X-chromosome inactivation in human liver: confirmation of X-linkage of ornithine transcarbamylase (Q35201500)

7 August 2017

title

X-chromosome inactivation in human liver: confirmation of X-linkage of ornithine transcarbamylase (English)

1 reference

7 August 2017

Ricciuti FC

1

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7 August 2017

Gelehrter TD

series ordinal

2

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7 August 2017

Rosenberg LE

series ordinal

3

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7 August 2017

language of work or name

English

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publication date

1 July 1976

1 reference

American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

28

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7 August 2017

issue

4

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7 August 2017

page(s)

332-338

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DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS

7 August 2017

cites work

1 reference

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Gene action in the X-chromosome of the mouse (Mus musculus L.)

13 July 2018

1 reference

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Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685051

Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685051

Expression of two X-linked genes in human hair follicles of double heterozygotes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685051

Partial expression of sex-linked recessive amelogenesis imperfecta in females compatible with the Lyon hypothesis

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685051

Use of Genetic Linkage for the Detection of Female Carriers of Hemophilia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685051

Urea Cycle Enzyme Adaptation to Dietary Protein in Primates

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685051

X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685051

Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685051

Evidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685051

X-chromosome inactivation and developmental patterns in mammals

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685051

Cytochemical demonstration of ornithine carbamoyltransferase activity in liver mitochondria of rat and mouse

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685051

Hyperammonaemia. A new instance of an inborn enzymatic defect of the biosynthesis of urea

13 July 2018

1 reference

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X Chromosome Inactivation in X-linked Hypohidrotic Ectodermal Dysplasia

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Time of X Chromosome Inactivation in Retinal Melanocytes of the Mouse

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12 December 2020

X-linked transmission of ornithine-transcarbamylase deficiency

1 reference

12 December 2020

X-linked transmission of structural gene mutations responsible for ornithine-transcarbamylase deficiencies

1 reference

12 December 2020

X-inactivation pattern in the epididymis of sex-reversed mice heterozygous for testicular feminization

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Heterogenous mutations of the structural gene of human ornithine carbamyltransferase as observed in five personal cases

1 reference

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Ornithine transcarbamylase deficiency: a cause of lethal neonatal hyperammonemia in males

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Human phosphoglycerate kinase and inactivation of the X chromosome

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Genetic Inactivation of the α-Galactosidase Locus in Carriers of Fabry's Disease

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Identifiers

PMC publication ID

1685051

1 reference

7 August 2017

1 reference