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Items: 4

1.
Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma
Isabelle Schrauwen, Béla I. Melegh, Imen Chakchouk, Anushree Acharya, Abdul Nasir, Alexis Poston, Diana M. Cornejo-Sanchez, Zsolt Szabo, Tamás Karosi, Judit Bene, Béla Melegh, Suzanne M. Leal
Eur J Hum Genet. 2019 Jun; 27(6): 869–878. Published online 2019 Mar 14. doi: 10.1038/s41431-019-0372-y
PMCID:
PMC6777543
AbstractArticlePDF–1.7M
2.
Absence of plastin 1 causes abnormal maintenance of hair cell stereocilia and a moderate form of hearing loss in mice
Ruth Taylor, Anwen Bullen, Stuart L. Johnson, Eva-Maria Grimm-Günter, Francisco Rivero, Walter Marcotti, Andrew Forge, Nicolas Daudet
Hum Mol Genet. 2015 Jan 1; 24(1): 37–49. Published online 2014 Aug 14. doi: 10.1093/hmg/ddu417
PMCID:
PMC4262491
AbstractArticlePDF–1.5M
3.
Plastin 1 Binds to Keratin and Is Required for Terminal Web Assembly in the Intestinal Epithelium
Eva-Maria S. Grimm-Günter, Céline Revenu, Sonia Ramos, Ilse Hurbain, Neil Smyth, Evelyne Ferrary, Daniel Louvard, Sylvie Robine, Francisco Rivero
Mol Biol Cell. 2009 May 15; 20(10): 2549–2562. doi: 10.1091/mbc.E08-10-1030
PMCID:
PMC2682596
AbstractArticlePDF–1.2M
4.
Identification of I-plastin, a human fimbrin isoform expressed in intestine and kidney.
C S Lin, W Shen, Z P Chen, Y H Tu, P Matsudaira
Mol Cell Biol. 1994 Apr; 14(4): 2457–2467. doi: 10.1128/mcb.14.4.2457
PMCID:
PMC358613
SummaryPage BrowsePDF–3.2M

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