(Q33492768)

27 July 2017

title

Bax-induced apoptosis in Leber's congenital amaurosis: a dual role in rod and cone degeneration (English)

1 reference

27 July 2017

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Daniel F Schorderet

2

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author name string

Séverine Hamann

series ordinal

1

1 reference

27 July 2017

Sandra Cottet

series ordinal

3

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27 July 2017

language of work or name

English

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publication date

12 August 2009

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27 July 2017

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27 July 2017

volume

4

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27 July 2017

issue

8

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27 July 2017

page(s)

e6616

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Creative Commons Attribution 4.0 International

27 July 2017

copyright license

start time

12 August 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Triggering of Bcl-2-related pathway is associated with apoptosis of photoreceptors in Rpe65-/- mouse model of Leber's congenital amaurosis.

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21 June 2018

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Susceptibility to neurodegeneration in a glaucoma is modified by Bax gene dosage

21 June 2018

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Major role of BAX in apoptosis during retinal development and in establishment of a functional postnatal retina

21 June 2018

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Proapoptotic bcl-2 family members, Bax and Bak, are essential for developmental photoreceptor apoptosis

21 June 2018

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21 June 2018

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Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy

21 June 2018

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Proapoptotic BAX and BAK: a requisite gateway to mitochondrial dysfunction and death

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 January 2018

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New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis.

21 January 2018

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Spontaneous activity of opsin apoprotein is a cause of Leber congenital amaurosis

21 January 2018

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Clinical phenotypes in carriers of Leber congenital amaurosis mutations

21 January 2018

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Cone opsin mislocalization in Rpe65-/- mice: a defect that can be corrected by 11-cis retinal

21 January 2018

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Apoptotic DNA fragmentation and upregulation of Bax induced by transient ischemia of the rat retina

21 January 2018

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Preventing retinal detachment-associated photoreceptor cell loss in Bax-deficient mice.

21 January 2018

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Deficiency of Bax and Bak protects photoreceptors from light damage in vivo.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0006616

Opsin activation as a cause of congenital night blindness.

21 January 2018

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Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy.

21 January 2018

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Evidence for two apoptotic pathways in light-induced retinal degeneration

21 January 2018

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Impaired opsin targeting and cone photoreceptor migration in the retina of mice lacking the cyclic nucleotide-gated channel CNGA3.

21 January 2018

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A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0006616

Ischemic preconditioning attenuates apoptotic cell death in the rat retina

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2720534

Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell loss.

31 October 2018

1 reference

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Biological characterization of gene response in Rpe65-/- mouse model of Leber's congenital amaurosis during progression of the disease

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19672311

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0006616

1 reference

27 July 2017

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27 July 2017

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