Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss

Mutations in CLDN14 are associated with different hearing thresholds

(2010) Rasheeda Bashir et al.   JOURNAL OF HUMAN GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Structure and Function of Extracellular Claudin Domains

(2009) Gerd Krause et al.   Annals of the New York Academy of Sciences

A Claudin-9–Based Ion Permeability Barrier Is Essential for Hearing

(2009) Yoko Nakano et al.   PLoS Genetics

A Key Claudin Extracellular Loop Domain is Critical for Epithelial Barrier Integrity

(2008) Randall J. Mrsny et al.   AMERICAN JOURNAL OF PATHOLOGY

SNAP predicts effect of mutations on protein function

(2008) Yana Bromberg et al.   BIOINFORMATICS

GPS 2.0, a Tool to Predict Kinase-specific Phosphorylation Sites in Hierarchy

(2008) Yu Xue et al.   MOLECULAR & CELLULAR PROTEOMICS

Prognostic significance of intestinal claudins in high-risk synchronous and metachronous multiple gastric epithelial neoplasias after initial endoscopic submucosal dissection

(2008) Shuho Semba et al.   PATHOLOGY INTERNATIONAL

CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

(2007) M. Konrad et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY