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Results: 1 to 20 of 160

Similar articles for PubMed (Select 11701636)

1.

DNA helicases, genomic instability, and human genetic disease.

van Brabant AJ, Stan R, Ellis NA.

Annu Rev Genomics Hum Genet. 2000;1:409-59. Review.

PMID:
11701636
2.

[Functional analysis of yeast homologue gene associated with human DNA helicase causative syndromes].

Miyajima A.

Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku. 2002;(120):53-74. Review. Japanese.

PMID:
12638184
3.

[DNA helicases and human diseases].

Uhring M, Poterszman A.

Med Sci (Paris). 2006 Dec;22(12):1087-94. Review. French.

4.
5.

Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases.

Gangloff S, Soustelle C, Fabre F.

Nat Genet. 2000 Jun;25(2):192-4.

PMID:
10835635
6.

Cloning of a human homolog of the yeast nucleotide excision repair gene MMS19 and interaction with transcription repair factor TFIIH via the XPB and XPD helicases.

Seroz T, Winkler GS, Auriol J, Verhage RA, Vermeulen W, Smit B, Brouwer J, Eker AP, Weeda G, Egly JM, Hoeijmakers JH.

Nucleic Acids Res. 2000 Nov 15;28(22):4506-13.

8.

The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor.

Weeda G, Rossignol M, Fraser RA, Winkler GS, Vermeulen W, van 't Veer LJ, Ma L, Hoeijmakers JH, Egly JM.

Nucleic Acids Res. 1997 Jun 15;25(12):2274-83.

9.

Premature aging and predisposition to cancers caused by mutations in RecQ family helicases.

Furuichi Y.

Ann N Y Acad Sci. 2001 Apr;928:121-31. Review.

PMID:
11795503
10.

DNA helicase deficiencies associated with cancer predisposition and premature ageing disorders.

Mohaghegh P, Hickson ID.

Hum Mol Genet. 2001 Apr;10(7):741-6. Review.

11.

Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases.

Siitonen HA, Kopra O, Kääriäinen H, Haravuori H, Winter RM, Säämänen AM, Peltonen L, Kestilä M.

Hum Mol Genet. 2003 Nov 1;12(21):2837-44. Epub 2003 Sep 2.

12.

Human diseases deficient in RecQ helicases.

Harrigan JA, Bohr VA.

Biochimie. 2003 Nov;85(11):1185-93.

PMID:
14726023
13.

Arabidopsis UVH6, a homolog of human XPD and yeast RAD3 DNA repair genes, functions in DNA repair and is essential for plant growth.

Liu Z, Hong SW, Escobar M, Vierling E, Mitchell DL, Mount DW, Hall JD.

Plant Physiol. 2003 Jul;132(3):1405-14.

14.
15.

TFIIH with inactive XPD helicase functions in transcription initiation but is defective in DNA repair.

Winkler GS, Araújo SJ, Fiedler U, Vermeulen W, Coin F, Egly JM, Hoeijmakers JH, Wood RD, Timmers HT, Weeda G.

J Biol Chem. 2000 Feb 11;275(6):4258-66.

16.

Human RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biology.

Monnat RJ Jr.

Semin Cancer Biol. 2010 Oct;20(5):329-39. doi: 10.1016/j.semcancer.2010.10.002. Epub 2010 Oct 8. Review.

17.
18.
19.

Transcription factor b (TFIIH) is required during nucleotide-excision repair in yeast.

Wang Z, Svejstrup JQ, Feaver WJ, Wu X, Kornberg RD, Friedberg EC.

Nature. 1994 Mar 3;368(6466):74-6.

PMID:
8107888
20.

Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases.

Yamagata K, Kato J, Shimamoto A, Goto M, Furuichi Y, Ikeda H.

Proc Natl Acad Sci U S A. 1998 Jul 21;95(15):8733-8.

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