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.
23. Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations. Arte S; Parmanen S; Pirinen S; Alaluusua S; Nieminen P PLoS One; 2013; 8(8):e73705. PubMed ID: 23991204 [TBL] [Abstract][Full Text] [Related]
24. Structural insights into pathogenic mechanism of hypohidrotic ectodermal dysplasia caused by ectodysplasin A variants. Yu K; Huang C; Wan F; Jiang C; Chen J; Li X; Wang F; Wu J; Lei M; Wu Y Nat Commun; 2023 Feb; 14(1):767. PubMed ID: 36765055 [TBL] [Abstract][Full Text] [Related]
25. Compound heterozygous WNT10A missense variations exacerbated the tooth agenesis caused by hypohidrotic ectodermal dysplasia. Liu Y; Sun J; Zhang C; Wu Y; Ma S; Li X; Wu X; Gao Q BMC Oral Health; 2024 Jan; 24(1):136. PubMed ID: 38280992 [TBL] [Abstract][Full Text] [Related]
26. Molecular aspects of hypohidrotic ectodermal dysplasia. Mikkola ML Am J Med Genet A; 2009 Sep; 149A(9):2031-6. PubMed ID: 19681132 [TBL] [Abstract][Full Text] [Related]
27. Molecular genetic analysis of patients from India with hypohidrotic ectodermal dysplasia reveals novel mutations in the EDA and EDAR genes. RamaDevi AR; Reddy EC; Ranjan S; Bashyam MD Br J Dermatol; 2008 Jan; 158(1):163-7. PubMed ID: 17970812 [No Abstract] [Full Text] [Related]
28. Novel mutations identified in patients with tooth agenesis by whole-exome sequencing. Zhao K; Lian M; Zou D; Huang W; Zhou W; Shen Y; Wang F; Wu Y Oral Dis; 2019 Mar; 25(2):523-534. PubMed ID: 30417976 [TBL] [Abstract][Full Text] [Related]
29. A compound heterozygous mutation in the EDAR gene in a Spanish family with autosomal recessive hypohidrotic ectodermal dysplasia. Moya-Quiles MR; Ballesta-Martínez MJ; López-González V; Glover G; Guillén-Navarro E Arch Dermatol Res; 2010 May; 302(4):307-10. PubMed ID: 20033817 [TBL] [Abstract][Full Text] [Related]
30. Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients. Zeng B; Xiao X; Li S; Lu H; Lu J; Zhu L; Yu D; Zhao W Genes (Basel); 2016 Sep; 7(9):. PubMed ID: 27657131 [TBL] [Abstract][Full Text] [Related]
31. [Whole exome sequencing and analysis of hypohidrotic ectodermal dysplasia patients]. Liu XY; Zhu JX; Zhao YM Zhonghua Kou Qiang Yi Xue Za Zhi; 2022 Feb; 57(2):155-161. PubMed ID: 35152651 [No Abstract] [Full Text] [Related]
32. Understanding the impact of missense mutations on the structure and function of the EDA gene in X-linked hypohidrotic ectodermal dysplasia: A bioinformatics approach. Ranjan P; Das P J Cell Biochem; 2022 Feb; 123(2):431-449. PubMed ID: 34817077 [TBL] [Abstract][Full Text] [Related]
33. Novel EDA mutation in X-linked hypohidrotic ectodermal dysplasia and genotype-phenotype correlation. Zeng B; Lu H; Xiao X; Zhou L; Lu J; Zhu L; Yu D; Zhao W Oral Dis; 2015 Nov; 21(8):994-1000. PubMed ID: 26411740 [TBL] [Abstract][Full Text] [Related]
34. Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus. Bal E; Baala L; Cluzeau C; El Kerch F; Ouldim K; Hadj-Rabia S; Bodemer C; Munnich A; Courtois G; Sefiani A; Smahi A Hum Mutat; 2007 Jul; 28(7):703-9. PubMed ID: 17354266 [TBL] [Abstract][Full Text] [Related]
35. Novel missense mutation in the EDA gene in a family affected by oligodontia. Ruiz-Heiland G; Jabir S; Wende W; Blecher S; Bock N; Ruf S J Orofac Orthop; 2016 Jan; 77(1):31-8. PubMed ID: 26753551 [TBL] [Abstract][Full Text] [Related]
36. Ectodysplasin A (EDA) - EDA receptor signalling and its pharmacological modulation. Kowalczyk-Quintas C; Schneider P Cytokine Growth Factor Rev; 2014 Apr; 25(2):195-203. PubMed ID: 24508088 [TBL] [Abstract][Full Text] [Related]
37. A novel frameshift mutation in the Rahbaran M; Hassani Doabsari M; Salavitabar S; Mokhberian N; Morovvati Z; Morovvati S Cell Mol Biol Lett; 2019; 24():54. PubMed ID: 31452656 [TBL] [Abstract][Full Text] [Related]
38. Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR- and EDA-associated nonsyndromic oligodontia. Zhang L; Yu M; Wong SW; Qu H; Cai T; Liu Y; Liu H; Fan Z; Zheng J; Zhou Y; Feng H; Han D Hum Mutat; 2020 Nov; 41(11):1957-1966. PubMed ID: 32906216 [TBL] [Abstract][Full Text] [Related]
39. Two novel mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia. Gunadi ; Miura K; Ohta M; Sugano A; Lee MJ; Sato Y; Matsunaga A; Hayashi K; Horikawa T; Miki K; Wataya-Kaneda M; Katayama I; Nishigori C; Matsuo M; Takaoka Y; Nishio H Pediatr Res; 2009 Apr; 65(4):453-7. PubMed ID: 19127222 [TBL] [Abstract][Full Text] [Related]
40. Oligodontia and curly hair occur with ectodysplasin-a mutations. Lee KE; Ko J; Shin TJ; Hyun HK; Lee SH; Kim JW J Dent Res; 2014 Apr; 93(4):371-5. PubMed ID: 24487376 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]