Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium. - sprookjes - yvandenbroek - TriplyDB

Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.

Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.

http://www.wikidata.org/entity/Q37281376

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Transplantation of reprogrammed embryonic stem cells improves visual function in a mouse model for retinitis pigmentosa.Taz-tead1 links cell-cell contact to zeb1 expression, proliferation, and dedifferentiation in retinal pigment epithelial cells Evaluation of multimodal imaging in carriers of X-linked retinitis pigmentosa.Generating iPSC-Derived Choroidal Endothelial Cells to Study Age-Related Macular Degeneration The Hippo pathway in biological control and cancer development.Silencing of tuberin enhances photoreceptor survival and function in a preclinical model of retinitis pigmentosa (an american ophthalmological society thesis).

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Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.

http://www.wikidata.org/entity/Q37281376

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article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on May 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.

@en

Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.

@nl

type

label

Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.

@en

Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.

@nl

prefLabel

Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.

@en

Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.

@nl

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J.OPHTHA.2008.10.032

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Cellular and molecular origin of circumpapillary dysgenesis of the pigment epithelium.

@en

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Chyuan-Sheng Lin

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J Mie Kasanuki

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Joaquin Tosi

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John T Flynn

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Kerstin M Janisch

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Nan-Kai Wang

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Stephen H Tsang

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P2860

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

TEAD/TEF transcription factors utilize the activation domain of YAP65, a Src/Yes-associated protein localized in the cytoplasm

A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)

Characterization of the mammalian YAP (Yes-associated protein) gene and its role in defining a novel protein module, the WW domain

Tead proteins activate the Foxa2 enhancer in the node in cooperation with a second factor

Defects in yolk sac vasculogenesis, chorioallantoic fusion, and embryonic axis elongation in mice with targeted disruption of Yap65

A Sveinsson's chorioretinal atrophy-associated missense mutation in mouse Tead1 affects its interaction with the co-factors YAP and TAZ

"Stemness": transcriptional profiling of embryonic and adult stem cells

Choroidal perfusion perturbations in non-neovascular age related macular degeneration.

The relationship between retrobulbar and choroidal hemodynamics in non-neovascular age-related macular degeneration.

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971-980

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scholarly article

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10.1016/J.OPHTHA.2008.10.032

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5

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116

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2009-05-01T00:00:00Z

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24397531

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19410955

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2717946

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