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1-7 of 7 results for ornithine aminotransferase gene

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Case report

First published 2021-9

First report of c.425-1G>A mutation in ornithine aminotransferase gene causing gyrate atrophy of the choroid and retina with hyperornithinemia

Hossein Jalali, Mojtaba Najafi, Atefeh Khoshaeen [...]

European Journal of Ophthalmology

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Research article

First published 1997-11

Retrovirus-Mediated Gene Transfer of Ornithine- δ -Aminotransferase into Keratinocytes from Gyrate Atrophy Patients

Thomas G. Jensen, Daniel M. Sullivan, Richard A. Morgan [...]

Human Gene Therapy

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Research article

First published 1994-06

Retrovirus-Mediated Gene Transfer and Expression of Human Ornithine δ-Aminotransferase into Embryonic Fibroblasts

J. Luis Rivero, H. Daniel Lacorazza, Alexander Kozhich [...]

Human Gene Therapy

Open access

Research article

First published 2016

Auxotrophy-Based Detection of Hyperornithinemia in Mouse Blood and Urine

Kenneth M. Palanza, Alex V. Nesta, Renukanandan Tumu [...]

Journal of Inborn Errors of Metabolism and Screening

Free access

Research article

First published 2024-1

Clinical characteristics of gyrate atrophy compared with a gyrate atrophy-like retinal phenotype

L. Pauleikhoff, N. Weisschuh, A. Lentzsch [...]

European Journal of Ophthalmology

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Research article

First published 1986-12

Investigation of Gyrate Atrophy Using a cDNA Clone for Human Ornithine Aminotransferase

Vijaya Ramesh, Marilee M. Shaffer, Julie M. Allaire [...]

DNA and Cell Biology

Open access

Research article

First published 2008

Pharmacodynamic Modeling of Acute and Chronic Effects of Methylprednisolone on Hepatic Urea Cycle Genes in Rats

Anasuya Hazra, Debra C. DuBois, Richard R. Almon [...]

Gene Regulation and Systems Biology