Jean Feunteun

Prof. Jean Feunteun

orcid

Research Focus & Metrics

Academic Career Length

58Years (1969-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
30 September 1994 in Science
Verified
Journal Article
Closed access
PDF file
RWRichard Wooster
Richard Wooster
SNSusan L. Neuhausen
Susan L. Neuhausen
JMJonathan Mangion
Jonathan Mangion
YQYvette Quirk
Yvette Quirk
DFDeborah Ford
Deborah Ford
AEAl. Et
Al. Et
A small proportion of breast cancer, in particular those cases arising at a young age, is due to the inheritance of dominant susceptibility genes conferring a high risk of the disease. A genomic linkage search was performed with 15 high-risk breast cancer families that were unlinked to the BRCA1 locus on chromosome 17q21. This analysis localized a second breast cancer susceptibility locus, BRCA2 , to a 6-centimorgan interval on chromosome 13q12-13. Preliminary evidence suggests that BRCA2 confers a high risk of breast cancer but, unlike BRCA1 , does not confer a substantially elevated risk of ovarian cancer.

1 January 1997 in Cell
Verified
Journal Article
Open access
RSRalph Scully
Ralph Scully
JCJunjie Chen
Junjie Chen
APAnnemieke Plug
Annemieke Plug
YXYonghong Xiao
Yonghong Xiao
DWDavid Weaver
David Weaver
DLDavid M Livingston
David M Livingston
BRCA1 immunostaining reveals discrete, nuclear foci during S phase of the cell cycle. Human Rad51, a homolog of bacterial RecA, behaves similarly. The two proteins were found to colocalize in vivo and to coimmunoprecipitate. BRCA1 residues 758-1064 alone formed Rad51-containing complexes in vitro. Rad51 is also specifically associated with developing synaptonemal complexes in meiotic cells, and BRCA1 and Rad51 were both detected on asynapsed (axial) elements of human synaptonemal complexes. These findings suggest a functional interaction between BRCA1 and Rad51 in the meiotic and mitotic cell cycles, which, in turn, suggests a role for BRCA1 in the control of recombination and of genome integrity.

1 August 1997 in Cell
Verified
Journal Article
Closed access
RSRalph Scully
Ralph Scully
JCJunjie Chen
Junjie Chen
RORobert L Ochs
Robert L Ochs
KKKathleen Keegan
Kathleen Keegan
MHMerl Hoekstra
Merl Hoekstra
DLDavid M Livingston
David M Livingston

1 November 1998 in Nature Genetics
Verified
Journal Article
Closed access
PDF file
FQFrédérique Quignon
Frédérique Quignon
FBFrédéric De Bels
Frédéric De Bels
MKMarcel H.M. Koken
Marcel H.M. Koken
JFJean Feunteun
Jean Feunteun
JAJean-Claude Ameisen
Jean-Claude Ameisen
HTHugues de Thé
Hugues de Thé

1 January 2001 in Journal of Medical Genetics
Verified
Journal Article
Open access
PDF file
ACAgnès Chompret
Agnès Chompret
AAAnne Abel
Anne Abel
DSDominique Stoppa-Lyonnet
Dominique Stoppa-Lyonnet
LBLaurence Brugières
Laurence Brugières
SPSabine Pagès
Sabine Pagès
CBCatherine Bonaïti-Pellié
Catherine Bonaïti-Pellié

18 December 2008 in New England Journal of Medicine
Verified
Journal Article
Open access
PDF file
CLCharline Ladroue
Charline Ladroue
RCRomain Carcenac
Romain Carcenac
MLMichel Leporrier
Michel Leporrier
SGSophie Gad
Sophie Gad
CHClaire Le Hello
Claire Le Hello
BGBetty Gardie
Betty Gardie
Prolyl hydroxylase domain (PHD) proteins play a major role in regulating the hypoxia-inducible factor (HIF) that induces expression of genes involved in angiogenesis, erythropoiesis, and cell metabolism, proliferation, and survival. Germ-line mutations in the prolyl hydroxylase domain 2 gene (PHD2) have been reported in patients with familial erythrocytosis but not in association with tumors. We describe a patient with erythrocytosis and recurrent paraganglioma who carries a newly discovered PHD2 mutation. This mutation affects PHD2 function and stabilizes HIF-α proteins. In addition, we demonstrate loss of heterozygosity of PHD2 in the tumor, suggesting that PHD2 could be a tumor-suppressor gene.