Results 191 to 200 of about 2,256,617 (260)

Cockayne syndrome A and B proteins regulate the timing of transcription arrest upon genotoxic stress through a ubiquitin/proteasome degradation process

, 2017
Alexey Epanchintsev
openalex   +1 more source

CSA-dependent degradation of CSB by the ubiquitin–proteasome pathway establishes a link between complementation factors of the Cockayne syndrome [PDF]

, 2006
Regina Groisman, Isao Kuraoka, Odile Chevallier, Nogaye Gaye, Thierry Magnaldo, Kiyoji Tanaka, Alexei F. Kisselev, Annick Harel‐Bellan, Yoshihiro Nakatani   +8 more
openalex   +1 more source

The ATPase Domain but Not the Acidic Region of Cockayne Syndrome Group B Gene Product Is Essential for DNA Repair

, 1999
Robert M. Brosh, Adayabalam S. Balajee, Rebecca R. Selzer, Morten Sunesen, Luca Proietti‐De‐Santis, Vilhelm A. Bohr   +5 more
openalex   +2 more sources

Molecular Analysis of Mutations in the CSB(ERCC6) Gene in Patients with Cockayne Syndrome [PDF]

, 1998
Donna L. Mallery, Bianca Tanganelli, Stefano Colella, Herdis Steingrimsdottir, Alain J. van Gool, Christine Troelstra, Miria Stefanini, Alan R. Lehmann   +7 more
openalex   +1 more source

Treatment outcomes of cochlear implantation in pediatric patients with Cockayne syndrome type I: a case series. [PDF]

J Surg Case Rep
Kostova M, Banerjee A.
europepmc   +1 more source

Perioperative Care of a Pediatric Patient With Cockayne Syndrome

, 2017
Asad A. Khawaja, Joseph D. Tobias
openalex   +2 more sources

Spectrum of ERCC6-Related Cockayne Syndrome (Type B): From Mild to Severe Forms. [PDF]

Genes (Basel)
Sartorelli J, Travaglini L, Macchiaiolo M, Garone G, Gonfiantini MV, Vecchio D, Sinibaldi L, Frascarelli F, Ceccatelli V, Petrillo S, Piemonte F, Piccolo G, Novelli A, Longo D, Pro S, D'Amico A, Bertini ES, Nicita F.   +17 more
europepmc   +1 more source

COCKAYNE SYNDROME – A CASE REPORT

, 2018
Prabakaran Palanisamy, Arunsantosh Pullabhota, Harshavardhana Kurubara Manjaneyadu, Phani Chakarvarty Mutnuru   +3 more
openalex   +2 more sources

Biallelic structural variants in three patients with ERCC8-related Cockayne syndrome and a potential pitfall of copy number variation analysis. [PDF]

Sci Rep
Watanabe D, Okamoto N, Kobayashi Y, Suzuki H, Kato M, Saitoh S, Kanemura Y, Takenouchi T, Yamada M, Nakato D, Sato M, Tsunoda T, Kosaki K, Miya F.   +13 more
europepmc   +1 more source

The identification and analysis of mutation in the Cockayne Syndrome B gene

, 1999
Donna L. Mallery
openalex   +1 more source