol.52 , pp. 1505-1511
    • Halverstadt, A.1    Phares, D.A.2    Ferrell, R.E.3    Wilund, K.R.4    Goldberg, A.P.5    Hagberg, J.M.6
  • 55
    • 0032231458 scopus 로고    scopus 로고
    • Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA
    • HANNA, M. G., I. P. NELSON, and S. RAHMAN. Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA. Am. J. Hum. Genet. 63:29-36, 1998.
    • (1998) Am. J. Hum. Genet. , vol.63 , pp. 29-36
    • Hanna, M.G.1    Nelson, I.P.2    Rahman, S.3
  • 56
    • 0028927272 scopus 로고
    • Segregation patterns of a novel mutation in the mitochondrial tRNA glutamic acid gene associated with myopathy and diabetes mellitus
    • HAO, H., E. BONILLA, G. MANFREDI, S. DIMAURO, and C. T. MORAES. Segregation patterns of a novel mutation in the mitochondrial tRNA glutamic acid gene associated with myopathy and diabetes mellitus. Am. J. Hum. Genet. 56:1017-1025, 1995.
    • (1995) Am. J. Hum. Genet. , vol.56 , pp. 1017-1025
    • Hao, H.1    Bonilla, E.2    Manfredi, G.3    DiMauro, S.4    Moraes, C.T.5
  • 57
    • 2942757356 scopus 로고    scopus 로고
    • Human ACE I/D polymorphism is associated with individual differences in exercise heat tolerance
    • HELED, Y., D. S. MORAN, L. MENDEL, A. LAOR, E. PRAS, and Y. SHAPIRO. Human ACE I/D polymorphism is associated with individual differences in exercise heat tolerance. J. Appl. Physiol. 97:72-76, 2004.
    • (2004) J. Appl. Physiol. , vol.97 , pp. 72-76
    • Heled, Y.1    Moran, D.S.2    Mendel, L.3    Laor, A.4    Pras, E.5    Shapiro, Y.6
  • 58
    • 3042654860 scopus 로고    scopus 로고
    • Glycerol kinase deficiency: Follow-up during 20 years, genetics, biochemistry and prognosis
    • HELLERUD, C., N. WRAMNER, A. ERIKSON, A. JOHANSSON, G. SAMUELSON, and S. LINDSTEDT. Glycerol kinase deficiency: follow-up during 20 years, genetics, biochemistry and prognosis. Acta Paediatr. 93:911-921, 2004.
    • (2004) Acta Paediatr. , vol.93 , pp. 911-921
    • Hellerud, C.1    Wramner, N.2    Erikson, A.3    Johansson, A.4    Samuelson, G.5    Lindstedt, S.6
  • 59
    • 4544347006 scopus 로고    scopus 로고
    • Angiotensin converting enzyme genotype and strength in chronic obstructive pulmonary disease
    • HOPKINSON, N. S., A. H. NICKOL, and J. PAYNE. Angiotensin converting enzyme genotype and strength in chronic obstructive pulmonary disease. Am. J. Respir. Crit. Care Med. 170:395-399, 2004.
    • (2004) Am. J. Respir. Crit. Care Med. , vol.170 , pp. 395-399
    • Hopkinson, N.S.1    Nickol, A.H.2    Payne, J.3
  • 60
    • 4544377426 scopus 로고    scopus 로고
    • The -55 C/T polymorphism within the UCP3 gene and performance during the South African Ironman Triathlon
    • HUDSON, D. E., G. G. MOKONE, T. D. NOAKES, and M. COLLINS. The -55 C/T polymorphism within the UCP3 gene and performance during the South African Ironman Triathlon. Int. J. Sports Med. 25:427-432, 2004.
    • (2004) Int. J. Sports Med. , vol.25 , pp. 427-432
    • Hudson, D.E.1    Mokone, G.G.2    Noakes, T.D.3    Collins, M.4
  • 61
    • 3042728655 scopus 로고    scopus 로고
    • Linkage of myostatin pathway genes with knee strength in humans
    • HUYGENS, W., M. A. THOMIS, and M. W. PEETERS. Linkage of myostatin pathway genes with knee strength in humans. Physiol. Genomics 17:264-270, 2004.
    • (2004) Physiol. Genomics , vol.17 , pp. 264-270
    • Huygens, W.1    Thomis, M.A.2    Peeters, M.W.3
  • 62
    • 10444256374 scopus 로고    scopus 로고
    • A quantitative trait locus on 13q14.2 for trunk strength
    • HUYGENS, W., M. A. THOMIS, and M. W. PEETERS. A quantitative trait locus on 13q14.2 for trunk strength. Twin Res. 7:603-606, 2004.
    • (2004) Twin Res. , vol.7 , pp. 603-606
    • Huygens, W.1    Thomis, M.A.2    Peeters, M.W.3
  • 63
    • 0034541394 scopus 로고    scopus 로고
    • Effects of age, gender, myostatin genotype on the hypertrophic response to heavy resistance strength training
    • IVEY, F. M., S. M. ROTH, and R. E. FERRELL. Effects of age, gender, myostatin genotype on the hypertrophic response to heavy resistance strength training. J. Gerontol. A. Biol. Sci. Med. Sci. 55:M641-648, 2000.
    • (2000) J. Gerontol. A. Biol. Sci. Med. Sci. , vol.55
    • Ivey, F.M.1    Roth, S.M.2    Ferrell, R.E.3
  • 64
    • 0037176933 scopus 로고    scopus 로고
    • Peroxisome proliferator-activated receptor alpha gene regulates left ventricular growth in response to exercise and hypertension
    • JAMSHIDI, Y., H. E. MONTGOMERY, and H. W. HENSE. Peroxisome proliferator-activated receptor alpha gene regulates left ventricular growth in response to exercise and hypertension. Circulation 105:950-955, 2002.
    • (2002) Circulation , vol.105 , pp. 950-955
    • Jamshidi, Y.1    Montgomery, H.E.2    Hense, H.W.3
  • 65
    • 2342626616 scopus 로고    scopus 로고
    • Gln27Glu polymorphism of the beta2 adrenergic receptor gene in healthy Japanese men is associated with the change of fructosamine level caused by exercise
    • KAHARA, T., T. HAYAKAWA, Y., NAGAI, A. SHIMIZU, and T. TAKAMURA. Gln27Glu polymorphism of the beta2 adrenergic receptor gene in healthy Japanese men is associated with the change of fructosamine level caused by exercise. Diabetes Res. Clin. Pract. 64:207-212, 2004.
    • (2004) Diabetes Res. Clin. Pract. , vol.64 , pp. 207-212
    • Kahara, T.1    Hayakawa, T.2    Nagai, Y.3    Shimizu, A.4    Takamura, T.5
  • 66
    • 0037313934 scopus 로고    scopus 로고
    • PPARgamma gene polymorphism is associated with exercise-mediated changes of insulin resistance in healthy men
    • KAHARA, T., T. TAKAMURA, and T. HAYAKAWA. PPARgamma gene polymorphism is associated with exercise-mediated changes of insulin resistance in healthy men. Metabolism 52:209-212, 2003.
    • (2003) Metabolism , vol.52 , pp. 209-212
    • Kahara, T.1    Takamura, T.2    Hayakawa, T.3
  • 67
    • 0036285677 scopus 로고    scopus 로고
    • Prediction of exercise-mediated changes in metabolic markers by gene polymorphism
    • KAHARA, T., T. TAKAMURA, and T. HAYAKAWA. Prediction of exercise-mediated changes in metabolic markers by gene polymorphism. Diabetes Res. Clin. Pract. 57:105-110, 2002.
    • (2002) Diabetes Res. Clin. Pract. , vol.57 , pp. 105-110
    • Kahara, T.1    Takamura, T.2    Hayakawa, T.3
  • 68
    • 0035347179 scopus 로고    scopus 로고
    • Altered intracellular processing and release of neuropeptide Y due to leucine 7 to proline 7 polymorphism in the signal peptide of preproneuropeptide Y in humans
    • KALLIO, J., U. PESONEN, and K. KAIPIO. Altered intracellular processing and release of neuropeptide Y due to leucine 7 to proline 7 polymorphism in the signal peptide of preproneuropeptide Y in humans. FASEB J. 15:1242-1244, 2001.
    • (2001) FASEB J. , vol.15 , pp. 1242-1244
    • Kallio, J.1    Pesonen, U.2    Kaipio, K.3
  • 69
    • 0035181764 scopus 로고    scopus 로고
    • Enhanced exercise-induced GH secretion in subjects with Pro7 substitution in the prepro-NPY
    • KALLIO, J., U. PESONEN, and M. K. KARVONEN. Enhanced exercise-induced GH secretion in subjects with Pro7 substitution in the prepro-NPY. J. Clin. Endocrinol. Metab. 86: 5348-5352, 2001.
    • (2001) J. Clin. Endocrinol. Metab. , vol.86 , pp. 5348-5352
    • Kallio, J.1    Pesonen, U.2    Karvonen, M.K.3
  • 70
    • 0038691852 scopus 로고    scopus 로고
    • Effects of captopril administration on pulmonary haemodynamics and tissue oxygenation during exercise in ACE gene subtypes in patients with COPD: A preliminary study
    • KANAZAWA, H., K. HIRATA, and J. YOSHIKAWA. Effects of captopril administration on pulmonary haemodynamics and tissue oxygenation during exercise in ACE gene subtypes in patients with COPD: a preliminary study. Thorax 58:629-631, 2003.
    • (2003) Thorax , vol.58 , pp. 629-631
    • Kanazawa, H.1    Hirata, K.2    Yoshikawa, J.3
  • 71
    • 0344825835 scopus 로고    scopus 로고
    • Influence of oxygen administration on pulmonary haemodynamics and tissue oxygenation during exercise in COPD patients with different ACE genotypes
    • KANAZAWA, H., K. HIRATA, and J. YOSHIKAWA. Influence of oxygen administration on pulmonary haemodynamics and tissue oxygenation during exercise in COPD patients with different ACE genotypes. Clin. Phvsiol. Fund. Imaging. 23:332-336, 2003.
    • (2003) Clin. Phvsiol. Fund. Imaging. , vol.23 , pp. 332-336
    • Kanazawa, H.1    Hirata, K.2    Yoshikawa, J.3
  • 72
    • 0033777672 scopus 로고    scopus 로고
    • Deletion polymorphisms in the angiotensin converting enzyme gene are associated with pulmonary hypertension evoked by exercise challenge in patients with chronic obstructive pulmonary disease
    • KANAZAWA, H., T. OKAMOTO, K. HIRATA, and J. YOSHIKAWA. Deletion polymorphisms in the angiotensin converting enzyme gene are associated with pulmonary hypertension evoked by exercise challenge in patients with chronic obstructive pulmonary disease. Am. J. Respir. Crit. Care Med. 162:1235-1238, 2000.
    • (2000) Am. J. Respir. Crit. Care Med. , vol.162 , pp. 1235-1238
    • Kanazawa, H.1    Okamoto, T.2    Hirata, K.3    Yoshikawa, J.4
  • 73
    • 0036207342 scopus 로고    scopus 로고
    • Association between the angiotensin-converting enzyme gene polymorphisms and tissue oxygenation during exercise in patients with COPD
    • KANAZAWA, H., T. OTSUKA, K. HIRATA, and J. YOSHIKAWA. Association between the angiotensin-converting enzyme gene polymorphisms and tissue oxygenation during exercise in patients with COPD. Chest 121:697-701, 2002.
    • (2002) Chest , vol.121 , pp. 697-701
    • Kanazawa, H.1    Otsuka, T.2    Hirata, K.3    Yoshikawa, J.4
  • 74
    • 4043062192 scopus 로고    scopus 로고
    • Acute effects of nifedipine administration in pulmonary haemodynamics and oxygen delivery during exercise in patients with chronic obstructive pulmonary disease: Implication of the angiotensin-converting enzyme gene polymorphisms
    • KANAZAWA, H., Y. TATEISHI, and J. YOSHIKAWA. Acute effects of nifedipine administration in pulmonary haemodynamics and oxygen delivery during exercise in patients with chronic obstructive pulmonary disease: implication of the angiotensin-converting enzyme gene polymorphisms. Clin. Physiol. Funct. Imaging. 24:224-228, 2004.
    • (2004) Clin. Physiol. Funct. Imaging. , vol.24 , pp. 224-228
    • Kanazawa, H.1    Tateishi, Y.2    Yoshikawa, J.3
  • 75
    • 0033811149 scopus 로고    scopus 로고
    • Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA
    • KARADIMAS, C. L., P. GREENSTEIN, and C. M. SUE. Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA. Neurology 55:644-649, 2000.
    • (2000) Neurology , vol.55 , pp. 644-649
    • Karadimas, C.L.1    Greenstein, P.2    Sue, C.M.3
  • 76
    • 0036837220 scopus 로고    scopus 로고
    • Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNA
    • KARADIMAS, C. L., L. SALVIATI, and S. SACCONI. Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNA. Neuromuscul. Disord. 12:865-868, 2002.
    • (2002) Neuromuscul. Disord. , vol.12 , pp. 865-868
    • Karadimas, C.L.1    Salviati, L.2    Sacconi, S.3
  • 77
    • 0033659683 scopus 로고    scopus 로고
    • Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene
    • KEIGHTLEY, J. A., R. ANITORI, M. D. BURTON, F. QUAN, N. R. BUIST, and N. G. KENNAWAY. Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene. Am. J. Hum. Genet. 67:1400-1410, 2000.
    • (2000) Am. J. Hum. Genet. , vol.67 , pp. 1400-1410
    • Keightley, J.A.1    Anitori, R.2    Burton, M.D.3    Quan, F.4    Buist, N.R.5    Kennaway, N.G.6
  • 78
    • 20244389989 scopus 로고    scopus 로고
    • Locomotor activity in D2 dopamine receptor-deficient mice is determined by gene dosage, genetic background, developmental adaptations
    • KELLY, M. A., M. RUBINSTEIN, and T. J. PHILLIPS. Locomotor activity in D2 dopamine receptor-deficient mice is determined by gene dosage, genetic background, developmental adaptations. J. Neurosci. 18:3470-3479, 1998.
    • (1998) J. Neurosci. , vol.18 , pp. 3470-3479
    • Kelly, M.A.1    Rubinstein, M.2    Phillips, T.J.3
  • 79
    • 0037318089 scopus 로고    scopus 로고
    • NOS3 genotype-dependent correlation between blood pressure and physical activity
    • KIMURA, T., T. YOKOYAMA, and Y. MATSUMURA. NOS3 genotype-dependent correlation between blood pressure and physical activity. Hypertension 41:355-360, 2003.
    • (2003) Hypertension , vol.41 , pp. 355-360
    • Kimura, T.1    Yokoyama, T.2    Matsumura, Y.3
  • 80
    • 34248564190 scopus 로고    scopus 로고
    • Interplay of physical activity and vitamin D receptor gene polymorphism on bone mineral density
    • KITAGAWA, I., Y. KITAGAWA, T. NAGAYA, and S. TOKUDOME. Interplay of physical activity and vitamin D receptor gene polymorphism on bone mineral density. J. Epidemiol. 11:229-232, 2001.
    • (2001) J. Epidemiol. , vol.11 , pp. 229-232
    • Kitagawa, I.1    Kitagawa, Y.2    Nagaya, T.3    Tokudome, S.4
  • 81
    • 0031816199 scopus 로고    scopus 로고
    • Correlation of M235T DNA polymorphism with cardiovascular and endocrine responses during physical exercise in healthy subjects
    • KRIZANOVA, O., J. KOSKA, M. VIGAS, and R. KVETNANSKY. Correlation of M235T DNA polymorphism with cardiovascular and endocrine responses during physical exercise in healthy subjects. Physiol. Res. 47:81-88, 1998.
    • (1998) Physiol. Res. , vol.47 , pp. 81-88
    • Krizanova, O.1    Koska, J.2    Vigas, M.3    Kvetnansky, R.4
  • 82
    • 0035849570 scopus 로고    scopus 로고
    • Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: Clinical features and assignment of the disease gene to chromosome 1p13-21
    • LAHAT, H., M. ELDAR, and E. LEVY-NISSENBAUM. Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21. Circulation 103:2822-2827, 2001.
    • (2001) Circulation , vol.103 , pp. 2822-2827
    • Lahat, H.1    Eldar, M.2    Levy-Nissenbaum, E.3
  • 83
    • 0035205336 scopus 로고    scopus 로고
    • A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel
    • LAHAT, H., E. PRAS, and T. OLENDER. A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel. Am. J. Hum. Genet. 69:1378-1384, 2001.
    • (2001) Am. J. Hum. Genet. , vol.69 , pp. 1378-1384
    • Lahat, H.1    Pras, E.2    Olender, T.3
  • 84
    • 0035969990 scopus 로고    scopus 로고
    • Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
    • LAITINEN, P. J., K. M. BROWN, and K. PUPPO. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation 103:485-490, 2001.
    • (2001) Circulation , vol.103 , pp. 485-490
    • Laitinen, P.J.1    Brown, K.M.2    Puppo, K.3
  • 85
    • 2542544450 scopus 로고    scopus 로고
    • Leptin and leptin receptor gene polymorphisms and changes in glucose homeostasis in response to regular exercise in nondiabetic individuals: The HERITAGE family study
    • LAKKA, T. A. T. RANKINEN, and S. J. WEISNAGEL. Leptin and leptin receptor gene polymorphisms and changes in glucose homeostasis in response to regular exercise in nondiabetic individuals: the HERITAGE family study. Diabetes 53:1603-1608, 2004.
    • (2004) Diabetes , vol.53 , pp. 1603-1608
    • Lakka, T.A.1    Rankinen, T.2    Weisnagel, S.J.3
  • 86
    • 0037644895 scopus 로고    scopus 로고
    • A quantitative trait locus on 7q31 for the changes in plasma insulin in response to exercise training: The HERITAGE Family Study
    • LAKKA, T. A., T. RANKINEN, and S. J. WEISNAGEL. A quantitative trait locus on 7q31 for the changes in plasma insulin in response to exercise training: the HERITAGE Family Study. Diabetes 52:1583-1587, 2003.
    • (2003) Diabetes , vol.52 , pp. 1583-1587
    • Lakka, T.A.1    Rankinen, T.2    Weisnagel, S.J.3
  • 87
    • 0036132671 scopus 로고    scopus 로고
    • A novel nonsense mutation (Q352X) in the mitochondrial cytochrome b gene associated with a combined deficiency of complexes I and III
    • LAMANTEA, E., F. CARRARA, C. MARIOTTI, L. MORANDI, V. TIRANTI, and M. ZEVIANI. A novel nonsense mutation (Q352X) in the mitochondrial cytochrome b gene associated with a combined deficiency of complexes I and III. Neuromuscul. Disord. 12:49-52, 2002.
    • (2002) Neuromuscul. Disord. , vol.12 , pp. 49-52
    • Lamantea, E.1    Carrara, F.2    Mariotti, C.3    Morandi, L.4    Tiranti, V.5    Zeviani, M.6
  • 88
    • 0036092736 scopus 로고    scopus 로고
    • Uncoupling protein 3 gene is associated with body composition changes with training in HERITAGE study
    • LANOUETTE, C. M., Y. C. CHAGNON, and T. RICE. Uncoupling protein 3 gene is associated with body composition changes with training in HERITAGE study. J Appl. Physiol 92:1111-1118, 2002.
    • (2002) J Appl. Physiol , vol.92 , pp. 1111-1118
    • Lanouette, C.M.1    Chagnon, Y.C.2    Rice, T.3
  • 89
    • 0346685841 scopus 로고    scopus 로고
    • Association of apolipoprotein e polymorphism with blood lipids and maximal oxygen uptake in the sedentary state and after exercise training in the HERITAGE family study
    • LEON, A. S., K. TOGASHI, and T. RANKINEN. Association of apolipoprotein E polymorphism with blood lipids and maximal oxygen uptake in the sedentary state and after exercise training in the HERITAGE family study. Metabolism 53:108-116, 2004.
    • (2004) Metabolism , vol.53 , pp. 108-116
    • Leon, A.S.1    Togashi, K.2    Rankinen, T.3
  • 90
    • 0036329369 scopus 로고    scopus 로고
    • Association of the Pro12Ala polymorphism in the PPAR-gamma2 gene with 3-year incidence of type 2 diabetes and body weight change in the Finnish Diabetes Prevention Study
    • LINDI, V. I., M. I. UUSITUPA, and J. LINDSTROM. Association of the Pro12Ala polymorphism in the PPAR-gamma2 gene with 3-year incidence of type 2 diabetes and body weight change in the Finnish Diabetes Prevention Study. Diabetes 51:2581-2586, 2002.
    • (2002) Diabetes , vol.51 , pp. 2581-2586
    • Lindi, V.I.1    Uusitupa, M.I.2    Lindstrom, J.3
  • 91
    • 0035063797 scopus 로고    scopus 로고
    • Calcium sensing receptor gene polymorphism, circulating calcium concentrations and bone mineral density in healthy adolescent girls
    • LORENTZON, M., R. LORENTZON, U. H. LERNER, and P. NORDSTROM. Calcium sensing receptor gene polymorphism, circulating calcium concentrations and bone mineral density in healthy adolescent girls. Eur. J. Endocrinol. 144:257-261, 2001.
    • (2001) Eur. J. Endocrinol. , vol.144 , pp. 257-261
    • Lorentzon, M.1    Lorentzon, R.2    Lerner, U.H.3    Nordstrom, P.4
  • 92
    • 0034859198 scopus 로고    scopus 로고
    • Vitamin D receptor gene polymorphism is related to bone density, circulating osteocalcin, parathyroid hormone in healthy adolescent girls
    • LORENTZON, M., R. LORENTZON, and P. NORDSTROM. Vitamin D receptor gene polymorphism is related to bone density, circulating osteocalcin, parathyroid hormone in healthy adolescent girls. J. Bone Miner. Metab. 19:302-307, 2001.
    • (2001) J. Bone Miner. Metab. , vol.19 , pp. 302-307
    • Lorentzon, M.1    Lorentzon, R.2    Nordstrom, P.3
  • 93
    • 0036592176 scopus 로고    scopus 로고
    • A maximal effort trial in obese women carrying the beta2-adrenoceptor Gln27Glu polymorphism
    • MACHO-AZCARATE, T., J. CALABUIG, A. MARTI, and J. A. MARTINEZ. A maximal effort trial in obese women carrying the beta2-adrenoceptor Gln27Glu polymorphism. J. Physiol. Biochem. 58: 103-108, 2002.
    • (2002) J. Physiol. Biochem. , vol.58 , pp. 103-108
    • Macho-Azcarate, T.1    Calabuig, J.2    Marti, A.3    Martinez, J.A.4
  • 94
    • 0037707717 scopus 로고    scopus 로고
    • Basal fat oxidation and after a peak oxygen consumption test in obese women with a beta2 adrenoceptor gene polymorphism
    • MACHO-AZCARATE, T., A. MARTI, J. CALABUIG, and J. A. MARTINEZ. Basal fat oxidation and after a peak oxygen consumption test in obese women with a beta2 adrenoceptor gene polymorphism. J. Nutr. Biochem. 14:275-279, 2003.
    • (2003) J. Nutr. Biochem. , vol.14 , pp. 275-279
    • Macho-Azcarate, T.1    Marti, A.2    Calabuig, J.3    Martinez, J.A.4
  • 95
    • 0036865752 scopus 로고    scopus 로고
    • Gln27Glu polymorphism in the beta2 adrenergic receptor gene and lipid metabolism during exercise in obese women
    • MACHO-AZCARATE, T., A. MARTI, A. GONZALEZ, J. A. MARTINEZ, and J. IBANEZ. Gln27Glu polymorphism in the beta2 adrenergic receptor gene and lipid metabolism during exercise in obese women. Int. J. Obes. Relat. Metab. Disord. 26:1434-1441, 2002.
    • (2002) Int. J. Obes. Relat. Metab. Disord. , vol.26 , pp. 1434-1441
    • Macho-Azcarate, T.1    Marti, A.2    Gonzalez, A.3    Martinez, J.A.4    Ibanez, J.5
  • 96
    • 0037447767 scopus 로고    scopus 로고
    • Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene
    • MANCUSO, M., M. FILOSTO, and J. C. STEVENS. Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene. J. Neurol. Sci. 209:61-63, 2003.
    • (2003) J. Neurol. Sci. , vol.209 , pp. 61-63
    • Mancuso, M.1    Filosto, M.2    Stevens, J.C.3
  • 97
    • 0034202223 scopus 로고    scopus 로고
    • Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiency
    • MARTIN, M. A., J. C. RUBIO, and P. DEL HOYO. Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiency. Hum. Mutat. 15:579-580, 2000.
    • (2000) Hum. Mutat. , vol.15 , pp. 579-580
    • Martin, M.A.1    Rubio, J.C.2    Del Hoyo, P.3
  • 98
    • 0348000622 scopus 로고    scopus 로고
    • Angiotensinogen M235T polymorphism associates with exercise hemodynamics in postmenopausal women
    • MCCOLE, S. D., M. D. BROWN, and G. E. MOORE. Angiotensinogen M235T polymorphism associates with exercise hemodynamics in postmenopausal women. Physiol. Genomics. 10:63-69, 2002.
    • (2002) Physiol. Genomics , vol.10 , pp. 63-69
    • McCole, S.D.1    Brown, M.D.2    Moore, G.E.3
  • 99
    • 0942265998 scopus 로고    scopus 로고
    • Beta2- and beta3-adrenergic receptor polymorphisms and exercise hemodynamics in postmenopausal women
    • MCCOLE, S. D., A. R. SHULDINER, and M. D. BROWN. Beta2- and beta3-adrenergic receptor polymorphisms and exercise hemodynamics in postmenopausal women. J. Appl. Physiol. 96:526-530, 2004.
    • (2004) J. Appl. Physiol. , vol.96 , pp. 526-530
    • McCole, S.D.1    Shuldiner, A.R.2    Brown, M.D.3
  • 100
    • 0347721039 scopus 로고    scopus 로고
    • A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis
    • MCFARLAND, R., R. W. TAYLOR, P. F. CHINNERY, N. HOWELL, and D. M. TURNBULL. A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis. Neuromuscul. Disord. 14:162-166, 2004.
    • (2004) Neuromuscul. Disord. , vol.14 , pp. 162-166
    • McFarland, R.1    Taylor, R.W.2    Chinnery, P.F.3    Howell, N.4    Turnbull, D.M.5
  • 101
    • 4644289990 scopus 로고    scopus 로고
    • Influence of the interleukin-6-174 G/C gene polymorphism on exercise training-induced changes in glucose tolerance indexes
    • MCKENZIE, J. A., E. P. WEISS, and I. A. GHIU. Influence of the interleukin-6-174 G/C gene polymorphism on exercise training-induced changes in glucose tolerance indexes. J. Appl. Physiol. 97:1338-1342, 2004.
    • (2004) J. Appl. Physiol. , vol.97 , pp. 1338-1342
    • McKenzie, J.A.1    Weiss, E.P.2    Ghiu, I.A.3
  • 102
    • 0033550795 scopus 로고    scopus 로고
    • Beta2-adrenoceptor gene polymorphism, body weight, physical activity
    • MEIRHAEGHE, A., N. HELBECQUE, D. COTTEL, and P. AMOUYEL. Beta2-adrenoceptor gene polymorphism, body weight, physical activity. Lancet 353:896, 1999.
    • (1999) Lancet , vol.353 , pp. 896
    • Meirhaeghe, A.1    Helbecque, N.2    Cottel, D.3    Amouyel, P.4
  • 103
    • 0035215987 scopus 로고    scopus 로고
    • The effect of the Gly 16Arg polymorphism of the beta(2)-adrenergic receptor gene on plasma free fatty acid levels is modulated by physical activity
    • MEIRHAEGHE, A., J. LUAN, and P. SELBERG-FRANKS. The effect of the Gly 16Arg polymorphism of the beta(2)-adrenergic receptor gene on plasma free fatty acid levels is modulated by physical activity. J. Clin. Endocrinol. Metab. 86:5881-5887, 2001.
    • (2001) J. Clin. Endocrinol. Metab. , vol.86 , pp. 5881-5887
    • Meirhaeghe, A.1    Luan, J.2    Selberg-Franks, P.3
  • 105
    • 0032994455 scopus 로고    scopus 로고
    • Angiotensin-converting-enzyme gene insertion/deletion polymorphism and response to physical training
    • MONTGOMERY, H., P. CLARKSON, and M. BARNARD. Angiotensin-converting- enzyme gene insertion/deletion polymorphism and response to physical training. Lancet 353:541-545, 1999.
    • (1999) Lancet , vol.353 , pp. 541-545
    • Montgomery, H.1    Clarkson, P.2    Barnard, M.3
  • 106
    • 0030840926 scopus 로고    scopus 로고
    • Association of angiotensin-converting enzyme gene I/D polymorphism with change in left ventricular mass in response to physical training
    • MONTGOMERY, H. E., P. CLARKSON, and C. M. DOLLERY. Association of angiotensin-converting enzyme gene I/D polymorphism with change in left ventricular mass in response to physical training. Circulation 96:741-747, 1997.
    • (1997) Circulation , vol.96 , pp. 741-747
    • Montgomery, H.E.1    Clarkson, P.2    Dollery, C.M.3
  • 107
    • 0029978105 scopus 로고    scopus 로고
    • The acute rise in plasma fibrinogen concentration with exercise is influenced by the G-453-A polymorphism of the beta-fibrinogen gene
    • MONTGOMERY, H. E., P. CLARKSON, and O. M. NWOSE. The acute rise in plasma fibrinogen concentration with exercise is influenced by the G-453-A polymorphism of the beta-fibrinogen gene. Arterioscler. Thromb. Vasc. Biol. 16:386-391, 1996.
    • (1996) Arterioscler. Thromb. Vasc. Biol. , vol.16 , pp. 386-391
    • Montgomery, H.E.1    Clarkson, P.2    Nwose, O.M.3
  • 108
    • 16744368147 scopus 로고    scopus 로고
    • Human gene for physical performance
    • MONTGOMERY, H. E., R. MARSHALL, and H. HEMINGWAY. Human gene for physical performance. Nature 393:221-222, 1998.
    • (1998) Nature , vol.393 , pp. 221-222
    • Montgomery, H.E.1    Marshall, R.2    Hemingway, H.3
  • 111
    • 2442701495 scopus 로고    scopus 로고
    • Variations in high-density lipoprotein cholesterol in relation to physical activity and Taq 1B polymorphism of the cholesteryl ester transfer protein gene
    • MUKHERJEE, M., and K. R. SHETTY. Variations in high-density lipoprotein cholesterol in relation to physical activity and Taq 1B polymorphism of the cholesteryl ester transfer protein gene. Clin. Genet. 65:412-418, 2004.
    • (2004) Clin. Genet. , vol.65 , pp. 412-418
    • Mukherjee, M.1    Shetty, K.R.2
  • 112
    • 0343674544 scopus 로고    scopus 로고
    • Lipomatosis, proximal myopathy, the mitochondrial 8344 mutation. A lipid storage myopathy?
    • MUNOZ-MALAGA, A., J. BAUTISTA, and J. A. SALAZAR. Lipomatosis, proximal myopathy, the mitochondrial 8344 mutation. A lipid storage myopathy? Muscle Nerve 23:538-542, 2000.
    • (2000) Muscle Nerve , vol.23 , pp. 538-542
    • Munoz-Malaga, A.1    Bautista, J.2    Salazar, J.A.3
  • 113
    • 0033910874 scopus 로고    scopus 로고
    • Intragenic inversion of mtDNA: A new type of pathogenic mutation in a patient with mitochondrial myopathy
    • MUSUMECI, O., A. L. ANDREU, and S. SHANSKE. Intragenic Inversion of mtDNA: A New Type of Pathogenic Mutation in a Patient with Mitochondrial Myopathy. Am. J. Hum. Genet. 66:1900-1904, 2000.
    • (2000) Am. J. Hum. Genet. , vol.66 , pp. 1900-1904
    • Musumeci, O.1    Andreu, A.L.2    Shanske, S.3
  • 115
    • 0035895320 scopus 로고    scopus 로고
    • Left ventricular hypertrophy with exercise and ACE gene insertion/deletion polymorphism: A randomized controlled trial with losartan
    • MYERSON, S. G., H. E. MONTGOMERY, and M. WHITTINGHAM. Left ventricular hypertrophy with exercise and ACE gene insertion/deletion polymorphism: a randomized controlled trial with losartan. Circulation 103:226-230, 2001.
    • (2001) Circulation , vol.103 , pp. 226-230
    • Myerson, S.G.1    Montgomery, H.E.2    Whittingham, M.3
  • 116
    • 0036892583 scopus 로고    scopus 로고
    • Potential role of vitamin D receptor gene polymorphism in determining bone phenotype in young male athletes
    • NAKAMURA, O., T. ISHII, and Y. ANDO. Potential role of vitamin D receptor gene polymorphism in determining bone phenotype in young male athletes. J. Appl. Physiol. 93:1973-1979, 2002.
    • (2002) J. Appl. Physiol. , vol.93 , pp. 1973-1979
    • Nakamura, O.1    Ishii, T.2    Ando, Y.3
  • 117
    • 0034750612 scopus 로고    scopus 로고
    • The angiotensin converting enzyme I/D polymorphism in Russian athletes
    • NAZAROV, I. B., D. R. WOODS, and H. E. MONTGOMERY. The angiotensin converting enzyme I/D polymorphism in Russian athletes. Eur. J. Hum. Genet. 9:797-801, 2001.
    • (2001) Eur. J. Hum. Genet. , vol.9 , pp. 797-801
    • Nazarov, I.B.1    Woods, D.R.2    Montgomery, H.E.3
  • 118
    • 5344258984 scopus 로고    scopus 로고
    • C-reactive protein genotypes affect baseline, but not exercise training-induced changes, in C-reactive protein levels
    • OBISESAN, T. O., C. LEEUWENBURGH, and T. PHILLIPS. C-reactive protein genotypes affect baseline, but not exercise training-induced changes, in C-reactive protein levels. Arterioscler. Thromb. Vasc. Biol. 24:1874-1879, 2004.
    • (2004) Arterioscler. Thromb. Vasc. Biol. , vol.24 , pp. 1874-1879
    • Obisesan, T.O.1    Leeuwenburgh, C.2    Phillips, T.3
  • 119
    • 0037783945 scopus 로고    scopus 로고
    • The vitamin D receptor gene variant and physical activity predicts fasting glucose levels in healthy young men
    • ORTLEPP, J. R., J. METRIKAT, M. ALBRECHT, A. VON KORFF, P. HANRATH, and R. HOFFMANN. The vitamin D receptor gene variant and physical activity predicts fasting glucose levels in healthy young men. Diabet. Med. 20:451-454, 2003.
    • (2003) Diabet. Med. , vol.20 , pp. 451-454
    • Ortlepp, J.R.1    Metrikat, J.2    Albrecht, M.3    Von Korff, A.4    Hanrath, P.5    Hoffmann, R.6
  • 120
    • 12444261670 scopus 로고    scopus 로고
    • The interleukin-6 promoter polymorphism is associated with elevated leukocyte, lymphocyte, monocyte counts and reduced physical fitness in young healthy smokers
    • ORTLEPP, J. R., J. METRIKAT, and K. VESPER. The interleukin-6 promoter polymorphism is associated with elevated leukocyte, lymphocyte, monocyte counts and reduced physical fitness in young healthy smokers. J. Mol Med. 81:578-584, 2003.
    • (2003) J. Mol Med. , vol.81 , pp. 578-584
    • Ortlepp, J.R.1    Metrikat, J.2    Vesper, K.3
  • 121
    • 0030771199 scopus 로고    scopus 로고
    • Natural behavior polymorphism due to a cGMP-dependent protein kinase of Drosophila
    • OSBORNE, K. A., A. ROBICHON, and E. BURGESS. Natural behavior polymorphism due to a cGMP-dependent protein kinase of Drosophila. Science 277:834-836, 1997.
    • (1997) Science , vol.277 , pp. 834-836
    • Osborne, K.A.1    Robichon, A.2    Burgess, E.3
  • 122
    • 0034003721 scopus 로고    scopus 로고
    • A genetic variation in the 5′ flanking region of the UCP3 gene is associated with body mass index in humans in interaction with physical activity
    • OTABE, S., K. CLEMENT, and C. DINA. A genetic variation in the 5′ flanking region of the UCP3 gene is associated with body mass index in humans in interaction with physical activity. Diabetologia 43:245-249, 2000.
    • (2000) Diabetologia , vol.43 , pp. 245-249
    • Otabe, S.1    Clement, K.2    Dina, C.3
  • 124
    • 0242635882 scopus 로고    scopus 로고
    • Angiotensin-converting enzyme genotype and the ventilatory response to exertional hypoxia
    • PATEL, S., D. R. WOODS, and N. J. MACLEOD. Angiotensin-converting enzyme genotype and the ventilatory response to exertional hypoxia. Eur. Respir. J. 22:755-760, 2003.
    • (2003) Eur. Respir. J. , vol.22 , pp. 755-760
    • Patel, S.1    Woods, D.R.2    MacLeod, N.J.3
  • 125
    • 20544471519 scopus 로고    scopus 로고
    • The human obesity gene map: The 2004 update
    • In press
    • PERUSSE, L., T. RANKINEN, and A. ZUBERI. The human obesity gene map: the 2004 update. Obes. Res. (In press), 2005.
    • (2005) Obes. Res.
    • Perusse, L.1    Rankinen, T.2    Zuberi, A.3
  • 126
    • 0037532401 scopus 로고    scopus 로고
    • Phenylethanolamine N-methyltransferase G-148A genetic variant and weight loss in obese women
    • PETERS, W. R., J. P. MACMURRY, J. WALKER, R. J. GIESE, JR., and D. E. COMINGS. Phenylethanolamine N-methyltransferase G-148A genetic variant and weight loss in obese women. Obes. Res. 11:415-419, 2003.
    • (2003) Obes. Res. , vol.11 , pp. 415-419
    • Peters, W.R.1    MacMurry, J.P.2    Walker, J.3    Giese Jr., R.J.4    Comings, D.E.5
  • 127
    • 4644292723 scopus 로고    scopus 로고
    • Association between body fat response to exercise training and multilocus ADR genotypes
    • PHARES, D. A., A. A. HALVERSTADT, and A. R. SHULDINER. Association between body fat response to exercise training and multilocus ADR genotypes. Obes. Res. 12:807-815, 2004.
    • (2004) Obes. Res. , vol.12 , pp. 807-815
    • Phares, D.A.1    Halverstadt, A.A.2    Shuldiner, A.R.3
  • 128
    • 1542494194 scopus 로고    scopus 로고
    • Physical activity modulates effects of some genetic polymorphisms affecting cardiovascular risk in men aged over 40 years
    • PISCIOTTA, L., A. CANTAFORA, and A. PIANA. Physical activity modulates effects of some genetic polymorphisms affecting cardiovascular risk in men aged over 40 years. Nutr. Metab. Cardiovasc. Dis. 13:202-210, 2003.
    • (2003) Nutr. Metab. Cardiovasc. Dis. , vol.13 , pp. 202-210
    • Pisciotta, L.1    Cantafora, A.2    Piana, A.3
  • 129
    • 0037131020 scopus 로고    scopus 로고
    • Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia
    • POSTMA, A. V., I. DENJOY, and T. M. HOORNTJE. Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia. Circ. Res. 91:e21-26, 2002.
    • (2002) Circ. Res. , vol.91
    • Postma, A.V.1    Denjoy, I.2    Hoorntje, T.M.3
  • 130
    • 0345871948 scopus 로고    scopus 로고
    • Sequence variation in hypoxia-inducible factor 1alpha (HIF1A): Association with maximal oxygen consumption
    • PRIOR, S. J., J. M. HAGBERG, and D. A. PHARES. Sequence variation in hypoxia-inducible factor 1alpha (HIF1A): association with maximal oxygen consumption. Physiol. Genomics 15:20-26, 2003.
    • (2003) Physiol. Genomics , vol.15 , pp. 20-26
    • Prior, S.J.1    Hagberg, J.M.2    Phares, D.A.3
  • 131
    • 0035895322 scopus 로고    scopus 로고
    • Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
    • PRIORI, S. G., C. NAPOLITANO, and N. TISO. Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia. Circulation 103:196-200, 2001.
    • (2001) Circulation , vol.103 , pp. 196-200
    • Priori, S.G.1    Napolitano, C.2    Tiso, N.3
  • 132
    • 0034711156 scopus 로고    scopus 로고
    • A novel mutation in the mitochondrial tRNA(TYr) gene associated with exercise intolerance
    • PULKES, T., A. SIDDIQUI, J. A. MORGAN-HUGHES, and M. G. HANNA. A novel mutation in the mitochondrial tRNA(TYr) gene associated with exercise intolerance. Neurology 55:1210-1212, 2000.
    • (2000) Neurology , vol.55 , pp. 1210-1212
    • Pulkes, T.1    Siddiqui, A.2    Morgan-Hughes, J.A.3    Hanna, M.G.4
  • 133
    • 0037077435 scopus 로고    scopus 로고
    • Genome-wide linkage scan for exercise stroke volume and cardiac output in the HERITAGE Family Study
    • RANKINEN, T., P. AN, and L. PERUSSE. Genome-wide linkage scan for exercise stroke volume and cardiac output in the HERITAGE Family Study. Physiol. Genomics 10:57-62, 2002.
    • (2002) Physiol. Genomics , vol.10 , pp. 57-62
    • Rankinen, T.1    An, P.2    Perusse, L.3
  • 134
    • 0035569033 scopus 로고    scopus 로고
    • Genomic scan for exercise blood pressure in the Health, Risk Factors, Exercise Training and Genetics (HERITAGE) Family Study
    • RANKINEN, T., P. AN, and T. RICE. Genomic scan for exercise blood pressure in the Health, Risk Factors, Exercise Training and Genetics (HERITAGE) Family Study. Hypertension 38:30-37, 2001.
    • (2001) Hypertension , vol.38 , pp. 30-37
    • Rankinen, T.1    An, P.2    Rice, T.3
  • 135
    • 0033866536 scopus 로고    scopus 로고
    • AGT M235T and ACE ID polymorphisms and exercise blood pressure in the HERITAGE Family Study
    • RANKINEN, T., J. GAGNON, and L. PERUSSE. AGT M235T and ACE ID polymorphisms and exercise blood pressure in the HERITAGE Family Study. Am. J. Physiol. Heart Circ. Physiol. 279: H368-374, 2000.
    • (2000) Am. J. Physiol. Heart Circ. Physiol. , vol.279
    • Rankinen, T.1    Gagnon, J.2    Perusse, L.3
  • 136
    • 0343820068 scopus 로고    scopus 로고
    • The Na(+)-K(+)-ATPase alpha2 gene and trainability of cardiorespiratory endurance: The HERITAGE family study
    • RANKINEN, T. L. PERUSSE, and I. BORECKI. The Na(+)-K(+)-ATPase alpha2 gene and trainability of cardiorespiratory endurance: the HERITAGE family study. J. Appl. Physiol. 88:346-351, 2000.
    • (2000) J. Appl. Physiol. , vol.88 , pp. 346-351
    • Rankinen, T.1    Perusse, L.2    Borecki, I.3
  • 137
    • 0342514705 scopus 로고    scopus 로고
    • Angiotensin-converting enzyme ID polymorphism and fitness phenotype in the HERITAGE Family Study
    • RANKINEN, T., L. PERUSSE, and J. GAGNON. Angiotensin-converting enzyme ID polymorphism and fitness phenotype in the HERITAGE Family Study. J. Appl. Physiol. 88:1029-1035, 2000.
    • (2000) J. Appl. Physiol. , vol.88 , pp. 1029-1035
    • Rankinen, T.1    Perusse, L.2    Gagnon, J.3
  • 140
    • 0347133174 scopus 로고    scopus 로고
    • Titin is a candidate gene for stroke volume response to endurance training: The HERITAGE Family Study
    • RANKINEN, T., T. RICE, and A. BOUDREAU. Titin is a candidate gene for stroke volume response to endurance training: the HERITAGE Family Study. Physiol. Genomics 15:27-33, 2003.
    • (2003) Physiol. Genomics , vol.15 , pp. 27-33
    • Rankinen, T.1    Rice, T.2    Boudreau, A.3
  • 141
    • 0037187042 scopus 로고    scopus 로고
    • G protein beta 3 polymorphism and hemodynamic and body composition phenotypes in the HERITAGE Family Study
    • RANKINEN, T., T. RICE, and A. S. LEON. G protein beta 3 polymorphism and hemodynamic and body composition phenotypes in the HERITAGE Family Study. Physiol. Genomics 8:151-157, 2002.
    • (2002) Physiol. Genomics , vol.8 , pp. 151-157
    • Rankinen, T.1    Rice, T.2    Leon, A.S.3
  • 142
    • 0033679202 scopus 로고    scopus 로고
    • NOS3 Glu298Asp genotype and blood pressure response to endurance training: The HERITAGE family study
    • RANKINEN, T., T. RICE, and L. PERUSSE. NOS3 Glu298Asp genotype and blood pressure response to endurance training: the HERITAGE family study. Hypertension 36:885-889, 2000.
    • (2000) Hypertension , vol.36 , pp. 885-889
    • Rankinen, T.1    Rice, T.2    Perusse, L.3
  • 143
    • 0348000623 scopus 로고    scopus 로고
    • Physical exercise and blood pressure with reference to the angiotensinogen M235T polymorphism
    • RAURAMAA, R., R. KUHANEN, and T. A. LAKKA. Physical exercise and blood pressure with reference to the angiotensinogen M235T polymorphism. Physiol. Genomics 10:71-77, 2002.
    • (2002) Physiol. Genomics , vol.10 , pp. 71-77
    • Rauramaa, R.1    Kuhanen, R.2    Lakka, T.A.3
  • 144
    • 1842365521 scopus 로고    scopus 로고
    • Physical activity, fibrinogen plasma level and gene polymorphisms in postmenopausal women
    • RAURAMAA, R., S. VAISANEN, and A. NISSINEN. Physical activity, fibrinogen plasma level and gene polymorphisms in postmenopausal women. Thromb. Haemost. 78:840-844, 1997.
    • (1997) Thromb. Haemost. , vol.78 , pp. 840-844
    • Rauramaa, R.1    Vaisanen, S.2    Nissinen, A.3
  • 145
    • 0343628026 scopus 로고    scopus 로고
    • The RsaI polymorphism in the alpha-fibrinogen gene and response of plasma fibrinogen to physical training-a controlled randomised clinical trial in men
    • RAURAMAA, R., S. B. VAISANEN, R. KUHANEN, I. PENTTILA, and C. BOUCHARD. The RsaI polymorphism in the alpha-fibrinogen gene and response of plasma fibrinogen to physical training-a controlled randomised clinical trial in men. Thromb. Haemost. 83: 803-806, 2000.
    • (2000) Thromb. Haemost. , vol.83 , pp. 803-806
    • Rauramaa, R.1    Vaisanen, S.B.2    Kuhanen, R.3    Penttila, I.4    Bouchard, C.5
  • 146
    • 0037383154 scopus 로고    scopus 로고
    • Aerobic exercise and bone mineral density in middle-aged finnish men: A controlled randomized trial with reference to androgen receptor, aromatase, estrogen receptor alpha gene polymorphisms
    • REMES, T., S. B. VAISANEN, and A. MAHONEN. Aerobic exercise and bone mineral density in middle-aged finnish men: a controlled randomized trial with reference to androgen receptor, aromatase, estrogen receptor alpha gene polymorphisms. Bone 32:412-420, 2003.
    • (2003) Bone , vol.32 , pp. 412-420
    • Remes, T.1    Vaisanen, S.B.2    Mahonen, A.3
  • 147
    • 0036310224 scopus 로고    scopus 로고
    • A genomewide linkage scan for abdominal subcutaneous and visceral fat in black and white families: The HERITAGE Family Study
    • RICE, T., Y. C. CHAGNON, and L. PERUSSE. A genomewide linkage scan for abdominal subcutaneous and visceral fat in black and white families: The HERITAGE Family Study. Diabetes 51: 848-855, 2002.
    • (2002) Diabetes , vol.51 , pp. 848-855
    • Rice, T.1    Chagnon, Y.C.2    Perusse, L.3
  • 148
    • 0036278171 scopus 로고    scopus 로고
    • Genomewide linkage scan of resting blood pressure: HERITAGE Family Study. Health, Risk Factors, Exercise Training, Genetics
    • RICE, T., T. RANKINEN, and Y. C. CHAGNON. Genomewide linkage scan of resting blood pressure: HERITAGE Family Study. Health, Risk Factors, Exercise Training, Genetics. Hypertension 39:1037-1043, 2002.
    • (2002) Hypertension , vol.39 , pp. 1037-1043
    • Rice, T.1    Rankinen, T.2    Chagnon, Y.C.3
  • 149
    • 0242270694 scopus 로고    scopus 로고
    • Associations between cardiorespiratory responses to exercise and the C34T AMPD1 gene polymorphism in the HERITAGE Family Study
    • RICO-SANZ, J., T. RANKINEN, and D. R. JOANISSE. Associations between cardiorespiratory responses to exercise and the C34T AMPD1 gene polymorphism in the HERITAGE Family Study. Physiol. Genomics 14:161-166, 2003.
    • (2003) Physiol. Genomics , vol.14 , pp. 161-166
    • Rico-Sanz, J.1    Rankinen, T.2    Joanisse, D.R.3
  • 150
    • 1442307658 scopus 로고    scopus 로고
    • Quantitative trait loci for maximal exercise capacity phenotypes and their responses to training in the HERITAGE Family Study
    • RICO-SANZ, J., T. RANKINEN, and T. RICE. Quantitative trait loci for maximal exercise capacity phenotypes and their responses to training in the HERITAGE Family Study. Physiol. Genomics 16:256-260, 2004.
    • (2004) Physiol. Genomics , vol.16 , pp. 256-260
    • Rico-Sanz, J.1    Rankinen, T.2    Rice, T.3
  • 151
    • 9244242571 scopus 로고    scopus 로고
    • Association of interleukin-15 protein and interleukin-15 receptor genetic variation with resistance exercise training responses
    • RIECHMAN, S. E., G. BALASEKARAN, S. M. ROTH, and R. E. FERRELL. Association of interleukin-15 protein and interleukin-15 receptor genetic variation with resistance exercise training responses. J. Appl. Physiol. 97:2214-2219, 2004.
    • (2004) J. Appl. Physiol. , vol.97 , pp. 2214-2219
    • Riechman, S.E.1    Balasekaran, G.2    Roth, S.M.3    Ferrell, R.E.4
  • 152
    • 3142677288 scopus 로고    scopus 로고
    • Steroid sulfatase gene variation and DHEA responsiveness to resistance exercise in MERET
    • RIECHMAN, S. E., T. J. FABIAN, P. D. KROBOTH, and R. E. FERRELL. Steroid sulfatase gene variation and DHEA responsiveness to resistance exercise in MERET. Physiol. Genomics 17:300-306, 2004.
    • (2004) Physiol. Genomics , vol.17 , pp. 300-306
    • Riechman, S.E.1    Fabian, T.J.2    Kroboth, P.D.3    Ferrell, R.E.4
  • 154
    • 0035100459 scopus 로고    scopus 로고
    • Angiogenin gene-race interaction for resting and exercise BP phenotypes: The HERITAGE Family Study
    • RIVERA, M. A., M. ECHEGARAY, and T. RANKINEN. Angiogenin gene-race interaction for resting and exercise BP phenotypes: the HERITAGE Family Study. J. Appl. Physiol. 90:1232-1238, 2001.
    • (2001) J. Appl. Physiol. , vol.90 , pp. 1232-1238
    • Rivera, M.A.1    Echegaray, M.2    Rankinen, T.3
  • 155
    • 0034807817 scopus 로고    scopus 로고
    • TGF-beta(1) gene-race interactions for resting and exercise blood pressure in the HERITAGE Family Study
    • RIVERA, M. A., M. ECHEGARAY, and T. RANKINEN. TGF-beta(1) gene-race interactions for resting and exercise blood pressure in the HERITAGE Family Study. J. Appl. Physiol. 91:1808-1813, 2001.
    • (2001) J. Appl. Physiol. , vol.91 , pp. 1808-1813
    • Rivera, M.A.1    Echegaray, M.2    Rankinen, T.3
  • 157
    • 0030933048 scopus 로고    scopus 로고
    • Could the A2A11 human leucocyte antigen locus correlate with maximal aerobic power?
    • RODAS, G., G. ERCILLA, and C. JAVIERRE. Could the A2A11 human leucocyte antigen locus correlate with maximal aerobic power? Clin. Sci. (Colch). 92:331-333, 1997.
    • (1997) Clin. Sci. (Colch). , vol.92 , pp. 331-333
    • Rodas, G.1    Ercilla, G.2    Javierre, C.3
  • 158
    • 0141679321 scopus 로고    scopus 로고
    • C174T polymorphism in the CNTF receptor gene is associated with fat-free mass in men and women
    • ROTH, S. M., E. J. METTER, M. R. LEE, B. F. HURLEY, and R. E. FERRELL. C174T polymorphism in the CNTF receptor gene is associated with fat-free mass in men and women. J. Appl. Physiol. 95:1425-1430, 2003.
    • (2003) J. Appl. Physiol. , vol.95 , pp. 1425-1430
    • Roth, S.M.1    Metter, E.J.2    Lee, M.R.3    Hurley, B.F.4    Ferrell, R.E.5
  • 159
    • 0035100458 scopus 로고    scopus 로고
    • CNTF genotype is associated with muscular strength and quality in humans across the adult age span
    • ROTH, S. M., M. A. SCHRAGER, and R. E. FERRELL. CNTF genotype is associated with muscular strength and quality in humans across the adult age span. J. Appl. Physiol. 90:1205-1210, 2001.
    • (2001) J. Appl. Physiol. , vol.90 , pp. 1205-1210
    • Roth, S.M.1    Schrager, M.A.2    Ferrell, R.E.3
  • 161
    • 0030731084 scopus 로고    scopus 로고
    • Effects of Trp64Arg mutation in the beta 3-adrenergic receptor gene on weight loss, body fat distribution, glycemic control, insulin resistance in obese type 2 diabetic patients
    • SAKANE, N., T. YOSHIDA, T. UMEKAWA, A. KOGURE, Y. TAKAKURA, and M. KONDO. Effects of Trp64Arg mutation in the beta 3-adrenergic receptor gene on weight loss, body fat distribution, glycemic control, insulin resistance in obese type 2 diabetic patients. Diabetes Care 20:1887-1890, 1997.
    • (1997) Diabetes Care , vol.20 , pp. 1887-1890
    • Sakane, N.1    Yoshida, T.2    Umekawa, T.3    Kogure, A.4    Takakura, Y.5    Kondo, M.6
  • 162
    • 0037713404 scopus 로고    scopus 로고
    • Relation of aromatase gene polymorphism and hormone replacement therapy to serum estradiol levels, bone mineral density, fracture risk in early postmenopausal women
    • SALMEN, T., A. M. HEIKKINEN, and A. MAHONEN. Relation of aromatase gene polymorphism and hormone replacement therapy to serum estradiol levels, bone mineral density, fracture risk in early postmenopausal women. Ann. Med. 35:282-288, 2003.
    • (2003) Ann. Med. , vol.35 , pp. 282-288
    • Salmen, T.1    Heikkinen, A.M.2    Mahonen, A.3
  • 163
    • 0036862978 scopus 로고    scopus 로고
    • Polymorphism of the IGF2 gene, birth weight and grip strength in adult men
    • SAYER, A. A., H. SYDDALL, and S. D. O'DELL. Polymorphism of the IGF2 gene, birth weight and grip strength in adult men. Age Ageing 31:468-470, 2002.
    • (2002) Age Ageing , vol.31 , pp. 468-470
    • Sayer, A.A.1    Syddall, H.2    O'Dell, S.D.3
  • 164
    • 0036801153 scopus 로고    scopus 로고
    • Increased frequency of the homozygous II ACE genotype in Italian Olympic endurance athletes
    • SCANAVINI, D., F. BERNARDI, E. CASTOLDI, F. CONCONI, and G. MAZZONI. Increased frequency of the homozygous II ACE genotype in Italian Olympic endurance athletes. Eur. J. Hum. Genet. 10:576-577, 2002.
    • (2002) Eur. J. Hum. Genet. , vol.10 , pp. 576-577
    • Scanavini, D.1    Bernardi, F.2    Castoldi, E.3    Conconi, F.4    Mazzoni, G.5
  • 165
    • 0032965656 scopus 로고    scopus 로고
    • Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: Clinical and biochemical differences with the fatal cardiac phenotype
    • SCHOLTE, H. R., R. N. VAN COSTER, and P. C. DE JONGE. Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype. Neuromuscul. Disord. 9:313-319, 1999.
    • (1999) Neuromuscul. Disord. , vol.9 , pp. 313-319
    • Scholte, H.R.1    Van Coster, R.N.2    De Jonge, P.C.3
  • 166
    • 9244251561 scopus 로고    scopus 로고
    • Insulin-like growth factor-2 (IGF2) genotype, fat-free mass, muscle performance across the adult life span
    • SCHRAGER, M. A., S. M. ROTH, and R. E. FERRELL. Insulin-like growth factor-2 (IGF2) genotype, fat-free mass, muscle performance across the adult life span. J. Appl. Physiol. 97:2176-2183, 2004.
    • (2004) J. Appl. Physiol. , vol.97 , pp. 2176-2183
    • Schrager, M.A.1    Roth, S.M.2    Ferrell, R.E.3
  • 167
    • 0036194222 scopus 로고    scopus 로고
    • Septo-optic dysplasia associated with a new mitochondrial cytochrome b mutation
    • SCHUELKE, M., H. KRUDE, and B. FINCKH. Septo-optic dysplasia associated with a new mitochondrial cytochrome b mutation. Ann. Neurol. 51:388-392, 2002.
    • (2002) Ann. Neurol. , vol.51 , pp. 388-392
    • Schuelke, M.1    Krude, H.2    Finckh, B.3
  • 168
    • 0035830365 scopus 로고    scopus 로고
    • Genotype-phenotype correlation in the long-QT syndrome: Gene-specific triggers for life-threatening arrhythmias
    • SCHWARTZ, P. J., S. G. PRIORI, and C. SPAZZOLINI. Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. Circulation 103:89-95, 2001.
    • (2001) Circulation , vol.103 , pp. 89-95
    • Schwartz, P.J.1    Priori, S.G.2    Spazzolini, C.3
  • 169
    • 0034867295 scopus 로고    scopus 로고
    • Polymorphic variation in the human myostatin (GDF-8) gene and association with strength measures in the Women's Health and Aging Study II cohort
    • SEIBERT, M. J., Q. L. XUE, L. P. FRIED, and J. D. WALSTON. Polymorphic variation in the human myostatin (GDF-8) gene and association with strength measures in the Women's Health and Aging Study II cohort. J. Am. Geriatr. Soc. 49:1093-1096, 2001.
    • (2001) J. Am. Geriatr. Soc. , vol.49 , pp. 1093-1096
    • Seibert, M.J.1    Xue, Q.L.2    Fried, L.P.3    Walston, J.D.4
  • 171
    • 0037339152 scopus 로고    scopus 로고
    • Clara cell protein 16 (CC16) gene polymorphism influences the degree of airway responsiveness in asthmatic children
    • SENGLER, C., A. HEINZMANN, and S. P. JERKIC. Clara cell protein 16 (CC16) gene polymorphism influences the degree of airway responsiveness in asthmatic children. J. Allergy Clin. Immunol. 111:515-519, 2003.
    • (2003) J. Allergy Clin. Immunol. , vol.111 , pp. 515-519
    • Sengler, C.1    Heinzmann, A.2    Jerkic, S.P.3
  • 172
    • 0034023655 scopus 로고    scopus 로고
    • Effect of physical activity on lipid levels in a population-based sample of men with and without the Arg192 variant of the human paraoxonase gene
    • SENTI, M., C. AUBO, R. ELOSUA, J. SALA, M. TOMAS, and J. MARRUGAT. Effect of physical activity on lipid levels in a population-based sample of men with and without the Arg192 variant of the human paraoxonase gene. Genet. Epidemiol. 18:276-286, 2000.
    • (2000) Genet. Epidemiol. , vol.18 , pp. 276-286
    • Senti, M.1    Aubo, C.2    Elosua, R.3    Sala, J.4    Tomas, M.5    Marrugat, J.6
  • 173
    • 0028100734 scopus 로고
    • Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII-and their population frequency
    • SHERMAN, J. B., N. RABEN, and C. NICASTRI. Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII-and their population frequency. Am. J. Hum. Genet. 55:305-313, 1994.
    • (1994) Am. J. Hum. Genet. , vol.55 , pp. 305-313
    • Sherman, J.B.1    Raben, N.2    Nicastri, C.3
  • 174
    • 0041317780 scopus 로고    scopus 로고
    • Difficulty in losing weight by behavioral intervention for women with Trp64Arg polymorphism of the beta3-adrenergic receptor gene
    • SHIWAKU, K., A. NOGI, and E. ANUURAD. Difficulty in losing weight by behavioral intervention for women with Trp64Arg polymorphism of the beta3-adrenergic receptor gene. Int. J. Obes. Relat. Metab. Disord. 27:1028-1036, 2003.
    • (2003) Int. J. Obes. Relat. Metab. Disord. , vol.27 , pp. 1028-1036
    • Shiwaku, K.1    Nogi, A.2    Anuurad, E.3
  • 175
    • 0038018264 scopus 로고    scopus 로고
    • A dopamine D2 receptor gene polymorphism and physical activity in two family studies
    • SIMONEN, R. L., T. RANKINEN, and L. PERUSSE. A dopamine D2 receptor gene polymorphism and physical activity in two family studies. Physiol Behav. 78:751-757, 2003.
    • (2003) Physiol Behav. , vol.78 , pp. 751-757
    • Simonen, R.L.1    Rankinen, T.2    Perusse, L.3
  • 176
    • 0041706248 scopus 로고    scopus 로고
    • Genome-wide linkage scan for physical activity levels in the Quebec Family study
    • SIMONEN, R. L., T. RANKINEN, and L. PERUSSE. Genome-wide linkage scan for physical activity levels in the Quebec Family study. Med. Sci. Sports Exerc. 35:1355-1359, 2003.
    • (2003) Med. Sci. Sports Exerc. , vol.35 , pp. 1355-1359
    • Simonen, R.L.1    Rankinen, T.2    Perusse, L.3
  • 177
    • 10844295737 scopus 로고    scopus 로고
    • Associations between BMI, energy intake, energy expenditure, VDR genotype and colon and rectal cancers (United States)
    • SLATTERY, M. L., M. MURTAUGH, B. CAAN, K. N. MA, R. WOLFF, and W. SAMOWITZ. Associations between BMI, energy intake, energy expenditure, VDR genotype and colon and rectal cancers (United States). Cancer Causes Control 15: 863-872, 2004.
    • (2004) Cancer Causes Control , vol.15 , pp. 863-872
    • Slattery, M.L.1    Murtaugh, M.2    Caan, B.3    Ma, K.N.4    Wolff, R.5    Samowitz, W.6
  • 178
    • 0036954311 scopus 로고    scopus 로고
    • The Gln223Arg polymorphism of the leptin receptor in Pima Indians: Influence on energy expenditure, physical activity and lipid metabolism
    • STEFAN, N., B. VOZAROVA, and A. DEL PARIGI. The Gln223Arg polymorphism of the leptin receptor in Pima Indians: influence on energy expenditure, physical activity and lipid metabolism. Int. J. Obes. Relat. Metab. Disord. 26:1629-1632, 2002.
    • (2002) Int. J. Obes. Relat. Metab. Disord. , vol.26 , pp. 1629-1632
    • Stefan, N.1    Vozarova, B.2    Del Parigi, A.3
  • 179
    • 0032833046 scopus 로고    scopus 로고
    • Association and linkage between an insulin-like growth factor-1 gene polymorphism and fat free mass in the HERITAGE Family Study
    • SUN, G., J. GAGNON, and Y. C. CHAGNON. Association and linkage between an insulin-like growth factor-1 gene polymorphism and fat free mass in the HERITAGE Family Study. Int. J. Obes. Relat. Metab. Disord. 23:929-935, 1999.
    • (1999) Int. J. Obes. Relat. Metab. Disord. , vol.23 , pp. 929-935
    • Sun, G.1    Gagnon, J.2    Chagnon, Y.C.3
  • 180
    • 0033025040 scopus 로고    scopus 로고
    • Novel mutations associated with carnitine palmitoyltransferase II deficiency
    • TAGGART, R. T., D. SMAIL, C. APOLITO, and G. D. VLADUTIU. Novel mutations associated with carnitine palmitoyltransferase II deficiency. Hum. Mutat. 13:210-220, 1999.
    • (1999) Hum. Mutat. , vol.13 , pp. 210-220
    • Taggart, R.T.1    Smail, D.2    Apolito, C.3    Vladutiu, G.D.4
  • 181
    • 0029950572 scopus 로고    scopus 로고
    • The effect of physical activity on serum total and low-density lipoprotein cholesterol concentrations varies with apolipoprotein e phenotype in male children and young adults: The Cardiovascular Risk in Young Finns Study
    • TAIMELA, S., T. LEHTIMAKI, K. V. PORKKA, L. RASANEN, and J. S. VIIKARI. The effect of physical activity on serum total and low-density lipoprotein cholesterol concentrations varies with apolipoprotein E phenotype in male children and young adults: The Cardiovascular Risk in Young Finns Study. Metabolism 45:797-803, 1996.
    • (1996) Metabolism , vol.45 , pp. 797-803
    • Taimela, S.1    Lehtimaki, T.2    Porkka, K.V.3    Rasanen, L.4    Viikari, J.S.5
  • 182
    • 0034006153 scopus 로고    scopus 로고
    • Interaction of the effects between vitamin D receptor polymorphism and exercise training on bone metabolism
    • TAJIMA, O., N, ASHIZAWA, and T. ISHII. Interaction of the effects between vitamin D receptor polymorphism and exercise training on bone metabolism. J. Appl. Physiol. 88:1271-1276, 2000.
    • (2000) J. Appl. Physiol. , vol.88 , pp. 1271-1276
    • Tajima, O.1    Ashizawa, N.2    Ishii, T.3
  • 183
    • 0027302901 scopus 로고
    • Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients
    • TARONI, F., E. VERDERIO, F. DWORZAK, P. J. WILLEMS, P. CAVADINI, and S. DIDONATO. Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients. Nat. Genet. 4:314-320, 1993.
    • (1993) Nat. Genet. , vol.4 , pp. 314-320
    • Taroni, F.1    Verderio, E.2    Dworzak, F.3    Willems, P.J.4    Cavadini, P.5    Didonato, S.6
  • 184
    • 4344717383 scopus 로고    scopus 로고
    • Exploration of myostatin polymorphisms and the angiotensin-converting enzyme insertion/deletion genotype in responses of human muscle to strength training
    • THOMIS, M. A., W. HUYGENS, and S. HEUNINCKX. Exploration of myostatin polymorphisms and the angiotensin-converting enzyme insertion/deletion genotype in responses of human muscle to strength training. Eur. J. Appl. Physiol. 92:267-274, 2004.
    • (2004) Eur. J. Appl. Physiol. , vol.92 , pp. 267-274
    • Thomis, M.A.1    Huygens, W.2    Heuninckx, S.3
  • 185
    • 10744225366 scopus 로고    scopus 로고
    • Apolipoprotein e genotype and changes in serum lipids and maximal oxygen uptake with exercise training
    • THOMPSON, P. D., G. J. TSONGALIS, and R. L. SEIP. Apolipoprotein E genotype and changes in serum lipids and maximal oxygen uptake with exercise training. Metabolism 53:193-202, 2004.
    • (2004) Metabolism , vol.53 , pp. 193-202
    • Thompson, P.D.1    Tsongalis, G.J.2    Seip, R.L.3
  • 186
    • 0032895749 scopus 로고    scopus 로고
    • The Lys198Asn polymorphism in the endothelin-1 gene is associated with blood pressure in overweight people
    • TIRET, L., O. POIRIER, and V. HALLET. The Lys198Asn polymorphism in the endothelin-1 gene is associated with blood pressure in overweight people. Hypertension 33:1169-1174, 1999.
    • (1999) Hypertension , vol.33 , pp. 1169-1174
    • Tiret, L.1    Poirier, O.2    Hallet, V.3
  • 187
    • 2442600044 scopus 로고    scopus 로고
    • The G-250A promoter polymorphism of the hepatic lipase gene predicts the conversion from impaired glucose tolerance to type 2 diabetes mellitus: The Finnish Diabetes Prevention Study
    • TODOROVA, B., A. KUBASZEK, and J. PIHLAJAMAKI. The G-250A promoter polymorphism of the hepatic lipase gene predicts the conversion from impaired glucose tolerance to type 2 diabetes mellitus: the Finnish Diabetes Prevention Study. J. Clin. Endocrinol. Metab. 89:2019-2023, 2004.
    • (2004) J. Clin. Endocrinol. Metab. , vol.89 , pp. 2019-2023
    • Todorova, B.1    Kubaszek, A.2    Pihlajamaki, J.3
  • 188
    • 0036244938 scopus 로고    scopus 로고
    • Paraoxonasel-192 polymorphism modulates the effects of regular and acute exercise on paraoxonasel activity
    • TOMAS, M., R. ELOSUA, and M. SENTI. Paraoxonasel-192 polymorphism modulates the effects of regular and acute exercise on paraoxonasel activity. J. Lipid Res. 43:713-720, 2002.
    • (2002) J. Lipid Res. , vol.43 , pp. 713-720
    • Tomas, M.1    Elosua, R.2    Senti, M.3
  • 189
    • 0029814303 scopus 로고    scopus 로고
    • Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the Italian kindred
    • TOSCANO, A., S. TSUJINO, G. VITA, S. SHANSKE, C. MESSINA, and S. DIMAURO. Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the Italian kindred. Muscle Nerve 19: 1134-1137, 1996.
    • (1996) Muscle Nerve , vol.19 , pp. 1134-1137
    • Toscano, A.1    Tsujino, S.2    Vita, G.3    Shanske, S.4    Messina, C.5    DiMauro, S.6
  • 190
    • 0028329868 scopus 로고
    • Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiency
    • TSUJINO, S., S. SERVIDEI, P. TONIN, S. SHANSKE, G. AZAN, and S. DIMAURO. Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiency. Am. J. Hum. Genet. 54:812-819, 1994.
    • (1994) Am. J. Hum. Genet. , vol.54 , pp. 812-819
    • Tsujino, S.1    Servidei, S.2    Tonin, P.3    Shanske, S.4    Azan, G.5    Dimauro, S.6
  • 191
    • 0028111774 scopus 로고
    • Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patients
    • TSUJINO, S., S. SHANSKE, A. K. BROWNELL, R. G. HALLER, and S. DIMAURO. Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patients. Ann. Neurol. 36:661-665, 1994.
    • (1994) Ann. Neurol. , vol.36 , pp. 661-665
    • Tsujino, S.1    Shanske, S.2    Brownell, A.K.3    Haller, R.G.4    DiMauro, S.5
  • 192
    • 0027194215 scopus 로고
    • Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease)
    • TSUJINO, S., S. SHANSKE, and S. DIMAURO. Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease). N. Engl. J. Med. 329:241-245, 1993.
    • (1993) N. Engl. J. Med. , vol.329 , pp. 241-245
    • Tsujino, S.1    Shanske, S.2    DiMauro, S.3
  • 193
    • 0029018845 scopus 로고
    • Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiency
    • TSUJINO, S., S. SHANSKE, and S. DIMAURO. Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiency. Muscle Nerve 3:S45-49, 1995.
    • (1995) Muscle Nerve , vol.3
    • Tsujino, S.1    Shanske, S.2    DiMauro, S.3
  • 194
    • 0027495730 scopus 로고
    • The molecular genetic basis of muscle phosphoglycerate mutase (PGAM) deficiency
    • TSUJINO, S., S. SHANSKE, S. SAKODA, G. FENICHEL, and S. DIMAURO. The molecular genetic basis of muscle phosphoglycerate mutase (PGAM) deficiency. Am. J. Hum. Genet. 52:472-477, 1993.
    • (1993) Am. J. Hum. Genet. , vol.52 , pp. 472-477
    • Tsujino, S.1    Shanske, S.2    Sakoda, S.3    Fenichel, G.4    DiMauro, S.5
  • 195
    • 0032464456 scopus 로고    scopus 로고
    • Does vitamin D receptor polymorphism influence the response of bone to brisk walking in postmenopausal women?
    • TSURITANI, I., K. S. BROOKE-WAVELL, S. S. MASTANA, P. R. JONES, A. E. HARDMAN, and Y. YAMADA. Does vitamin D receptor polymorphism influence the response of bone to brisk walking in postmenopausal women? Horm. Res. 50:315-319, 1998.
    • (1998) Horm. Res. , vol.50 , pp. 315-319
    • Tsuritani, I.1    Brooke-Wavell, K.S.2    Mastana, S.S.3    Jones, P.R.4    Hardman, A.E.5    Yamada, Y.6
  • 196
    • 4944258307 scopus 로고    scopus 로고
    • The angiotensin converting enzyme I/D polymorphism in Turkish athletes and sedentary controls
    • TURGUT, G., S. TURGUT, O. GENC, A. ATALAY, and E. O. ATALAY. The angiotensin converting enzyme I/D polymorphism in Turkish athletes and sedentary controls. Acta Medica (Hradec Kralove). 47:133-136, 2004.
    • (2004) Acta Medica (Hradec Kralove) , vol.47 , pp. 133-136
    • Turgut, G.1    Turgut, S.2    Genc, O.3    Atalay, A.4    Atalay, E.O.5
  • 197
    • 4644338633 scopus 로고    scopus 로고
    • The effect of CYP19 and COMT polymorphisms on exercise-induced fat loss in postmenopausal women
    • TWOROGER, S. S., J. CHUBAK, and E. J. AIELLO. The effect of CYP19 and COMT polymorphisms on exercise-induced fat loss in postmenopausal women. Obes. Res. 12:972-981, 2004.
    • (2004) Obes. Res. , vol.12 , pp. 972-981
    • Tworoger, S.S.1    Chubak, J.2    Aiello, E.J.3
  • 198
    • 0032883038 scopus 로고    scopus 로고
    • Regular exercise, plasminogen activator inhibitor-1 (PAI-1) activity and the 4G/5G promoter polymorphism in the PAI-1 gene
    • VAISANEN, S. B., S. E. HUMPHRIES, L. A. LUONG, I. PENTTILA, C. BOUCHARD, and R. RAURAMAA. Regular exercise, plasminogen activator inhibitor-1 (PAI-1) activity and the 4G/5G promoter polymorphism in the PAI-1 gene. Thromb. Haemost. 82:1117-1120, 1999.
    • (1999) Thromb. Haemost. , vol.82 , pp. 1117-1120
    • Vaisanen, S.B.1    Humphries, S.E.2    Luong, L.A.3    Penttila, I.4    Bouchard, C.5    Rauramaa, R.6
  • 199
    • 0035191848 scopus 로고    scopus 로고
    • Association of the type I collagen alpha1 Sp1 polymorphism, bone density and upper limb muscle strength in community-dwelling elderly men
    • VAN POTTELBERGH, I., S. GOEMAERE, L. NUYTINCK, A. DE PAEPE, and J. M. KAUFMAN. Association of the type I collagen alpha1 Sp1 polymorphism, bone density and upper limb muscle strength in community-dwelling elderly men. Osteoporos. Int. 12:895-901, 2001.
    • (2001) Osteoporos. Int. , vol.12 , pp. 895-901
    • Van Pottelbergh, I.1    Goemaere, S.2    Nuytinck, L.3    De Paepe, A.4    Kaufman, J.M.5
  • 200
    • 4043105100 scopus 로고    scopus 로고
    • The ER22/23EK polymorphism in the glucocorticoid receptor gene is associated with a beneficial body composition and muscle strength in young adults
    • VAN ROSSUM, E. F., P. G. VOORHOEVE, and S. J. TE VELDE. The ER22/23EK polymorphism in the glucocorticoid receptor gene is associated with a beneficial body composition and muscle strength in young adults. J. Clin. Endocrinol. Metab. 89:4004-4009, 2004.
    • (2004) J. Clin. Endocrinol. Metab. , vol.89 , pp. 4004-4009
    • Van Rossum, E.F.1    Voorhoeve, P.G.2    Te Velde, S.J.3
  • 202
    • 0031801084 scopus 로고    scopus 로고
    • A new mitochondrial tRNA(Met) gene mutation in a patient with dystrophic muscle and exercise intolerance
    • VISSING, J., M. B. SALAMON, and P. ARLIEN-SOBORG. A new mitochondrial tRNA(Met) gene mutation in a patient with dystrophic muscle and exercise intolerance. Neurology 50:1875-1878, 1998.
    • (1998) Neurology , vol.50 , pp. 1875-1878
    • Vissing, J.1    Salamon, M.B.2    Arlien-Soborg, P.3
  • 203
    • 0034791307 scopus 로고    scopus 로고
    • Exercise intolerance resulting from a muscle-restricted mutation in the mitochondrial tRNA(Leu (CUN)) gene
    • VIVES-BAUZA, C., J. GAMEZ, and M. ROIG. Exercise intolerance resulting from a muscle-restricted mutation in the mitochondrial tRNA(Leu (CUN)) gene. Ann. Med. 33:493-496, 2001.
    • (2001) Ann. Med. , vol.33 , pp. 493-496
    • Vives-Bauza, C.1    Gamez, J.2    Roig, M.3
  • 204
    • 0036788659 scopus 로고    scopus 로고
    • Phenotypic variability among first-degree relatives with carnitine palmitoyltransferase II deficiency
    • VLADUTIU, G. D., M. J. BENNETT, and N. M. FISHER. Phenotypic variability among first-degree relatives with carnitine palmitoyltransferase II deficiency. Muscle Nerve 26:492-498, 2002.
    • (2002) Muscle Nerve , vol.26 , pp. 492-498
    • Vladutiu, G.D.1    Bennett, M.J.2    Fisher, N.M.3
  • 205
    • 0033910749 scopus 로고    scopus 로고
    • A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene
    • VLADUTIU, G. D., M. J. BENNETT, D. SMAIL, L. J. WONG, R. T. TAGGART, and H. B. LINDSLEY. A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene. Mol. Genet. Metab. 70:134-141, 2000.
    • (2000) Mol. Genet. Metab. , vol.70 , pp. 134-141
    • Vladutiu, G.D.1    Bennett, M.J.2    Smail, D.3    Wong, L.J.4    Taggart, R.T.5    Lindsley, H.B.6
  • 206
    • 0030587554 scopus 로고    scopus 로고
    • Muscle phosphofructokinase deficiency in two generations
    • VORGERD, M., J. KARTTZKY, and M. RISTOW. Muscle phosphofructokinase deficiency in two generations. J. Neurol. Sci. 141:95-99, 1996.
    • (1996) J. Neurol. Sci. , vol.141 , pp. 95-99
    • Vorgerd, M.1    Karttzky, J.2    Ristow, M.3
  • 207
    • 17444439098 scopus 로고    scopus 로고
    • Polymorphisms of the beta(2)-adrenergic receptor determine exercise capacity in patients with heart failure
    • WAGONER, L. E., L. L. CRAFT, and B. SINGH. Polymorphisms of the beta(2)-adrenergic receptor determine exercise capacity in patients with heart failure. Circ. Res. 86:834-840, 2000.
    • (2000) Circ. Res. , vol.86 , pp. 834-840
    • Wagoner, L.E.1    Craft, L.L.2    Singh, B.3
  • 208
    • 0036826922 scopus 로고    scopus 로고
    • Polymorphisms of the beta1-adrenergic receptor predict exercise capacity in heart failure
    • WAGONER, L. E., L. L. CRAFT, and P. ZENGEL. Polymorphisms of the beta1-adrenergic receptor predict exercise capacity in heart failure. Am. Heart J. 144:840-846, 2002.
    • (2002) Am. Heart J. , vol.144 , pp. 840-846
    • Wagoner, L.E.1    Craft, L.L.2    Zengel, P.3
  • 209
    • 9044240040 scopus 로고    scopus 로고
    • Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
    • WANG, Q., M. E. CURRAN, and I. SPLAWSKI. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat. Genet. 12:17-23, 1996.
    • (1996) Nat. Genet. , vol.12 , pp. 17-23
    • Wang, Q.1    Curran, M.E.2    Splawski, I.3
  • 210
    • 10744227665 scopus 로고    scopus 로고
    • Bradykinin receptor gene variant and human physical performance
    • WILLIAMS, A. G., S. S. DHAMRAIT, and P. T. WOOTTON. Bradykinin receptor gene variant and human physical performance. J. Appl. Physiol. 96:938-942, 2004.
    • (2004) J. Appl. Physiol. , vol.96 , pp. 938-942
    • Williams, A.G.1    Dhamrait, S.S.2    Wootton, P.T.3
  • 211
    • 0034628406 scopus 로고    scopus 로고
    • The ACE gene and muscle performance
    • WILLIAMS, A. G., M. P. RAYSON, and M. JUBB. The ACE gene and muscle performance. Nature 403:614, 2000.
    • (2000) Nature , vol.403 , pp. 614
    • Williams, A.G.1    Rayson, M.P.2    Jubb, M.3
  • 212
    • 0036281792 scopus 로고    scopus 로고
    • Changes in high-density lipoprotein-cholesterol subfractions with exercise training may be dependent on cholesteryl ester transfer protein (CETP) genotype
    • WILUND, K. R., R. E. FERRELL, D. A. PHARES, A. P. GOLDBERG, and J. M. HAGBERG. Changes in high-density lipoprotein-cholesterol subfractions with exercise training may be dependent on cholesteryl ester transfer protein (CETP) genotype. Metabolism 51: 774-778, 2002.
    • (2002) Metabolism , vol.51 , pp. 774-778
    • Wilund, K.R.1    Ferrell, R.E.2    Phares, D.A.3    Goldberg, A.P.4    Hagberg, J.M.5
  • 213
    • 10744228245 scopus 로고    scopus 로고
    • Physical activity and angiotensin-converting enzyme gene polymorphism in mild hypertensives
    • WINNICKI, M., V. ACCURSO, and M. HOFFMANN. Physical activity and angiotensin-converting enzyme gene polymorphism in mild hypertensives. Am. J. Med. Genet. A. 125:38-44, 2004.
    • (2004) Am. J. Med. Genet. A. , vol.125 , pp. 38-44
    • Winnicki, M.1    Accurso, V.2    Hoffmann, M.3
  • 214
    • 0033626603 scopus 로고    scopus 로고
    • A polymorphism in the alpha2a-adrenoceptor gene and endurance athlete status
    • WOLFARTH, B., M. A. RIVERA, and J. M. OPPERT. A polymorphism in the alpha2a-adrenoceptor gene and endurance athlete status. Med. Sci. Sports Exerc. 32:1709-1712, 2000.
    • (2000) Med. Sci. Sports Exerc. , vol.32 , pp. 1709-1712
    • Wolfarth, B.1    Rivera, M.A.2    Oppert, J.M.3
  • 215
    • 2642544952 scopus 로고    scopus 로고
    • Apolipoprotein C-III SstI genotypes modulate exercise-induced hypotriglyceridemia
    • WOO, S. K., and H. S. KANG. Apolipoprotein C-III SstI genotypes modulate exercise-induced hypotriglyceridemia. Med. Sci. Sports Exerc. 36:955-959, 2004.
    • (2004) Med. Sci. Sports Exerc. , vol.36 , pp. 955-959
    • Woo, S.K.1    Kang, H.S.2
  • 216
    • 0035072230 scopus 로고    scopus 로고
    • Elite swimmers and the D allele of the ACE I/D polymorphism
    • WOODS, D., M. HICKMAN, and Y. JAMSHIDI. Elite swimmers and the D allele of the ACE I/D polymorphism. Hum. Genet. 108: 230-232, 2001.
    • (2001) Hum. Genet. , vol.108 , pp. 230-232
    • Woods, D.1    Hickman, M.2    Jamshidi, Y.3
  • 217
    • 0035023621 scopus 로고    scopus 로고
    • Angiotensin-I converting enzyme genotype-dependent benefit from hormone replacement therapy in isometric muscle strength and bone mineral density
    • WOODS, D., G. ONAMBELE, and R. WOLEDGE. Angiotensin-I converting enzyme genotype-dependent benefit from hormone replacement therapy in isometric muscle strength and bone mineral density. J. Clin. Endocrinol. Metab. 86:2200-2204, 2001.
    • (2001) J. Clin. Endocrinol. Metab. , vol.86 , pp. 2200-2204
    • Woods, D.1    Onambele, G.2    Woledge, R.3
  • 218
    • 1542315578 scopus 로고    scopus 로고
    • The serum angiotensin-converting enzyme and angiotensin II response to altered posture and acute exercise, the influence of ACE genotype
    • WOODS, D., J. SANDERS, and A. JONES. The serum angiotensin-converting enzyme and angiotensin II response to altered posture and acute exercise, the influence of ACE genotype. Eur. J. Appl. Physiol. 91:342-348, 2004.
    • (2004) Eur. J. Appl. Physiol. , vol.91 , pp. 342-348
    • Woods, D.1    Sanders, J.2    Jones, A.3
  • 219
    • 0036939239 scopus 로고    scopus 로고
    • Endurance enhancement related to the human angiotensin I-converting enzyme I-D polymorphism is not due to differences in the cardiorespiratory response to training
    • WOODS, D. R., M. WORLD, and M. P. RAYSON. Endurance enhancement related to the human angiotensin I-converting enzyme I-D polymorphism is not due to differences in the cardiorespiratory response to training. Eur. J. Appl. Physiol. 86:240-244, 2002.
    • (2002) Eur. J. Appl. Physiol. , vol.86 , pp. 240-244
    • Woods, D.R.1    World, M.2    Rayson, M.P.3
  • 220
    • 0041385595 scopus 로고    scopus 로고
    • ACTN3 genotype is associated with human elite athletic performance
    • YANG, N., D. G. MACARTHUR, and J. P. GULBIN. ACTN3 genotype is associated with human elite athletic performance. Am. J. Hum. Genet. 73:627-631, 2003.
    • (2003) Am. J. Hum. Genet. , vol.73 , pp. 627-631
    • Yang, N.1    MacArthur, D.G.2    Gulbin, J.P.3
  • 221
    • 0036822068 scopus 로고    scopus 로고
    • Association of angiotensin-converting-enzyme gene polymorphism with the depressor response to mild exercise therapy in patients with mild to moderate essential hypertension
    • ZHANG, B., T. SAKAI, and S. MIURA. Association of angiotensin-converting- enzyme gene polymorphism with the depressor response to mild exercise therapy in patients with mild to moderate essential hypertension. Clin. Genet. 62:328-333, 2002.
    • (2002) Clin. Genet. , vol.62 , pp. 328-333
    • Zhang, B.1    Sakai, T.2    Miura, S.3


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