COL4A6 is dispensable for autosomal recessive Alport syndrome. - Wikidata - awgldk - TriplyDB

COL4A6 is dispensable for autosomal recessive Alport syndrome.

COL4A6 is dispensable for autosomal recessive Alport syndrome.

http://www.wikidata.org/entity/Q37063978

about

Type IV collagen α6 chain is a regulator of keratin 10 in keratinization of oral mucosal epithelium.

P2860

Q50107229-D9193B8A-F456-4E73-9785-E2E1C66E9778

P2860

COL4A6 is dispensable for autosomal recessive Alport syndrome.

http://www.wikidata.org/entity/Q37063978

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 05 July 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

COL4A6 is dispensable for autosomal recessive Alport syndrome.

@en

COL4A6 is dispensable for autosomal recessive Alport syndrome.

@nl

type

label

COL4A6 is dispensable for autosomal recessive Alport syndrome.

@en

COL4A6 is dispensable for autosomal recessive Alport syndrome.

@nl

prefLabel

COL4A6 is dispensable for autosomal recessive Alport syndrome.

@en

COL4A6 is dispensable for autosomal recessive Alport syndrome.

@nl

P1433

Q37063978-3B545DCC-CC37-4115-BCCA-EC06AD59EB05

P1476

Q37063978-E6046B52-EF76-41E0-ACA3-056D7855EEAA

P2093

Q37063978-0C4765A9-D1B4-4A32-90A3-779A1D487CEF

Q37063978-3395820C-76EC-488F-BFCF-9B64F0F23853

Q37063978-679CA8F3-7F63-4B5F-8D3F-808940FA7892

Q37063978-6E64FE32-9BAE-42E9-A8BF-47ADF8605306

Q37063978-6F5A1BED-F2E5-49B4-BBED-918FDC92CF21

Q37063978-9CB9C550-825F-46F1-BA33-307BEF1E0B1A

Q37063978-CEE331C3-F734-4845-80B4-3693F7503F68

Q37063978-E88BF5FB-9939-4109-BEA4-3A9BBD932926

Q37063978-F2FB7260-F6A7-4DCF-A22A-E73499E34468

Q37063978-FCFD4B55-4004-4976-BBE3-6F952D2A38FC

P2860

Q37063978-12BD72FF-658F-4FB3-922F-127FCFC0507D

Q37063978-17B568C2-D7F5-4757-999F-9F9AC9191D10

Q37063978-29A3F321-F439-4225-816C-248EF7180455

Q37063978-2EDFDBCB-9B53-451F-9565-6D0250F4B14F

Q37063978-3C9B0924-73F1-4F23-ABEE-346A3CCDD40C

Q37063978-41F3367A-AC10-4BEA-9DBD-8A4AF26D3C44

Q37063978-55A652C7-7BEB-46FD-8BDA-03AB34AE08BB

Q37063978-5708E3AB-8F26-4B17-BC0B-016B6A92AD70

Q37063978-6A5B2F5D-CF3E-4263-A777-99E3B3454AA7

Q37063978-6C3511EA-39DF-4F80-8862-D51860D21ED4

P2888

Q37063978-A171F68C-109D-426A-96D3-CBE46DECA374

P304

Q37063978-98B073D9-638C-49CB-9953-7D1B67A2687D

P31

Q37063978-15EAC3D5-8E63-494F-98CF-CDB21C59B60E

P356

Q37063978-80E6FAC4-3E0C-4F7F-BBE6-F5DE5AB3F30A

P407

Q37063978-413B8F6A-E7B0-4DDF-8C23-076650B1AAE3

P478

Q37063978-3C4BD174-93F0-4665-BA02-B60ED4F190B1

P577

Q37063978-0B4A6082-FDE9-401A-BC8C-2CC706B08404

P698

Q37063978-AFC68CD7-3866-452E-921A-AB34E28DF218

P932

Q37063978-F17D92BA-8A46-4862-9918-54B7AA22BE87

P356

P1433

Scientific Reports

P1476

COL4A6 is dispensable for autosomal recessive Alport syndrome.

@en

P2093

Eiji Ishikawa

http://www.w3.org/2001/XMLSchema#string

Kan Katayama

http://www.w3.org/2001/XMLSchema#string

Karl Tryggvason

http://www.w3.org/2001/XMLSchema#string

Masaaki Ito

http://www.w3.org/2001/XMLSchema#string

Shinsuke Nomura

http://www.w3.org/2001/XMLSchema#string

Timo Jahnukainen

http://www.w3.org/2001/XMLSchema#string

Tomohiro Murata

http://www.w3.org/2001/XMLSchema#string

Tomoko Yonezawa

http://www.w3.org/2001/XMLSchema#string

Toshitaka Oohashi

http://www.w3.org/2001/XMLSchema#string

Yoshikazu Sado

http://www.w3.org/2001/XMLSchema#string

P2860

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

The genes COL4A5 and COL4A6, coding for basement membrane collagen chains alpha 5(IV) and alpha 6(IV), are located head-to-head in close proximity on human chromosome Xq22 and COL4A6 is transcribed from two alternative promoters

Deletion of the paired alpha 5(IV) and alpha 6(IV) collagen genes in inherited smooth muscle tumors

Distinct target-derived signals organize formation, maturation, and maintenance of motor nerve terminals

Collagen IV alpha 3, alpha 4, and alpha 5 chains in rodent basal laminae: sequence, distribution, association with laminins, and developmental switches

Searching for a treatment for Alport syndrome using mouse models

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

Irradiation prolongs survival of Alport mice

Isoform switching of type IV collagen is developmentally arrested in X-linked Alport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis.

Nitric oxide inhibition induces early activation of type I collagen gene in renal resistance vessels and glomeruli in transgenic mice. Role of endothelin.

P2888

P304

29450

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/SREP29450

http://www.w3.org/2001/XMLSchema#string

P407

P478

6

http://www.w3.org/2001/XMLSchema#string

P577

2016-07-05T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

27377778

http://www.w3.org/2001/XMLSchema#string

P932

4932521

http://www.w3.org/2001/XMLSchema#string