Mouse eye enucleation for remote high-throughput phenotyping. - Wikidata - wikimedia - TriplyDB

Mouse eye enucleation for remote high-throughput phenotyping.

Mouse eye enucleation for remote high-throughput phenotyping.

http://www.wikidata.org/entity/Q42575435

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Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome Mcph1-deficient mice reveal a role for MCPH1 in otitis media Whole mount immunofluorescent staining of the neonatal mouse retina to investigate angiogenesis in vivo Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss.CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model Translational vitreous proteomics.CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa.A highly reproducible and straightforward method to perform in vivo ocular enucleation in the mouse after eye opening.Silencing of tuberin enhances photoreceptor survival and function in a preclinical model of retinitis pigmentosa (an american ophthalmological society thesis).Mouse Models of Corneal Scarring.Acute vitreoretinal trauma and inflammation after traumatic brain injury in mice.

P2860

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P2860

Mouse eye enucleation for remote high-throughput phenotyping.

http://www.wikidata.org/entity/Q42575435

description

2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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2011年论文

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2011年论文

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name

Mouse eye enucleation for remote high-throughput phenotyping.

@en

Mouse eye enucleation for remote high-throughput phenotyping.

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type

label

Mouse eye enucleation for remote high-throughput phenotyping.

@en

Mouse eye enucleation for remote high-throughput phenotyping.

@nl

prefLabel

Mouse eye enucleation for remote high-throughput phenotyping.

@en

Mouse eye enucleation for remote high-throughput phenotyping.

@nl

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P1433

Journal of Visualized Experiments

P1476

Mouse eye enucleation for remote high-throughput phenotyping.

@en

P2093

Amir H Assefnia

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Jessica M Skeie

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Maryann Mahajan

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Stephen H Tsang

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Vinit B Mahajan

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P2860

Retinal degeneration mutants in the mouse

Mouse model resources for vision research.

Results from screening over 9000 mutation-bearing mice for defects in the electroretinogram and appearance of the fundus.

Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness.

Retinal degeneration in mice lacking the gamma subunit of the rod cGMP phosphodiesterase.

Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice.

Screening for mouse retinal degenerations. I. Correlation of indirect ophthalmoscopy, electroretinograms, and histology.

P31

scholarly article

P356

10.3791/3184

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57

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2011-11-19T00:00:00Z

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51839654

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22126835

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3308585

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