Citations for
1FANCC, UNC5A
FANCC localizes with UNC5A at neurite outgrowth and promotes neuritogenesis.
Huang F, Ben Aissa M, Lévesque G, Carreau M.
BMC Res Notes. Sep 12;11(1):662. doi: 10.1186/s13104-018-3763-1. 2018
2FANCC, UNC5A
The Fanconi anemia group C protein interacts with uncoordinated 5A and delays apoptosis.
Huang F, Ben Aissa M, Magron A, Huard CC, Godin C, Lévesque G, Carreau M.
PLoS One. Mar 27;9(3):e92811. doi: 10.1371/journal.pone.0092811. eCollection 2014 2014
3FANCA, FANCC
FANCA and FANCC modulate TLR and p38 MAPK-dependent expression of IL-1β in macrophages.
Garbati MR, Hays LE, Keeble W, Yates JE, Rathbun RK, Bagby GC.
Blood 122(18):3197-205. doi: 10.1182/blood-2013-02-484816. Epub 2013 Sep 17. 2013
4FANCC, HELQ
Helq acts in parallel to Fancc to suppress replication-associated genome instability.
Luebben SW, Kawabata T, Akre MK, Lee WL, Johnson CS, O'Sullivan MG, Shima N.
Nucleic Acids Res 41(22):10283-97. doi: 10.1093/nar/gkt676. Epub 2013 Sep 4. 2013
5FANCC, PTCH1
Association of FANCC and PTCH1 with the development of early dysplastic lesions of the head and neck.
Ghosh A, Ghosh S, Maiti GP, Mukherjee S, Mukherjee N, Chakraborty J, Roy A, Roychoudhury S, Panda CK.
Ann Surg Oncol 19 Suppl 3:S528-38. doi: 10.1245/s10434-011-1991-x. Epub 2011 Aug 23. 2012
6FANCC
Human FANCC is hypomorphic in murine Fancc-deficient cells.
Hays LE, Keeble WW, Yates JE, Rathbun RK, Koretsky T, Olson SB, Sun Z, Clapp DW, Bagby GC Jr.
Blood lood. 2010 Jun 16. [Epub ahead of print]PMID: 20554974 2010
7FANCC, XRCC3
FANCC suppresses short telomere-initiated telomere sister chromatid exchange.
Rhee DB, Wang Y, Mizesko M, Zhou F, Haneline L, Liu Y.
Hum Mol Genet 19(5):879-87. Epub 2009 Dec 18.PMID: 20022886 2010
8FANCC
Correct mRNA processing at a mutant TT splice donor in FANCC ameliorates the clinical phenotype in patients and is enhanced by delivery of suppressor U1 snRNAs.
Hartmann L, Neveling K, Borkens S, Schneider H, Freund M, Grassman E, Theiss S, Wawer A, Burdach S, Auerbach AD, Schindler D, Hanenberg H, Schaal H.
Am J Hum Genet 87(4):480-93.PMID: 20869034 2010
9FANCA, FANCC
Cytoplasmic FANCA-FANCC complex interacts and stabilizes the cytoplasm-dislocalized leukemic nucleophosmin protein (NPMc).
Du W, Li J, Sipple J, Chen J, Pang Q.
J Biol Chem 285(48):37436-44. doi: 10.1074/jbc.M110.113209. Epub 2010 Sep 23. 2010
10(FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, FANCJ, FANCL, FANCM, FANCN, FNACI
A possible approach for stem cell gene therapy of Fanconi anemia.
Song L.
Curr Gene Ther 9(1):26-32. Review.PMID: 19275569 2009
11FANCC, FANCL
Hypermethylation of the FANCC and FANCL promoter regions in sporadic acute leukaemia.
Hess CJ, Ameziane N, Schuurhuis GJ, Errami A, Denkers F, Kaspers GJ, Cloos J, Joenje H, Reinhardt D, Ossenkoppele GJ, Zwaan CM, Waisfisz Q.
Cell Oncol 30(4):299-306.PMID: 18607065 2008
12FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ, FANCL, FANCM, FANCN,
Endocrine abnormalities in patients with Fanconi anemia.
Giri N, Batista DL, Alter BP, Stratakis CA.
J Clin Endocrinol Metab 92(7):2624-31. Epub 2007 Apr 10. 2007
13FANCC
Loss of FANCC function is associated with failure to inhibit late firing replication origins after DNA cross-linking.
Phelps RA, Gingras H, Hockenbery DM.
Exp Cell Res 313(11):2283-92. Epub 2007 Apr 6.PMID: 17490643 2007
14CHARGE, CHD7, DEL22Q11, FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, FANCJ, MYCN, ODED1, SALL1, TBS, TBX1, VACTERLH
Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology.
Shaw-Smith C.
J Med Genet 43(7):545-54. Epub 2005 Nov 18. Review. 2006
15FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCM, FANCL
Fanconi anemia proteins are required to prevent accumulation of replication-associated DNA double-strand breaks.
Sobeck A, Stone S, Costanzo V, de Graaf B, Reuter T, de Winter J, Wallisch M, Akkari Y, Olson S, Wang W, Joenje H, Christian JL, Lupardus PJ, Cimprich KA, Gautier J, Hoatlin ME.
Mol Cell Biol 26(2):425-37. 2006
16FANCC,FANCD2,FANCE
FANCC, FANCE, and FANCD2 form a ternary complex essential to the integrity of the Fanconi anemia DNA damage response pathway.
Gordon SM, Alon N, Buchwald M.
J Biol Chem 280(43):36118-25. Epub 2005 Aug 26. 2005
17FANCA, FANCC, FANCE, FANCG, FANCD2
The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC.
Taniguchi T, D'Andrea AD.
Blood 100(7):2457-62. 2002
18FANCA, FANCC, FANCE, FANCF, FANCG
Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway.
Medhurst AL, Huber PA, Waisfisz Q, de Winter JP, Mathew CG.
Hum Mol Genet 10(4):423-9. 2001
19FANCC, HSPA4
FANCC interacts with Hsp70 to protect hematopoietic cells from IFN-gamma/TNF-alpha-mediated cytotoxicity.
Pang Q, Keeble W, Christianson TA, Faulkner GR, Bagby GC.
EMBO J 20(16):4478-89. 2001
20FANCC
The Fanconi anemia complementation group C gene product: structural evidence of multifunctionality.
Pang Q, Christianson TA, Keeble W, Diaz J, Faulkner GR, Reifsteck C, Olson S, Bagby GC.
Blood 98(5):1392-401. 2001
21FANCA, FANCG, FANCC
Fanconi anemia proteins FANCA, FANCC, and FANCG/XRCC9 interact in a functional nuclear complex.
Garcia-Higuera I, et al.
Mol Cell Biol 19(7):4866-73. 1999
22FANCC
The Fanconi anemia group C gene product is located in both the nucleus and cytoplasm of human cells.
Hoatlin ME, Christianson TA, Keeble WW, Hammond AT, Zhi Y, Heinrich MC, Tower PA, Bagby GC Jr.
Blood 91(4):1418-25. 1998
23FANCC
Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joining.
Escarceller M, et al.
J Mol Biol 279 : 375-385. 1998
24FANCC
Involvement of the Fanconi anemia protein Fa-C in repair processes of oxidative DNA damages.
Lackinger D, et al.
FEBS Lett 440 : 103-106. 1998
25FANCC
VACTERL with hydrocephalus in twins due to Fanconi anemia (FA) : mutation in the FAC gene.
Cox PM, et al.
Am J Med Genet 68 : 86-90. 1997
26FANCC, NBCCS2, ZNF169
Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 region.
Levanat S, Chidambaram A, Wicking C, Bray-Ward P, Pressman C, Toftgard R, Gailani MR, Myers JC, Wainwright B, Dean M, Bale AE.
Cytogenet Cell Genet 76(3-4):208-13. 1997
27FANCA, FANCC
Phenotypic consequences of mutations in the Fanconi anemia FAC gene: an International Fanconi Anemia Registry study.
Gillio AP, Verlander PC, Batish SD, Giampietro PF, Auerbach AD.
Blood 90(1):105-10. 1997
28FANCA, FANCC
The Fanconi anaemia proteins, FAA and FAC, interact fo form a nuclear complex.
Kupfer GM, Naf D, Suliman A, Pulsipher M, D'Andrea AD.
Nat Genet 17(4):487-90. 1997
29FANCC
Developmental expression of the Fac gene correlates with congenital defects in Fanconi anemia patients.
Krasnoshtein F, et al.
Hum Mol Genet 5 : 85-93. 1996
30FANCC
Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia.
Chen M, et al.
Nat Genet 12 : 448-451. 1996
31FANCC
Induction of Fanconi anemia cellular phenotype in human 293 cells by overexpression of a mutant FAC allele.
Youssoufian H, et al.
J Clin Invest 97 : 957-962. 1996
32FANCC
Novel frameshift mutation (180insA) in exon 14 of the Fanconi anemia C gene, FAC.
Lo Ten Foe JR, et al.
Hum Mutat 7 : 264-265. 1996
33FANCC
Molecular characterization of Fanconi anaemia group C, (FAC) gene polymorphisms.
Savoia A, et al.
Mol Cell Probes 10 : 213-218. 1996
34FANCC
Sequence variations in the Fanconi anaemia gene, FAC : pathogenicity of 1806insA and R548X and recognition of D195V as a polymorphic variant.
Lo Ten Foe JR, et al.
Hum Genet 98 : 522-523. 1996
35FANCC
Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cells.
Youssoufian H.
J Clin Invest 97 : 2003-2010. 1996
36FANCC
Characterization of the 5' region of the Fanconi anaemia group C (FACC) gene.
Savoia A, et al.
Hum Mol Genet 4 : 1321-1326. 1995
37FANCC
Mutation analysis of the fanconi anemia gene FACC.
Verlander PC, et al.
Am J Hum Genet 54 : 595-601. 1994
38FANCC
The Ashkenazi Jewish fanconi anemia mutation : incidence among patients and carrier frequency in the at-risk population.
Whitney MA, et al.
Hum Mutat 3 : 339-341. 1994
39FANCC, NBCCS2, XPA
A YAC contig spanning the nevoid basal cell carcinoma syndrome, Fanconi anaemia group C, and xeroderma pigmentosum group A loci on chromosome 9q.
Morris DJ, et al.
Genomics 23 : 23-29. 1994
40FANCC, MSSE, NBCCS2, XPA
Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3.
Farndon PA, et al.
Genomics 23 : 486-489. 1994
41FANCC
Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families.
Gibson RA, et al.
J Med Genet 31 : 868-871. 1994
42FANCC
The Fanconi anemia polypeptide FACC is localized to the cytoplasm.
Yamashita T, Barber DL, Zhu Y, Wu N, D'Andrea AD.
Proc Natl Acad Sci U S A 91(14):6712-6.PMID: 7517562 1994
43FANCC
A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews.
Whitney MA, et al.
Nat Genet 4 : 202-205. 1993
44FANCC
A nonsense mutation and exon skipping in the Fanconi anaemia group C gene.
Gibson RA, et al.
Hum Mol Genet 2 : 797-799. 1993
45FANCC
EcoRI RFLP in the Fanconi anaemia complementation group C gene (FACC).
Gibson RA, et al.
Hum Mol Genet 2 : 1509. 1993
46FANCC
Characterisation of the exon structure of the Fanconi anaemia group C gene by vectorette PCR.
Gibson RA, et al.
Hum Mol Genet 2 : 35-38. 1993
47FANCC
A Leu554-to-Pro substitution completely abolishes the functional complementing activity of the Fanconi anemia (FACC) protein.
Gavish H, et al.
Hum Mol Genet 2 : 123-126. 1993
48FANCA, FANCC
Cloning of cDNAs for Fanconi's anaemia by functional complementation. (Correction of Nature 1992 ; 356 : 763-767.)
Strathdee CA, et al.
Nature 358 : 434. 1992
49FANCA, FANCC
Fanconi anemia : linkage analysis with chromosome 9q and 20q markers.
Verlander PC, et al.
Am J Hum Genet 51 : A204. 1992
50FANCC
Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9.
Strathdee CA, et al.
Nat Genet 1 : 196-198. 1992
51FANCC
Cloning of cDNAs for Fanconi's anaemia by functional complementation.
Strathdee CA, et al.
Nature 356 : 763-767. 1992