| References |
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| REF 1 |
Evidence for subcomplexes in the Fanconi anemia pathway. Blood. 2006 Sep 15;108(6):2072-80.
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| REF 2 |
Modularized functions of the Fanconi anemia core complex. Cell Rep. 2014 Jun 26;7(6):1849-57.
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| REF 3 |
Mechanism of Ubiquitination and Deubiquitination in the Fanconi Anemia Pathway. Mol Cell. 2017 Jan 19;65(2):247-259.
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| REF 4 |
HSP90 Shapes the Consequences of Human Genetic Variation. Cell. 2017 Feb 23;168(5):856-866.e12.
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| REF 5 |
The Fanconi anemia gene product FANCF is a flexible adaptor protein. J Biol Chem. 2004 Sep 17;279(38):39421-30.
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| REF 6 |
The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG. Hum Mol Genet. 2000 Nov 1;9(18):2665-74.
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| REF 7 |
Physical and functional crosstalk between Fanconi anemia core components and the GINS replication complex. DNA Repair (Amst). 2011 Feb 7;10(2):149-58.
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| REF 8 |
FANCM connects the genome instability disorders Bloom's Syndrome and Fanconi Anemia. Mol Cell. 2009 Dec 25;36(6):943-53.
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| REF 9 |
Structural determinants of human FANCF protein that function in the assembly of a DNA damage signaling complex. J Biol Chem. 2007 Jan 19;282(3):2047-55.
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| REF 10 |
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M. Nat Genet. 2005 Sep;37(9):958-63.
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| REF 11 |
Several tetratricopeptide repeat (TPR) motifs of FANCG are required for assembly of the BRCA2/D1-D2-G-X3 complex, FANCD2 monoubiquitylation and phleomycin resistance. Mutat Res. 2010 Jul 7;689(1-2):12-20.
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| REF 12 |
Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems. Blood. 2003 Jul 1;102(1):136-41.
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| REF 13 |
Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway. Hum Mol Genet. 2001 Feb 15;10(4):423-9.
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| REF 14 |
Analysis of a FANCE Splice Isoform in Regard to DNA Repair. J Mol Biol. 2015 Sep 25;427(19):3056-73.
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