(Q48812831)

English

The metallothionein-I gene maps to mouse chromosome 8: implications for human Menkes' disease.

scientific article published in January 1983

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scholarly article

1 reference

Europe PubMed Central

15 February 2018

http://europepmc.org/abstract/MED/6683708

The metallothionein-I gene maps to mouse chromosome 8: implications for human Menkes' disease. (English)

1 reference

Europe PubMed Central

15 February 2018

http://europepmc.org/abstract/MED/6683708

author name string

D R Cox

1

1 reference

Europe PubMed Central

15 February 2018

http://europepmc.org/abstract/MED/6683708

R D Palmiter

2

1 reference

Europe PubMed Central

15 February 2018

http://europepmc.org/abstract/MED/6683708

publication date

1 January 1983

1 reference

Europe PubMed Central

15 February 2018

http://europepmc.org/abstract/MED/6683708

1 reference

Europe PubMed Central

15 February 2018

http://europepmc.org/abstract/MED/6683708

64

1 reference

Europe PubMed Central

15 February 2018

http://europepmc.org/abstract/MED/6683708

61-64

1 reference

Europe PubMed Central

15 February 2018

http://europepmc.org/abstract/MED/6683708

1

1 reference

Europe PubMed Central

15 February 2018

http://europepmc.org/abstract/MED/6683708

https://scigraph.springernature.com/pub.10.1007/bf00289481

0 references

Isolation and characterization of the mouse metallothionein-I gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased copper metallothionein in Menkes cultured skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal copper-thionein synthesis and impaired copper utilization in mutated brindled mice: model for Menkes' disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the gene for beta 2-microglobulin (B2m) to mouse chromosome 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene order in linkage group XVI of the house mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA methylation controls the inducibility of the mouse metallothionein-I gene in lymphoid cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptional regulation of the mouse metallothionein-I gene by heavy metals

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary defect in copper transport underlies mottled mutants in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the committee on comparative mapping. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Menkes's kinky hair syndrome. An inherited defect in copper absorption with widespread effects

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amplification of the metallothionein-I gene in cadmium-resistant mouse cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucocorticoid regulation of metallothionein-I mRNA synthesis in cultured mouse cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/6683708

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00289481

1 reference

Europe PubMed Central

15 February 2018

http://europepmc.org/abstract/MED/6683708

1 reference

Europe PubMed Central

15 February 2018

http://europepmc.org/abstract/MED/6683708

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