(Q42521637)

1 November 2017

title

Inner ear defects and hearing loss in mice lacking the collagen receptor DDR1. (English)

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1 November 2017

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Angela M Meyer zum Gottesberge

1

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1 November 2017

Oliver Gross

2

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1 November 2017

Ursula Becker-Lendzian

3

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1 November 2017

Thomas Massing

4

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1 November 2017

Wolfgang F Vogel

5

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1 November 2017

language of work or name

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19 November 2007

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1 November 2017

published in

Laboratory Investigation

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1 November 2017

volume

88

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1 November 2017

issue

1

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1 November 2017

page(s)

27-37

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Type IX collagen is crucial for normal hearing

1 November 2017

cites work

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Ultrastructural organization of proteoglycans and fibrillar matrix of the tectorial membrane.

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The presence and arrangement of type II collagen in the basilar membrane.

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Collagen of accessory structures of organ of Corti

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7 January 2021

Abnormal basement membrane in the inner ear and the kidney of the Mpv17-/- mouse strain: ultrastructural and immunohistochemical investigations

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7 January 2021

Structure and innervation of the cochlea

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7 January 2021

The Development of the Stria Vascularis in the Mouse

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Localization of actin in basal cells of stria vascularis

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7 January 2021

The molecular architecture of the inner ear.

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7 January 2021

KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential

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7 January 2021

Inner ear defects induced by null mutation of the isk gene

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Ear and kidney syndromes: molecular versus clinical approach

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The Alport nephropathy: clinicopathological correlations

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Ultrastructural, physiological, and molecular defects in the inner ear of a gene-knockout mouse model for autosomal Alport syndrome

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7 January 2021

The inner ear of dogs with X-linked nephritis provides clues to the pathogenesis of hearing loss in X-linked Alport syndrome

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7 January 2021

The discoidin domain receptor tyrosine kinases are activated by collagen

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7 January 2021

An orphan receptor tyrosine kinase family whose members serve as nonintegrin collagen receptors

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7 January 2021

Sensing extracellular matrix: an update on discoidin domain receptor function

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7 January 2021

Discoidin domain receptor 1-deficient mice are resistant to bleomycin-induced lung fibrosis

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7 January 2021

Discoidin domain receptor-1a (DDR1a) promotes glioma cell invasion and adhesion in association with matrix metalloproteinase-2.

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7 January 2021

The discoidin domain receptor tyrosine kinase DDR1 in arterial wound repair

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7 January 2021

Discoidin domain receptor 1 tyrosine kinase has an essential role in mammary gland development

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7 January 2021

DDR1 signaling is essential to sustain Stat5 function during lactogenesis

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7 January 2021

DDR1-deficient mice show localized subepithelial GBM thickening with focal loss of slit diaphragms and proteinuria.

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7 January 2021

Discoidin domain receptor 1 null mice are protected against hypertension-induced renal disease

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7 January 2021

Ultrastructural and physiological defects in the cochlea of the Mpv17 mouse strain. A comparison between young and old adult animals

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7 January 2021

Endocochlear potential generation is associated with intercellular communication in the stria vascularis: structural analysis in the viable dominant spotting mouse mutant

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7 January 2021

Lateral wall histopathology and endocochlear potential in the noise-damaged mouse cochlea

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7 January 2021

Pathologic changes of presbycusis begin in secondary processes and spread to primary processes of strial marginal cells

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7 January 2021

Novel structures in marginal and intermediate cells presumably relate to functions of apical versus basal strial strata

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7 January 2021

Immunohistochemical localization of brain type glucose transporter in mammalian inner ears: comparison of developmental and adult stages

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7 January 2021

Interaction of discoidin domain receptor 1 with collagen type 1.

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7 January 2021

Role of discoidin domain receptors 1 and 2 in human smooth muscle cell-mediated collagen remodeling: potential implications in atherosclerosis and lymphangioleiomyomatosis

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7 January 2021

Discoidin domain receptor 1 controls growth and adhesion of mesangial cells

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7 January 2021

Gene discovery in the auditory system using a tissue specific approach

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7 January 2021

A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous family.

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7 January 2021

A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene

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https://api.crossref.org/works/10.1038%2FLABINVEST.3700692

7 January 2021

Molecular and functional defects in kidneys of mice lacking collagen alpha 3(IV): implications for Alport syndrome

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.3700692

7 January 2021

Immunocytochemical localization of contractile and contraction associated proteins in the spiral ligament of the cochlea

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.3700692

7 January 2021

Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9

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7 January 2021

Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.3700692

7 January 2021

10.1038/LABINVEST.3700692

Identifiers

DOI

1 reference

1 November 2017

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