(Q42748347)

English

Cerebellar expression of copper chaperone for superoxide, cytosolic cu/zn-superoxide dismutase, 4-hydroxy-2-nonenal, acrolein and heat shock protein 32 in patients with menkes kinky hair disease: immunohistochemical study

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Europe PubMed Central

PMC publication ID

6 November 2017

Cerebellar expression of copper chaperone for superoxide, cytosolic cu/zn-superoxide dismutase, 4-hydroxy-2-nonenal, acrolein and heat shock protein 32 in patients with menkes kinky hair disease: immunohistochemical study (English)

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

molecular chaperones

0 references

immunohistochemistry

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Atsushi Yokoyama

1

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

Kousaku Ohno

2

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

Asao Hirano

3

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

Masayuki Shintaku

4

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

Masako Kato

5

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

Kazuhiko Hayashi

6

1 reference

Europe PubMed Central

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6 November 2017

Shinsuke Kato

7

1 reference

Europe PubMed Central

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6 November 2017

publication date

1 March 2014

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

Yonago Acta Medica

1 reference

Europe PubMed Central

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6 November 2017

57

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

1

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

23-35

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

Variable response of selected cuproproteins in rat choroid plexus and cerebellum following perinatal copper deficiency

1 reference

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27 May 2018

A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

Copper deficiency induces the upregulation of the copper chaperone for Cu/Zn superoxide dismutase in weanling male rats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

Copper-stimulated endocytosis and degradation of the human copper transporter, hCtr1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

Copper chaperone for superoxide dismutase is essential to activate mammalian Cu/Zn superoxide dismutase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

A delicate balance: homeostatic control of copper uptake and distribution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

Undetectable intracellular free copper: the requirement of a copper chaperone for superoxide dismutase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

The copper chaperone CCS is abundant in neurons and astrocytes in human and rodent brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

The copper chaperone CCS directly interacts with copper/zinc superoxide dismutase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

The copper chaperone for superoxide dismutase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

Pathological characterization of astrocytic hyaline inclusions in familial amyotrophic lateral sclerosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

Menkes' kinky hair disease. II. A clinicopathological report of three cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

Trichopoliodystrophy. II. Pathological changes in skeletal muscle and nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

Polydendritic Purkinje cells in X-chromosome linked copper malabsorption: a Golgi study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

Thalamic degeneration in X-chromosome-linked copper malabsorption

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

27 May 2018

Hypoxic changes in Purkinje cells of the human cerebellum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

16 August 2018

Redox system expression in the motor neurons in amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS, superoxide dismutase 1 (SOD1)-mutated familial ALS, and SOD1-mutated ALS animal models

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

16 August 2018

Histological evidence of redox system breakdown caused by superoxide dismutase 1 (SOD1) aggregation is common to SOD1-mutated motor neurons in humans and animal models

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

16 August 2018

Metallochaperone for Cu,Zn-superoxide dismutase (CCS) protein but not mRNA is higher in organs from copper-deficient mice and rats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

16 August 2018

Immunohistochemical expression of inducible nitric oxide synthase (iNOS) in human brain tumors: relationships of iNOS to superoxide dismutase (SOD) proteins (SOD1 and SOD2), Ki-67 antigen (MIB-1) and p53 protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

16 August 2018

Temporospatial relationship between the expressions of superoxide dismutase and nitric oxide synthase in the developing human brain: immunohistochemical and immunoblotting analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

16 August 2018

Purkinje cells in olivopontocerebellar atrophy and granule cell-type cerebellar degeneration: an immunohistochemical study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

16 August 2018

Familial amyotrophic lateral sclerosis with a two base pair deletion in superoxide dismutase 1: gene multisystem degeneration with intracytoplasmic hyaline inclusions in astrocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

16 August 2018

Kinky hair disease. I. Clinical and pathological features.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

16 August 2018

Atypical form of Menkes kinky hair disease with mitochondrial NADH-CoQ reductase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4110693

16 August 2018

Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions: an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/25067875

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebellar superoxide dismutase expression in Menkes' kinky hair disease: an immunohistochemical investigation

1 reference

https://pubmed.ncbi.nlm.nih.gov/25067875

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Degeneration of the cerebellar system in X-chromosome?linked copper malabsorption

1 reference

https://pubmed.ncbi.nlm.nih.gov/25067875

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Astrocytic hyaline inclusions contain advanced glycation endproducts in familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation: immunohistochemical and immunoelectron microscopical analyses

1 reference

https://pubmed.ncbi.nlm.nih.gov/25067875

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Superoxide dismutases

1 reference

https://pubmed.ncbi.nlm.nih.gov/25067875

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/25067875

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

6 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

6 November 2017

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