Results 111 to 120 of about 85,361 (267)

Advances in the understanding of the Fanconi anemia tumor suppressor pathway [PDF]

open access: bronze, 2013
Anna Pickering   +3 more
openalex   +1 more source

Data from Disabling the Fanconi Anemia Pathway in Stem Cells Leads to Radioresistance and Genomic Instability

open access: gold, 2023
Xinzhu Deng   +9 more
openalex   +1 more source

Concepts of multi-level dynamical modelling: understanding mechanisms of squamous cell carcinoma development in Fanconi anemia [PDF]

open access: gold, 2023
Eunike Velleuer   +4 more
openalex   +1 more source

Investigation of FANCA mutations in greek patients [PDF]

open access: yes, 2013
Background: Fanconi anemia (FA) is a rare genetic disease characterized by considerable heterogeneity. Fifteen subtypes are currently recognised and deletions of the Fanconi anemia complementation group A (FANCA) gene account for more than 65% of FA ...
Fryssira, Elena   +8 more
core  

FANCONI ANEMIA PRESENTING LATE AS MALIGNANT BUCCAL CARCINOMA; A CASE REPORT

open access: yesPakistan Armed Forces Medical Journal, 2020
Fanconi anemia (FA) is a rare, genetically and phenotypically heterogeneous autosomal recessive disorder. It is characterized by various congenital malformations, progressive bone marrow failure usually at a very young age and of tumor development.
Taimoor Ashraf Khan   +3 more
doaj  

Pregnancy after allogeneic hematopoietic stem cell transplantation in a Fanconi anemia patient

open access: yesInternational Medical Case Reports Journal, 2017
Simin Atashkhoei, Solmaz Fakhari, Eissa Bilehjani, Haleh Farzin Department of Anesthesiology, Al-Zahra Hospital, Tabriz University of Medical Sciences, Tabriz, Iran Abstract: Pregnancy in patients with Fanconi anemia (FA) is rare. However,
Atashkhoei S   +3 more
doaj  

Data from Defects in the Fanconi Anemia Pathway in Head and Neck Cancer Cells Stimulate Tumor Cell Invasion through DNA-PK and Rac1 Signaling

open access: gold, 2023
Lindsey E. Romick‐Rosendale   +13 more
openalex   +1 more source

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