(Q35882120)

English

Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency.

scientific article published in October 1996

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scholarly article

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19 October 2019

Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency (English)

1 reference

Europe PubMed Central

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19 October 2019

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Filosa S

1

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19 October 2019

Giacometti N

2

1 reference

Europe PubMed Central

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19 October 2019

Wangwei C

3

1 reference

Europe PubMed Central

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19 October 2019

De Mattia D

4

1 reference

Europe PubMed Central

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19 October 2019

Pagnini D

5

1 reference

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19 October 2019

Alfinito F

6

1 reference

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19 October 2019

Schettini F

7

1 reference

Europe PubMed Central

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19 October 2019

Luzzatto L

8

1 reference

Europe PubMed Central

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19 October 2019

Martini G

9

1 reference

Europe PubMed Central

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19 October 2019

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publication date

1 October 1996

1 reference

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19 October 2019

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

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19 October 2019

59

1 reference

Europe PubMed Central

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19 October 2019

4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8808605%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

887-895

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8808605%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

In vitro generation of lymphoid precursors from embryonic stem cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Suppression of apoptosis allows differentiation and development of a multipotent hemopoietic cell line in the absence of added growth factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Application of carrier testing to genetic counseling for X-linked agammaglobulinemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Targeted disruption of the housekeeping gene encoding glucose 6-phosphate dehydrogenase (G6PD): G6PD is dispensable for pentose synthesis but essential for defense against oxidative stress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Biochemical variants of glucose-6-phosphate dehydrogenase giving rise to congenital nonspherocytic hemolytic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Inheritance of quantitative expression of erythrocyte glucose-6-phosphate dehydrogenase activity in the negro--a twin study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Selection of Escherichia coli Mutants Lacking Glucose-6-Phosphate Dehydrogenase or Gluconate-6-Phosphate Dehydrogenase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Primordial cell pool size and lineage relationships of five human cell types

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

A new glucose-6-phosphate dehydrogenase variant, Gd(-) Tepic, characterized by moderate enzyme deficiency and mild episodes of hemolytic anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Genetic variation of glucose-6-phosphate dehydrogenase: a catalog and future prospects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Isolation and characterization of the ZWF1 gene of Saccharomyces cerevisiae, encoding glucose-6-phosphate dehydrogenase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Intragenic interspecific complementation of glucose 6-phosphate dehydrogenase in human-hamster cell hybrids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Identification of the structural gene for glucose-6-phosphate dehydrogenase in yeast. Inactivation leads to a nutritional requirement for organic sulfur

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

X-chromosome inactivation patterns using HPRT and PGK polymorphisms in haematologically normal and post-chemotherapy females.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Molecular basis of chronic non-spherocytic haemolytic anaemia: a new G6PD variant (393 Arg----His) with abnormal KmG6P and marked in vivo instability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Role of the pentose phosphate pathway in metabolism of Drosophila melanogaster elucidated by mutations affecting glucose 6-phosphate and 6-phosphogluconate dehydrogenases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Three new electrophoretically normal glucose-6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: G6PD Ogikubo, Yokohama, and Akita

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

?Gd(-) H�tel Dieu?: A new G-6PD variant with chronic hemolysis in a Negro patient from Senegal

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Genetic Rescue of a Lethal "Null" Activity Allele of 6-Phosphogluconate Dehydrogenase in Drosophila melanogaster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

Genetics of red cells and susceptibility to malaria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

G-6-PD Long Prairie: a new glucose-6-phosphate dehydrogenase mutant exhibiting normal sensitivity to inhibition by NADPH and accompanied by nonspherocytic hemolytic anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

11 July 2018

G6PD San Francisco: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

24 September 2018

A new glucose-6-phosphate dehydrogenase variant (G6PD Nagano) associated with congenital hemolytic anemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914807

24 September 2018

GENETIC TESTS WITH A SEX-LINKED MARKER: GLUCOSE-6-PHOSPHATE DEHYDROGENASE

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucose-6-phosphate dehydrogenase variants: reexamination of G6PD Chicago and Cornell and a new variant (G6PD Pea Ridge) resembling G6PD Chicago

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new glucose-6-phosphate dehydrogenase deficient variant in a patient with Chediak-Higashi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gd(-) Rennes, a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia found in France

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe-glucose-6-phosphate dehydrogenase (G6PD) deficiency associated with chronic hemolytic anemia, granulocyte dysfunction, and increased susceptibility to infections: description of a new molecular variant (G6PD Barcelona)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucose 6-Phosphate dehydrogenase variants: A unique variant (G6PD Kobe) showed an extremely increased affinity for galactose 6-phosphate and a new variant (G6PD Sapporo) resembling G6PD Pea Ridge

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G6PD-Puerto Limón: a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA in heritable disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gd(-) Gifu and Gd(-) Fukuoka. Two new variants of glucose-6-phosphate dehydrogenase found in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A glucose-6-phosphate dehydrogenase variant, Gd(-) Santamaria found in Costa Rica

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of Glucose-6-phosphate Dehydrogenase among Chinese

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G-6PD Bangkok: a new variant found in congenital nonspherocytic hemolytic disease (CNHD)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of non-random X chromosome activity in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucose 6-phosphate dehydrogenase: identity of erythrocyte and leukocyte enzyme with report of a new variant in Chinese

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new variant of glucose-6-phosphate dehydrogenase deficiency hereditary hemolytic anemia, G6PD Cornell: erythrocyte, leukocyte, and platelet studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G-6-PD tripler: a unique variant associated with chronic hemolytic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G6PD deficiency and chronic hemolysis: four new mutants--relationships between clinical syndrome and enzyme kinetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in southern Italy: a study on the population of Naples

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G-6-PD Walter Reed: possible insight into "structural" NADP in G-6-PD

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two new variants of glucose-6-phosphate dehydrogenase associated with hereditary non-spherocytic hemolytic anemia: G6PD Wayne and G6PD Huron

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new glucose-6-phosphate dehydrogenase variant (G6PD Tsukui) associated with congenital hemolytic anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G6PD Huntsville: a new glucose-6-phosphate dehydrogenase associated with chronic hemolytic anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new glucose-6-phosphate dehydrogenase variant with congenital nonspherocytic hemolytic anemia (G6PD Genova). Biochemical characterization and mosaicism expression in the heterozygote

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studying X inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptional analysis of the active X-chromosome in normal and clonal hematopoiesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Some milestones in the history of X-chromosome inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G6PD Nara: a new class 1 glucose-6-phosphate dehydrogenase variant with an eight amino acid deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased induction of apoptosis in mononuclear cells of a glucose-6-phosphate dehydrogenase deficient patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SELECTION IN MAMMALIAN MOSAIC CELL POPULATIONS

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GENE INACTIVATION: THE DISTRIBUTION OF GENE PRODUCTS AMONG POPULATIONS OF CELLS IN HETEROZYGOUS HUMANS

1 reference

https://pubmed.ncbi.nlm.nih.gov/8808605

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8808605%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8808605%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

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