Large is required for normal astrocyte migration and retinal vasculature development (Q33568370)

28428837

28 July 2017

title

Large is required for normal astrocyte migration and retinal vasculature development (English)

1 reference

28 July 2017

0 references

5

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7 June 2020

Gezhi Xu

7

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7 June 2020

author name string

Min Zhou

1

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7 June 2020

Herui Wang

2

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7 June 2020

Hui Ren

3

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7 June 2020

Rui Jiang

4

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7 June 2020

Xiaohui Wu

6

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7 June 2020

publication date

17 April 2017

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28 July 2017

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7 June 2020

volume

7

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7 June 2020

page(s)

18

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Laminins containing the β2 and γ3 chains regulate astrocyte migration and angiogenesis in the retina

7 June 2020

cites work

1 reference

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Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE

21 June 2018

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Lama1 mutations lead to vitreoretinal blood vessel formation, persistence of fetal vasculature, and epiretinal membrane formation in mice.

21 June 2018

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A developmental defect in astrocytes inhibits programmed regression of the hyaloid vasculature in the mammalian eye.

21 June 2018

1 reference

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Mutations in Lama1 disrupt retinal vascular development and inner limiting membrane formation

21 June 2018

1 reference

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Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study

21 June 2018

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PBmice: an integrated database system of piggyBac (PB) insertional mutations and their characterizations in mice

21 June 2018

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Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome.

21 June 2018

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Development of the retinal vasculature

21 June 2018

1 reference

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WNT7b mediates macrophage-induced programmed cell death in patterning of the vasculature

21 June 2018

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Efficient transposition of the piggyBac (PB) transposon in mammalian cells and mice

21 June 2018

1 reference

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Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan

21 June 2018

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Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

21 June 2018

1 reference

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Origin and turnover of ECM proteins from the inner limiting membrane and vitreous body

21 June 2018

1 reference

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Dystroglycan in development and disease.

21 January 2018

1 reference

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Reactive gliosis of astrocytes and Müller glial cells in retina of POMGnT1-deficient mice.

21 January 2018

1 reference

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Ocular abnormalities in Large(myd) and Large(vls) mice, spontaneous models for muscle, eye, and brain diseases.

21 January 2018

1 reference

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Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders

21 January 2018

1 reference

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Abnormal maturation of the retinal vasculature in type XVIII collagen/endostatin deficient mice and changes in retinal glial cells due to lack of collagen types XV and XVIII.

21 January 2018

1 reference

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Retinal vascular development is mediated by endothelial filopodia, a preexisting astrocytic template and specific R-cadherin adhesion.

31 October 2018

1 reference

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A novel rat model to study the functions of macrophages during normal development and pathophysiology of the eye

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28428837

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S13578-017-0143-9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28428837%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

7 June 2020

0 references

1 reference

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7 June 2020

28428837

1 reference