Inner ear defects and hearing loss in mice lacking the collagen receptor DDR1

[1]  G. Agarwal,et al.  Interaction of discoidin domain receptor 1 with collagen type 1. , 2007, Journal of molecular biology.

[2]  W. Vogel,et al.  Discoidin domain receptor 1 null mice are protected against hypertension-induced renal disease. , 2006, Journal of the American Society of Nephrology : JASN.

[3]  J. van den Ende,et al.  A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene. , 2006, American journal of human genetics.

[4]  W. Vogel,et al.  Discoidin domain receptor 1-deficient mice are resistant to bleomycin-induced lung fibrosis. , 2006, American journal of respiratory and critical care medicine.

[5]  C. Ford,et al.  Sensing extracellular matrix: an update on discoidin domain receptor function. , 2006, Cellular signalling.

[6]  W. Vogel,et al.  DDR1 signaling is essential to sustain Stat5 function during lactogenesis , 2006, Journal of cellular biochemistry.

[7]  K. Nikolich,et al.  Discoidin Domain Receptor-1a (DDR1a) Promotes Glioma Cell Invasion and Adhesion in Association with Matrix Metalloproteinase-2 , 2006, Journal of Neuro-Oncology.

[8]  L. Ala‐Kokko,et al.  A Novel Autosomal Recessive Non-Syndromic Deafness Locus, DFNB66, Maps to Chromosome 6p21.2-22.3 in a Large Tunisian Consanguineous Family , 2006, Human Heredity.

[9]  A. Aszódi,et al.  Type IX collagen is crucial for normal hearing , 2005, Neuroscience.

[10]  Fatima Regina Abreu Alves,et al.  Revisão sobre a perda auditiva na Síndrome de Alport, analisando os aspectos clínicos, genéticos e biomoleculares , 2005 .

[11]  Fátima Alves,et al.  Revision about hearing loss in the Alport's syndrome, analyzing the clinical, genetic and bio-molecular aspects. , 2005, Brazilian journal of otorhinolaryngology.

[12]  H. Felix,et al.  Abnormal basement membrane in the inner ear and the kidney of the Mpv17-/- mouse strain: ultrastructural and immunohistochemical investigations , 2005, Histochemistry and Cell Biology.

[13]  S. Spicer,et al.  Pathologic changes of presbycusis begin in secondary processes and spread to primary processes of strial marginal cells , 2005, Hearing Research.

[14]  D. Milford,et al.  The Alport nephropathy: clinicopathological correlations , 2005, Pediatric Nephrology.

[15]  S. Spicer,et al.  Novel structures in marginal and intermediate cells presumably relate to functions of apical versus basal strial strata , 2005, Hearing Research.

[16]  C. Morton.  Gene discovery in the auditory system using a tissue specific approach , 2004, American journal of medical genetics. Part A.

[17]  W. Vogel,et al.  DDR1-deficient mice show localized subepithelial GBM thickening with focal loss of slit diaphragms and proteinuria. , 2004, Kidney international.

[18]  N. Carragher,et al.  Role of discoidin domain receptors 1 and 2 in human smooth muscle cell-mediated collagen remodeling: potential implications in atherosclerosis and lymphangioleiomyomatosis. , 2004, The American journal of pathology.

[19]  Hassane Izzedine,et al.  Ear and kidney syndromes: molecular versus clinical approach. , 2004, Kidney international.

[20]  K. Steel,et al.  Endocochlear potential generation is associated with intercellular communication in the stria vascularis: Structural analysis in the viable dominant spotting mouse mutant , 1990, Cell and Tissue Research.

[21]  Yehoash Raphael,et al.  Structure and innervation of the cochlea , 2003, Brain Research Bulletin.

[22]  M. Liberman,et al.  Lateral Wall Histopathology and Endocochlear Potential in the Noise-Damaged Mouse Cochlea , 2003, Journal of the Association for Research in Otolaryngology.

[23]  W. Vogel,et al.  Discoidin domain receptor 1 controls growth and adhesion of mesangial cells. , 2002, Journal of the American Society of Nephrology : JASN.

[24]  A. Forge,et al.  The molecular architecture of the inner ear. , 2002, British medical bulletin.

[25]  O. Henson,et al.  The presence and arrangement of type II collagen in the basilar membrane , 2002, Hearing Research.

[26]  P. Wangemann,et al.  KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential. , 2002, American journal of physiology. Cell physiology.

[27]  W. Vogel,et al.  Collagen-receptor signaling in health and disease. , 2001, European journal of dermatology : EJD.

[28]  J. White,et al.  Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes. , 2001, American journal of human genetics.

[29]  I. Naito,et al.  The inner ear of dogs with X-linked nephritis provides clues to the pathogenesis of hearing loss in X-linked Alport syndrome. , 2001, The American journal of pathology.

[30]  H. Weiher,et al.  Ultrastructural and physiological defects in the cochlea of the Mpv17 mouse strain A comparison between young and old adult animals , 2001, Hearing Research.

[31]  T. Pawson,et al.  Discoidin Domain Receptor 1 Tyrosine Kinase Has an Essential Role in Mammary Gland Development , 2001, Molecular and Cellular Biology.

[32]  W. Vogel,et al.  The discoidin domain receptor tyrosine kinase DDR1 in arterial wound repair. , 2001, The Journal of clinical investigation.

[33]  M. Kelley,et al.  Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9. , 2000, American journal of human genetics.

[34]  J. McGee,et al.  Ultrastructural, physiological, and molecular defects in the inner ear of a gene-knockout mouse model for autosomal Alport syndrome , 1998, Hearing Research.

[35]  T. Pawson,et al.  The discoidin domain receptor tyrosine kinases are activated by collagen. , 1997, Molecular cell.

[36]  G. Yancopoulos,et al.  An orphan receptor tyrosine kinase family whose members serve as nonintegrin collagen receptors. , 1997, Molecular cell.

[37]  P. Santi,et al.  Ultrastructural organization of proteoglycans and fibrillar matrix of the tectorial membrane , 1997, Hearing Research.

[38]  S. Heinemann,et al.  Inner Ear Defects Induced by Null Mutationof the isk Gene , 1996, Neuron.

[39]  J. Sanes,et al.  Molecular and functional defects in kidneys of mice lacking collagen alpha 3(IV): implications for Alport syndrome , 1996, The Journal of cell biology.

[40]  D. Cosgrove,et al.  Immunohistochemical localization of basement membrane collagens and associated proteins in the murine cochlea , 1996, Hearing Research.

[41]  S. Spicer,et al.  Localization of actin in basal cells of stria vascularis , 1996, Hearing Research.

[42]  J. Claes,et al.  Osteogenesis imperfecta and hearing loss. , 1996, Acta oto-rhino-laryngologica Belgica.

[43]  S. Spicer,et al.  Immunohistochemical localization of brain type glucose transporter in mammalian inner ears: Comparison of developmental and adult stages , 1993, Hearing Research.

[44]  I. Thalmann,et al.  Collagen of accessory structures of organ of Corti. , 1993, Connective tissue research.

[45]  D. B. Jenkins,et al.  Immunocytochemical localization of contractile and contraction associated proteins in the spiral ligament of the cochlea , 1985, Hearing Research.

[46]  D. Hilding,et al.  Pigmentation of the stria vascularis. The contribution of neural crest melanocytes. , 1977, Acta oto-laryngologica.

[47]  K. Jahnke,et al.  The fine structure of freeze-fractured intercellular junctions in the guinea pig inner ear. , 1975, Acta oto-laryngologica. Supplementum.

[48]  D. Hilding,et al.  The development of the stria vascularis in the mouse. , 1966, Acta oto-laryngologica.