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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Disease and EDA[original query]
Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study.
PLoS genetics 2009 Jan 5 (1): e1000338.
Tanaka Toshiko, Shen Jian, Abecasis Gonçalo R, Kisialiou Aliaksei, Ordovas Jose M, Guralnik Jack M, Singleton Andrew, Bandinelli Stefania, Cherubini Antonio, Arnett Donna, Tsai Michael Y, Ferrucci Lui
Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia.
Journal of medical genetics 2011 Jun 48 (6): 426-32.
Schneider Holm, Hammersen Johanna, Preisler-Adams Sabine, Huttner Kenneth, Rascher Wolfgang, Bohring Ax
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
[Mutation screening and functional analysis for 8 patients with ectodermal dysplasia].
Shanghai kou qiang yi xue = Shanghai journal of stomatology 2019 9 28 (3): 268-274.
Zhao Kai, Yu Kang, Wang Feng, Sun Yuan-Yuan, Wu Yi-Q
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
Elevated plasma EDA fibronectin in primary myelofibrosis is determined by high allele burden of JAK2V617F mutation and strongly predicts splenomegaly progression.
Frontiers in oncology 2022 10 12 987643.
Malara Alessandro, Gruppi Cristian, Massa Margherita, Tira Maria Enrica, Rosti Vittorio, Balduini Alessandra, Barosi Giovan
DNA Methylation in the Anti-Mullerian Hormone Gene and the Risk of Disease Activity in Multiple Sclerosis.
Annals of neurology 2024 5 .
Antonino Giordano, Béatrice Pignolet, Elisabetta Mascia, Ferdinando Clarelli, Melissa Sorosina, Kaalindi Misra, Florence Bucciarelli, Laura Ferrè, Lucia Moiola, Roland Liblau, Massimo Filippi, Federica Esposi
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