Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Disease and EDAR[original query] |
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| Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia. American journal of medical genetics. Part A 2013 Apr 161A (4): 671-8. Plaisancié Julie, Bailleul-Forestier Isabelle, Gaston Véronique, Vaysse Fréderic, Lacombe Didier, Holder-Espinasse Muriel, Abramowicz Marc, Coubes Christine, Plessis Ghislaine, Faivre Laurence, Demeer Bénédicte, Vincent-Delorme Catherine, Dollfus Hélène, Sigaudy Sabine, Guillén-Navarro Encarna, Verloes Alain, Jonveaux Philippe, Martin-Coignard Dominique, Colin Estelle, Bieth Eric, Calvas Patrick, Chassaing Nicol |
| Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis. European journal of medical genetics 2016 Jun 59 (8): 377-385. Shahid Mohammad, Balto Hanan A, Al-Hammad Nouf, Joshi S, Khalil Hesham Saleh, Somily Ali Mohammed, Sinjilawi Nasr Abdul-Aziz, Al-Ghamdi Sameer, Faiyaz-Ul-Haque Muhammad, Dhillon Varinderpal |
| Downstream activation of NF-?B in the EDA-A1/EDAR signalling in Sjögren's syndrome and its regulation by the ubiquitin-editing enzyme A20. Clinical and experimental immunology 2016 Jan . Sisto Margherita, Barca Amilcare, Lofrumento Dario Domenico, Lisi Sabri |
| Geographic Variation in EGFR Mutation Frequency in Lung Adenocarcinoma May Be Explained by Interethnic Genetic Variation. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2018 03 13 (3): 454-458. Soraas Lars, Stebbing Just |
| Relation of Odor Identification with Alzheimer's Disease Markers in Cerebrospinal Fluid and Cognition. Journal of Alzheimer's disease : JAD 2017 60 (3): 1025-1034. Reijs Babette L R, Ramakers Inez H G B, Elias-Sonnenschein Lyzel, Teunissen Charlotte E, Koel-Simmelink Marleen, Tsolaki Magda, Wahlund Lars-Olof, Waldemar Gunhild, Hausner Lucrezia, Johannsen Peter, Vanderstichele Hugo, Verhey Frans, Devanand D P, Visser Pieter Jel |
| A novel EDAR missense mutation identified by whole-exome sequencing with non-syndromic tooth agenesis in a Chinese family. Molecular genetics & genomic medicine 2021 5 9 (6): e1684. Zhang Hongyu, Kong Xuanting, Ren Jiabao, Yuan Shuo, Liu Chunyan, Hou Yan, Liu Ye, Meng Lingqiang, Zhang Guozhong, Du Qingqing, Shen Wenji |
- Page last reviewed:Feb 1, 2024
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