Related references
Note: Only part of the references are listed.Individuals with &ITFANCM&IT biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility
Irene Catucci et al.
GENETICS IN MEDICINE (2018)
Biallelic truncating &ITFANCM&IT mutations cause early-onset cancer but not Fanconi anemia
Massimo Bogliolo et al.
GENETICS IN MEDICINE (2018)
Human foetal ovary shares meiotic preventing factors with the developing testis
Nelly Frydman et al.
HUMAN REPRODUCTION (2017)
Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer
Guido Neidhardt et al.
JAMA ONCOLOGY (2017)
A novel action of follicle-stimulating hormone in the ovary promotes estradiol production without inducing excessive follicular growth before puberty
Charlotte M. Francois et al.
SCIENTIFIC REPORTS (2017)
A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency
F. Fauchereau et al.
CLINICAL GENETICS (2016)
Interplay between Fanconi anemia and homologous recombination pathways in genome integrity
Johanna Michl et al.
EMBO JOURNAL (2016)
Premature Ovarian Insufficiency: New Perspectives on Genetic Cause and Phenotypic Spectrum
Elena J. Tucker et al.
ENDOCRINE REVIEWS (2016)
FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome
Johanna I. Kiiski et al.
INTERNATIONAL JOURNAL OF CANCER (2016)
The Fanconi anaemia pathway: newyplayers and new functions
Raphael Ceccaldi et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2016)
FANCD2 functions as a critical factor downstream of MiTF to maintain the proliferation and survival of melanoma cells
Julie Bourseguin et al.
SCIENTIFIC REPORTS (2016)
BRCA Mutations, DNA Repair Deficiency, and Ovarian Aging
Kutluk Oktay et al.
BIOLOGY OF REPRODUCTION (2015)
Fanconi anemia: a model disease for studies on human genetics and advanced therapeutics
Massimo Bogliolo et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2015)
Whole exome sequencing reveals concomitant mutations of multiple FA genes in individual Fanconi anemia patients
Lixian Chang et al.
BMC MEDICAL GENOMICS (2014)
Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer
Johanna I. Kiiski et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Hypersensitivity of Primordial Germ Cells to Compromised Replication-Associated DNA Repair Involves ATM-p53-p21 Signaling
Yunhai Luo et al.
PLOS GENETICS (2014)
Cellular and Molecular Effect of MEHP Involving LXRα in Human Fetal Testis and Ovary
Vincent Muczynski et al.
PLOS ONE (2012)
The Fission Yeast FANCM Ortholog Directs Non-Crossover Recombination During Meiosis
Alexander Lorenz et al.
SCIENCE (2012)
FANCM Limits Meiotic Crossovers
Wayne Crismani et al.
SCIENCE (2012)
Association of BRCA1 Mutations With Occult Primary Ovarian Insufficiency: A Possible Explanation for the Link Between Infertility and Breast/Ovarian Cancer Risks
Kutluk Oktay et al.
JOURNAL OF CLINICAL ONCOLOGY (2010)
Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M
Thiyam Ramsing Singh et al.
BLOOD (2009)
Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M
Sietske T. Bakker et al.
HUMAN MOLECULAR GENETICS (2009)
Emergence of a DNA-damage response network consisting of Fanconi anaemia and BRCA proteins
Weidong Wang
NATURE REVIEWS GENETICS (2007)
Thrombopoietin regulates IEX-1 gene expression through ERK-induced AML1 phosphorylation
V Hamelin et al.
BLOOD (2006)
DNA-PK, ATM and ATR as sensors of DNA damage: variations on a theme?
D Durocher et al.
CURRENT OPINION IN CELL BIOLOGY (2001)