Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss

Tricellulin deficiency affects tight junction architecture and cochlear hair cells

(2013) Gowri Nayak et al.   JOURNAL OF CLINICAL INVESTIGATION

Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing

(2013) Tao Yang et al.   Orphanet Journal of Rare Diseases

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

(2012) Kwanghyuk Lee et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Analysis of the 'angulin' proteins LSR, ILDR1 and ILDR2 - tricellulin recruitment, epithelial barrier function and implication in deafness pathogenesis

(2012) T. Higashi et al.   JOURNAL OF CELL SCIENCE

Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

(2011) Guntram Borck et al.   AMERICAN JOURNAL OF HUMAN GENETICS

DFNB49 is an important cause of non-syndromic deafness in Czech Roma patients but not in the general Czech population

(2011) D Šafka Brožková et al.   CLINICAL GENETICS

Tricellulin forms homomeric and heteromeric tight junctional complexes

(2010) Julie K. Westphal et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Dynamics and functions of tight junctions

(2010) Emily Steed et al.   TRENDS IN CELL BIOLOGY

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

(2009) Yoko Nakano et al.   PLoS Genetics

Tight junction-based epithelial microenvironment and cell proliferation

(2008) S Tsukita et al.   ONCOGENE