(Q43627980)

25 November 2017

title

A comparison of phenotype and copper distribution in blotchy and brindled mutant mice and in nutritionally copper deficient controls (English)

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25 November 2017

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M Phillips

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25 November 2017

J Camakaris

series ordinal

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25 November 2017

D M Danks

series ordinal

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25 November 2017

publication date

1 April 1991

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Biological Trace Element Research

25 November 2017

published in

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25 November 2017

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25 November 2017

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25 November 2017

page(s)

11-29

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Copper metabolism in mottled mouse mutants: copper therapy of brindled (Mobr) mice

25 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FBF03032670

Copper metabolism in mottled mouse mutants: distribution of 64Cu in brindled (Mobr) mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03032670

Comparisons of copper deficiency states in the murine mutants blotchy and brindled. Changes in copper-dependent enzyme activity in 13-day-old mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03032670

Copper metabolism in mottled mouse mutants. Copper concentrations in tissues during development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03032670

Autoradiographic demonstration of the copper-accumulating tissues in mice with a defect homologous to Menkes' Kinky Hair disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03032670

Abnormal copper metabolism and deficient lysyl oxidase activity in a heritable connective tissue disorder.

21 January 2018

1 reference

12 December 2020

Mutations in humans and animals which affect copper metabolism

1 reference

12 December 2020

Report of the American Institute of Nurtition ad hoc Committee on Standards for Nutritional Studies

1 reference

12 December 2020

Altered copper metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutants

1 reference

12 December 2020

A study of copper treatment and tissue copper levels in the murine congenital copper deficiency, mottled

1 reference

12 December 2020

Type IX Ehlers-Danlos syndrome and Menkes syndrome: the decrease in lysyl oxidase activity is associated with a corresponding deficiency in the enzyme protein.

1 reference

12 December 2020

Alterations in copper and collagen metabolism in Menkes' syndrome and a new subtype of Ehlers-Danlos syndrome

1 reference

12 December 2020

Copper metabolism in mottled mouse (Mus musculus) mutants. Studies of blotchy (Moblo) mice and a comparison with brindled (Mobr) mice

1 reference

12 December 2020

A sex-linked defect in the cross-linking of collagen and elastin associated with the mottled locus in mice

1 reference

12 December 2020

Primary defect in copper transport underlies mottled mutants in the mouse

1 reference

12 December 2020

Catecholamine biosynthesis and the activity of a number of copper-dependent enzymes in the copper deficient mottled mouse mutants

1 reference

12 December 2020

Congenital copper deficiency: copper therapy and dopamine-beta-hydroxylase activity in the mottled (brindled) mouse

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03032670

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Dimensions Publication ID

25 November 2017

1041884995

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1 reference