Search Results - "Nishina, Patsy M."

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Deficiency in Lyst function leads to accumulation of secreted proteases and reduced retinal adhesion.

Authors: Ji, Xiaojie Zhao, Lihong Umapathy, Ankita et al.

Source: PLoS ONE. 3/3/2022, Vol. 17 Issue 3, p1-19. 19p.

PROGRESS TOWARD UNDERSTANDING THE GENETIC AND BIOCHEMICAL MECHANISMS OF INHERITED PHOTORECEPTOR DEGENERATIONS.

Authors: Pacione, Laura R. Szego, Michael J. Ikeda, Sakae et al.

Source: Annual Review of Neuroscience. 2003, Vol. 26 Issue 1, p657-700. 46p.

Subjects: Photoreceptors, Genes, Cells, Retina, Genetic mutation

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A Dpagt1 Missense Variant Causes Degenerative Retinopathy without Myasthenic Syndrome in Mice.

Authors: Hyde, Lillian F. Kong, Yang Zhao, Lihong et al.

Source: International Journal of Molecular Sciences. Oct2022, Vol. 23 Issue 19, p12005. 15p.

Single-Cell RNA Sequencing Reveals Molecular Features of Heterogeneity in the Murine Retinal Pigment Epithelium.

Authors: Pandey, Ravi S. Krebs, Mark P. Bolisetty, Mohan T. et al.

Source: International Journal of Molecular Sciences. Sep2022, Vol. 23 Issue 18, pN.PAG-N.PAG. 23p.

A Splicing Mutation in Slc4a5 Results in Retinal Detachment and Retinal Pigment Epithelium Dysfunction.

Authors: Collin, Gayle B. Shi, Lanying Yu, Minzhong et al.

Source: International Journal of Molecular Sciences. Feb2022, Vol. 23 Issue 4, p2220. 1p.

Genetic Interaction between Mfrp and Adipor1 Mutations Affect Retinal Disease Phenotypes.

Authors: Gogna, Navdeep Weatherly, Sonia Zhao, Fuxin et al.

Source: International Journal of Molecular Sciences. Feb2022, Vol. 23 Issue 3, p1615-N.PAG. 1p.

Mouse models of human ocular disease for translational research.

Authors: Krebs, Mark P. Collin, Gayle B. Hicks, Wanda L. et al.

Source: PLoS ONE. 8/31/2017, Vol. 12 Issue 8, p1-33. 33p.

Requirement of Smad4 from Ocular Surface Ectoderm for Retinal Development.

Authors: Li, Jing Wang, Shusheng Anderson, Chastain et al.

Source: PLoS ONE. 8/5/2016, Vol. 11 Issue 8, p1-18. 18p.

Gene Profiling of Postnatal Mfrp^rd6 Mutant Eyes Reveals Differential Accumulation of Prss56, Visual Cycle and Phototransduction mRNAs.

Authors: Soundararajan, Ramani Won, Jungyeon Stearns, Timothy M. et al.

Source: PLoS ONE. Oct2014, Vol. 9 Issue 10, p1-13. 13p.

From Vivarium to Bedside: Lessons Learned from Animal Models.

Authors: Budzynski, Ewa Lee, Yongsuk Sakamoto, Kenji et al.

Source: Ophthalmic Genetics. Dec2006, Vol. 27 Issue 4, p123-137. 15p. 3 Charts, 1 Graph.

A novel ENU-induced mutation, peewee, causes dwarfism in the mouse.

Authors: Lee, Bokryeon Kano, Kiyoshi Young, Jay et al.

Source: Mammalian Genome. Jul2009, Vol. 20 Issue 7, p455-455. 1p.

Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss.

Authors: Collin, Gayle B. Gogna, Navdeep Chang, Bo et al.

Source: Cells (2073-4409). Apr2020, Vol. 9 Issue 4, p931. 1p.

Aberrant actin cytoskeleton leads to accelerated proliferation of corneal epithelial cells in mice deficient for destrin (actin depolymerizing factor).

Authors: Ikeda, Sakae Cunningham, Leslie A. Boggess, Dawnalyn et al.

Source: Human molecular genetics Jun2003; Vol. 12 (11).

Journal Info: Publisher: Oxford University Press / USA ISSN: 0964-6906

Eye, Retina, and Visual System of the Mouse

Authors: Leo M. Chalupa Robert W. Williams

Resource Type: eBook.

Subjects: Visual pathways, Eye, Mice--Sense organs

Categories: MEDICAL / Neuroscience, HEALTH & FITNESS / Vision

Not quite type 1 or type 2, what now? Review of monogenic, mitochondrial, and syndromic diabetes.

Authors: Yeung RO Hannah-Shmouni F Niederhoffer K et al.

Source: Reviews in endocrine & metabolic disorders [Rev Endocr Metab Disord] 2018 Mar; Vol. 19 (1), pp. 35-52.

Publication Type: Journal Article; Review

Journal Info: Publisher: Springer Country of Publication: Germany NLM ID: 100940588 Publication Model: Print Cited Medium: Internet ISSN: 1573-2606 (Electronic) Linking ISSN: 13899155 NLM ISO Abbreviation: Rev Endocr Metab Disord Subsets: MEDLINE