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Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics.
Nat Genet. 2015 Sep;47(9):969-978. doi: 10.1038/ng.3360. Epub 2015 Jul 27.
Nat Genet. 2015.
PMID: 26214591
Free PMC article.
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.
Bowl MR, Simon MM, Ingham NJ, Greenaway S, Santos L, Cater H, Taylor S, Mason J, Kurbatova N, Pearson S, Bower LR, Clary DA, Meziane H, Reilly P, Minowa O, Kelsey L; International Mouse Phenotyping Consortium; Tocchini-Valentini GP, Gao X, Bradley A, Skarnes WC, Moore M, Beaudet AL, Justice MJ, Seavitt J, Dickinson ME, Wurst W, de Angelis MH, Herault Y, Wakana S, Nutter LMJ, Flenniken AM, McKerlie C, Murray SA, Svenson KL, Braun RE, West DB, Lloyd KCK, Adams DJ, White J, Karp N, Flicek P, Smedley D, Meehan TF, Parkinson HE, Teboul LM, Wells S, Steel KP, Mallon AM, Brown SDM.
Bowl MR, et al.
Nat Commun. 2017 Oct 12;8(1):886. doi: 10.1038/s41467-017-00595-4.
Nat Commun. 2017.
PMID: 29026089
Free PMC article.
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Silencing of the Ca2+ Channel ORAI1 Improves the Multi-Systemic Phenotype of Tubular Aggregate Myopathy (TAM) and Stormorken Syndrome (STRMK) in Mice.
Silva-Rojas R, Pérez-Guàrdia L, Lafabrie E, Moulaert D, Laporte J, Böhm J.
Silva-Rojas R, et al. Among authors: moulaert d.
Int J Mol Sci. 2022 Jun 23;23(13):6968. doi: 10.3390/ijms23136968.
Int J Mol Sci. 2022.
PMID: 35805973
Free PMC article.
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