Anterior segment dysgenesis and early-onset glaucoma in nee mice with mutation of Sh3pxd2b - Test2 - elhamkhani - TriplyDB

Anterior segment dysgenesis and early-onset glaucoma in nee mice with mutation of Sh3pxd2b

Anterior segment dysgenesis and early-onset glaucoma in nee mice with mutation of Sh3pxd2b

http://www.wikidata.org/entity/Q34936970

about

Aqueous outflow - A continuum from trabecular meshwork to episcleral veins Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome.Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucoma Genetic dissection of anterior segment dysgenesis caused by a Col4a1 mutation in mouse.Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure.Ketamine/Xylazine-Induced Corneal Damage in Mice.Adoptive transfer of immune cells from glaucomatous mice provokes retinal ganglion cell loss in recipients.Using genetic mouse models to gain insight into glaucoma: Past results and future possibilities.Quantitative measurement of retinal ganglion cell populations via histology-based random forest classification.Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.Transplantation of iPSC-derived TM cells rescues glaucoma phenotypes in vivo.YBR/EiJ mice: a new model of glaucoma caused by genes on chromosomes 4 and 17.Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma.The role of Tks adaptor proteins in invadopodia formation, growth and metastasis of melanoma.Development of diagnostic and treatment strategies for glaucoma through understanding and modification of scleral and lamina cribrosa connective tissue The Trabecular Meshwork: A Basic Review of Form and Function Segmental outflow of aqueous humor in mouse and human.Invadosomes are coming: new insights into function and disease relevance.Automated Axon Counting in Rodent Optic Nerve Sections with AxonJ.Tks adaptor proteins at a glance.The In Vivo Effects of the CB1-Positive Allosteric Modulator GAT229 on Intraocular Pressure in Ocular Normotensive and Hypertensive Mice.Transgenic TBK1 mice have features of normal tension glaucoma.

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Anterior segment dysgenesis and early-onset glaucoma in nee mice with mutation of Sh3pxd2b

http://www.wikidata.org/entity/Q34936970

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2011 nî lūn-bûn

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2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2011 թվականի ապրիլին հրատարակված գիտական հոդված

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2011年の論文

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Anterior segment dysgenesis an ...... mice with mutation of Sh3pxd2b

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Anterior segment dysgenesis an ...... mice with mutation of Sh3pxd2b

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Investigative Ophthalmology & Visual Science

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Anterior segment dysgenesis an ...... mice with mutation of Sh3pxd2b

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Adam Hedberg-Buenz

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Demelza Koehn

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Mao Mao

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Simon W M John

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P2860

Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure

Disruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar Syndrome

Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma

The novel adaptor protein Tks4 (SH3PXD2B) is required for functional podosome formation

PITX2 regulates procollagen lysyl hydroxylase (PLOD) gene expression: implications for the pathology of Rieger syndrome

Molecular mechanisms of invadopodium formation: the role of the N-WASP-Arp2/3 complex pathway and cofilin

The number of people with glaucoma worldwide in 2010 and 2020

Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice

The mouse anterior chamber angle and trabecular meshwork develop without cell death

Elevated oxidative membrane damage associated with genetic modifiers of Lyst-mutant phenotypes

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2679-2688

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10.1167/IOVS.10-5993

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Michael Anderson

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49799618

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