Related references
Note: Only part of the references are listed.HES1 is a novel interactor of the Fanconi anemia core complex
Cedric S. Tremblay et al.
BLOOD (2008)
FANCM of the Fanconi anemia core complex is required for both monoubiquitination and DNA repair
Yutong Xue et al.
HUMAN MOLECULAR GENETICS (2008)
Control of the reversibility of cellular quiescence by the transcriptional repressor HES1
Liyun Sang et al.
SCIENCE (2008)
Notch activation is associated with tetraploidy and enhanced chromosomal instability in meningiomas
Gilson Baia et al.
NEOPLASIA (2008)
Neurological defects in trichothiodystrophy reveal a coactivator function of TFIIH
Emmanuel Compe et al.
NATURE NEUROSCIENCE (2007)
Endocrine abnormalities in patients with fanconi anemia
Neelam Giri et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2007)
FANCI is a second monoubiquitinated member of the Fanconi anemia pathway
Ashley E. Sims et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2007)
Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair
Agata Smogorzewska et al.
CELL (2007)
The Hes gene family: repressors and oscillators that orchestrate embryogenesis
Ryoichiro Kageyama et al.
DEVELOPMENT (2007)
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2
Bing Xia et al.
NATURE GENETICS (2007)
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
Sarah Reid et al.
NATURE GENETICS (2007)
Tetraploidy, aneuploidy and cancer
Neil J. Ganem et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2007)
Hes6 inhibits astrocyte differentiation and promotes neurogenesis through different mechanisms
Sumit Jhas et al.
JOURNAL OF NEUROSCIENCE (2006)
Hrt and Hes negatively regulate Notch signaling through interactions with RBP-Jκ
Isabelle N. King et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
CSL: A notch above the rest
SE Pursglove et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2005)
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
O Levran et al.
NATURE GENETICS (2005)
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M
AR Meetei et al.
NATURE GENETICS (2005)
The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway
G Mosedale et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2005)
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J
M Levitus et al.
NATURE GENETICS (2005)
The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair
WL Bridge et al.
NATURE GENETICS (2005)
Regulation of the Fanconi anemia group C protein through proteolytic modification
I Brodeur et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Activating the PARP-1 sensor component of the Groucho/TLE1 corepressor complex mediates a CaMKinase IIδ-dependent neurogenic gene activation pathway
BG Ju et al.
CELL (2004)
X-linked inheritance of Fanconi anemia complementation group B
AR Meetei et al.
NATURE GENETICS (2004)
A novel ubiquitin ligase is deficient in Fanconi anemia
AR Meetei et al.
NATURE GENETICS (2003)
Hes6 promotes cortical neurogenesis and inhibits Hes1 transcription repression activity by multiple mechanisms
MO Gratton et al.
MOLECULAR AND CELLULAR BIOLOGY (2003)
Presenilin-1 is indirectly implicated in Notch1 cleavage
C Godin et al.
NEUROREPORT (2003)
Presenilin-1 interacts directly with the β-site amyloid protein precursor cleaving enzyme (BACE1)
SS Hébert et al.
NEUROBIOLOGY OF DISEASE (2003)
HES and HERP families: Multiple effectors of the Notch signaling pathway
T Iso et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2003)
Biallelic inactivation of BRCA2 in Fanconi anemia
NG Howlett et al.
SCIENCE (2002)
Overexpression of the Notch target genes Hes in vivo induces lymphoid and myeloid alterations
S Kawamata et al.
ONCOGENE (2002)
XPD mutations prevent TFIIH-dependent transactivation by nuclear receptors and phosphorylation of RARα
A Keriel et al.
CELL (2002)
Role of Smad1 and Smad4 proteins in the induction of p21(WAF1,Cip1) during bone morphogenetic protein-induced growth arrest in human breast cancer cells
F Pouliot et al.
JOURNAL OF ENDOCRINOLOGY (2002)
Functional correction of FA-C cells with FANCC suppresses the expression of interferon γ-inducible genes
SR Fagerlie et al.
BLOOD (2001)
Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry
MP Wajnrajch et al.
PEDIATRICS (2001)
Notch pathway: Making sense of suppressor of hairless
S Bray et al.
CURRENT BIOLOGY (2001)
Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway
AL Medhurst et al.
HUMAN MOLECULAR GENETICS (2001)
Positional cloning of a novel fanconi anemia gene, FANCD2
C Timmers et al.
MOLECULAR CELL (2001)
Association with the nuclear matrix and interaction with Groucho and RUNX proteins regulate the transcription repression activity of the basic helix loop helix factor Hes1
FW McLarrent et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Requirement for presenilin 1 in facilitating lagged 2-mediated endoproteolysis and signaling of notch 1
JL Martys-Zage et al.
JOURNAL OF MOLECULAR NEUROSCIENCE (2000)
Isolation of a cDNA representing the Fanconi anemia complementation group E gene
JP de Winter et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG
JP de Winter et al.
HUMAN MOLECULAR GENETICS (2000)
The genetics of Fanconi's anaemia
I Dokal
BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY (2000)
HES-1 repression of differentiation and proliferation in PC12 cells: Role for the helix 3-helix 4 domain in transcription repression
P Castella et al.
MOLECULAR AND CELLULAR BIOLOGY (2000)
The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM
JP de Winter et al.
NATURE GENETICS (2000)