(Q41713542)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9484600%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

review article

1 reference

title

Intermediate filaments and their associated proteins: multiple dynamic personalities (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9484600%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9484600%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

author name string

M K Houseweart

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9484600%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

publication date

1 February 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9484600%20AND%20SRC:MED&resulttype=core&format=json

Current Opinion in Cell Biology

9 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9484600%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9484600%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

page(s)

93-101

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9484600%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9484600%20AND%20SRC:MED&resulttype=core&format=json

The function of intermediate filaments in cell shape and cytoskeletal integrity

9 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Cytoskeleton-associated plectin: in situ localization, in vitro reconstitution, and binding to immobilized intermediate filament proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Protein kinase A- and protein kinase C-regulated interaction of plectin with lamin B and vimentin

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Plectin sidearms mediate interaction of intermediate filaments with microtubules and other components of the cytoskeleton

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Basic amino acid residue cluster within nuclear targeting sequence motif is essential for cytoplasmic plectin-vimentin network junctions

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

An essential cytoskeletal linker protein connecting actin microfilaments to intermediate filaments.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

M-phase-specific phosphorylation and structural rearrangement of the cytoplasmic cross-linking protein plectin involve p34cdc2 kinase

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Dynamic organisation of intermediate filaments and associated proteins during the cell cycle

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Human plectin: organization of the gene, sequence analysis, and chromosome localization (8q24)

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Cloning and characterization of mouse ACF7, a novel member of the dystonin subfamily of actin binding proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

The plakin family: versatile organizers of cytoskeletal architecture

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Homozygous deletion mutations in the plectin gene (PLEC1) in patients with epidermolysis bullosa simplex associated with late-onset muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Targeted inactivation of plectin reveals essential function in maintaining the integrity of skin, muscle, and heart cytoarchitecture

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Identification of a 450-kDa human epidermal autoantigen as a new member of the plectin family

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Developmental expression of BPAG1-n: insights into the spastic ataxia and gross neurologic degeneration in dystonia musculorum mice

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Dystonin expression in the developing nervous system predominates in the neurons that degenerate in dystonia musculorum mutant mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Neuronal intermediate filaments

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Hereditary hypotrophic axonopathy with neurofilament deficiency in a mutant strain of the Japanese quail

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Neurofilament-deficient axons and perikaryal aggregates in viable transgenic mice expressing a neurofilament-beta-galactosidase fusion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Delayed maturation of regenerating myelinated axons in mice lacking neurofilaments

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Neurofilament subunit NF-H modulates axonal diameter by selectively slowing neurofilament transport

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Subunit composition of neurofilaments specifies axonal diameter.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Overexpression of the human NFM subunit in transgenic mice modifies the level of endogenous NFL and the phosphorylation state of NFH subunits

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

A mutant neurofilament subunit causes massive, selective motor neuron death: implications for the pathogenesis of human motor neuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Sequence variants in human neurofilament proteins: absence of linkage to familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Analysis of the KSP repeat of the neurofilament heavy subunit in familiar amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Disruption of muscle architecture and myocardial degeneration in mice lacking desmin

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Cardiovascular lesions and skeletal myopathy in mice lacking desmin.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Desmin is essential for the tensile strength and integrity of myofibrils but not for myogenic commitment, differentiation, and fusion of skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Suppression by antisense mRNA demonstrates a requirement for the glial fibrillary acidic protein in the formation of stable astrocytic processes in response to neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Mice devoid of the glial fibrillary acidic protein develop normally and are susceptible to scrapie prions

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Targeted deletion in astrocyte intermediate filament (Gfap) alters neuronal physiology

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

GFAP is necessary for the integrity of CNS white matter architecture and long-term maintenance of myelination

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Deficient cerebellar long-term depression, impaired eyeblink conditioning, and normal motor coordination in GFAP mutant mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Disrupted glial fibrillary acidic protein network in astrocytes from vimentin knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Mice lacking vimentin develop and reproduce without an obvious phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Disruption of nuclear lamin organization alters the distribution of replication factors and inhibits DNA synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

1 reference

7 January 2021

The genetic basis of epidermolysis bullosa simplex with mottled pigmentation

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

A novel H1 mutation in the keratin 1 chain in epidermolytic hyperkeratosis

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

The cytoskeleton and disease: genetic disorders of intermediate filaments

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Mutation of human keratin 18 in association with cryptogenic cirrhosis

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

A transgenic mouse model with an inducible skin blistering disease phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

Transgenic studies with a keratin promoter-driven growth hormone transgene: prospects for gene therapy

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980091-4

7 January 2021

10.1016/S0955-0674(98)80091-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9484600%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference