-
1
-
-
8744279211
-
Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalities
-
DOI 10.1210/jc.2003-031658
-
MC Vantyghem P Pigny CA Maurage N Rouaix-Emery T Stojkovic JM Cuisset A Millaire O Lascols P Vermersch JL Wemeau, et al. 2004 Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalities J Clin Endocrinol Metab 89 5337 5346 10.1210/jc.2003-031658 1:CAS:528:DC%2BD2cXhtVSisb%2FM 15531479 (Pubitemid 39518406)
-
(2004)
Journal of Clinical Endocrinology and Metabolism
, vol.89
, Issue.11
, pp. 5337-5346
-
-
Vantyghem, M.C.1
Pigny, P.2
Maurage, C.A.3
Rouaix-Emery, N.4
Stojkovic, T.5
Cuisset, J.M.6
Millaire, A.7
Lascols, O.8
Vermersch, P.9
Wemeau, J.L.10
Capeau, J.11
Vigouroux, C.12
-
2
-
-
33845286555
-
Human laminopathies: Nuclei gone genetically awry
-
DOI 10.1038/nrg1906, PII NRG1906
-
BC Capell FS Collins 2006 Human laminopathies: nuclei gone genetically awry Nat Rev Genet 7 940 952 10.1038/nrg1906 1:CAS:528:DC%2BD28Xht1KisrzN 17139325 (Pubitemid 44871397)
-
(2006)
Nature Reviews Genetics
, vol.7
, Issue.12
, pp. 940-952
-
-
Capell, B.C.1
Collins, F.S.2
-
3
-
-
32144442169
-
Nuclear lamin A inhibits adipocyte differentiation: Implications for Dunnigan-type familial partial lipodystrophy
-
DOI 10.1093/hmg/ddi480
-
RL Boguslavsky CL Stewart HJ Worman 2006 Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy Hum Mol Genet 15 653 663 10.1093/hmg/ddi480 1:CAS:528: DC%2BD28XhtFaitbc%3D 16415042 (Pubitemid 43205428)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.4
, pp. 653-663
-
-
Boguslavsky, R.L.1
Stewart, C.L.2
Worman, H.J.3
-
4
-
-
0036537888
-
A novel interaction between lamin A and SREBP1: Implications for partial lipodystrophy and other laminopathies
-
10.1093/hmg/11.7.769 1:CAS:528:DC%2BD38Xjt1Grsbo%3D 11929849
-
DJ Lloyd RC Trembath S Shackleton 2002 A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies Hum Mol Genet 11 769 777 10.1093/hmg/11.7.769 1:CAS:528:DC%2BD38Xjt1Grsbo%3D 11929849
-
(2002)
Hum Mol Genet
, vol.11
, pp. 769-777
-
-
Lloyd, D.J.1
Trembath, R.C.2
Shackleton, S.3
-
5
-
-
33847709027
-
SREBP in signal transduction: Cholesterol metabolism and beyond
-
DOI 10.1016/j.ceb.2007.02.004, PII S095506740700018X
-
MT Bengoechea-Alonso J Ericsson 2007 SREBP in signal transduction: cholesterol metabolism and beyond Curr Opin Cell Biol 19 215 222 10.1016/j.ceb.2007.02.004 1:CAS:528:DC%2BD2sXjt1Sksr0%3D 17303406 (Pubitemid 46386402)
-
(2007)
Current Opinion in Cell Biology
, vol.19
, Issue.2
, pp. 215-222
-
-
Bengoechea-Alonso, M.T.1
Ericsson, J.2
-
6
-
-
36649036187
-
Evaluating the association of common LMNA variants with type 2 diabetes and quantitative metabolic phenotypes in French Europids
-
DOI 10.1007/s00125-007-0857-z
-
K Duesing G Charpentier M Marre J Tichet S Hercberg P Froguel F Gibson 2008 Evaluating the association of common LMNA variants with type 2 diabetes and quantitative metabolic phenotypes in French Europids Diabetologia 51 76 81 10.1007/s00125-007-0857-z 1:STN:280:DC%2BD2sjgvFCktg%3D%3D 17994215 (Pubitemid 50002202)
-
(2008)
Diabetologia
, vol.51
, Issue.1
, pp. 76-81
-
-
Duesing, K.1
Charpentier, G.2
Marre, M.3
Tichet, J.4
Hercberg, S.5
Froguel, P.6
Gibson, F.7
-
7
-
-
33847419918
-
Common variation in LMNA increases susceptibility to type 2 diabetes and associates with elevated fasting glycemia and estimates of body fat and height in the general population: Studies of 7,495 Danish whites
-
DOI 10.2337/db06-0927
-
L Wegner G Andersen T Sparso N Grarup C Glümer K Borch-Johnsen T Jørgensen T Hansen O Pedersen 2007 Common variation in LMNA increases susceptibility to type 2 diabetes and associates with elevated fasting glycemia and estimates of body fat and height in the general population: studies of 7,495 Danish whites Diabetes 56 694 698 10.2337/db06-0927 1:CAS:528: DC%2BD2sXis12it7g%3D 17327437 (Pubitemid 46348468)
-
(2007)
Diabetes
, vol.56
, Issue.3
, pp. 694-698
-
-
Wegner, L.1
Andersen, G.2
Sparso, T.3
Grarup, N.4
Glumer, C.5
Borch-Johnsen, K.6
Jorgensen, T.7
Hansen, T.8
Pedersen, O.9
-
8
-
-
4444384648
-
Variation in the lamin A/C gene: Associations with metabolic syndrome
-
DOI 10.1161/01.ATV.0000136384.53705.c9
-
NI Steinle R Kazlauskaite IG Imumorin WC Hsueh TI Pollin JR O'Connell BD Mitchell AR Shuldiner 2004 Variation in the lamin A/C gene: associations with metabolic syndrome Arterioscler Thromb Vasc Biol 24 1708 1713 10.1161/01.ATV.0000136384.53705.c9 1:CAS:528:DC%2BD2cXntVCrtbY%3D 15205219 (Pubitemid 39180899)
-
(2004)
Arteriosclerosis, Thrombosis, and Vascular Biology
, vol.24
, Issue.9
, pp. 1708-1713
-
-
Steinle, N.I.1
Kazlauskaite, R.2
Imumorin, I.G.3
Hsueh, W.-C.4
Pollin, T.I.5
O'Connell, J.R.6
Mitchell, B.D.7
Shuldiner, A.R.8
-
9
-
-
0034729587
-
Genetic variation in LMNA modulates plasma leptin and indices of obesity in aboriginal Canadians
-
1:CAS:528:DC%2BD3cXlt12qs7k%3D 11015599
-
RA Hegele H Cao SB Harris B Zinman AJ Hanley CM Anderson 2000 Genetic variation in LMNA modulates plasma leptin and indices of obesity in aboriginal Canadians Physiol Genomics 3 39 44 1:CAS:528:DC%2BD3cXlt12qs7k%3D 11015599
-
(2000)
Physiol Genomics
, vol.3
, pp. 39-44
-
-
Hegele, R.A.1
Cao, H.2
Harris, S.B.3
Zinman, B.4
Hanley, A.J.5
Anderson, C.M.6
-
10
-
-
24144462222
-
Association of LMNA 1908C/T polymorphism with cerebral vascular disease and diabetic nephropathy in Japanese men with type 2 diabetes
-
DOI 10.1111/j.1365-2265.2005.02344.x
-
H Liang Y Murase Y Katuta A Asano J Kobayashi H Mabuchi 2005 Association of LMNA 1908C/T polymorphism with cerebral vascular disease and diabetic nephropathy in Japanese men with type 2 diabetes Clin Endocrinol 63 317 322 10.1111/j.1365-2265.2005.02344.x 1:CAS:528:DC%2BD2MXhtVyisbzO (Pubitemid 41233450)
-
(2005)
Clinical Endocrinology
, vol.63
, Issue.3
, pp. 317-322
-
-
Liang, H.1
Murase, Y.2
Katuta, Y.3
Asano, A.4
Kobayashi, J.5
Mabuchi, H.6
-
11
-
-
0036344930
-
An LMNA variant is associated with dyslipidemia and insulin resistance in the Japanese
-
10.1053/meta.2002.34030 1:CAS:528:DC%2BD38XlvV2hsLo%3D 12145775
-
Y Murase K Yagi Y Katsuda A Asano J Koizumi H Mabuchi 2002 An LMNA variant is associated with dyslipidemia and insulin resistance in the Japanese Metabolism 51 1017 1021 10.1053/meta.2002.34030 1:CAS:528:DC%2BD38XlvV2hsLo%3D 12145775
-
(2002)
Metabolism
, vol.51
, pp. 1017-1021
-
-
Murase, Y.1
Yagi, K.2
Katsuda, Y.3
Asano, A.4
Koizumi, J.5
Mabuchi, H.6
-
12
-
-
0034974846
-
Common genomic variation in LMNA modulates indexes of obesity in Inuit
-
DOI 10.1210/jc.86.6.2747
-
R Hegele MW Huff TK Young 2001 Common genomic variation in LMNA modulates indexes of obesity in Inuit J Clin Endocrinol Metab 86 2747 2751 10.1210/jc.86.6.2747 1:CAS:528:DC%2BD3MXktlKiu70%3D 11397881 (Pubitemid 32545733)
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, Issue.6
, pp. 2747-2751
-
-
Hegele, R.A.1
Huff, M.W.2
Young, T.K.3
-
13
-
-
0035715144
-
Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21-q23 and is associated with a common polymorphism in LMNA in Pima Indians
-
DOI 10.1006/mgme.2001.3147
-
C Weyer JK Wolford RL Hanson JE Foley PA Tataranni C Bogardus RE Pratley 2001 Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21-q23 and is associated with a common polymorphism in LMNA in Pima Indians Mol Genet Metab 72 231 238 10.1006/mgme.2001.3147 1:CAS:528:DC%2BD3MXhslSnu7k%3D 11243729 (Pubitemid 34171440)
-
(2001)
Molecular Genetics and Metabolism
, vol.72
, Issue.3
, pp. 231-238
-
-
Weyer, C.1
Wolford, J.K.2
Hanson, R.L.3
Foley, J.E.4
Tataranni, P.A.5
Bogardus, C.6
Pratley, R.E.7
-
14
-
-
33847357832
-
Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: Association analyses in 9,518 subjects
-
DOI 10.2337/db06-0930
-
KR Owen CJ Groves RL Hanson WC Knowler AR Shuldiner SC Elbein BD Mitchell P Froguel MC Ng JC Chan, et al. 2007 Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9, 518 subjects Diabetes 56 879 883 10.2337/db06-0930 1:CAS:528:DC%2BD2sXis12iur4%3D 17327460 (Pubitemid 46348473)
-
(2007)
Diabetes
, vol.56
, Issue.3
, pp. 879-883
-
-
Owen, K.R.1
Groves, C.J.2
Hanson, R.L.3
Knowler, W.C.4
Shuldiner, A.R.5
Elbein, S.C.6
Mitchell, B.D.7
Froguel, P.8
Ng, M.C.Y.9
Chan, J.C.10
Jia, W.11
Deloukas, P.12
Hitman, G.A.13
Walker, M.14
Frayling, T.M.15
Hattersley, A.T.16
Zeggini, E.17
McCarthy, M.I.18
-
15
-
-
33847339384
-
Lamin A/C polymorphisms, type 2 diabetes, and the metabolic syndrome: Case-control and quantitative trait studies
-
DOI 10.2337/db06-1055
-
JL Mesa RJ Loos PW Franks KK Ong J Luan S O'Rahilly NJ Wareham I Barroso 2007 Lamin A/C polymorphisms, type 2 diabetes, and the metabolic syndrome: case-control and quantitative trait studies Diabetes 56 884 889 10.2337/db06-1055 1:CAS:528:DC%2BD2sXis12iur8%3D 17327461 (Pubitemid 46348474)
-
(2007)
Diabetes
, vol.56
, Issue.3
, pp. 884-889
-
-
Mesa, J.L.1
Loos, R.J.F.2
Franks, P.W.3
Ong, K.K.4
Luan, J.5
O'Rahilly, S.6
Wareham, N.J.7
Barroso, I.8
-
16
-
-
0034856615
-
Analysis of the Lamin A/C gene as a candidate for Type II diabetes susceptibility in Pima Indians
-
DOI 10.1007/s001250051688
-
JK Wolford RL Hanson C Bogardus M Prochazka 2001 Analysis of the lamin A/C gene as a candidate for type II diabetes susceptibility in Pima Indians Diabetologia 44 779 782 10.1007/s001250051688 1:CAS:528:DC%2BD3MXjs1ylu7Y%3D 11440372 (Pubitemid 32846034)
-
(2001)
Diabetologia
, vol.44
, Issue.6
, pp. 779-782
-
-
Wolford, J.K.1
Hanson, R.L.2
Bogardus, C.3
Prochazka, M.4
-
17
-
-
30844434561
-
Prelamin A, Zmpste24, misshapen cell nuclei, and progeria - New evidence suggesting that protein farnesylation could be important for disease pathogenesis
-
DOI 10.1194/jlr.R500011-JLR200
-
SG Young LG Fong S Michaelis 2005 Prelamin A, Zmpste24, misshapen cell nuclei, and progeria-new evidence suggesting that protein farnesylation could be important for disease pathogenesis J Lipid Res 46 2531 2558 10.1194/jlr.R500011-JLR200 1:CAS:528:DC%2BD2MXhtlWmsLbI 16207929 (Pubitemid 43107466)
-
(2005)
Journal of Lipid Research
, vol.46
, Issue.12
, pp. 2531-2558
-
-
Young, S.G.1
Fong, L.G.2
Michaelis, S.3
-
18
-
-
46249086799
-
Premature aging in mice activates a systemic metabolic response involving autophagy induction
-
DOI 10.1093/hmg/ddn120
-
G Marino AP Ugalde N Salvador-Montoliu I Varela PM Quirós J Cadiñanos I vander Pluijm JM Freije C López-Otín 2008 Premature aging in mice activates a systemic metabolic response involving autophagy induction Hum Mol Genet 17 2196 2211 10.1093/hmg/ddn120 1:CAS:528:DC%2BD1cXnvV2qtrk%3D 18443001 (Pubitemid 351911988)
-
(2008)
Human Molecular Genetics
, vol.17
, Issue.14
, pp. 2196-2211
-
-
Marino, G.1
Ugalde, A.P.2
Salvador-Montoliu, N.3
Varela, I.4
Quiros, P.M.5
Cadinanos, J.6
Van Der Pluijm, I.7
Freije, J.M.P.8
Lopez-Otin, C.9
-
19
-
-
0035937112
-
Isoprenylcysteine carboxyl methyltransferase deficiency in mice
-
10.1074/jbc.C000831200 1:CAS:528:DC%2BD3MXhs1KmtLo%3D 11121396
-
MO Bergo GK Leung P Ambroziak JC Otto PJ Casey AQ Gomes MC Seabra SG Young 2001 Isoprenylcysteine carboxyl methyltransferase deficiency in mice J Biol Chem 276 5841 5845 10.1074/jbc.C000831200 1:CAS:528:DC%2BD3MXhs1KmtLo%3D 11121396
-
(2001)
J Biol Chem
, vol.276
, pp. 5841-5845
-
-
Bergo, M.O.1
Leung, G.K.2
Ambroziak, P.3
Otto, J.C.4
Casey, P.J.5
Gomes, A.Q.6
Seabra, M.C.7
Young, S.G.8
-
20
-
-
24644459728
-
Blocking protein farnesyltransferase improves nuclear shape in fibroblasts from humans with progeroid syndromes
-
DOI 10.1073/pnas.0505767102
-
JI Toth SH Yang X Qiao AP Beigneux MH Gelb CL Moulson JH Miner SG Young LG Fong 2005 Blocking protein farnesyltransferase improves nuclear shape in fibroblasts from humans with progeroid syndromes Proc Natl Acad Sci U S A 102 12873 12878 10.1073/pnas.0505767102 1:CAS:528:DC%2BD2MXhtVWktb7L 16129834 (Pubitemid 41279458)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.36
, pp. 12873-12878
-
-
Toth, J.I.1
Yang, S.H.2
Qiao, X.3
Beigneux, A.P.4
Gelb, M.H.5
Moulson, C.L.6
Miner, J.H.7
Young, S.G.8
Fong, L.G.9
-
21
-
-
9844229896
-
Proposed criteria for the diagnosis of diabetes: Evidence from a French epidemiological study (D.E.S.I.R.)
-
1:STN:280:DyaK1c%2FnvVeqsA%3D%3D 9416436
-
B Balkau E Eschwege J Tichet M Marre 1997 Proposed criteria for the diagnosis of diabetes: evidence from a French epidemiological study (D.E.S.I.R.) Diabetes Metab 23 428 434 1:STN:280:DyaK1c%2FnvVeqsA%3D%3D 9416436
-
(1997)
Diabetes Metab
, vol.23
, pp. 428-434
-
-
Balkau, B.1
Eschwege, E.2
Tichet, J.3
Marre, M.4
-
22
-
-
39849107884
-
Analysis of novel risk loci for type 2 diabetes in a general French population: The D.E.S.I.R. study
-
10.1007/s00109-007-0295-x 1:CAS:528:DC%2BD1cXitlGnuro%3D 18210030
-
S Cauchi C Proença H Choquet S Gaget F De Graeve M Marre B Balkau J Tichet D Meyre M Vaxillaire, et al. 2008 Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study J Mol Med 86 341 348 10.1007/s00109-007-0295-x 1:CAS:528:DC%2BD1cXitlGnuro%3D 18210030
-
(2008)
J Mol Med
, vol.86
, pp. 341-348
-
-
Cauchi, S.1
Proença, C.2
Choquet, H.3
Gaget, S.4
De Graeve, F.5
Marre, M.6
Balkau, B.7
Tichet, J.8
Meyre, D.9
Vaxillaire, M.10
-
23
-
-
27444443876
-
Diagnosis and management of the metabolic syndrome: An American Heart Association/National Heart, Lung, and Blood Institute scientific statement
-
DOI 10.1161/CIRCULATIONAHA.105.169404
-
KRM DJ PJ Savage SC Smith Jr JA Spertus, et al. 2005 Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement Circulation 112 2735 2752 10.1161/CIRCULATIONAHA.105.169404 (Pubitemid 41532612)
-
(2005)
Circulation
, vol.112
, Issue.17
, pp. 2735-2752
-
-
Grundy, S.M.1
Cleeman, J.I.2
Daniels, S.R.3
Donato, K.A.4
Eckel, R.H.5
Franklin, B.A.6
Gordon, D.J.7
Krauss, R.M.8
Savage, P.J.9
Smith Jr., S.C.10
Spertus, J.A.11
Costa, F.12
-
24
-
-
0021813187
-
Homeostasis model assessment: Insulin resistance and β-cell function from fasting plasma glucose and insulin concentrations in man
-
DOI 10.1007/BF00280883
-
D Matthews JP Hosker AS Rudenski BA Naylor DF Treacher RC Turner 1985 Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man Diabetologia 28 412 419 10.1007/BF00280883 1:CAS:528:DyaL2MXlslKnu7k%3D 3899825 (Pubitemid 15018832)
-
(1985)
Diabetologia
, vol.28
, Issue.7
, pp. 412-419
-
-
Matthews, D.R.1
Hosker, J.P.2
Rudenski, A.S.3
-
25
-
-
34447137327
-
Ferritin and transferrin are associated with metabolic syndrome abnormalities and their change over time in a general population: Data from an Epidemiological Study on the Insulin Resistance syndrome (DESIR)
-
DOI 10.2337/dc06-2312
-
IS Vari B Balkau A Kettaneh P Andre J Tichet F Fumeron E Caces M Marre B Grandchamp P Ducimetiere 2007 Ferritin and transferrin are associated with metabolic syndrome abnormalities and their change over time in a general population: Data from an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) Diabetes Care 30 1795 1801 10.2337/dc06-2312 1:CAS:528:DC%2BD2sXotlWhsbY%3D 17416791 (Pubitemid 47036354)
-
(2007)
Diabetes Care
, vol.30
, Issue.7
, pp. 1795-1801
-
-
Vari, I.S.1
Balkau, B.2
Kettaneh, A.3
Andre, P.4
Tichet, J.5
Fumeron, F.6
Caces, E.7
Marre, M.8
Grandchamp, B.9
Ducimetiere, P.10
-
26
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
DOI 10.1093/bioinformatics/bth457
-
JC Barrett B Fry J Maller MJ Daly 2005 Haploview: analysis and visualization of LD and haplotype maps Bioinformatics 21 263 265 10.1093/bioinformatics/bth457 1:CAS:528:DC%2BD2MXkt1WitQ%3D%3D 15297300 (Pubitemid 40202029)
-
(2005)
Bioinformatics
, vol.21
, Issue.2
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
27
-
-
34249662218
-
A new JAVA interface implementation of THESIAS: Testing haplotype effects in association studies
-
DOI 10.1093/bioinformatics/btm058
-
DA Tregouet V Garelle 2007 A new JAVA interface implementation of THESIAS: testing haplotype effects in association studies Bioinformatics 23 1038 1039 10.1093/bioinformatics/btm058 1:CAS:528:DC%2BD2sXmtVKqtbs%3D 17308338 (Pubitemid 47050595)
-
(2007)
Bioinformatics
, vol.23
, Issue.8
, pp. 1038-1039
-
-
Tregouet, D.A.1
Garelle, V.2
-
28
-
-
1642313766
-
A new algorithm for haplotype-based association analysis: The Stochastic-EM algorithm
-
DOI 10.1046/j.1529-8817.2003.00085.x
-
DA Tregouet S Escolano L Tiret A Mallet JL Golmard 2004 A new algorithm for haplotype-based association analysis: the Stochastic-EM algorithm Ann Hum Genet 68 165 77 10.1046/j.1529-8817.2003.00085.x 1:STN:280: DC%2BD2c7hvVOiug%3D%3D 15008795 (Pubitemid 38379847)
-
(2004)
Annals of Human Genetics
, vol.68
, Issue.2
, pp. 165-177
-
-
Tregouet, D.-A.1
Escolano, S.2
Tiret, L.3
Mallet, A.4
Golmard, J.L.5
-
29
-
-
0042024864
-
Automated detection of informative combined effects in genetic association studies of complex traits
-
1:CAS:528:DC%2BD3sXmsVWqtbo%3D 12902385
-
N Tahri-Daizadeh DA Tregouet V Nicaud N Manuel F Cambien L Tiret 2003 Automated detection of informative combined effects in genetic association studies of complex traits Genome Res 13 1952 1960 1:CAS:528:DC%2BD3sXmsVWqtbo%3D 12902385
-
(2003)
Genome Res
, vol.13
, pp. 1952-1960
-
-
Tahri-Daizadeh, N.1
Tregouet, D.A.2
Nicaud, V.3
Manuel, N.4
Cambien, F.5
Tiret, L.6
-
30
-
-
35449001001
-
Polymorphisms in 33 inflammatory genes and risk of myocardial infarction - A system genetics approach
-
DOI 10.1007/s00109-007-0234-x
-
S Barbaux DA Tregouet V Nicaud O Poirier C Perret T Godefroy C Francomme C Combadiere D Arveiler G Luc, et al. 2007 Polymorphisms in 33 inflammatory genes and risk of myocardial infarction-a system genetics approach J Mol Med 85 1271 1280 10.1007/s00109-007-0234-x 1:CAS:528:DC%2BD2sXhtFyrurzF 17634906 (Pubitemid 47622225)
-
(2007)
Journal of Molecular Medicine
, vol.85
, Issue.11
, pp. 1271-1280
-
-
Barbaux, S.1
Tregouet, D.-A.2
Nicaud, V.3
Poirier, O.4
Perret, C.5
Godefroy, T.6
Francomme, C.7
Combadiere, C.8
Arveiler, D.9
Luc, G.10
Ruidavets, J.-B.11
Evans, A.E.12
Kee, F.13
Morrison, C.14
Tiret, L.15
Brand-Herrmann, S.M.16
Cambien, F.17
-
31
-
-
0027257461
-
Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C
-
1:CAS:528:DyaK3sXlsFeiu7g%3D 8344919
-
F Lin HJ Worman 1993 Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C J Biol Chem 268 16321 16326 1:CAS:528:DyaK3sXlsFeiu7g%3D 8344919
-
(1993)
J Biol Chem
, vol.268
, pp. 16321-16326
-
-
Lin, F.1
Worman, H.J.2
-
32
-
-
10044244767
-
Genetic epidemiology and haplotypes
-
DOI 10.1002/gepi.20046
-
DJ Schaid 2004 Genetic epidemiology and haplotypes Genet Epidemiol 27 317 320 10.1002/gepi.20046 15543637 (Pubitemid 39602316)
-
(2004)
Genetic Epidemiology
, vol.27
, Issue.4
, pp. 317-320
-
-
Schaid, D.J.1
-
33
-
-
61349137526
-
-
10.1038/ng.314
-
DA Trégout IR König J Erdmann A Munteanu PS Braund AS Hall A Grosshennig P Linsel-Nitschke C Perret M DeSuremain, et al. 2009 Nat Genet 41 283 285 10.1038/ng.314
-
(2009)
Nat Genet
, vol.41
, pp. 283-285
-
-
Trégout, D.A.1
König, I.R.2
Erdmann, J.3
Munteanu, A.4
Braund, P.S.5
Hall, A.S.6
Grosshennig, A.7
Linsel-Nitschke, P.8
Perret, C.9
Desuremain, M.10
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