The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17. - Test2 - elhamkhani - TriplyDB

The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17.

The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17.

http://www.wikidata.org/entity/Q33535689

about

Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans Epithelial sheet movement requires the cooperation of c-Jun and MAP3K1 Ectodomain Shedding by ADAM17: Its Role in Neutrophil Recruitment and the Impairment of This Process during Sepsis Genetic variants of Adam17 differentially regulate TGFβ signaling to modify vascular pathology in mice and humans.Waved with open eyelids 2 (woe2) is a novel spontaneous mouse mutation in the protein phosphatase 1, regulatory (inhibitor) subunit 13 like (Ppp1r13l) gene.A1 adenosine receptor-stimulated exocytosis in bladder umbrella cells requires phosphorylation of ADAM17 Ser-811 and EGF receptor transactivation.Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice.Anterior segment dysgenesis and early-onset glaucoma in nee mice with mutation of Sh3pxd2b LPA-producing enzyme PA-PLA₁α regulates hair follicle development by modulating EGFR signalling.Functional analysis of the Hsf4(lop11) allele responsible for cataracts in lop11 mice.A spontaneous mutation in Srebf2 leads to cataracts and persistent skin wounds in the lens opacity 13 (lop13) mouse.Genomic copy number variation in Mus musculus A Disintegrin and Metalloproteinase10 (ADAM10) Regulates NOTCH Signaling during Early Retinal Development.ADAM17 transactivates EGFR signaling during embryonic eyelid closure.Endothelial deletion of ADAM17 in mice results in defective remodeling of the semilunar valves and cardiac dysfunction in adults.Proteolytic Activity Matrix Analysis (PrAMA) for simultaneous determination of multiple protease activities Genetically modified laboratory mice with sebaceous glands abnormalities.TBC1D20 mediates autophagy as a key regulator of autophagosome maturation.Meibomian gland morphogenesis requires developmental eyelid closure and lid fusion.Loss of Krox20 results in aortic valve regurgitation and impaired transcriptional activation of fibrillar collagen genes.

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The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17.

http://www.wikidata.org/entity/Q33535689

description

2010 nî lūn-bûn

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2010 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի մարտին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17.

@ast

The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17.

@en

The waved with open eyelids

@nl

type

label

The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17.

@ast

The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17.

@en

The waved with open eyelids

@nl

prefLabel

The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17.

@ast

The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17.

@en

The waved with open eyelids

@nl

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GENETICS.109.113167

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P1476

The waved with open eyelids (woe) locus is a hypomorphic mouse mutation in Adam17.

@en

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B Chang

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

C J Zeiss

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

C P Blobel

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

D J Sidjanin

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

E L Hassemer

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

M McNally

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

R D Dubielzig

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

R Liegel

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

S M Le Gall

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

T Kimura

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

P2860

A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells

ADAMs: key components in EGFR signalling and development

c-Jun is essential for organization of the epidermal leading edge

Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice

ESEfinder: A web resource to identify exonic splicing enhancers

Listening to silence and understanding nonsense: exonic mutations that affect splicing

Distinct roles for ADAM10 and ADAM17 in ectodomain shedding of six EGFR ligands

A continuous fluorimetric assay for tumor necrosis factor-alpha converting enzyme.

EGF receptor ligands.

Mice lacking the metalloprotease-disintegrin MDC9 (ADAM9) have no evident major abnormalities during development or adult life.

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245-255

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scholarly article

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10.1534/GENETICS.109.113167

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1

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185

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Keisuke Horiuchi

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2010-03-01T00:00:00Z

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41657049

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20194968

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2870960

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