(Q40167522)

English

The functional alteration of mutant GFAP depends on the location of the domain: morphological and functional studies using astrocytoma-derived cells

scientific article published on 22 February 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

The functional alteration of mutant GFAP depends on the location of the domain: morphological and functional studies using astrocytoma-derived cells (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

author name string

Tomokatsu Yoshida

1

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Yasuko Tomozawa

2

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Takayo Arisato

3

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Yuji Okamoto

4

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Hirofumi Hirano

5

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Masanori Nakagawa

6

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

publication date

22 February 2007

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

52

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

362-369

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

https://scigraph.springernature.com/pub.10.1007/s10038-007-0124-7

0 references

Molecular findings in symptomatic and pre-symptomatic Alexander disease patients.

1 reference

https://api.crossref.org/works/10.1007%2FS10038-007-0124-7

21 January 2018

Desmin mutation responsible for idiopathic dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1007%2FS10038-007-0124-7

21 January 2018

Juvenile form of Alexander disease with GFAP mutation and mitochondrial abnormality.

1 reference

https://api.crossref.org/works/10.1007%2FS10038-007-0124-7

21 January 2018

Mutant NDUFV1 subunit of mitochondrial complex I causes leukodystrophy and myoclonic epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atypical focal MRI lesions in a case of juvenile Alexander's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant palatal myoclonus and spinal cord atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plectin regulates the organization of glial fibrillary acidic protein in Alexander disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On-grid immunogold labeling of glial intermediate filaments in epoxy-embedded tissue

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular interactions in intermediate-sized filaments revealed by chemical cross-linking. Heteropolymers of vimentin and glial filament protein in cultured human glioma cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proliferating cell nuclear antigen (PCNA) immunolocalization in paraffin sections: an index of cell proliferation with evidence of deregulated expression in some neoplasms.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of adult-onset Alexander disease with Arg416Trp human glial fibrillary acidic protein gene mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Alexander disease-causing glial fibrillary acidic protein mutant, R416W, accumulates into Rosenthal fibers by a pathway that involves filament aggregation and the association of alpha B-crystallin and HSP27

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GFAP mutations in Alexander disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disruption of intermediate filament organization leads to structural defects at the intersomite junction in Xenopus myotomal muscle.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alexander disease: ventricular garlands and abnormalities of the medulla and spinal cord.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alexander's disease: unique presentation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile Alexander disease with a novel mutation in glial fibrillary acidic protein gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytoskeletal catastrophe causes brain degeneration.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alpha B-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mutation in glial fibrillary acidic protein gene in a patient with Alexander disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case of infantile Alexander disease with a milder phenotype and a novel GFAP mutation, L90P.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rosenthal fibers share epitopes with alpha B-crystallin, glial fibrillary acidic protein, and ubiquitin, but not with vimentin. Immunoelectron microscopy with colloidal gold

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cytoskeleton and disease: genetic disorders of intermediate filaments

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alexander-disease mutation of GFAP causes filament disorganization and decreased solubility of GFAP

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fluctuation of computed tomographic findings in white matter in Alexander's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17318298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-007-0124-7

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 September 2017

ResearchGate publication ID

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