(Q28591745)

31 January 2017

title

Fdp, a new fibrocyte-derived protein related to MIA/CD-RAP, has an in vitro effect on the early differentiation of the inner ear mesenchyme (English)

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31 January 2017

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GOA release 2020-03-11

M. Cohen-Salmon

1

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Christine Petit

object named as

C. Petit

6

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author name string

D. Frenz

2

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31 January 2017

W. Liu

3

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31 January 2017

E. Verpy

4

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31 January 2017

S. Voegeling

5

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31 January 2017

language of work or name

English

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publication date

22 December 2000

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Journal of Biological Chemistry

31 January 2017

published in

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31 January 2017

volume

275

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31 January 2017

issue

51

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31 January 2017

page(s)

40036–40041

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Genes responsible for human hereditary deafness: symphony of a thousand

31 January 2017

cites work

1 reference

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The mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system

21 January 2018

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Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

21 January 2018

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Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss.

21 January 2018

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An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

21 January 2018

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Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening

21 January 2018

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Otogelin: a glycoprotein specific to the acellular membranes of the inner ear

21 January 2018

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Characterization of otoconin-95, the major protein of murine otoconia, provides insights into the formation of these inner ear biominerals

21 January 2018

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A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

21 January 2018

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Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9

21 January 2018

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Targeted disruption of otog results in deafness and severe imbalance

21 January 2018

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A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

21 January 2018

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Epithelial control of periotic mesenchyme chondrogenesis.

21 January 2018

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Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

21 January 2018

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A new method for predicting signal sequence cleavage sites

21 January 2018

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The structure and biosynthesis of glycosyl phosphatidylinositol protein anchors

21 January 2018

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Cloning of a retinoic acid-sensitive mRNA expressed in cartilage and during chondrogenesis

21 January 2018

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Mouse CD-RAP/MIA gene: structure, chromosomal localization, and expression in cartilage and chondrosarcoma

21 January 2018

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21 January 2018

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SPECIFIC STAINING OF SULPHATE GROUPS WITH ALCIAN BLUE AT LOW pH

21 January 2018

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Trans-activation of the mouse cartilage-derived retinoic acid-sensitive protein gene by Sox9.

21 January 2018

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Sox9 is required for cartilage formation

21 January 2018

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Structure and promoter analysis of the gene encoding the human melanoma-inhibiting protein MIA

21 January 2018

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Expression of cartilage extracellular matrix and potential regulatory genes in a new human chondrosarcoma cell line

21 January 2018

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The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency

21 January 2018

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Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

21 January 2018

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Expression of the gap-junction connexins 26 and 30 in the rat cochlea

21 January 2018

1 reference

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Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness.

21 January 2018

1 reference

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Transforming growth factor beta 1 is an epithelial-derived signal peptide that influences otic capsule formation

21 January 2018

1 reference

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Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

21 January 2018

1 reference

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Changes in the subcellular localization of the Brn4 gene product precede mesenchymal remodeling of the otic capsule

21 January 2018

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21 January 2018

1 reference

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Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002876200

Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

21 January 2018

1 reference

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Gap Junction Systems in the Rat Vestibular Labyrinth: Immunohistochemical and Ultrastructural Analysis

21 January 2018

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Towards high resolution maps of the mouse and human genomes—a facility for ordering markers to 0.1 cM resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002876200

21 January 2018

Identifiers

DOI

10.1074/JBC.M002876200

1 reference

31 January 2017

1 reference