(Q35882337)

English

Homozygosity mapping of the gene for Chediak-Higashi syndrome to chromosome 1q42-q44 in a segment of conserved synteny that includes the mouse beige locus (bg)

scientific article published in September 1996

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Homozygosity mapping of the gene for Chediak-Higashi syndrome to chromosome 1q42-q44 in a segment of conserved synteny that includes the mouse beige locus (bg) (English)

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Chediak-Higashi syndrome

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Richard A Spritz

8

object named as

R A Spritz

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

author name string

K Fukai

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

J Oh

2

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

M A Karim

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

K J Moore

4

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

H H Kandil

5

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

H Ito

6

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

J Bürger

7

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

language of work or name

0 references

publication date

1 September 1996

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

59

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

620-624

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

THE FAMILIAL OCCURRENCE OF THE CHEDIAK-HIGASHI SYNDROME IN MINK AND CATTLE

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

Congenital gigantism of peroxidase granules; the first case ever reported of qualitative abnormity of peroxidase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

Integration of the cytogenetic, genetic, and physical maps of the human genome by FISH mapping of CEPH YAC clones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

Identification of the murine beige gene by YAC complementation and positional cloning

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

Chédiak-Higashi syndrome: report of a case and review of the Japanese literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

The giant organelles in beige and Chediak-Higashi fibroblasts are derived from late endosomes and mature lysosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

Melanosomes are specialized members of the lysosomal lineage of organelles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

The Chediak-Higashi Syndrome and the Homologous Trait in Animals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

Human gamma-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

The accelerated phase of Chediak-Higashi syndrome. An expression of the virus-associated hemophagocytic syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

Relationship of the genes for Chediak-Higashi syndrome (beige) and the T-cell receptor gamma chain in mouse and man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

Human nidogen: cDNA cloning, cellular expression, and mapping of the gene to chromosome Iq43

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

Colour genes, oncogenes and melanocyte differentiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

The Chediak-Higashi syndrome of cats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

27 July 2018

Linkage disequilibrium mapping of the gene for Hermansky-Pudlak syndrome to chromosome 10q23.1-q23.3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

24 September 2018

A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914913

24 September 2018

Giant granules in leukocytes of the beige mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unrelated donor bone marrow transplantation for correction of lethal congenital immunodeficiencies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Chediak-Higashi syndrome: a possible lysosomal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Chediak-Higashi syndrome: electrophysiological and electron microscopic observations on the peripheral neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beige rat: a new animal model of Chediak-Higashi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chédiak-Higashi syndrome; a lethal familial disease with anomalous inclusions in the leukocytes and constitutional stigmata: report of a case with necropsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chediak-Higashi syndrome: reversal of increased susceptibility to infection by bone marrow transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

STUDIES OF ABNORMAL LEUKOCYTE BODIES IN THE MINK

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[New leukocyte anomaly of constitutional and familial character]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chédiak and Higashi's Disease. Probable Identity of “A New Leucocytal Anomaly (Chédiak)” and “Congenital Gigantism of Peroxidase Granules (Higashi)”

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

T-cell lymphoma and the Chediak-Higashi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of loci associated with two pigment mutations on mouse chromosome 13

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nidogen/entactin (Nid) maps to the proximal end of mouse chromosome 13 linked to beige (bg) and identifies a new region of homology between mouse and human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chediak-Higashi syndrome: hereditary gigantism of cytoplasmic organelles

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Chediak-Higashi syndrome: formation of giant melanosomes and the basis of hypopigmentation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complementation analysis of Chediak-Higashi Syndrome: The same gene may be responsible for the defect in all patients and species

1 reference

https://pubmed.ncbi.nlm.nih.gov/8751863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

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