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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 - 3 (of 3 Records)

Query Trace: Disease and LIMK1[original query]
Common genetic polymorphisms in moyamoya and atherosclerotic disease in Europeans.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2011 Feb 27 (2): 245-52.
Roder Constantin, Peters Vera, Kasuya Hidetoshi, Nishizawa Tsutomu, Takehara Yayoi, Berg Daniela, Schulte Claudia, Khan Nadia, Tatagiba Marcos, Krischek Bor
A mutation in Nischarin causes otitis media via LIMK1 and NF-?B pathways.
PLoS genetics 2017 Aug 13 (8): e1006969.
Crompton Michael, Purnell Tom, Tyrer Hayley E, Parker Andrew, Ball Greg, Hardisty-Hughes Rachel E, Gale Richard, Williams Debbie, Dean Charlotte H, Simon Michelle M, Mallon Ann-Marie, Wells Sara, Bhutta Mahmood F, Burton Martin J, Tateossian Hilda, Brown Steve D
Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases. GWAS Catalog
Annals of the rheumatic diseases 2019 Mar 78 (3): 311-319.
Acosta-Herrera Marialbert, Kerick Martin, González-Serna David, , , Wijmenga Cisca, Franke Andre, Gregersen Peter K, Padyukov Leonid, Worthington Jane, Vyse Timothy James, Alarcón-Riquelme Marta Eugenia, Mayes Maureen D, Martin Javi
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