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European Journal of Internal Medicine|April 7, 2004
Warfarin therapy is feasible in CYP2C9*3 homozygous patientsJacob Ablin, Shaltiel Cabili, Amiram Eldor, et al.
Cell and Tissue Research|July 30, 2008
Double gene deletion reveals lack of cooperation between claudin 11 and claudin 14 tight junction proteinsLiron Elkouby-Naor, Zaid Abassi, Ayala Lagziel, et al.
Molecular Vision|September 17, 2009
Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1DAyala Lagziel, Nora Overlack, Steven L Bernstein, et al.
Genomics|October 20, 2006
Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner earLinda M Peters, Inna A Belyantseva, Ayala Lagziel, et al.
Developmental Biology|May 11, 2005
Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell developmentAyala Lagziel, Zubair M Ahmed, Julie M Schultz, et al.
Molecular Genetics and Metabolism|March 21, 2007
Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuriaHava Peretz, Meirav Shtauber Naamati, David Levartovsky, et al.
Hearing Research|March 27, 2013
A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunctionSue I Lee, Travis Conrad, Sherri M Jones, et al.
The Journal of Clinical Investigation|February 7, 2018
Modifier variant of METTL13 suppresses human GAB1-associated profound deafnessRizwan Yousaf, Zubair M Ahmed, Arnaud Pj Giese, et al.
The New England Journal of Medicine|April 15, 2005
Modification of human hearing loss by plasma-membrane calcium pump PMCA2Julie M Schultz, Yandan Yang, Ariel J Caride, et al.
American Journal of Human Genetics|December 23, 2006
Tricellulin is a tight-junction protein necessary for hearingSaima Riazuddin, Zubair M Ahmed, Alan S Fanning, et al.
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