Independent association of an APOE gene promoter polymorphism with increased risk of myocardial infarction and decreased APOE plasma concentrations--the ECTIM Study (English)
- New search for: Lambert, Jean-Charles
- New search for: Brousseau, Thierry
- New search for: Defosse, Véronique
- New search for: Evans, Alun
- New search for: Arveiler, Dominique
- New search for: Ruidavets, Jean-Bernard
- New search for: Haas, Bernadette
- New search for: Cambou, Jean-Pierre
- New search for: Luc, Gérald
- New search for: Ducimetière, Pierre
- New search for: Cambien, François
- New search for: Chartier-Harlin, Marie-Christine
- New search for: Amouyel, Philippe
- New search for: Lambert, Jean-Charles
- New search for: Brousseau, Thierry
- New search for: Defosse, Véronique
- New search for: Evans, Alun
- New search for: Arveiler, Dominique
- New search for: Ruidavets, Jean-Bernard
- New search for: Haas, Bernadette
- New search for: Cambou, Jean-Pierre
- New search for: Luc, Gérald
- New search for: Ducimetière, Pierre
- New search for: Cambien, François
- New search for: Chartier-Harlin, Marie-Christine
- New search for: Amouyel, Philippe
In:
Human molecular genetics
;
9
, 1
;
57-
;
2000
- Article (Journal) / Electronic Resource
-
Title:Independent association of an APOE gene promoter polymorphism with increased risk of myocardial infarction and decreased APOE plasma concentrations--the ECTIM Study
-
Contributors:Lambert, Jean-Charles ( author ) / Brousseau, Thierry ( author ) / Defosse, Véronique ( author ) / Evans, Alun ( author ) / Arveiler, Dominique ( author ) / Ruidavets, Jean-Bernard ( author ) / Haas, Bernadette ( author ) / Cambou, Jean-Pierre ( author ) / Luc, Gérald ( author ) / Ducimetière, Pierre ( author )
-
Published in:Human molecular genetics ; 9, 1 ; 57-
-
Publisher:
- New search for: Oxford University Press
-
Publication date:2000-01-01
-
ISSN:
-
DOI:
-
Type of media:Article (Journal)
-
Type of material:Electronic Resource
-
Language:English
-
Source:
Table of contents – Volume 9, Issue 1
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1
-
Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax21Neu +/- mutant micePorteous, Sarah / Torban, Elena / Cho, Nam-Pyo / Cunliffe, Heather / Chua, Lin / McNoe, Les / Ward, Teresa / Souza, Carolina / Gus, Patricia / Giugliani, Roberto et al. | 2000
- 13
-
Expanded polyglutamine peptides alone are intrinsically cytotoxic and cause neurodegeneration in DrosophilaMarsh, J. Lawrence / Walker, Heli / Theisen, Heidi / Zhu, Ya-Zhen / Fielder, Tom / Purcell, Judy / Thompson, Leslie M. et al. | 2000
- 27
-
A frameshift mutation in prominin (mouse)-like 1 causes human retinal degenerationMaw, Marion A. / Corbeil, Denis / Koch, Julia / Hellwig, Andrea / Wilson-Wheeler, Jane C. / Bridges, Robyn J. / Kumaramanickavel, Govindasamy / John, Sheila / Nancarrow, Derek / Röper, Katja et al. | 2000
- 35
-
NF1 microdeletion breakpoints are clustered at flanking repetitive sequencesDorschner, Michael O. / Sybert, Virginia P. / Weaver, Molly / Pletcher, Beth A. / Stephens, Karen et al. | 2000
- 47
-
Subcellular localization and axonal transport of the survival motor neuron (SMN) protein in the developing rat spinal cordPagliardini, Silvia / Giavazzi, Alessio / Setola, Veronica / Lizier, Carlotta / Di Luca, Monica / DeBiasi, Silvia / Battaglia, Giorgio et al. | 2000
- 57
-
Independent association of an APOE gene promoter polymorphism with increased risk of myocardial infarction and decreased APOE plasma concentrations--the ECTIM StudyLambert, Jean-Charles / Brousseau, Thierry / Defosse, Véronique / Evans, Alun / Arveiler, Dominique / Ruidavets, Jean-Bernard / Haas, Bernadette / Cambou, Jean-Pierre / Luc, Gérald / Ducimetière, Pierre et al. | 2000
- 63
-
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing lossLiu, Xue-Zhong / Xia, Xia Juan / Xu, Li Rong / Pandya, Arti / Liang, Chuan Yu / Blanton, Susan H. / Brown, Steve D.M. / Steel, Karen P. / Nance, Walter E. et al. | 2000
- 69
-
Cell cycle arrest enhances the in vitro cellular toxicity of the truncated Machado-Joseph disease gene product with an expanded polyglutamine stretchYoshizawa, Toshihiro / Yamagishi, Yasuaki / Koseki, Naoteru / Goto, Jun / Yoshida, Hideaki / Shibasaki, Futoshi / Shoji, Shinichi / Kanazawa, Ichiro et al. | 2000
- 79
-
The sex-linked fidget mutation abolishes Brn4/Pou3f4 gene expression in the embryonic inner earPhippard, Deborah / Boyd, Yvonne / Reed, Vivienne / Fisher, Graham / Masson, Walter K. / Evans, Edward P. / Saunders, James C. / Crenshaw III, E. Bryan et al. | 2000
- 87
-
Significant evidence for linkage of febrile seizures to chromosome 5q14-q15Nakayama, Junko / Hamano, Kenzo / Iwasaki, Nobuaki / Nakahara, Satoko / Horigome, Yumi / Saitoh, Hisako / Aoki, Takeshi / Maki, Takako / Kikuchi, Masahiro / Migita, Takuo et al. | 2000
- 93
-
CGG/CCG repeats exhibit orientation-dependent instability and orientation-independent fragility in Saccharomyces cerevisiaeBalakumaran, Bala S. / Freudenreich, Catherine H. / Zakian, Virginia A. et al. | 2000
- 101
-
Profound obesity associated with a balanced translocation that disrupts the SIM1 geneHolder, J. Lloyd / Butte, Nancy F. / Zinn, Andrew R. et al. | 2000
- 109
-
Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophyCao, Henian / Hegele, Robert A. et al. | 2000
- 113
-
Molecular structure and evolution of an alpha satellite/non-alpha satellite junction at 16p11Horvath, Juliann E. / Viggiano, Luigi / Loftus, Brendan J. / Adams, Mark D. / Archidiacono, Nicoletta / Rocchi, Mariano / Eichler, Evan E. et al. | 2000
- 125
-
Ser298 of MITF, a mutation site in Waardenburg syndrome type 2, is a phosphorylation site with functional significanceTakeda, Kazuhisa / Takemoto, Clifford / Kobayashi, Ichiro / Watanabe, Atsushi / Nobukuni, Yoshitaka / Fisher, David E. / Tachibana, Masayoshi et al. | 2000
- 133
-
Motoneuronal cell death is not correlated with aggregate formation of androgen receptors containing an elongated polyglutamine tractSimeoni, Silvia / Mancini, Michael A. / Stenoien, David L. / Marcelli, Marco / Weigel, Nancy L. / Zanisi, Mariarosa / Martini, Luciano / Poletti, Angelo et al. | 2000