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fanconi anemia complementation group g
Known as:
FANCG
, FANCONI ANEMIA, COMPLEMENTATION GROUP G
Fanconi anemia caused by mutations of the FANCG gene.
National Institutes of Health
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Related topics
Related topics
5 relations
Anemia
Bone Marrow
FANCG gene
FANCG protein, human
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Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Novel Founder Mutation in FANCA Gene (c.3446_3449dupCCCT) Among Romani Patients from the Balkan Region
M. Dimishkovska
,
V. Kotori
,
Z. Gucev
,
S. Kocheva
,
M. Polenaković
,
D. Plaseska‐Karanfilska
Balkan Medical Journal
2017
Corpus ID: 3924488
Background: Fanconi anemia is a rare autosomal recessive or X-linked disorder characterised by clinical and genetic heterogeneity…
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2015
2015
Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia.
C. Feben
,
J. Kromberg
,
+4 authors
A. Krause
Blood Cells, Molecules & Diseases
2015
Corpus ID: 205959557
2014
2014
Interleukin 8/KC enhances G-CSF induced hematopoietic stem/progenitor cell mobilization in Fancg deficient mice.
Yan Li
,
W. Xing
,
+11 authors
Feng-Chun Yang
Stem Cell Investigation
2014
Corpus ID: 8906665
BACKGROUND Fanconi anemia (FA) is a heterogeneous genetic disorder characterized by a progressive bone marrow aplasia…
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2013
2013
Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation.
T. Wainstein
,
R. Kerr
,
+6 authors
A. Krause
South African medical journal = Suid-Afrikaanse…
2013
Corpus ID: 33902262
BACKGROUND Fanconi anaemia (FA) is an autosomal recessive, genetically heterogeneous disorder, characterised by interstrand…
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Review
2011
Review
2011
Fanconi anemia.
J. Soulier
Hematology. American Society of Hematology…
2011
Corpus ID: 265716813
Fanconi anemia (FA) is the most frequent inherited cause of BM failure (BMF). Fifteen FANC genes have been identified to date…
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2006
2006
Estudo das mutações do gene FANCG em pacientes com quadro clinico sugestivo de anemia de Fanconi
Lucila Gobby Amstalden
,
C. Bertuzzo
2006
Corpus ID: 161886828
A Anemia de Fanconi (AF) e uma doenca caracterizada por multiplas anomalias congenitas, progressiva falha da medula ossea e alto…
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2005
2005
α II Spectrin Interacts with Specific Proteins in the Nucleus: Relevance to Fanconi Anemia.
M. W. Lambert
,
Laura W. McMahon
,
D. Sridharan
2005
Corpus ID: 208484846
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure, a predisposition to cancer, congenital…
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2003
2003
Role of Fanconi Anemia FANCG in Preventing Double-Strand Breakage and Chromosomal Rearrangement during DNA Replication
R. Tebbs
,
J. M. Hinz
,
+6 authors
L. Thompson
2003
Corpus ID: 82676449
The Fanconi anemia (FA) proteins overlap with those of homologous recombination through FANCD1/BRCA2, but the biochemical…
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Review
2002
Review
2002
Molecular biology of Fanconi anaemia—an old problem, a new insight
Shamim I. Ahmad
,
F. Hanaoka
,
S. Kirk
Bioessays
2002
Corpus ID: 40955296
Fanconi anaemia (FA) comprises a group of autosomal recessive disorders resulting from mutations in one of eight genes (FANCA…
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2001
2001
[Chart 48: FANCG/XRCC9 (type G Fanconi's anemia)].
T. Soussi
Bulletin du Cancer
2001
Corpus ID: 20215260
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