BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons.

about

Two novel mutations identified in ADCC families impair crystallin protein distribution and induce apoptosis in human lens epithelial cells.A Triple Mutation of BetaB2-Crystallin is Necessary to Develop Cataract and Glaucoma.

P2860

Q47125740-2C775639-835B-4F93-84A1-4C41ABCEFDE4 Q55005982-A32F6752-1D7F-43EA-A7E7-55BD43556BB2

P2860

BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons.

Item

http://www.wikidata.org/entity/Q38993774

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

BetaB2-crystallin mutations as ...... ial cells and retinal neurons.

@en

type

Item

label

BetaB2-crystallin mutations as ...... ial cells and retinal neurons.

@en

prefLabel

BetaB2-crystallin mutations as ...... ial cells and retinal neurons.

@en

P1476

BetaB2-crystallin mutations as ...... ial cells and retinal neurons.

@en

P2093

Anne Rübsam

http://www.w3.org/2001/XMLSchema#string

Hemant S Pawar

http://www.w3.org/2001/XMLSchema#string

Jennifer E Dulle

http://www.w3.org/2001/XMLSchema#string

Sarah J Garnai

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations in the RNA granule component TDRD7 cause cataract and glaucoma

Crybb2 coding for βB2-crystallin affects sensorimotor gating and hippocampal function.

Proteome analysis of lens epithelia, fibers, and the HLE B-3 cell line.

Deletion mutation in an eye lens beta-crystallin. An animal model for inherited cataracts.

Elongation of axons during regeneration involves retinal crystallin beta b2 (crybb2).

Mitochondrial proteomics in experimental autoimmune uveitis oxidative stress

Cataractogenic lens injury prevents traumatic ganglion cell death and promotes axonal regeneration both in vivo and in culture.

Posttranslational modification of differentially expressed mitochondrial proteins in the retina during early experimental autoimmune uveitis.

Congenital cataract causing mutants of αA-crystallin/sHSP form aggregates and aggresomes degraded through ubiquitin-proteasome pathway.

Cataract-causing defect of a mutant γ-crystallin proceeds through an aggregation pathway which bypasses recognition by the α-crystallin chaperone.

P304

85-90

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1016/J.EXER.2017.01.005

http://www.w3.org/2001/XMLSchema#string

P478

155

http://www.w3.org/2001/XMLSchema#string

P50

Patrice E. Fort

P577

2017-01-25T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28131617

http://www.w3.org/2001/XMLSchema#string

P932

5390483

http://www.w3.org/2001/XMLSchema#string

BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons.

about

P2860

P2860

BetaB2-crystallin mutations associated with cataract and glaucoma leads to mitochondrial alterations in lens epithelial cells and retinal neurons.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P932