Mice lacking ornithine-delta-aminotransferase have paradoxical neonatal hypoornithinaemia and retinal degeneration (Q71721181)

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20 October 2019

title

Mice lacking ornithine-delta-aminotransferase have paradoxical neonatal hypoornithinaemia and retinal degeneration (English)

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20 October 2019

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Wang T

1

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20 October 2019

Lawler AM

2

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20 October 2019

Steel G

3

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20 October 2019

Sipila I

4

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20 October 2019

Milam AH

5

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20 October 2019

Valle D

6

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20 October 2019

publication date

1 October 1995

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20 October 2019

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20 October 2019

volume

11

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20 October 2019

issue

2

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20 October 2019

page(s)

185-190

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https://scigraph.springernature.com/pub.10.1038/ng1095-185

20 October 2019

exact match

0 references

cites work

An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina

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7 January 2021

Strand-separating conformational polymorphism analysis: efficacy of detection of point mutations in the human ornithine delta-aminotransferase gene

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7 January 2021

Ocular clinicopathologic study of gyrate atrophy

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The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

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7 January 2021

Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes

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7 January 2021

Genomic DNA microextraction: A method to screen numerous samples

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7 January 2021

Introduction and expression of the 400 kilobase amyloid precursor protein gene in transgenic mice [corrected]

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7 January 2021

Conversion of glutamate to ornithine and proline: pyrroline-5-carboxylate, a possible modulator of arginine requirements

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7 January 2021

Development of ornithine metabolism in the mouse intestine

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7 January 2021

Ammonia Intoxication in the Near-Adult Cat as a Result of a Dietary Deficiency of Arginine

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7 January 2021

Arginine: an essential amino acid for the cat

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7 January 2021

Intestinal metabolism of glutamine and glutamate from the lumen as compared to glutamine from blood

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7 January 2021

Enzymological evidence for the indispensability of small intestine in the synthesis of arginine from glutamate. I. Pyrroline-5-carboxylate synthase

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7 January 2021

The arginine-nitric oxide pathway: a target for new drugs.

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7 January 2021

Allopurinol-induced orotidinuria. A test for mutations at the ornithine carbamoyltransferase locus in women

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7 January 2021

At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.

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7 January 2021

Amino acid compositions of body and milk protein change during the suckling period in rats

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7 January 2021

An arginine-deficient diet in humans does not evoke hyperammonemia or orotic aciduria

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7 January 2021

Generation of a mouse model for citrullinemia by targeted disruption of the argininosuccinate synthetase gene

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7 January 2021

Mice deficient in cystathionine beta-synthase: animal models for mild and severe homocyst(e)inemia

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7 January 2021

Disruption of the adenosine deaminase gene causes hepatocellular impairment and perinatal lethality in mice

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7 January 2021

Adenosine-deaminase-deficient mice die perinatally and exhibit liver-cell degeneration, atelectasis and small intestinal cell death

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7 January 2021

Identifiers

DOI

10.1038/NG1095-185

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7550347%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

1 reference