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FANCONI ANEMIA, COMPLEMENTATION GROUP C

Known as: FAC, FANCONI PANCYTOPENIA, TYPE 3, FANCC 
Fanconi anemia caused by mutations of the FANCC gene. This gene provides instructions for making a protein that delays the onset of apoptosis and… 
National Institutes of Health

Related topics

Related topics

6 relations
AnemiaBone MarrowFANCC geneFANCC wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Continental carbonate facies of a Neoproterozoic panglaciation , 1 NE Svalbard 2
2015
2015
SPCTPD/ACC/AAP/AHA Training Guidelines for Pediatric Cardiology Fellowship Programs (Revision of the 2005 Training Guidelines for Pediatric Cardiology Fellowship Programs)
  • L. Wilkins
  • Pediatric Clinical Practice Guidelines & Policies
  • 2015
  • Corpus ID: 78936636
Introduction/Steering Committee Robert D. Ross, MD, FAAP, FACC, Chair Michael Brook, MD, Co-Chair Peter Koenig, MD, FACC… 
2011
2011
Depositional Architecture of a Near-Slope Turbidite Succession: Upper Kaza Group, Windermere Supergroup, Castle Creek, British Columbia, Canada
An expansive panel of well exposed (periglacial) strata of the Upper Kaza Group permitted a detailed study of the stratal… 
2002
2002
Hematopoietic Stem Cells from Fancc−/− Mice Have Lower Growth and Differentiation Potential in Response to Growth Factors
Fanconi anemia (FA) is a complex recessive genetic disease characterized by progressive bone marrow (BM) failure. We have… 
Highly Cited
1996
Highly Cited
1996
The effect of the Fanconi anemia polypeptide, FAC, upon p53 induction and G2 checkpoint regulation.
Fanconi anemia (FA) is an autosomal recessive disease marked by developmental defects, bone marrow failure, and cancer… 
1996
1996
Sequence variations in the Fanconi anaemia gene, FAC: pathogenicity of 1806insA and R548X and recognition of D195V as a polymorphic variant
Abstract Fanconi anaemia (FA) is a rare autosomal recessive disorder associated with diverse clinical symptoms, increased… 
1996
1996
Novel frameshift mutation (1806insA) in exon 14 of the Fanconi anemia c gene, FAC
1994
1994
Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families.
Fanconi anaemia is an autosomal recessive disorder associated with increased chromosome breakage and progressive bone marrow… 
1991
1991
Developmental analysis of the facets, a group of intronic mutations at the Notch locus of Drosophila melanogaster that affect postembryonic development.
The activity of the Notch locus of Drosophila melanogaster during embryogenesis is necessary for the correct segregation of… 
1989
1989
Phenotypic and molecular analysis of the facets, a group of intronic mutations at the Notch locus of Drosophila melanogaster which affect postembryonic development.
The function of the Notch locus of Drosophila melanogaster is essential for normal development both during embryogenesis and… 
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