(Q48324994)

10 February 2018

title

Characterization of ADAMTS14, a novel member of the ADAMTS metalloproteinase family. (English)

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10 February 2018

author

Alfredo Ramirez

2

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10 February 2018

author name string

H Bolz

1

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10 February 2018

B von Brederlow

3

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10 February 2018

C Kubisch

4

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10 February 2018

publication date

1 December 2001

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10 February 2018

Biochimica et Biophysica Acta

published in

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10 February 2018

volume

1522

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10 February 2018

issue

3

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10 February 2018

page(s)

221-225

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10 February 2018

Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10.

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

ADAM-TS5, ADAM-TS6, and ADAM-TS7, novel members of a new family of zinc metalloproteases. General features and genomic distribution of the ADAM-TS family

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

ADAMTS: a novel family of extracellular matrix proteases

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

Metalloprotease-disintegrins: links to cell adhesion and cleavage of TNF alpha and Notch

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

The ADAM gene family: surface proteins with adhesion and protease activity

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

Cloning and characterization of ADAMTS11, an aggrecanase from the ADAMTS family

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

Purification and cloning of aggrecanase-1: a member of the ADAMTS family of proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

Extracellular matrix and cell adhesion molecules in the developing inner ear

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

A novel locus for autosomal recessive peripheral neuropathy in the EGR2 region on 10q23.

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

Genetic fine mapping of the gene for nonsyndromic congenital retinal nonattachment

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

Procollagen II amino propeptide processing by ADAMTS-3. Insights on dermatosparaxis

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4781%2801%2900329-3

7 January 2021

10.1016/S0167-4781(01)00329-3

Identifiers

DOI

1 reference

10 February 2018

1 reference

10 February 2018