Literature DB >> 7587084

Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome.

W Vermeulen1, A J van Vuuren, M Chipoulet, L Schaeffer, E Appeldoorn, G Weeda, N G Jaspers, A Priestley, C F Arlett, A R Lehmann.   

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Year:  1994        PMID： 7587084     DOI： 10.1101/sqb.1994.059.01.036

Source DB:  PubMed          Journal:  Cold Spring Harb Symp Quant Biol        ISSN： 0091-7451


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  37 in total

1.  Scanning confocal fluorescence microscopy for single molecule analysis of nucleotide excision repair complexes.

Authors:  G M J Segers-Nolten; C Wyman; N Wijgers; W Vermeulen; A T M Lenferink; J H J Hoeijmakers; J Greve; C Otto
Journal:  Nucleic Acids Res       Date:  2002-11-01       Impact factor: 16.971

2.  Substrate specificity of the cdk-activating kinase (CAK) is altered upon association with TFIIH.

Authors:  M Rossignol; I Kolb-Cheynel; J M Egly
Journal:  EMBO J       Date:  1997-04-01       Impact factor: 11.598

3.  Single-stranded DNA binding activity of XPBI, but not XPBII, from Sulfolobus tokodaii causes double-stranded DNA melting.

Authors:  Xiaoqing Ma; Ye Hong; Wenyuan Han; Duohong Sheng; Jinfeng Ni; Guihua Hou; Yulong Shen
Journal:  Extremophiles       Date:  2010-12-05       Impact factor: 2.395

Review 4.  Cockayne syndrome: defective repair of transcription?

Authors:  A J van Gool; G T van der Horst; E Citterio; J H Hoeijmakers
Journal:  EMBO J       Date:  1997-07-16       Impact factor: 11.598

5.  Functional TFIIH is required for UV-induced translocation of CSA to the nuclear matrix.

Authors:  Masafumi Saijo; Tamami Hirai; Akiko Ogawa; Aki Kobayashi; Shinya Kamiuchi; Kiyoji Tanaka
Journal:  Mol Cell Biol       Date:  2007-01-22       Impact factor: 4.272

6.  Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism.

Authors:  Satoshi Makino; Ryuji Kaji; Satoshi Ando; Maiko Tomizawa; Katsuhito Yasuno; Satoshi Goto; Shinnichi Matsumoto; Maria Daisy Tabuena; Elma Maranon; Marita Dantes; Lillian V Lee; Kazumasa Ogasawara; Ikuo Tooyama; Hiroyasu Akatsu; Masataka Nishimura; Gen Tamiya
Journal:  Am J Hum Genet       Date:  2007-01-23       Impact factor: 11.025

7.  Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy.

Authors:  Jennifer Boyle; Takahiro Ueda; Kyu-Seon Oh; Kyoko Imoto; Deborah Tamura; Jared Jagdeo; Sikandar G Khan; Carine Nadem; John J Digiovanna; Kenneth H Kraemer
Journal:  Hum Mutat       Date:  2008-10       Impact factor: 4.878

8.  Cockayne syndrome group B protein enhances elongation by RNA polymerase II.

Authors:  C P Selby; A Sancar
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-14       Impact factor: 11.205

9.  Mechanism of open complex and dual incision formation by human nucleotide excision repair factors.

Authors:  E Evans; J G Moggs; J R Hwang; J M Egly; R D Wood
Journal:  EMBO J       Date:  1997-11-03       Impact factor: 11.598

10.  The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex.

Authors:  A J van Gool; E Citterio; S Rademakers; R van Os; W Vermeulen; A Constantinou; J M Egly; D Bootsma; J H Hoeijmakers
Journal:  EMBO J       Date:  1997-10-01       Impact factor: 11.598
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