Pages that link to "Q41771953"

The following pages link to Xeroderma pigmentosum--Cockayne syndrome complex: a further case (Q41771953):

Displaying 30 items.

• Retracted: A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function (Q24678938) (← links)
• First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure (Q24680149) (← links)
• Diseases associated with defective responses to DNA damage (Q26997852) (← links)
• Mammalian transcription-coupled excision repair (Q27022616) (← links)
• Physiological consequences of defects in ERCC1–XPF DNA repair endonuclease (Q28238547) (← links)
• Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G (Q28302894) (← links)
• Identification of the XPG region that causes the onset of Cockayne syndrome by using Xpg mutant mice generated by the cDNA-mediated knock-in method (Q28506081) (← links)
• Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene (Q28592787) (← links)
• Developmental defects and male sterility in mice lacking the ubiquitin-like DNA repair gene mHR23B (Q28863975) (← links)
• Xeroderma pigmentosum group A protein loads as a separate factor onto DNA lesions (Q30974742) (← links)
• Anti-tumour compounds illudin S and Irofulven induce DNA lesions ignored by global repair and exclusively processed by transcription- and replication-coupled repair pathways. (Q31126129) (← links)
• Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy (Q32067170) (← links)
• Cockayne syndrome and xeroderma pigmentosum (Q34143455) (← links)
• The ERCC1 and ERCC4 (XPF) genes and gene products (Q35663361) (← links)
• A Rare Case of Cockayne Syndrome-MRI Features (Q36481448) (← links)
• Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage? (Q36690915) (← links)
• Ocular manifestations of xeroderma pigmentosum: long-term follow-up highlights the role of DNA repair in protection from sun damage (Q36986273) (← links)
• Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome (Q37593459) (← links)
• Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damage (Q37684033) (← links)
• Xeroderma pigmentosum-Cockayne syndrome complex (Q37736827) (← links)
• Recruitment of the nucleotide excision repair endonuclease XPG to sites of UV-induced dna damage depends on functional TFIIH. (Q39127506) (← links)
• Novel XPG (ERCC5) mutations affect DNA repair and cell survival after ultraviolet but not oxidative stress. (Q39223156) (← links)
• Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing (Q39393194) (← links)
• Disruption of Xpg increases spontaneous mutation frequency, particularly A:T to C:G transversion (Q40764618) (← links)
• Homozygous R788W Point Mutation in the XPF Gene of a Patient with Xeroderma Pigmentosum and Late-Onset Neurologic Disease (Q42454862) (← links)
• Purkinje cell degeneration in mice lacking the xeroderma pigmentosum group G gene (Q48887750) (← links)
• Rapid switching of TFIIH between RNA polymerase I and II transcription and DNA repair in vivo (Q51841369) (← links)
• Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy (Q55670525) (← links)
• Heritable genetic alterations in a xeroderma pigmentosum group G/Cockayne syndrome pedigree (Q74107895) (← links)
• A comprehensive description of the severity groups in Cockayne syndrome (Q83824079) (← links)