Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells (Q24633620)

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English	Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells	scientific article

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instance of

scholarly article

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title

Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells (English)

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main subject

heterozygosity

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based on heuristic

inferred from title

author name string

B R Migeon

series ordinal

1

author given names

B R

author last names

Migeon

1 reference

stated in

PubMed

PubMed publication ID

6795626

retrieved

19 October 2023

H W Moser

series ordinal

2

author given names

H W

author last names

Moser

1 reference

stated in

PubMed

PubMed publication ID

6795626

retrieved

19 October 2023

A B Moser

series ordinal

3

author given names

A B

author last names

Moser

1 reference

stated in

PubMed

PubMed publication ID

6795626

retrieved

19 October 2023

J Axelman

series ordinal

4

author given names

J

author last names

Axelman

1 reference

stated in

PubMed

PubMed publication ID

6795626

retrieved

19 October 2023

D Sillence

series ordinal

5

author given names

D

author last names

Sillence

1 reference

stated in

PubMed

PubMed publication ID

6795626

retrieved

19 October 2023

R A Norum

series ordinal

6

author given names

R A

author last names

Norum

1 reference

stated in

PubMed

PubMed publication ID

6795626

retrieved

19 October 2023

language of work or name

English

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publication date

August 1981

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full work available at URL

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC320333

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published in

Proceedings of the National Academy of Sciences of the United States of America

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volume

78

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issue

8

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page(s)

5066-70

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cites work

Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=320333

retrieved

7 April 2017

Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=320333

retrieved

27 September 2017

X-chromosome inactivation and developmental patterns in mammals

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=320333

retrieved

27 September 2017

Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=320333

retrieved

27 September 2017

Adrenoleukodystrophy and adrenomyeloneuropathy associated with partial adrenal insufficiency in three generations of a kindred

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=320333

retrieved

27 September 2017

Adrenomyeloneuropathy: A probable variant of adrenoleukodystrophy I. Clinical and endocrinologic aspects

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=320333

retrieved

27 September 2017

Adrenoleukodystrophy. A clinical and pathological study of 17 cases

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=320333

retrieved

27 September 2017

Locus on human X chromosome for dihydrotestosterone receptor and androgen insensitivity

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=320333

retrieved

27 September 2017

Adrenoleukodystrophy (Siemerling-creutzfeldt disease): Heterozygote with two clonal fibroblast populations

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=320333

retrieved

30 May 2018

Selection and cell communication as determinants of female phenotype

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=320333

retrieved

30 May 2018

Imbalance in X-chromosome expression: evidence for a human X-linked gene affecting growth of hemopoietic cells

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=320333

retrieved

30 May 2018

Adrenoleukodystrophy: studies of the phenotype, genetics and biochemistry

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6795626

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High concentration of hexacosanoate in cultured skin fibroblast lipids from adrenoleukodystrophy patients

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6795626

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adrenoleukodystrophy: Elevated C26 fatty acid in cultured skin fibroblasts

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6795626

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wiskott-Aldrich syndrome: cellular impairments and their implication for carrier detection

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6795626

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.78.8.5066

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ADS bibcode

1981PNAS...78.5066M

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PMC publication ID

320333

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PubMed publication ID

6795626

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ResearchGate publication ID

16402639

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