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23篇 您的检索式：作者名="Caburet"

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	题名	作者	年代	出处	被引量
1	The identification and characterization of a foxl2 response element provides insights into the pathogenesis of mutant alleles 显示文摘	Benayoun BA Caburet S Dipietromaria A	2008	Hum Mol Genet2008，17，20：	1
2	Forkhead transcription factors: key players in health and disease 显示文摘	Benayoun BA Caburet S Veitia RA	2011	Trends Genet2011，27，6：	1
3	Forkhead transcription factors:key players in health and disease显示文摘	Benayoun BA Caburet S Veitia RA		0，，：	1
4	The transcription factorF0XL2 : at the crossroads of ovarian physiology and pathology 显示文摘	Caburet S Georges A L Hote D	2012	Mol Cell Endocrinol2012，356，12：	1
5	A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation显示文摘	CABURET S DEMAREZ A MOUMNE L	2004	J Med Genet2004，41，：	1
6	A recurrent polyalanine expansion in the transcription factor foxl2 induces extensive nuclear and cytoplasmic protein aggregation 显示文摘	Caburet S Demarez A Moumne L	2004	J Med Genet2004，41，12：	1
7	Forkhead transcription factors:key players in health and disease显示文摘	Benayoun BA Caburet S Veitia RA	2011	Trends Genet2011，27，6：	1
8	Forkhead transcription factors: key players in health and disease显示文摘	Benayoun B A Caburet S eitia R A	2011	Trends Genet2011，27，6：	1
9	The posttranslational modification profile of the forkhead transcription factor FOXL2 suggests the existence of parallel processive/concerted modifica- tion parhways 显示文摘	Benayoun B A Auer J Caburet S	2008	Proteomics2008，8，15：	1
10	Mutant eohesin in premature ovarian failure显示文摘	Caburet S Arboleda VA Llano E	2014	N Engl J Med2014，370，10：	1
11	Premature ovarian failure and forkhead transcription factor FOXL2 : blepharophimosis- ptosis-epicanthus inversus syndrome and ovarian dysfunction 显示文摘	DE BAERE E ICOPELLI S CABURET S	2005	Pediatr Endocrinol Rev2005，2，：	1
12	The transcription factor FOXL2: At the crossroads of ovarian physiology and pathology 显示文摘	Caburet S Georges A L'hote D	2012	Mol Cell Endocrinol2012，356，12：	1
13	Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial premature ovarian failure 显示文摘	Caburet S Zavadakova P Ben-Neriah Z	2012	PloS one2012，7，33：	1
14	Eucaryotic genome evolution through the spontaneous duplication of large chromosomal segments显示文摘	Koszul R Caburet S Dujon B	2004	The EMBO Journal2004，23，1：	1
15	A reverse polymerase chain reaction method for detection of human cytomegalovirus late transcripts in cells infected in vitro显示文摘	Gozlan J Caburet F Tamcrede C	1992	J Virol Method1992，40，：	1
16	Genome- wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromicfamilial Premature Ovarian Failure 显示文摘	Caburet S Zavadakova P Ben-Neriah Z	2012	PLoS 0ne2012，7，33：	1
17	Premature ovarian failure and forkhead transcription factor FOXL2 : blepharophimosisptosis-epicanthus inversus syndrome and ovarian dysfunction 显示文摘	Caburet S Laissue P Beysen D	2005	Pediatr Endocrinol Rev2005，2，4：	1
18	Forkhead transcription factors: key players in health and disease 显示文摘	Benayoun BA Caburet S Veitia RA	2011	Trends Genet2011，27，6：	1
19	The identification and characterization of a FOXL2 re- sponse element provides insights into the pathogene- sis of mutant alleles显示文摘	Benayoun B A Caburet S Dipietromaria A	2008	Hum Mol Genet2008，17，：	1
20	Generic binding sites, generic DNA-binding domains: Where does specific promoter recognition come from 显示文摘	Georges A B Benayoun B A Caburet S	2009	FASEB2009，24，：	1

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