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Zebrafish: Housing and husbandry recommendations

Laboratory animals (London), 2020-06, Vol.54 (3), p.213-224

2020

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Hmx1 regulates urfh1 expression in the craniofacial region in zebrafish

PloS one, 2021-01, Vol.16 (1), p.e0245239-e0245239

2021

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Piperlongumine promotes death of retinoblastoma cancer cells

Oncotarget, 2021-04, Vol.12 (9), p.907-916

2021

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Mechanisms of apoptosis in retinitis pigmentosa

Current molecular medicine, 2009-04, Vol.9 (3), p.375

2009

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A dimerized HMX1 inhibits EPHA6/epha4b in mouse and zebrafish retinas

PloS one, 2014-06, Vol.9 (6), p.e100096-e100096

2014

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NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP)

Human mutation, 2009-11, Vol.30 (11), p.1475-1485

2009

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A peptide inhibitor of c-Jun N-terminal kinase protects against excitotoxicity and cerebral ischemia

Nature medicine, 2003-09, Vol.9 (9), p.1180-1186

2003

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Acute hypoglycemia induces retinal cell death in mouse

PloS one, 2011-06, Vol.6 (6), p.e21586-e21586

2011

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Analysis of the cytoprotective role of α-crystallins in cell survival and implication of the αA-crystallin C-terminal extension domain in preventing Bax-induced apoptosis

PloS one, 2013-02, Vol.8 (2), p.e55372-e55372

2013

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Mutation update: TGFBI pathogenic and likely pathogenic variants in corneal dystrophies

Human mutation, 2019-06, Vol.40 (6), p.675-693

2019

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MAP kinase pathways in UV-induced apoptosis of retinal pigment epithelium ARPE19 cells

Apoptosis (London), 2008-03, Vol.13 (3), p.343-353

2008

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Dental phenotype in Jalili syndrome due to a c.1312 dupC homozygous mutation in the CNNM4 gene

PloS one, 2013-10, Vol.8 (10), p.e78529-e78529

2013

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Mutations in the SPARC-Related Modular Calcium-Binding Protein 1 Gene, SMOC1, Cause Waardenburg Anophthalmia Syndrome

American journal of human genetics, 2011-01, Vol.88 (1), p.92-98

2011

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Autosomal-Recessive Posterior Microphthalmos Is Caused by Mutations in PRSS56, a Gene Encoding a Trypsin-Like Serine Protease

American journal of human genetics, 2011-03, Vol.88 (3), p.382-390

2011

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Autophagy defect is associated with low glucose-induced apoptosis in 661W photoreceptor cells

PloS one, 2013-09, Vol.8 (9), p.e74162-e74162

2013

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Genetic spectrum of retinal dystrophies in Tunisia

Scientific reports, 2020-07, Vol.10 (1), p.11199-11199, Article 11199

2020

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Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia

Advances in experimental medicine and biology, 2019, Vol.1185, p.221-226

2019

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Shaken, Not Stirred Collagen in Corneal Dystrophy

Human mutation, 2015-04, Vol.36 (4), p.v-v

Schorderet, Daniel F.

2015

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

PloS one, 2009-08, Vol.4 (8), p.e6616-e6616

2009

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New COL6A6 Variant Causes Autosomal Dominant Retinitis Pigmentosa in a Four-Generation Family

Investigative ophthalmology & visual science, 2022-03, Vol.63 (3), p.23-23

2022

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Mutations in the DNA-binding domain of NR2E3 affect in vivo dimerization and interaction with CRX

PloS one, 2009-10, Vol.4 (10), p.e7379-e7379

2009

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ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm

Human molecular genetics, 2013-08, Vol.22 (16), p.3250-3258

2013

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Tgfbi/Bigh3 silencing activates ERK in mouse retina

Experimental eye research, 2015-11, Vol.140, p.159-170

2015

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Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants

International journal of molecular sciences, 2022-04, Vol.23 (8), p.4294

2022

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JNK Inhibition Reduced Retinal Ganglion Cell Death after Ischemia/Reperfusion In Vivo and after Hypoxia In Vitro

Advances in experimental medicine and biology, 2016-01, Vol.854, p.677-683

2016

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Zebrafish: Housing and husbandry recommendations

Hmx1 regulates urfh1 expression in the craniofacial region in zebrafish

Piperlongumine promotes death of retinoblastoma cancer cells

Mechanisms of apoptosis in retinitis pigmentosa

A dimerized HMX1 inhibits EPHA6/epha4b in mouse and zebrafish retinas

NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP)

A peptide inhibitor of c-Jun N-terminal kinase protects against excitotoxicity and cerebral ischemia

Acute hypoglycemia induces retinal cell death in mouse

Analysis of the cytoprotective role of α-crystallins in cell survival and implication of the αA-crystallin C-terminal extension domain in preventing Bax-induced apoptosis

Mutation update: TGFBI pathogenic and likely pathogenic variants in corneal dystrophies

MAP kinase pathways in UV-induced apoptosis of retinal pigment epithelium ARPE19 cells

Dental phenotype in Jalili syndrome due to a c.1312 dupC homozygous mutation in the CNNM4 gene

Mutations in the SPARC-Related Modular Calcium-Binding Protein 1 Gene, SMOC1, Cause Waardenburg Anophthalmia Syndrome

Autosomal-Recessive Posterior Microphthalmos Is Caused by Mutations in PRSS56, a Gene Encoding a Trypsin-Like Serine Protease

Autophagy defect is associated with low glucose-induced apoptosis in 661W photoreceptor cells

Genetic spectrum of retinal dystrophies in Tunisia

Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia

Shaken, Not Stirred Collagen in Corneal Dystrophy

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

New COL6A6 Variant Causes Autosomal Dominant Retinitis Pigmentosa in a Four-Generation Family

Mutations in the DNA-binding domain of NR2E3 affect in vivo dimerization and interaction with CRX

ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm

Tgfbi/Bigh3 silencing activates ERK in mouse retina

Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants

JNK Inhibition Reduced Retinal Ganglion Cell Death after Ischemia/Reperfusion In Vivo and after Hypoxia In Vitro

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