These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
25. The AP-2 Transcription Factor APTF-2 Is Required for Neuroblast and Epidermal Morphogenesis in Caenorhabditis elegans Embryogenesis. Budirahardja Y; Tan PY; Doan T; Weisdepp P; Zaidel-Bar R PLoS Genet; 2016 May; 12(5):e1006048. PubMed ID: 27176626 [TBL] [Abstract][Full Text] [Related]
26. Wnt1-Cre-mediated deletion of AP-2alpha causes multiple neural crest-related defects. Brewer S; Feng W; Huang J; Sullivan S; Williams T Dev Biol; 2004 Mar; 267(1):135-52. PubMed ID: 14975722 [TBL] [Abstract][Full Text] [Related]
27. The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia. Mollaaghababa R; Pavan WJ Oncogene; 2003 May; 22(20):3024-34. PubMed ID: 12789277 [TBL] [Abstract][Full Text] [Related]
28. Familial occurrence of patent ductus arteriosus. Sletten LJ; Pierpont ME Am J Med Genet; 1995 May; 57(1):27-30. PubMed ID: 7645594 [TBL] [Abstract][Full Text] [Related]
29. Familial patent ductus arteriosus and bicuspid aortic valve with hand anomalies: a novel heart-hand syndrome. Gelb BD; Zhang J; Sommer RJ; Wasserman JM; Reitman MJ; Willner JP Am J Med Genet; 1999 Nov; 87(2):175-9. PubMed ID: 10533032 [TBL] [Abstract][Full Text] [Related]
30. Congenital corneal anesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and mental retardation: a new syndrome? Ramos-Arroyo MA; Clark GG; Saksena SS; Hodes ME Am J Med Genet; 1987 Feb; 26(2):345-54. PubMed ID: 2433942 [TBL] [Abstract][Full Text] [Related]
31. Comparative analysis of the FOXL2 gene and characterization of mutations in BPES patients. Udar N; Yellore V; Chalukya M; Yelchits S; Silva-Garcia R; Small K; Hum Mutat; 2003 Sep; 22(3):222-8. PubMed ID: 12938087 [TBL] [Abstract][Full Text] [Related]
32. AP-2β is a transcriptional regulator for determination of digit length in tetrapods. Seki R; Kitajima K; Matsubara H; Suzuki T; Saito D; Yokoyama H; Tamura K Dev Biol; 2015 Nov; 407(1):75-89. PubMed ID: 26277217 [TBL] [Abstract][Full Text] [Related]
33. [Clinical characteristics and genetic analysis of a child with Char syndrome caused by TFAP2B gene variant]. Hu B; Liu Z; Zhang X; Yang D; Li Y; Li H; Fang S Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Aug; 41(8):936-940. PubMed ID: 39097275 [TBL] [Abstract][Full Text] [Related]
34. The NMR solution structure of a mutant of the Max b/HLH/LZ free of DNA: insights into the specific and reversible DNA binding mechanism of dimeric transcription factors. Sauvé S; Tremblay L; Lavigne P J Mol Biol; 2004 Sep; 342(3):813-32. PubMed ID: 15342239 [TBL] [Abstract][Full Text] [Related]
35. A BMAL1 mutant with arginine 91 substituted with alanine acts as a dominant negative inhibitor. Hosoda H; Motohashi J; Kato H; Masushige S; Kida S Gene; 2004 Sep; 338(2):235-41. PubMed ID: 15315827 [TBL] [Abstract][Full Text] [Related]
36. Expression of a truncated Sall1 transcriptional repressor is responsible for Townes-Brocks syndrome birth defects. Kiefer SM; Ohlemiller KK; Yang J; McDill BW; Kohlhase J; Rauchman M Hum Mol Genet; 2003 Sep; 12(17):2221-7. PubMed ID: 12915476 [TBL] [Abstract][Full Text] [Related]
37. Solution structure of the K50 class homeodomain PITX2 bound to DNA and implications for mutations that cause Rieger syndrome. Chaney BA; Clark-Baldwin K; Dave V; Ma J; Rance M Biochemistry; 2005 May; 44(20):7497-511. PubMed ID: 15895993 [TBL] [Abstract][Full Text] [Related]
38. KCTD1 mutants in scalp‑ear‑nipple syndrome and AP‑2α P59A in Char syndrome reciprocally abrogate their interactions, but can regulate Wnt/β‑catenin signaling. Hu L; Chen L; Yang L; Ye Z; Huang W; Li X; Liu Q; Qiu J; Ding X Mol Med Rep; 2020 Nov; 22(5):3895-3903. PubMed ID: 33000225 [TBL] [Abstract][Full Text] [Related]
39. Identification of two novel mutations of IRF6 in Korean families affected with Van der Woude syndrome. Kim Y; Park JY; Lee TJ; Yoo HW Int J Mol Med; 2003 Oct; 12(4):465-8. PubMed ID: 12964020 [TBL] [Abstract][Full Text] [Related]