A mutation ofMET, encoding hepatocyte growth factor receptor, is associated with humanDFNB97hearing loss

Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation

(2013) Sarah Doss et al.   JOURNAL OF NEUROLOGY

Hepatocyte Growth Factor Signaling in Intrapancreatic Ductal Cells Drives Pancreatic Morphogenesis

(2013) Ryan M. Anderson et al.   PLoS Genetics

HGF Accelerates Wound Healing by Promoting the Dedifferentiation of Epidermal Cells throughβ1-Integrin/ILK Pathway

(2013) Jin-Feng Li et al.   Biomed Research International

Autosomal recessive nonsyndromic deafness genes: a review

(2012) Duygu Duman   Frontiers in Bioscience-Landmark

An overview of the c-MET signaling pathway

(2011) Shawna Leslie Organ et al.   Therapeutic Advances in Medical Oncology

Hearing Impairment: A Panoply of Genes and Functions

(2010) Amiel A. Dror et al.   NEURON

Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

(2009) Julie M. Schultz et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A High Affinity Hepatocyte Growth Factor-binding Site in the Immunoglobulin-like Region of Met

(2008) Cristina Basilico et al.   JOURNAL OF BIOLOGICAL CHEMISTRY