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searching for RECQL4 7 found (24 total)

alternate case: rECQL4

UBR1 (899 words) [view diff] exact match in snippet view article find links to article

PMC 514446. PMID 15302935. Yin J, Kwon YT, Varshavsky A, Wang W (2005). "RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with

List of genes mutated in cutaneous conditions (108 words) [view diff] case mismatch in snippet view article find links to article

(WRN) DNA helicase Werner syndrome RecQL3 (BLM) DNA helicase Bloom syndrome RecQL4 DNA helicase Rothmund–Thomson syndrome RET MEN2A, MEN2B SAMD9 Familial tumoral

UBR2 (584 words) [view diff] exact match in snippet view article find links to article

1038/ng1285. PMID 14702039. Yin J, Kwon YT, Varshavsky A, Wang W (2005). "RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with

FAM13B (842 words) [view diff] case mismatch in snippet view article find links to article

functions. N-terminal homeodomain-like domain of metazoan RecQ protein-like 4 (RecQL4_SLD2_NTD) - involved in various cellular process, including DNA replication

Xenopus (5,807 words) [view diff] case mismatch in snippet view article find links to article

BRCA1 inherited breast and ovarian cancer, Nbs1 Nijmegen breakage syndrome, RecQL4 Rothmund-Thomson syndrome, c-Myc oncogene and FANC proteins (Fanconi anemia)

Progeroid syndromes (8,748 words) [view diff] exact match in snippet view article find links to article

encoding RecQ in humans (RECQ1-5), and defects in RECQL2/WRN, RECQL3/BLM and RECQL4 lead to Werner syndrome (WS), Bloom syndrome (BS), and Rothmund–Thomson

Gluten-sensitive enteropathy–associated conditions (7,562 words) [view diff] exact match in snippet view article find links to article

congenitale, is a rare disorder, generally attributed to mutations of the RECQL4 helicase gene on 8q24 with features that include photosensitivity and poikilodermatous