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Items: 1 to 20 of 145

1.

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. 1994 Jul 5;91(14):6712-6.

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Phenotypic correction of Fanconi anemia in human hematopoietic cells with a recombinant adeno-associated virus vector.

Walsh CE, Nienhuis AW, Samulski RJ, Brown MG, Miller JL, Young NS, Liu JM.

J Clin Invest. 1994 Oct;94(4):1440-8.

4.

Localization of Fanconi anemia C protein to the cytoplasm of mammalian cells.

Youssoufian H.

Proc Natl Acad Sci U S A. 1994 Aug 16;91(17):7975-9.

5.

A functionally active retrovirus vector for gene therapy in Fanconi anemia group C.

Walsh CE, Grompe M, Vanin E, Buchwald M, Young NS, Nienhuis AW, Liu JM.

Blood. 1994 Jul 15;84(2):453-9.

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A patient-derived mutant form of the Fanconi anemia protein, FANCA, is defective in nuclear accumulation.

Kupfer G, Naf D, Garcia-Higuera I, Wasik J, Cheng A, Yamashita T, Tipping A, Morgan N, Mathew CG, D'Andrea AD.

Exp Hematol. 1999 Apr;27(4):587-93.

PMID:
10210316
8.

Cloning and analysis of the murine Fanconi anemia group C cDNA.

Wevrick R, Clarke CA, Buchwald M.

Hum Mol Genet. 1993 Jun;2(6):655-62.

PMID:
7689006
9.

A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews.

Whitney MA, Saito H, Jakobs PM, Gibson RA, Moses RE, Grompe M.

Nat Genet. 1993 Jun;4(2):202-5.

PMID:
8348157
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The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG.

de Winter JP, van der Weel L, de Groot J, Stone S, Waisfisz Q, Arwert F, Scheper RJ, Kruyt FA, Hoatlin ME, Joenje H.

Hum Mol Genet. 2000 Nov 1;9(18):2665-74.

13.

A nonsense mutation and exon skipping in the Fanconi anaemia group C gene.

Gibson RA, Hajianpour A, Murer-Orlando M, Buchwald M, Mathew CG.

Hum Mol Genet. 1993 Jun;2(6):797-9.

PMID:
7689011
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Function of the Fanconi anemia pathway in Fanconi anemia complementation group F and D1 cells.

Siddique MA, Nakanishi K, Taniguchi T, Grompe M, D'Andrea AD.

Exp Hematol. 2001 Dec;29(12):1448-55.

PMID:
11750104
16.

Fanconi anemia group A and C double-mutant mice: functional evidence for a multi-protein Fanconi anemia complex.

Noll M, Battaile KP, Bateman R, Lax TP, Rathbun K, Reifsteck C, Bagby G, Finegold M, Olson S, Grompe M.

Exp Hematol. 2002 Jul;30(7):679-88.

PMID:
12135664
17.

Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.

Faivre L, Guardiola P, Lewis C, Dokal I, Ebell W, Zatterale A, Altay C, Poole J, Stones D, Kwee ML, van Weel-Sipman M, Havenga C, Morgan N, de Winter J, Digweed M, Savoia A, Pronk J, de Ravel T, Jansen S, Joenje H, Gluckman E, Mathew CG.

Blood. 2000 Dec 15;96(13):4064-70.

18.

Heterogeneous activation of the Fanconi anemia pathway by patient-derived FANCA mutants.

Adachi D, Oda T, Yagasaki H, Nakasato K, Taniguchi T, D'Andrea AD, Asano S, Yamashita T.

Hum Mol Genet. 2002 Dec 1;11(25):3125-34.

19.

Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.

Hussain S, Witt E, Huber PA, Medhurst AL, Ashworth A, Mathew CG.

Hum Mol Genet. 2003 Oct 1;12(19):2503-10.

20.

The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC.

Taniguchi T, D'Andrea AD.

Blood. 2002 Oct 1;100(7):2457-62.

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