-
1
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is unstable on Huntington's disease chromosomes
-
The Huntington's Disease Collaborative Research Group
-
A novel gene containing a trinucleotide repeat that is unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group, Cell 1993 26 971 983
-
(1993)
Cell
, vol.26
, pp. 971-983
-
-
-
2
-
-
0027261537
-
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease
-
DOI 10.1038/ng0893-393
-
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease. RG Snell JC MacMillan JP Cheadle I Fenton LP Lazarou P Davies ME MacDonald JF Gusella PS Harper DJ Shaw, Nat Genet 1993 4 393 397 10.1038/ng0893-393 8401588 (Pubitemid 23231489)
-
(1993)
Nature Genetics
, vol.4
, Issue.4
, pp. 393-397
-
-
Snell, R.G.1
MacMillan, J.C.2
Cheadle, J.P.3
Fenton, I.4
Lazarou, L.P.5
Davies, P.6
MacDonald, M.E.7
Gusella, J.F.8
Harper, P.S.9
Shaw, D.J.10
-
3
-
-
0027176364
-
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease
-
DOI 10.1038/ng0893-398
-
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease. SE Andrew YP Goldberg B Kremer H Telenius J Theilmann S Adam E Starr F Squitieri B Lin MA Kalchman,, et al. Nat Genet 1993 4 398 403 10.1038/ng0893-398 8401589 (Pubitemid 23231490)
-
(1993)
Nature Genetics
, vol.4
, Issue.4
, pp. 398-403
-
-
Andrew, S.E.1
Goldberg, Y.P.2
Kremer, B.3
Telenius, H.4
Theilmann, J.5
Adam, S.6
Starr, E.7
Squitieri, F.8
Lin, B.9
Kalchman, M.A.10
Graham, R.K.11
Hayden, M.R.12
-
4
-
-
0027240431
-
Trinucleotide repeat length instability and age of onset in Huntington's disease
-
DOI 10.1038/ng0893-387
-
Trinucleotide repeat length instability and age of onset in Huntington's disease. M Duyao C Ambrose R Myers A Noveletto F Persichetti M Frontali S Folstein C Ross M Franz M Abbott,, et al. Nat Genet 1993 4 387 392 10.1038/ng0893-387 8401587 (Pubitemid 23231488)
-
(1993)
Nature Genetics
, vol.4
, Issue.4
, pp. 387-392
-
-
Duyao, M.1
Ambrose, C.2
Myers, R.3
Novelletto, A.4
Persichetti, F.5
Frontali, M.6
Folstein, S.7
Ross, C.8
Franz, M.9
Abbott, M.10
Gray, J.11
Conneally, P.12
Young, A.13
Penney, J.14
Hollingsworth, Z.15
Shoulson, I.16
Lazzarini, A.17
Falek, A.18
MacDonald, M.19
-
5
-
-
77951252744
-
Huntington's disease: The case for genetic modifiers
-
10.1186/gm80. 19725930
-
Huntington's disease: the case for genetic modifiers. JF Gusella ME Macdonald, Genome Med 2009 1 80 10.1186/gm80 19725930
-
(2009)
Genome Med
, vol.1
, pp. 80
-
-
Gusella, J.F.1
MacDonald, M.E.2
-
6
-
-
33846436448
-
Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds
-
DOI 10.1136/jmg.2006.045153
-
Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds. JM Andresen J Gaya'n SS Cherny D Brocklebank G Alkorta-Aranburu EA Addis US-Venezuela Collaborative Research Group LR Cardon DE Housman NS Wexler, J Med Genet 2007 44 44 50 17018562 (Pubitemid 46142838)
-
(2007)
Journal of Medical Genetics
, vol.44
, Issue.1
, pp. 44-50
-
-
Andresen, J.M.1
Gayan, J.2
Cherny, S.S.3
Brocklebank, D.4
Alkorta-Aranburu, G.5
Addis, E.A.6
Cardon, L.R.7
Housman, D.E.8
Wexler, N.S.9
-
7
-
-
15444363304
-
NR2A and NR2B receptor gene variations modify age at onset in Huntington disease
-
DOI 10.1007/s10048-004-0198-8
-
NR2A and NR2B receptor gene variations modify age at onset in Huntington disease. L Arning PH Kraus S Valentin C Saft J Andrich JT Epplen, Neurogenetics 2005 6 25 28 10.1007/s10048-004-0198-8 15742215 (Pubitemid 40394827)
-
(2005)
Neurogenetics
, vol.6
, Issue.1
, pp. 25-28
-
-
Arning, L.1
Kraus, P.H.2
Valentin, S.3
Saft, C.4
Andrich, J.5
Epplen, J.T.6
-
8
-
-
42449161835
-
ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease
-
10.1007/s00109-007-0299-6. 18327563
-
ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease. L Arning D Monté W Hansen S Wieczorek P Jagiello DA Akkad J Andrich PH Kraus C Saft JT Epplen, J Mol Med 2008 86 485 490 10.1007/s00109-007-0299-6 18327563
-
(2008)
J Mol Med
, vol.86
, pp. 485-490
-
-
Arning, L.1
Monté, D.2
Hansen, W.3
Wieczorek, S.4
Jagiello, P.5
Akkad, D.A.6
Andrich, J.7
Kraus, P.H.8
Saft, C.9
Epplen, J.T.10
-
9
-
-
41849097772
-
Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease
-
DOI 10.1093/hmg/ddn003
-
Huntingtin-associated protein-1 is a modifier of the ageat - onset of Huntington's disease. S Metzger J Rong HP Nguyen A Cape J Tomiuk AS Soehn P Propping Y Freudenberg-Hua J Freudenberg L Tong,, et al. Hum Mol Genet 2008 17 1137 1146 10.1093/hmg/ddn003 18192679 (Pubitemid 351494185)
-
(2008)
Human Molecular Genetics
, vol.17
, Issue.8
, pp. 1137-1146
-
-
Metzger, S.1
Rong, J.2
Nguyen, H.-P.3
Cape, A.4
Tomiuk, J.5
Soehn, A.S.6
Propping, P.7
Freudenberg-hua, Y.8
Freudenberg, J.9
Tong, L.10
Li, S.-H.11
Li, X.-J.12
Riess, O.13
-
10
-
-
78650059716
-
Age at onset in Huntington's disease: Replication study on the associations of ADORA2A, HAP1 and OGG1
-
Age at onset in Huntington's disease: replication study on the associations of ADORA2A, HAP1 and OGG1. E Taherzadeh-Fard C Saft S Wieczorek JT Epplen L Arning, Neurogenetics 2010 4 435 439
-
(2010)
Neurogenetics
, vol.4
, pp. 435-439
-
-
Taherzadeh-Fard, E.1
Saft, C.2
Wieczorek, S.3
Epplen, J.T.4
Arning, L.5
-
11
-
-
58649094617
-
The gene coding for PGC-1alpha modifies age at onset in Huntington's disease
-
10.1186/1750-1326-4-3. 19133136
-
The gene coding for PGC-1alpha modifies age at onset in Huntington's disease. P Weydt SM Soyal C Gellera S Didonato C Weidinger H Oberkofler GB Landwehrmeyer W Patsch, Mol Neurodegener 2009 4 3 10.1186/1750-1326-4-3 19133136
-
(2009)
Mol Neurodegener
, vol.4
, pp. 3
-
-
Weydt, P.1
Soyal, S.M.2
Gellera, C.3
Didonato, S.4
Weidinger, C.5
Oberkofler, H.6
Landwehrmeyer, G.B.7
Patsch, W.8
-
13
-
-
77951256226
-
Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease
-
Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease. L Arning A Haghikia E Taherzadeh-Fard C Saft J Andrich B Pula S Höxtermann S Wieczorek DA Akkad M Perrech R Gold JT Epplen A Chan, J Mol Med 2010 4 431 436
-
(2010)
J Mol Med
, vol.4
, pp. 431-436
-
-
Arning, L.1
Haghikia, A.2
Taherzadeh-Fard, E.3
Saft, C.4
Andrich, J.5
Pula, B.6
Höxtermann, S.7
Wieczorek, S.8
Akkad, D.A.9
Perrech, M.10
Gold, R.11
Epplen, J.T.12
Chan, A.13
-
14
-
-
78650865385
-
Localization of sequence variations in PGC-1 influence their modifying effect in Huntington disease
-
10.1186/1750-1326-6-1. 21211002
-
Localization of sequence variations in PGC-1 influence their modifying effect in Huntington disease. HV Che S Metzger E Portal C Deyle O Riess HP Nguyen, Mol Neurodegener 2011 6 1 10.1186/1750-1326-6-1 21211002
-
(2011)
Mol Neurodegener
, vol.6
, pp. 1
-
-
Che, H.V.1
Metzger, S.2
Portal, E.3
Deyle, C.4
Riess, O.5
Nguyen, H.P.6
-
15
-
-
77958020160
-
The role of PGC-1 in the pathogenesis of neurodegenerative disorders
-
The role of PGC-1 in the pathogenesis of neurodegenerative disorders. K Rána-Vörös P Weydt, Curr Drug Targets 2010 10 1262 1269
-
(2010)
Curr Drug Targets
, vol.10
, pp. 1262-1269
-
-
Rána-Vörös, K.1
Weydt, P.2
-
16
-
-
5344252327
-
Defects in adaptive energy metabolism with CNS-linked hyperactivity in PGC-1α null mice
-
DOI 10.1016/j.cell.2004.09.013, PII S0092867404008864
-
Defects in adaptive energy metabolism with CNS-linked hyperactivity in PGC-1alpha null mice. J Lin PH Wu PT Tarr KS Lindenberg J St-Pierre CY Zhang VK Mootha S Jäger CR Vianna RM Reznick,, et al. Cell 2004 119 121 135 10.1016/j.cell.2004.09.013 15454086 (Pubitemid 39349325)
-
(2004)
Cell
, vol.119
, Issue.1
, pp. 121-135
-
-
Lin, J.1
Wu, P.-H.2
Tarr, P.T.3
Lindenberg, K.S.4
St-Pierre, J.5
Zhang, C.-Y.6
Mootha, V.K.7
Jager, S.8
Vianna, C.R.9
Reznick, R.M.10
Cui, L.11
Manieri, M.12
Donovan, M.X.13
Wu, Z.14
Cooper, M.P.15
Fan, M.C.16
Rohas, L.M.17
Zavacki, A.M.18
Cinti, S.19
Shulman, G.I.20
Lowell, B.B.21
Krainc, D.22
Spiegelman, B.M.23
more..
-
17
-
-
21144446106
-
PGC-1alpha deficiency causes multi-system energy metabolic derangements: Muscle dysfunction, abnormal weight control and hepatic steatosis
-
PGC-1alpha deficiency causes multi-system energy metabolic derangements: muscle dysfunction, abnormal weight control and hepatic steatosis. TC Leone JJ Lehman BN Finck PJ Schaeffer AR Wende S Boudina M Courtois DF Wozniak N Sambandam C Bernal-Mizrachi,, et al. PLoS Biol 2005 4 101
-
(2005)
PLoS Biol
, vol.4
, pp. 101
-
-
Leone, T.C.1
Lehman, J.J.2
Finck, B.N.3
Schaeffer, P.J.4
Wende, A.R.5
Boudina, S.6
Courtois, M.7
Wozniak, D.F.8
Sambandam, N.9
Bernal-Mizrachi, C.10
-
18
-
-
33749042331
-
Transcriptional repression of PGC-1α by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration
-
DOI 10.1016/j.cell.2006.09.015, PII S0092867406012050
-
Transcriptional repression of PGC-1α by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration. L Cui H Jeong F Borovecki CN Parkhurst N Tanese D Krainc, Cell 2006 127 59 69 10.1016/j.cell.2006.09.015 17018277 (Pubitemid 44466642)
-
(2006)
Cell
, vol.127
, Issue.1
, pp. 59-69
-
-
Cui, L.1
Jeong, H.2
Borovecki, F.3
Parkhurst, C.N.4
Tanese, N.5
Krainc, D.6
-
19
-
-
33750437278
-
Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1α in Huntington's disease neurodegeneration
-
DOI 10.1016/j.cmet.2006.10.004, PII S1550413106003329
-
Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1alpha in Huntington's disease neurodegeneration. P Weydt VV Pineda AE Torrence RT Libby TF Satterfield ER Lazarowski ML Gilbert GJ Morton TK Bammler AD Strand,, et al. Cell Metab 2006 4 349 362 10.1016/j.cmet.2006.10. 004 17055784 (Pubitemid 44645069)
-
(2006)
Cell Metabolism
, vol.4
, Issue.5
, pp. 349-362
-
-
Weydt, P.1
Pineda, V.V.2
Torrence, A.E.3
Libby, R.T.4
Satterfield, T.F.5
Lazarowski, EduardoR.6
Gilbert, M.L.7
Morton, G.J.8
Bammler, T.K.9
Strand, A.D.10
Cui, L.11
Beyer, R.P.12
Easley, C.N.13
Smith, A.C.14
Krainc, D.15
Luquet, S.16
Sweet, IanR.17
Schwartz, M.W.18
La Spada, A.R.19
-
20
-
-
67650061723
-
Impaired PGC-1alpha function in muscle in Huntington's disease
-
Impaired PGC-1alpha function in muscle in Huntington's disease. RK Chaturvedi P Adhihetty S Shukla T Hennessy N Calingasan L Yang A Starkov M Kiaei M Cannella J Sassone A Ciammola F Squitieri MF Beal, Hum Mol Genet 2009 16 3048 3065
-
(2009)
Hum Mol Genet
, vol.16
, pp. 3048-3065
-
-
Chaturvedi, R.K.1
Adhihetty, P.2
Shukla, S.3
Hennessy, T.4
Calingasan, N.5
Yang, L.6
Starkov, A.7
Kiaei, M.8
Cannella, M.9
Sassone, J.10
Ciammola, A.11
Squitieri, F.12
Beal, M.F.13
-
21
-
-
77955017449
-
Impairment of PGC-1alpha expression, neuropathology and hepatic steatosis in a transgenic mouse model of Huntington's disease following chronic energy deprivation
-
Impairment of PGC-1alpha expression, neuropathology and hepatic steatosis in a transgenic mouse model of Huntington's disease following chronic energy deprivation. RK Chaturvedi NY Calingasan L Yang T Hennessey A Johri MF Beal, Hum Mol Genet 2010 16 3190 3205
-
(2010)
Hum Mol Genet
, vol.16
, pp. 3190-3205
-
-
Chaturvedi, R.K.1
Calingasan, N.Y.2
Yang, L.3
Hennessey, T.4
Johri, A.5
Beal, M.F.6
-
22
-
-
77955660387
-
Resveratrol protects against peripheral deficits in a mouse model of Huntington's disease
-
Resveratrol protects against peripheral deficits in a mouse model of Huntington's disease. DJ Ho NY Calingasan E Wille M Dumont MF Beal, Exp Neurol 2010 1 74 84
-
(2010)
Exp Neurol
, vol.1
, pp. 74-84
-
-
Ho, D.J.1
Calingasan, N.Y.2
Wille, E.3
Dumont, M.4
Beal, M.F.5
-
23
-
-
0037036115
-
Nuclear activators and coactivators in mammalian mitochondrial biogenesis
-
DOI 10.1016/S0167-4781(02)00343-3, PII S0167478102003433
-
Nuclear activators and coactivators in mammalian mitochondrial biogenesis. RC Scarpulla, Biochim Biophys Acta 2002 1-2 1 14 (Pubitemid 34597079)
-
(2002)
Biochimica et Biophysica Acta - Gene Structure and Expression
, vol.1576
, Issue.1-2
, pp. 1-14
-
-
Scarpulla, R.C.1
-
24
-
-
79959357562
-
Metabolic control of mitochondrial biogenesis through the PGC-1 family regulatory network
-
Metabolic control of mitochondrial biogenesis through the PGC-1 family regulatory network. RC Scarpulla, Biochim Biophys Acta 2010
-
(2010)
Biochim Biophys Acta
-
-
Scarpulla, R.C.1
-
25
-
-
1542373685
-
Transcriptional regulatory circuits controlling mitochondrial biogenesis and function
-
DOI 10.1101/gad.1177604
-
Transcriptional regulatory circuits controlling mitochondrial biogenesis and function. DP Kelly RC Scarpulla, Genes Dev 2004 4 357 368 (Pubitemid 38316342)
-
(2004)
Genes and Development
, vol.18
, Issue.4
, pp. 357-368
-
-
Kelly, D.P.1
Scarpulla, R.C.2
-
26
-
-
33847635184
-
NRF-2 transcription factor is required for human TOMM20 gene expression
-
DOI 10.1016/j.gene.2006.12.024, PII S037811190700008X
-
NRF-2 transcription factor is required for human TOMM20 gene expression. JR Blesa JA Prieto-Ruiz JM Hernndez J Hernndez-Yago, Gene 2007 1-2 198 208 (Pubitemid 46356798)
-
(2007)
Gene
, vol.391
, Issue.1-2
, pp. 198-208
-
-
Blesa, J.R.1
Prieto-Ruiz, J.A.2
Hernandez, J.M.3
Hernandez-Yago, J.4
-
27
-
-
0037407143
-
Quantitative analysis of circulating mitochondrial DNA in plasma
-
DOI 10.1373/49.5.719
-
Quantitative analysis of circulating mitochondrial DNA in plasma. RW Chiu LY Chan NY Lam NB Tsui EK Ng TH Rainer YM Lo, Clin Chem 2003 5 719 726 (Pubitemid 36513249)
-
(2003)
Clinical Chemistry
, vol.49
, Issue.5
, pp. 719-726
-
-
Chiu, R.W.K.1
Chan, L.Y.S.2
Lam, N.Y.L.3
Tsui, N.B.Y.4
Ng, E.K.O.5
Rainer, T.H.6
Lo, Y.M.D.7
-
28
-
-
0033837739
-
Physical activity as a metabolic stressor
-
Physical activity as a metabolic stressor. EF Coyle, Am J Clin Nutr 2000 72 512S 520S 10919953 (Pubitemid 30650049)
-
(2000)
American Journal of Clinical Nutrition
, vol.72
, Issue.2 SUPPL.
-
-
Coyle, E.F.1
-
29
-
-
43949120748
-
NRF-1 genotypes and endurance exercise capacity in young Chinese men
-
DOI 10.1136/bjsm.2007.042945
-
NRF-1 genotypes and endurance exercise capacity in young Chinese men. Z He Y Hu L Feng Y Li G Liu Y Xi L Wen A Lucia, Br J Sports Med 2008 5 361 366 (Pubitemid 351702683)
-
(2008)
British Journal of Sports Medicine
, vol.42
, Issue.5
, pp. 361-366
-
-
He, Z.1
Hu, Y.2
Feng, L.3
Li, Y.4
Liu, G.5
Xi, Y.6
Wen, L.7
Lucia, A.8
-
30
-
-
21644444035
-
PPARGC1A genotype (Gly482Ser) predicts exceptional endurance capacity in European men
-
DOI 10.1152/japplphysiol.00037.2005
-
PPARGC1A genotype (Gly482Ser) predicts exceptional endurance capacity in European men. A Lucia F Gámez-Gallego I Barroso M Rabadn F Bandrés AF San Juan JL Chicharro U Ekelund S Brage CP Earnest,, et al. J Appl Physiol 2005 1 344 348 (Pubitemid 40934501)
-
(2005)
Journal of Applied Physiology
, vol.99
, Issue.1
, pp. 344-348
-
-
Lucia, A.1
Gomez-Gallego, F.2
Barroso, I.3
Rabadan, M.4
Bandres, F.5
San Juan, A.F.6
Chicharro, J.L.7
Ekelund, U.8
Brage, S.9
Earnest, C.P.10
Wareham, N.J.11
Franks, P.W.12
-
31
-
-
23644445367
-
Mitochondrial DNA and ACTN3 genotypes in Finnish elite endurance and sprint athletes
-
DOI 10.1038/sj.ejhg.5201438
-
Mitochondrial DNA and ACTN3 genotypes in Finnish elite endurance and sprint athletes. AK Niemi K Majamaa, Eur J Hum Genet 2005 13 965 969 10.1038/sj.ejhg.5201438 15886711 (Pubitemid 41131745)
-
(2005)
European Journal of Human Genetics
, vol.13
, Issue.8
, pp. 965-969
-
-
Niemi, A.-K.1
Majamaa, K.2
-
32
-
-
34548154271
-
Mitochondrial haplogroup T is negatively associated with the status of elite endurance athlete
-
DOI 10.1016/j.mito.2007.06.002, PII S1567724907001134
-
Mitochondrial haplogroup T is negatively associated with the status of elite endurance athlete. MG Castro N Terrados JR Reguero V Alvarez E Coto, Mitochondrion 2007 7 354 357 10.1016/j.mito.2007.06.002 17660050 (Pubitemid 47307255)
-
(2007)
Mitochondrion
, vol.7
, Issue.5
, pp. 354-357
-
-
Castro, M.G.1
Terrados, N.2
Reguero, J.R.3
Alvarez, V.4
Coto, E.5
-
33
-
-
34249852535
-
Genetic variations in PPARD and PPARGC1A determine mitochondrial function and change in aerobic physical fitness and insulin sensitivity during lifestyle intervention
-
DOI 10.1210/jc.2006-1785
-
Genetic variations in PPARD and PPARGC1A determine mitochondrial function and change in aerobic physical fitness and insulin sensitivity during lifestyle intervention. N Stefan C Thamer H Staiger F Machicao J Machann F Schick C Venter A Niess M Laakso A Fritsche,, et al. J Clin Endocrinol Metab 2007 92 1827 1833 10.1210/jc.2006-1785 17327385 (Pubitemid 46997196)
-
(2007)
Journal of Clinical Endocrinology and Metabolism
, vol.92
, Issue.5
, pp. 1827-1833
-
-
Stefan, N.1
Thamer, C.2
Staiger, H.3
Machicao, F.4
Machann, J.5
Schick, F.6
Venter, C.7
Niess, A.8
Laakso, M.9
Fritsche, A.10
Haring, H.-U.11
-
34
-
-
77951742677
-
Association of mitochondrial transcription factor (TFAM) gene polymorphism with physical performance in athletes
-
10.1134/S0362119710020155
-
Association of mitochondrial transcription factor (TFAM) gene polymorphism with physical performance in athletes. II Ahmetov DV Popov SS Missina OL Vinogradova VA Rogozkin, Human Physiology 2010 36 229 233 10.1134/S0362119710020155
-
(2010)
Human Physiology
, vol.36
, pp. 229-233
-
-
Ahmetov, I.I.1
Popov, D.V.2
Missina, S.S.3
Vinogradova, O.L.4
Rogozkin, V.A.5
-
35
-
-
68649109608
-
The biology of PGC-1alpha and its therapeutic potential
-
The biology of PGC-1alpha and its therapeutic potential. C Handschin, Trends Pharmacol Sci 2009 6 322 329
-
(2009)
Trends Pharmacol Sci
, vol.6
, pp. 322-329
-
-
Handschin, C.1
-
36
-
-
35348969404
-
Targeting PGC-1α to control energy homeostasis
-
DOI 10.1517/14728222.11.10.1329
-
Targeting PGC-1 alpha to control energy homeostasis. Z Wu O Boss, Expert Opin Ther Targets 2007 10 1329 1338 (Pubitemid 47604072)
-
(2007)
Expert Opinion on Therapeutic Targets
, vol.11
, Issue.10
, pp. 1329-1338
-
-
Wu, Z.1
Boss, O.2
-
37
-
-
2542495951
-
New genomic region for Wegener's granulomatosis as revealed by an extended association screen with 202 apoptosis-related genes
-
DOI 10.1007/s00439-004-1092-z
-
New genomic region for Wegener's granulomatosis as revealed by an extended association screen with 202 apoptosis-related genes. P Jagiello M Gencik L Arning S Wieczorek E Kunstmann E Csernok WL Gross JT Epplen, Hum Genet 2004 5 468 477 (Pubitemid 38678925)
-
(2004)
Human Genetics
, vol.114
, Issue.5
, pp. 468-477
-
-
Jagiello, P.1
Gencik, M.2
Arning, L.3
Wieczorek, S.4
Kunstmann, E.5
Csernok, E.6
Gross, W.L.7
Epplen, J.T.8
-
38
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
DOI 10.1126/science.1069424
-
The structure of haplotype blocks in the human genome. SB Gabriel SF Schaffner H Nguyen JM Moore J Roy B Blumenstiel J Higgins M DeFelice A Lochner M Faggart,, et al. Science 2002 296 2225 2229 10.1126/science.1069424 12029063 (Pubitemid 34680308)
-
(2002)
Science
, vol.296
, Issue.5576
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
DeFelice, M.8
Lochner, A.9
Faggart, M.10
Liu-Cordero, S.N.11
Rotimi, C.12
Adeyemo, A.13
Cooper, R.14
Ward, R.15
Lander, E.S.16
Daly, M.J.17
Altshuler, D.18
-
39
-
-
34548703847
-
NRF2 genotype improves endurance capacity in response to training
-
DOI 10.1055/s-2007-964913
-
NRF2 genotype improves endurance capacity in response to training. Z He Y Hu L Feng Y Lu G Liu Y Xi L Wen LR McNaughton, Int J Sports Med 2007 9 717 721 (Pubitemid 47414159)
-
(2007)
International Journal of Sports Medicine
, vol.28
, Issue.9
, pp. 717-721
-
-
He, Z.1
Hu, Y.2
Feng, L.3
Lu, Y.4
Liu, C.5
Xi, Y.6
Wen, L.7
McNaughton, L.R.8
-
40
-
-
34948846024
-
SIRT1 gene, age-related diseases, and mortality: The Leiden 85-plus study
-
SIRT1 gene, age-related diseases, and mortality: the Leiden 85-plus study. M Kuningas M Putters RG Westendorp PE Slagboom D van Heemst, J Gerontol A Biol Sci Med Sci 2007 9 960 965 (Pubitemid 47531211)
-
(2007)
Journals of Gerontology - Series A Biological Sciences and Medical Sciences
, vol.62
, Issue.9
, pp. 960-965
-
-
Kuningas, M.1
Putters, M.2
Westendorp, R.G.J.3
Slagboom, P.E.4
Van Heemst, D.5
|