scholarly journals Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3

2000 ◽  
Vol 66 (5) ◽  
pp. 1540-1551 ◽  
Author(s):  
James A. Hejna ◽  
Cynthia D. Timmers ◽  
Carol Reifsteck ◽  
Donald A. Bruun ◽  
Lora W. Lucas ◽  
...  
Keyword(s):  
Fanconi Anemia ◽  
Complementation Group ◽  
Group D

scholarly journals A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M

2005 ◽  
Vol 37 (9) ◽  
pp. 958-963 ◽  
Author(s):  
Amom Ruhikanta Meetei ◽  
Annette L Medhurst ◽  
Chen Ling ◽  
Yutong Xue ◽  
Thiyam Ramsing Singh ◽  
...  
Keyword(s):  
Dna Repair ◽  
Fanconi Anemia ◽  
Complementation Group ◽  
Repair Protein ◽  
Dna Repair Protein ◽  
Human Ortholog

Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2

2006 ◽  
Vol 601 (1-2) ◽  
pp. 191-201 ◽  
Author(s):  
Barbara C. Godthelp ◽  
Paul P.W. van Buul ◽  
Nicolaas G.J. Jaspers ◽  
Elhaam Elghalbzouri-Maghrani ◽  
Annemarie van Duijn-Goedhart ◽  
...  
Keyword(s):  
Fanconi Anemia ◽  
Complementation Group

scholarly journals Identification of Cytosolic Proteins That Bind to the Fanconi Anemia Complementation Group C Polypeptidein Vitro

1995 ◽  
Vol 270 (17) ◽  
pp. 9876-9882 ◽  
Author(s):  
Hagop Youssoufian ◽  
Arleen D. Auerbach ◽  
Peter C. Verlander ◽  
Viktor Steimle ◽  
Bernard Mach
Keyword(s):  
Fanconi Anemia ◽  
Complementation Group ◽  
Cytosolic Proteins

Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia

2018 ◽  
Vol 98 (2) ◽  
pp. 271-280 ◽  
Author(s):  
Miharu Yabe ◽  
Takashi Koike ◽  
Keisuke Ohtsubo ◽  
Eri Imai ◽  
Tsuyoshi Morimoto ◽  
...  
Keyword(s):  
Fanconi Anemia ◽  
Japanese Patients ◽  
Complementation Group ◽  
Clonal Abnormalities

SNX5, a New Member of the Sorting Nexin Family, Binds to the Fanconi Anemia Complementation Group A Protein

1999 ◽  
Vol 265 (3) ◽  
pp. 630-635 ◽  
Author(s):  
Tetsuya Otsuki ◽  
Sachiko Kajigaya ◽  
Keiya Ozawa ◽  
Johnson M. Liu
Keyword(s):  
Fanconi Anemia ◽  
Complementation Group ◽  
Sorting Nexin ◽  
Group A

scholarly journals Polymorphism ofXRCC1,XRCC3, andXPDGenes and Risk of Chronic Myeloid Leukemia

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Claudia Bănescu ◽  
Adrian P. Trifa ◽  
Smaranda Demian ◽  
Erzsebeth Benedek Lazar ◽  
Delia Dima ◽  
...  
Keyword(s):  
Complementation Group ◽  
Control Group ◽  
X Ray ◽  
Genotype Frequencies ◽  
Significant Difference ◽  
Variant Genotype ◽  
Group 3 ◽  
And Control ◽  
Group D ◽  
Repair Genes

The genetic polymorphisms of X-ray repair cross complementing group 1 (XRCC1), X-ray repair cross complementing group 3 (XRCC3), and xeroderma pigmentosum complementation group D (XPD) repair genes may lead to genetic instability and leukemogenesis. The purpose of the study was to evaluate the association betweenXRCC1Arg399Gln, Arg280His and Arg194Trp,XRCC3Thr241Met, andXPDLys751Gln polymorphisms and the risk of developing CML in Romanian patients. A total of 156 patients diagnosed with CML and 180 healthy controls were included in this study. We found no association between CML andXRCC1orXRCC3variant genotypes in any of the investigated cases. A significant difference was observed in the variant genotype frequencies of theXPDLys751Gln polymorphism between the patients with CML and control group (for variant homozygous genotypes,OR=2.37; 95%CI=1.20–4.67;Pvalue = 0.016 and for combined heterozygous and variant homozygous genotypes,OR=1.72; 95%CI=1.10–2.69;Pvalue = 0.019). This was also observed when analyzing the variant 751Gln allele (OR=1.54; 95%CI=1.13–2.11;Pvalue = 0.008). Our results suggest that theXPDLys751Gln variant genotype increases the risk of CML.

Complementation group assignments in fanconi anemia fibroblast cell lines from North America

1997 ◽  
Vol 23 (1) ◽  
pp. 1-7 ◽  
Author(s):  
P. M. Jakobs ◽  
E. Fiddler-Odell ◽  
C. Reifsteck ◽  
S. Olson ◽  
R. E. Moses ◽  
...  
Keyword(s):  
North America ◽  
Cell Lines ◽  
Fanconi Anemia ◽  
Fibroblast Cell ◽  
Complementation Group ◽  
Fibroblast Cell Lines
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