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Blood
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January 7, 2006
Natural gene therapy in monozygotic twins with Fanconi anemia
Anuj Mankad, Toshiyasu Taniguchi, Barbara Cox, et al.
Molecular and Cellular Biology
|
October 7, 2009
XPF-ERCC1 participates in the Fanconi anemia pathway of cross-link repair
Nikhil Bhagwat, Anna L Olsen, Anderson T Wang, et al.
British Journal of Haematology
|
November 18, 2003
Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia
Marc Tischkowitz, Najim Ameziane, Quinten Waisfisz, et al.
Nature Genetics
|
April 26, 2016
Somatic ERCC2 mutations are associated with a distinct genomic signature in urothelial tumors
Jaegil Kim, Kent W Mouw, Paz Polak, et al.
Stem Cells (Dayton, Ohio)
|
May 28, 2010
Hematopoietic stem cell defects in mice with deficiency of Fancd2 or Usp1
Kalindi Parmar, Jungmin Kim, Stephen M Sykes, et al.
Plos One
|
October 31, 2025
A porcine model of Fanconi anemia
Brandon Hergert, Kristin M Whitworth, Devorah C Goldman, et al.
Plos Genetics
|
September 21, 2011
PCNA ubiquitination is important, but not essential for translesion DNA synthesis in mammalian cells
Ayal Hendel, Peter H L Krijger, Noam Diamant, et al.
Nature
|
September 6, 2013
HELQ promotes RAD51 paralogue-dependent repair to avert germ cell loss and tumorigenesis
Carrie A Adelman, Rafal L Lolo, Nicolai J Birkbak, et al.
Molecular Cell
|
March 27, 2012
BRCA1 functions independently of homologous recombination in DNA interstrand crosslink repair
Samuel F Bunting, Elsa Callén, Marina L Kozak, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 12, 2022
Phase 1b Clinical Trial with Alpelisib plus Olaparib for Patients with Advanced Triple-Negative Breast Cancer
Felipe Batalini, Niya Xiong, Nabihah Tayob, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 39) with videos related to
Sort By:
Page
of 4
Blood
|
January 7, 2006
Natural gene therapy in monozygotic twins with Fanconi anemia
Anuj Mankad, Toshiyasu Taniguchi, Barbara Cox, et al.
Molecular and Cellular Biology
|
October 7, 2009
XPF-ERCC1 participates in the Fanconi anemia pathway of cross-link repair
Nikhil Bhagwat, Anna L Olsen, Anderson T Wang, et al.
British Journal of Haematology
|
November 18, 2003
Bi-allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia
Marc Tischkowitz, Najim Ameziane, Quinten Waisfisz, et al.
Nature Genetics
|
April 26, 2016
Somatic ERCC2 mutations are associated with a distinct genomic signature in urothelial tumors
Jaegil Kim, Kent W Mouw, Paz Polak, et al.
Stem Cells (Dayton, Ohio)
|
May 28, 2010
Hematopoietic stem cell defects in mice with deficiency of Fancd2 or Usp1
Kalindi Parmar, Jungmin Kim, Stephen M Sykes, et al.
Plos One
|
October 31, 2025
A porcine model of Fanconi anemia
Brandon Hergert, Kristin M Whitworth, Devorah C Goldman, et al.
Plos Genetics
|
September 21, 2011
PCNA ubiquitination is important, but not essential for translesion DNA synthesis in mammalian cells
Ayal Hendel, Peter H L Krijger, Noam Diamant, et al.
Nature
|
September 6, 2013
HELQ promotes RAD51 paralogue-dependent repair to avert germ cell loss and tumorigenesis
Carrie A Adelman, Rafal L Lolo, Nicolai J Birkbak, et al.
Molecular Cell
|
March 27, 2012
BRCA1 functions independently of homologous recombination in DNA interstrand crosslink repair
Samuel F Bunting, Elsa Callén, Marina L Kozak, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 12, 2022
Phase 1b Clinical Trial with Alpelisib plus Olaparib for Patients with Advanced Triple-Negative Breast Cancer
Felipe Batalini, Niya Xiong, Nabihah Tayob, et al.
Page
of 4