메뉴 건너뛰기




Volumn 27, Issue 5, 2009, Pages 983-990

A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany

(15)  Hoffmann, Katrin a,b,c   Planitz, Christian d   Rüschendorf, Franz c   Müller Myhsok, Bertram e   Stassen, Hans H f   Lucke, Barbara a,c   Mattheisen, Manuel g   Stumvoll, Michael h   Bochmann, Rolf d   Zschornackj, Martin i   Wienker, Thomas F c,g   Nürnberg, Peter c,j   Reis, André k   Luft, Friedrich C a   Lindner, Tom H h  


Author keywords

Essential hypertension; Genetics; Germans; Hypertension; Isolated population; Linkage analysis; Primary hypertension; Sorbs

Indexed keywords

ADULT; ARTICLE; BODY MASS; CHROMOSOME 1P; CHROMOSOME MAP; CONTROLLED STUDY; DIABETES MELLITUS; FEMALE; GENE LOCUS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC TRAIT; GENOTYPE; GERMANY; HUMAN; HYPERLIPIDEMIA; HYPERTENSION; MAJOR CLINICAL STUDY; MALE; METABOLIC SYNDROME X; MICROSATELLITE MARKER; OBESITY; PRIORITY JOURNAL;

EID: 67649635079     PISSN: 02636352     EISSN: None     Source Type: Journal    
DOI: 10.1097/HJH.0b013e328328123d     Document Type: Article
Times cited : (11)

References (64)
  • 1
    • 27744463911 scopus 로고    scopus 로고
    • Comparison of risk factors for the competing risks of coronary heart disease, stroke, and venous thromboembolism
    • Glynn RJ, Rosner B. Comparison of risk factors for the competing risks of coronary heart disease, stroke, and venous thromboembolism. Am J Epidemiol 2005; 162:975-982.
    • (2005) Am J Epidemiol , vol.162 , pp. 975-982
    • Glynn, R.J.1    Rosner, B.2
  • 2
    • 0028942436 scopus 로고
    • Prevalence of hypertension in the US adult population. Results from the Third Nation al Health and Nutrition Examination Survey, 1988-1991
    • Burt VL, Whelton P, Roccella EJ, Brown C, Cutler JA, Higgins M, et al. Prevalence of hypertension in the US adult population. Results from the Third Nation al Health and Nutrition Examination Survey, 1988-1991. Hypertension 1995; 25:305-313.
    • (1995) Hypertension , vol.25 , pp. 305-313
    • Burt, V.L.1    Whelton, P.2    Roccella, E.J.3    Brown, C.4    Cutler, J.A.5    Higgins, M.6
  • 3
    • 18244379376 scopus 로고    scopus 로고
    • Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP)
    • FBPP Investigators
    • FBPP Investigators. Multi-center genetic study of hypertension: the Family Blood Pressure Program (FBPP). Hypertension 2002; 39:3-9.
    • (2002) Hypertension , vol.39 , pp. 3-9
  • 4
    • 0344718782 scopus 로고    scopus 로고
    • World Health Organization (WHO)/International Society of Hypertension (ISH) statement on management of hypertension
    • Whitworth JA. 2003 World Health Organization (WHO)/International Society of Hypertension (ISH) statement on management of hypertension. J Hypertens 2003; 21:1983-1992.
    • (2003) J Hypertens , vol.2003 , Issue.21 , pp. 1983-1992
    • Whitworth, J.A.1
  • 7
    • 0028238365 scopus 로고
    • Epidemiology of hypertension
    • Whelton PK. Epidemiology of hypertension. Lancet 1994; 344:101-106.
    • (1994) Lancet , vol.344 , pp. 101-106
    • Whelton, P.K.1
  • 8
    • 0031409125 scopus 로고    scopus 로고
    • Peltonen L Molecular background of the Finnish disease heritage. Ann Med 1997; 29:553-556.
    • Peltonen L Molecular background of the Finnish disease heritage. Ann Med 1997; 29:553-556.
  • 9
    • 0033992497 scopus 로고    scopus 로고
    • Peltonen L Positional cloning of disease genes: advantages of genetic isolates. Hum Hered 2000; 50:66-75.
    • Peltonen L Positional cloning of disease genes: advantages of genetic isolates. Hum Hered 2000; 50:66-75.
  • 10
    • 0032869123 scopus 로고    scopus 로고
    • Molecular genetics of the Finnish disease heritage
    • Peltonen L, Jalanko A, Varilo T. Molecular genetics of the Finnish disease heritage. Hum Mol Genet 1999; 8:1913-1923.
    • (1999) Hum Mol Genet , vol.8 , pp. 1913-1923
    • Peltonen, L.1    Jalanko, A.2    Varilo, T.3
  • 11
    • 0036556373 scopus 로고    scopus 로고
    • Genetics of population isolates
    • Arcos-Burgos M, Muenke M. Genetics of population isolates. Clin Genet 2002; 61:233-247.
    • (2002) Clin Genet , vol.61 , pp. 233-247
    • Arcos-Burgos, M.1    Muenke, M.2
  • 12
    • 84969213492 scopus 로고    scopus 로고
    • Genome-wide association study of 14000 cases of seven common diseases and 3000 shared controls
    • The Wellcome Trust Case Control Consortium
    • The Wellcome Trust Case Control Consortium. Genome-wide association study of 14000 cases of seven common diseases and 3000 shared controls. Nature 2007; 447:661-678.
    • (2007) Nature , vol.447 , pp. 661-678
  • 13
    • 42649084334 scopus 로고    scopus 로고
    • Rare independent mutations in renal salt handling genes contribute to blood pressure variation
    • Ji W, Foo JN, O'Roak BJ, Zhao H, Larson MG, Simon DB, et al. Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nat Genet 2008; 40:592-599.
    • (2008) Nat Genet , vol.40 , pp. 592-599
    • Ji, W.1    Foo, J.N.2    O'Roak, B.J.3    Zhao, H.4    Larson, M.G.5    Simon, D.B.6
  • 16
    • 67649732239 scopus 로고    scopus 로고
    • Nielsen GR. In search of a home: nineteenth-century Wendish immigration. 1st ed. College Station, TX: Texas A & M University Press; 1989.
    • Nielsen GR. In search of a home: nineteenth-century Wendish immigration. 1st ed. College Station, TX: Texas A & M University Press; 1989.
  • 17
    • 34347125488 scopus 로고
    • Blood group and blood factor distribution in the Sorbs of Lusatia
    • in German
    • Pettenkofer HJ, Thomas K, Voigt GE. Blood group and blood factor distribution in the Sorbs of Lusatia [in German]. Blut 1958; 4:128-130.
    • (1958) Blut , vol.4 , pp. 128-130
    • Pettenkofer, H.J.1    Thomas, K.2    Voigt, G.E.3
  • 18
    • 67649793062 scopus 로고
    • The frequency of the blood group marker S (Walsh and Montgomery) of the MNSs blood group system in the Sorbian population of Lusatia
    • in German
    • Thomas K. The frequency of the blood group marker S (Walsh and Montgomery) of the MNSs blood group system in the Sorbian population of Lusatia [in German]. Dtsch Gesundh Wes 1962; 17:613-614.
    • (1962) Dtsch Gesundh Wes , vol.17 , pp. 613-614
    • Thomas, K.1
  • 19
    • 0032231877 scopus 로고    scopus 로고
    • Comprehensive human genetic maps: Individual and sex-specific variation in recombination
    • Broman KW, Murray JC, Sheffield VC, White RL, Weber JL. Comprehensive human genetic maps: individual and sex-specific variation in recombination. Am J Hum Genet 1998; 63:861-869.
    • (1998) Am J Hum Genet , vol.63 , pp. 861-869
    • Broman, K.W.1    Murray, J.C.2    Sheffield, V.C.3    White, R.L.4    Weber, J.L.5
  • 20
    • 0036699522 scopus 로고    scopus 로고
    • Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly)
    • Hoffmann K, Dreger CK, Olins AL, Olins DE, Shultz LD, Lucke B, et al. Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly). Nat Genet 2002; 31:410-414.
    • (2002) Nat Genet , vol.31 , pp. 410-414
    • Hoffmann, K.1    Dreger, C.K.2    Olins, A.L.3    Olins, D.E.4    Shultz, L.D.5    Lucke, B.6
  • 21
    • 0032231941 scopus 로고    scopus 로고
    • PedCheck: A program for identification of genotype incompatibilities in linkage analysis
    • O'Connell JR, Weeks DE. PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 1998; 63:259-266.
    • (1998) Am J Hum Genet , vol.63 , pp. 259-266
    • O'Connell, J.R.1    Weeks, D.E.2
  • 23
    • 0028877463 scopus 로고
    • Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
    • Lander E, Kruglyak L Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 1995; 11:241-247.
    • (1995) Nat Genet , vol.11 , pp. 241-247
    • Lander, E.1    Kruglyak, L.2
  • 24
    • 0036338150 scopus 로고    scopus 로고
    • Merlin: Rapid analysis of dense genetic maps using sparse gene flow trees
    • Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin: rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002; 30:97-101.
    • (2002) Nat Genet , vol.30 , pp. 97-101
    • Abecasis, G.R.1    Cherny, S.S.2    Cookson, W.O.3    Cardon, L.R.4
  • 25
    • 0036842918 scopus 로고    scopus 로고
    • Evaluating the results of genomewide linkage scans of complex traits by locus counting
    • Wiltshire S, Cardon LR, McCarthy MI. Evaluating the results of genomewide linkage scans of complex traits by locus counting. Am J Hum Genet 2002; 71:1175-1182.
    • (2002) Am J Hum Genet , vol.71 , pp. 1175-1182
    • Wiltshire, S.1    Cardon, L.R.2    McCarthy, M.I.3
  • 26
    • 0032754452 scopus 로고    scopus 로고
    • Linkage analysis in heterogeneous and complex traits
    • Ott J, Bhat A. Linkage analysis in heterogeneous and complex traits. Eur Child Adolesc Psychiatry 1999; 8 (Suppl 3):43-46.
    • (1999) Eur Child Adolesc Psychiatry , vol.8 , Issue.SUPPL. 3 , pp. 43-46
    • Ott, J.1    Bhat, A.2
  • 27
    • 13844266053 scopus 로고    scopus 로고
    • easyLINKAGE: A PERL script for easy and automated two-/multipoint linkage analyses
    • Lindner TH, Hoffmann K. easyLINKAGE: a PERL script for easy and automated two-/multipoint linkage analyses. Bioinformatics 2005; 21:405-407.
    • (2005) Bioinformatics , vol.21 , pp. 405-407
    • Lindner, T.H.1    Hoffmann, K.2
  • 28
    • 0034098774 scopus 로고    scopus 로고
    • Gudbjartsson DF, Jonasson K, Frigge ML, Kong A. Allegro, a new computer program for multipoint linkage analysis. Nat Genet 2000; 25:12-13.
    • Gudbjartsson DF, Jonasson K, Frigge ML, Kong A. Allegro, a new computer program for multipoint linkage analysis. Nat Genet 2000; 25:12-13.
  • 29
    • 0032928542 scopus 로고    scopus 로고
    • Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans
    • Cox NJ, Frigge M, Nicolae DL, Concannon P, Hanis CL, Bell GI, Kong A. Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans. Nat Genet 1999; 21:213-215.
    • (1999) Nat Genet , vol.21 , pp. 213-215
    • Cox, N.J.1    Frigge, M.2    Nicolae, D.L.3    Concannon, P.4    Hanis, C.L.5    Bell, G.I.6    Kong, A.7
  • 30
    • 0028301661 scopus 로고
    • A class of tests for linkage using affected pedigree members
    • Whittemore AS, Halpern J. A class of tests for linkage using affected pedigree members. Biometrics 1994; 50:118-127.
    • (1994) Biometrics , vol.50 , pp. 118-127
    • Whittemore, A.S.1    Halpern, J.2
  • 31
    • 0030728925 scopus 로고    scopus 로고
    • Allele-sharing models: LOD scores and accurate linkage tests
    • Kong A, Cox NJ. Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 1997; 61:1179-1188.
    • (1997) Am J Hum Genet , vol.61 , pp. 1179-1188
    • Kong, A.1    Cox, N.J.2
  • 34
    • 38649091662 scopus 로고    scopus 로고
    • The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
    • Helgadottir A, Thorleifsson G, Magnusson KP, Gretarsdottir S, Steinthorsdottir V, Manolescu A, et al. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet 2008; 40:217-224.
    • (2008) Nat Genet , vol.40 , pp. 217-224
    • Helgadottir, A.1    Thorleifsson, G.2    Magnusson, K.P.3    Gretarsdottir, S.4    Steinthorsdottir, V.5    Manolescu, A.6
  • 35
    • 0034641601 scopus 로고    scopus 로고
    • Linkage and association of tumor necrosis factor receptor 2 locus with hypertension, hypercholesterolemia and plasma shed receptor
    • Glenn CL, Wang WY, Benjafield AV, Morris BJ. Linkage and association of tumor necrosis factor receptor 2 locus with hypertension, hypercholesterolemia and plasma shed receptor. Hum Mol Genet 2000; 9:1943-1949.
    • (2000) Hum Mol Genet , vol.9 , pp. 1943-1949
    • Glenn, C.L.1    Wang, W.Y.2    Benjafield, A.V.3    Morris, B.J.4
  • 36
    • 19744370778 scopus 로고    scopus 로고
    • Genome-wide scan for hypertension in Sydney sibships: The GENIHUSS study
    • Benjafield AV, Wang WY, Speirs HJ, Morris BJ. Genome-wide scan for hypertension in Sydney sibships: the GENIHUSS study. Am J Hypertens 2005; 18:828-832.
    • (2005) Am J Hypertens , vol.18 , pp. 828-832
    • Benjafield, A.V.1    Wang, W.Y.2    Speirs, H.J.3    Morris, B.J.4
  • 38
    • 31944435805 scopus 로고    scopus 로고
    • Genome-wide scan for linkage to obesity-associated hypertension in French Canadians
    • Pausova Z, Gaudet D, Gossard F, Bernard M, Kaldunski ML, Jomphe M, et al. Genome-wide scan for linkage to obesity-associated hypertension in French Canadians. Hypertension 2005; 46:1280-1285.
    • (2005) Hypertension , vol.46 , pp. 1280-1285
    • Pausova, Z.1    Gaudet, D.2    Gossard, F.3    Bernard, M.4    Kaldunski, M.L.5    Jomphe, M.6
  • 40
    • 34748889585 scopus 로고    scopus 로고
    • Genome-wide scan for serum ghrelin detects linkage on chromosome 1 p36 in Hispanic children: Results from the Viva La Familia study
    • Voruganti VS, Goring HH, Diego VP, Cai G, Mehta NR, Haack K, et al. Genome-wide scan for serum ghrelin detects linkage on chromosome 1 p36 in Hispanic children: results from the Viva La Familia study. Pediatr Res 2007; 62:445-450.
    • (2007) Pediatr Res , vol.62 , pp. 445-450
    • Voruganti, V.S.1    Goring, H.H.2    Diego, V.P.3    Cai, G.4    Mehta, N.R.5    Haack, K.6
  • 41
    • 33344471915 scopus 로고    scopus 로고
    • A genomewide search finds major susceptibility loci for gall bladder disease on chromosome 1 in Mexican Americans
    • Puppala S, Dodd GD, Fowler S, Arya R, Schneider J, Farook VS, et al. A genomewide search finds major susceptibility loci for gall bladder disease on chromosome 1 in Mexican Americans. Am J Hum Genet 2006; 78:377-392.
    • (2006) Am J Hum Genet , vol.78 , pp. 377-392
    • Puppala, S.1    Dodd, G.D.2    Fowler, S.3    Arya, R.4    Schneider, J.5    Farook, V.S.6
  • 42
    • 13844302007 scopus 로고    scopus 로고
    • Principal component for metabolic syndrome risk maps to chromosome 4p in Mexican Americans: The San Antonio Family Heart Study
    • Cai G, Cole SA, Freeland-Graves JH, MacCluer JW, Blangero J, Comuzzie AG. Principal component for metabolic syndrome risk maps to chromosome 4p in Mexican Americans: the San Antonio Family Heart Study. Hum Biol 2004; 76:651-665.
    • (2004) Hum Biol , vol.76 , pp. 651-665
    • Cai, G.1    Cole, S.A.2    Freeland-Graves, J.H.3    MacCluer, J.W.4    Blangero, J.5    Comuzzie, A.G.6
  • 43
    • 0037219259 scopus 로고    scopus 로고
    • Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects
    • Iwasaki N, Cox NJ, Wang YQ, Schwarz PE, Bell GI, Honda M, et al. Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects. Diabetes 2003; 52:209-213.
    • (2003) Diabetes , vol.52 , pp. 209-213
    • Iwasaki, N.1    Cox, N.J.2    Wang, Y.Q.3    Schwarz, P.E.4    Bell, G.I.5    Honda, M.6
  • 44
    • 34249936215 scopus 로고    scopus 로고
    • A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1 p36.13 and a type 2 diabetes locus on chromosome 16p12.2
    • Hoffmann K, Mattheisen M, Dahm S, Nurnberg P, Roe C, Johnson J, et al. A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1 p36.13 and a type 2 diabetes locus on chromosome 16p12.2. Diabetologia 2007; 50:1418-1422.
    • (2007) Diabetologia , vol.50 , pp. 1418-1422
    • Hoffmann, K.1    Mattheisen, M.2    Dahm, S.3    Nurnberg, P.4    Roe, C.5    Johnson, J.6
  • 45
    • 20244390026 scopus 로고    scopus 로고
    • Quantitative founder-effect analysis of French Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension
    • Hamet P, Merlo E, Seda O, Broeckel U, Tremblay J, Kaldunski M, et al. Quantitative founder-effect analysis of French Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension. Am J Hum Genet 2005; 76:815-832.
    • (2005) Am J Hum Genet , vol.76 , pp. 815-832
    • Hamet, P.1    Merlo, E.2    Seda, O.3    Broeckel, U.4    Tremblay, J.5    Kaldunski, M.6
  • 47
    • 0037305164 scopus 로고    scopus 로고
    • Genome scans for hypertension and blood pressure regulation
    • Samani NJ. Genome scans for hypertension and blood pressure regulation. Am J Hypertens 2003; 16:167-171.
    • (2003) Am J Hypertens , vol.16 , pp. 167-171
    • Samani, N.J.1
  • 48
    • 0035936780 scopus 로고    scopus 로고
    • Molecular mechanisms of human hypertension
    • Lifton RP, Gharavi AG, Geller DS. Molecular mechanisms of human hypertension. Cell 2001; 104:545-556.
    • (2001) Cell , vol.104 , pp. 545-556
    • Lifton, R.P.1    Gharavi, A.G.2    Geller, D.S.3
  • 49
    • 0029160972 scopus 로고
    • Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase
    • Mune T, Rogerson FM, Nikkila H, Agarwal AK, White PC. Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase. Nat Genet 1995; 10:394-399.
    • (1995) Nat Genet , vol.10 , pp. 394-399
    • Mune, T.1    Rogerson, F.M.2    Nikkila, H.3    Agarwal, A.K.4    White, P.C.5
  • 50
    • 0030049329 scopus 로고    scopus 로고
    • Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 beta-hydroxysteroid dehydrogenase type 2 gene
    • Stewart PM, Krozowski ZS, Gupta A, Milford DV, Howie AJ, Sheppard MC, Whorwood CB. Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 beta-hydroxysteroid dehydrogenase type 2 gene. Lancet 1996; 347:88-91.
    • (1996) Lancet , vol.347 , pp. 88-91
    • Stewart, P.M.1    Krozowski, Z.S.2    Gupta, A.3    Milford, D.V.4    Howie, A.J.5    Sheppard, M.C.6    Whorwood, C.B.7
  • 51
    • 33847644921 scopus 로고    scopus 로고
    • Polymorphic variation in the 11 beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency
    • Barr M, MacKenzie SM, Friel EC, Holloway CD, Wilkinson DM, Brain NJ, et al. Polymorphic variation in the 11 beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency. Hypertension 2007; 49:113-119.
    • (2007) Hypertension , vol.49 , pp. 113-119
    • Barr, M.1    MacKenzie, S.M.2    Friel, E.C.3    Holloway, C.D.4    Wilkinson, D.M.5    Brain, N.J.6
  • 52
    • 0034617130 scopus 로고    scopus 로고
    • Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy
    • Geller DS, Farhi A, Pinkerton N, Fradley M, Moritz M, Spitzer A, et al. Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy. Science 2000; 289:119-123.
    • (2000) Science , vol.289 , pp. 119-123
    • Geller, D.S.1    Farhi, A.2    Pinkerton, N.3    Fradley, M.4    Moritz, M.5    Spitzer, A.6
  • 54
    • 0029092801 scopus 로고
    • Hypertension caused by a truncated epithelial sodium channel gamma subunit: Genetic heterogeneity of Liddle syndrome
    • Hansson JH, Nelson-Williams C, Suzuki H, Schild L, Shimkets R, Lu Y, et al. Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome. Nat Genet 1995; 11:76-82.
    • (1995) Nat Genet , vol.11 , pp. 76-82
    • Hansson, J.H.1    Nelson-Williams, C.2    Suzuki, H.3    Schild, L.4    Shimkets, R.5    Lu, Y.6
  • 55
    • 0027946089 scopus 로고
    • Liddle's syndrome: Heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel
    • Shimkets RA, Warnock DG, Bositis CM, Nelson-Williams C, Hansson JH, Schambelan M, et al. Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel. Cell 1994; 79:407-414.
    • (1994) Cell , vol.79 , pp. 407-414
    • Shimkets, R.A.1    Warnock, D.G.2    Bositis, C.M.3    Nelson-Williams, C.4    Hansson, J.H.5    Schambelan, M.6
  • 56
    • 0029918734 scopus 로고    scopus 로고
    • Liddle disease caused by a missense mutation of beta subunit of the epithelial sodium channel gene
    • Tamura H, Schild L, Enomoto N, Matsui N, Marumo F, Rossier BC. Liddle disease caused by a missense mutation of beta subunit of the epithelial sodium channel gene. J Clin Invest 1996; 97:1780-1784.
    • (1996) J Clin Invest , vol.97 , pp. 1780-1784
    • Tamura, H.1    Schild, L.2    Enomoto, N.3    Matsui, N.4    Marumo, F.5    Rossier, B.C.6
  • 58
    • 0037457965 scopus 로고    scopus 로고
    • Molecular pathogenesis of inherited hypertension with hyperkalemia: The Na-Cl cotransporter is inhibited by wild-type but not mutant WNK4
    • Wilson FH, Kahle KT, Sabath E, Lalioti MD, Rapson AK, Hoover RS, et al. Molecular pathogenesis of inherited hypertension with hyperkalemia: the Na-Cl cotransporter is inhibited by wild-type but not mutant WNK4. Proc Natl Acad Sci U S A 2003; 100:680-684.
    • (2003) Proc Natl Acad Sci U S A , vol.100 , pp. 680-684
    • Wilson, F.H.1    Kahle, K.T.2    Sabath, E.3    Lalioti, M.D.4    Rapson, A.K.5    Hoover, R.S.6
  • 59
    • 33746977635 scopus 로고    scopus 로고
    • Role of with-no-lysine [K] kinases in the pathogenesis of Gordon's syndrome
    • Xie J, Craig L, Cobb MH, Huang CL. Role of with-no-lysine [K] kinases in the pathogenesis of Gordon's syndrome. Pediatr Nephrol 2006; 21:1231-1236.
    • (2006) Pediatr Nephrol , vol.21 , pp. 1231-1236
    • Xie, J.1    Craig, L.2    Cobb, M.H.3    Huang, C.L.4
  • 60
    • 12444257322 scopus 로고    scopus 로고
    • Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p
    • Gong M, Zhang H, Schulz H, Lee YA, Sun K, Bahring S, etal. Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p. Hum Mol Genet 2003; 12:1273-1277.
    • (2003) Hum Mol Genet , vol.12 , pp. 1273-1277
    • Gong, M.1    Zhang, H.2    Schulz, H.3    Lee, Y.A.4    Sun, K.5    Bahring, S.6
  • 61
    • 56749149825 scopus 로고    scopus 로고
    • Replication of the Wellcome Trust genome-wide association study of essential hypertension: The Family Blood Pressure Program
    • Ehret GB, Morrison AC, O'Connor AA, Grove ML, Baird L, Schwander K, et al. Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program. Eur J Hum Genet 2008; 16:1507-1511.
    • (2008) Eur J Hum Genet , vol.16 , pp. 1507-1511
    • Ehret, G.B.1    Morrison, A.C.2    O'Connor, A.A.3    Grove, M.L.4    Baird, L.5    Schwander, K.6
  • 64
    • 2542446307 scopus 로고    scopus 로고
    • Isolates and their potential use in complex gene mapping efforts
    • Varilo T, Peltonen L. Isolates and their potential use in complex gene mapping efforts. Curr Opin Genet Dev 2004; 14:316-323.
    • (2004) Curr Opin Genet Dev , vol.14 , pp. 316-323
    • Varilo, T.1    Peltonen, L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.