دنبال کردن
VEITIA Reiner A.
VEITIA Reiner A.
Professor, Université de Paris. Head François Jacob Institute, CEA. Editor In Chief Clinical Genet
ایمیل تأیید شده در ijm.fr - صفحهٔ اصلی
عنوان
نقل شده توسط
نقل شده توسط
سال
Heterosis‏
JA Birchler, H Yao, S Chudalayandi, D Vaiman, RA Veitia‏
The Plant Cell 22 (7), 2105-2112, 2010‏
6722010
Gene balance hypothesis: connecting issues of dosage sensitivity across biological disciplines‏
JA Birchler, RA Veitia‏
Proceedings of the National Academy of Sciences 109 (37), 14746-14753, 2012‏
5802012
The gene balance hypothesis: from classical genetics to modern genomics‏
JA Birchler, RA Veitia‏
The Plant Cell 19 (2), 395-402, 2007‏
4672007
Dosage balance in gene regulation: biological implications‏
JA Birchler, NC Riddle, DL Auger, RA Veitia‏
Trends in Genetics 21 (4), 219-226, 2005‏
4202005
Forkhead transcription factors: key players in health and disease‏
BA Benayoun, S Caburet, RA Veitia‏
Trends in Genetics 27 (6), 224-232, 2011‏
3762011
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure‏
P Laissue, S Christin-Maitre, P Touraine, F Kuttenn, O Ritvos, K Aittomaki, ...‏
European Journal of Endocrinology 154 (5), 739-744, 2006‏
3502006
Evolution and expression of FOXL2‏
J Cocquet, E Pailhoux, F Jaubert, N Servel, X Xia, M Pannetier, ...‏
Journal of medical genetics 39 (12), 916-921, 2002‏
3392002
The gene balance hypothesis: implications for gene regulation, quantitative traits and evolution‏
JA Birchler, RA Veitia‏
New Phytologist 186 (1), 54-62, 2010‏
3372010
Exploring the etiology of haploinsufficiency‏
RA Veitia‏
Bioessays 24 (2), 175-184, 2002‏
3372002
Cellular reactions to gene dosage imbalance: genomic, transcriptomic and proteomic effects‏
RA Veitia, S Bottani, JA Birchler‏
Trends in Genetics 24 (8), 390-397, 2008‏
3312008
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype–phenotype correlation‏
E De Baere, MJ Dixon, KW Small, EW Jabs, BP Leroy, K Devriendt, ...‏
Human molecular genetics 10 (15), 1591-1600, 2001‏
3262001
Mutant cohesin in premature ovarian failure‏
S Caburet, VA Arboleda, E Llano, PA Overbeek, JL Barbero, K Oka, ...‏
New England Journal of Medicine 370 (10), 943-949, 2014‏
3202014
Reverse transcriptase template switching and false alternative transcripts‏
J Cocquet, A Chong, G Zhang, RA Veitia‏
Genomics 88 (1), 127-131, 2006‏
3072006
FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation‏
E De Baere, D Beysen, C Oley, B Lorenz, J Cocquet, P De Sutter, ...‏
The American Journal of Human Genetics 72 (2), 478-487, 2003‏
2942003
The transience of transient overexpression‏
TJ Gibson, M Seiler, RA Veitia‏
Nature methods 10 (8), 715-721, 2013‏
2802013
FOXL2 activates P450 aromatase gene transcription: towards a better characterization of the early steps of mammalian ovarian development‏
M Pannetier, S Fabre, F Batista, A Kocer, L Renault, G Jolivet, ...‏
Journal of molecular endocrinology 36 (3), 399-413, 2006‏
2752006
An evolutionary and functional analysis of FoxL2 in rainbow trout gonad differentiation‏
D Baron, J Cocquet, X Xia, M Fellous, Y Guiguen, RA Veitia‏
Journal of molecular endocrinology 33 (3), 705-715, 2004‏
2412004
Transcription factors: specific DNA binding and specific gene regulation‏
AL Todeschini, A Georges, RA Veitia‏
Trends in genetics 30 (6), 211-219, 2014‏
2242014
FOXL2: a central transcription factor of the ovary‏
A Georges, A Auguste, L Bessiere, A Vanet, AL Todeschini, RA Veitia‏
Journal of molecular endocrinology 52 (1), R17-R33, 2014‏
2012014
Structure, evolution and expression of the FOXL2 transcription unit‏
J Cocquet, E De Baere, M Gareil, M Pannetier, X Xia, M Fellous, RA Veitia‏
Cytogenetic and genome research 101 (3-4), 206-211, 2003‏
1822003
سیستم در حال حاضر قادر به انجام عملکرد نیست. بعداً دوباره امتحان کنید.
مقاله‌ها 1–20