Fancm has dual roles in the limiting of meiotic crossovers and germ cell maintenance in mammals

V Tsui, R Lyu, S Novakovic, JM Stringer, JEM Dunleavy… - Cell Genomics, 2023 - cell.com
Meiotic crossovers are required for accurate chromosome segregation and producing new
allelic combinations. Meiotic crossover numbers are tightly regulated within a narrow range …

FANCM Gene Variants in a Male Diagnosed with Sertoli Cell-Only Syndrome and Diffuse Astrocytoma

ML Klarić, T Marić, L Žunić, L Trgovec-Greif, F Rokić… - Genes, 2024 - mdpi.com
Azoospermia is a form of male infertility characterized by a complete lack of spermatozoa in
the ejaculate. Sertoli cell-only syndrome (SCOS) is the most severe form of azoospermia …

Myelodysplastic syndrome and multiple solid tumours in an individual with compound heterozygous deleterious FANCM variants: A case report and review of the …

JY Ng, L Warwick, P Craft, L Austen… - British Journal of …, 2023 - search.ebscohost.com
Most cases reported chemotherapy and radiotherapy toxicities including myelosuppression,
and mucositis. Individuals with FANCM biallelic mutations do not develop Fanconi anemia …

Grade 5 Radiation Necrosis After Whole-Brain Radiation Therapy

A Tam, YR Li, T Williams, S Yoon - Practical Radiation Oncology, 2024 - Elsevier
Whole-brain radiation treatment is often considered for patients with leptomeningeal
disease. There are limited reports of the development of radiation necrosis after whole-brain …

Fancm regulates meiotic double-strand break repair pathway choice in mammals

V Tsui, R Lyu, S Novakovic, JM Stringer, JEM Dunleavy… - bioRxiv, 2022 - biorxiv.org
Meiotic crossovers are required for accurate chromosome segregation and to produce new
allelic combinations. Meiotic crossover numbers are tightly regulated within a narrow range …

[PDF][PDF] Homozygous FANCM variant c. 5101C> T p.(Gln1701*) in a patient with early onset breast cancer, chemotherapy toxicity, and chromosome fragility

S Sulkava, AH Hakonen, M Pöyhönen… - Authorea …, 2024 - authorea.com
Homozygous FANCM variant c. 5101C> T p.(Gln1701*) in a patient with early onset breast
cancer, chemotherapy toxicity, and chromosome fragilitySonja Sulkava1, 2*, Anna H …