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Journal Article

Novel mutations in malonyl-CoA-acyl carrier protein transacylase provoke autosomal recessive optic neuropathy

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Huiping Li and others

Human Molecular Genetics, Volume 29, Issue 3, 1 February 2020, Pages 444–458, https://doi.org/10.1093/hmg/ddz311

Published: 09 January 2020

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Journal Article

Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma

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Yukihiro Shiga and others

Human Molecular Genetics, Volume 27, Issue 8, 15 April 2018, Pages 1486–1496, https://doi.org/10.1093/hmg/ddy053

Published: 14 February 2018

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Journal Article

A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration

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Pooja Biswas and others

Human Molecular Genetics, Volume 25, Issue 12, 15 June 2016, Pages 2483–2497, https://doi.org/10.1093/hmg/ddw113

Published: 22 April 2016

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Journal Article

Enhanced optineurin E50K–TBK1 interaction evokes protein insolubility and initiates familial primary open-angle glaucoma Get access

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Yuriko Minegishi and others

Human Molecular Genetics, Volume 22, Issue 17, 1 September 2013, Pages 3559–3567, https://doi.org/10.1093/hmg/ddt210

Published: 12 May 2013

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Journal Article

Mutant WDR36 directly affects axon growth of retinal ganglion cells leading to progressive retinal degeneration in mice

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Zai-Long Chi and others

Human Molecular Genetics, Volume 19, Issue 19, 1 October 2010, Pages 3806–3815, https://doi.org/10.1093/hmg/ddq299

Published: 14 July 2010

Journal Article

Overexpression of optineurin E50K disrupts Rab8 interaction and leads to a progressive retinal degeneration in mice

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Zai-Long Chi and others

Human Molecular Genetics, Volume 19, Issue 13, 1 July 2010, Pages 2606–2615, https://doi.org/10.1093/hmg/ddq146

Published: 13 April 2010

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Novel mutations in malonyl-CoA-acyl carrier protein transacylase provoke autosomal recessive optic neuropathy

Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma

A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration

Enhanced optineurin E50K–TBK1 interaction evokes protein insolubility and initiates familial primary open-angle glaucoma Get access

Mutant WDR36 directly affects axon growth of retinal ganglion cells leading to progressive retinal degeneration in mice

Overexpression of optineurin E50K disrupts Rab8 interaction and leads to a progressive retinal degeneration in mice

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Novel mutations in malonyl-CoA-acyl carrier protein transacylase provoke autosomal recessive optic neuropathy Free

Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma Free

A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration Free

Enhanced optineurin E50K–TBK1 interaction evokes protein insolubility and initiates familial primary open-angle glaucoma Get access

Mutant WDR36 directly affects axon growth of retinal ganglion cells leading to progressive retinal degeneration in mice Open Access

Overexpression of optineurin E50K disrupts Rab8 interaction and leads to a progressive retinal degeneration in mice Open Access

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Novel mutations in malonyl-CoA-acyl carrier protein transacylase provoke autosomal recessive optic neuropathy

Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma

A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration

Mutant WDR36 directly affects axon growth of retinal ganglion cells leading to progressive retinal degeneration in mice

Overexpression of optineurin E50K disrupts Rab8 interaction and leads to a progressive retinal degeneration in mice