Fyn kinase genetic ablation causes structural abnormalities in mature retina and defective Müller cell function-Reference-Cited by-同舟云学术

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Fyn kinase genetic ablation causes structural abnormalities in mature retina and defective Müller cell function

Published:2016-04 Issue: Volume:72 Page:91-100
ISSN:1044-7431
Container-title:Molecular and Cellular Neuroscience
language:en
Short-container-title:Molecular and Cellular Neuroscience

Author:

Chavez-Solano Marbella,Ibarra-Sanchez Alfredo,Treviño Mario,Gonzalez-Espinosa Claudia,Lamas Monica

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Elsevier BV

Subject

Cell Biology,Cellular and Molecular Neuroscience,Molecular Biology

Reference63 articles.

1. The optomotor response: a robust first-line visual screening method for mice;Abdeljalil;Vis. Res.,2005

2. Shape diversity among chick retina Müller cells and their postnatal differentiation;Anezary;J. Comp. Neurol.,2001

3. Cell adhesion molecules, signal transduction and cell growth;Aplin;Curr. Opin. Cell Biol.,1999

4. The diverse roles and multiple forms of focal adhesion kinase in brain;Armendáriz;Eur. J. Neurosci.,2014

5. Decreased dendritic spine density and abnormal spine morphology in Fyn knockout mice;Babus;Brain Res.,2011

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1. Müller Cell Molecular Heterogeneity: Facts and Predictions;ASN Neuro;2022-01

2. Maternal separation induces retinal and peripheral blood mononuclear cell alterations across the lifespan of female rats;Brain Research;2020-12

3. Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss;Cells;2020-04-10

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