A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene (Q24538715)

5 July 2017

title

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene (English)

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Charcot-Marie-Tooth disease type 2

5 July 2017

main subject

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Mersiyanova IV

1

1 reference

5 July 2017

Perepelov AV

2

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5 July 2017

Polyakov AV

3

1 reference

5 July 2017

Sitnikov VF

4

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5 July 2017

Dadali EL

5

1 reference

5 July 2017

Oparin RB

6

1 reference

5 July 2017

Petrin AN

7

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5 July 2017

Evgrafov OV

8

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5 July 2017

language of work or name

English

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publication date

7 June 2000

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American Journal of Human Genetics

5 July 2017

published in

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5 July 2017

volume

67

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5 July 2017

issue

1

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5 July 2017

page(s)

37-46

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Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies

5 July 2017

cites work

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24 March 2017

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Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

24 March 2017

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

24 March 2017

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24 March 2017

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Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies

24 March 2017

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Delayed Maturation of Regenerating Myelinated Axons in Mice Lacking Neurofilaments

24 March 2017

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

24 March 2017

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24 March 2017

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24 March 2017

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27 September 2017

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27 September 2017

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Localization of the giant axonal neuropathy gene to chromosome 16q24.

27 September 2017

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Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family

27 September 2017

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Neurofilament triplet protein interactions: evidence for the preferred formation of NF-L-containing dimers and a putative function for the end domains.

27 September 2017

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Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D).

27 September 2017

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A role for neurofilaments in the pathogenesis of amyotrophic lateral sclerosis

27 September 2017

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Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q.

27 September 2017

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Alzheimer disease tangles share immunological similarities with multiphosphorylation repeats in the two large neurofilament proteins

27 September 2017

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Epitope map of neurofilament protein domains in cortical and peripheral nervous system Lewy bodies

27 September 2017

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Cytopathology of amyotrophic lateral sclerosis

27 September 2017

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A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse

27 September 2017

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Mechanisms of selective motor neuron death in transgenic mouse models of motor neuron disease.

27 September 2017

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The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype

27 September 2017

1 reference

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X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study

30 May 2018

1 reference

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Myelin-Associated Glycoprotein Is a Myelin Signal that Modulates the Caliber of Myelinated Axons

30 May 2018

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The phenotypic manifestations of chromosome 17p11.2 duplication

30 May 2018

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

30 May 2018

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Subunit composition of neurofilaments specifies axonal diameter.

30 May 2018

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Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene

30 May 2018

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Characterization of a shared epitope in cortical Lewy body fibrils and Alzheimer paired helical filaments

30 May 2018

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Comparative epitope analysis of neuronal cytoskeletal proteins in Alzheimer's disease senile plaque neurites and neuropil threads.

30 May 2018

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Trembler mouse carries a point mutation in a myelin gene

30 May 2018

1 reference

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The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

30 May 2018

1 reference

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Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A

30 May 2018

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Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287099

Charcot-Marie-Tooth disease type 2 associated with mutation of the myelin protein zero gene

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287099

Pathogenesis of two axonopathies does not require axonal neurofilaments.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287099

Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287099

Self-assembly in Vitro of the 68,000 molecular weight component of the mammalian neurofilament triplet proteins into intermediate-sized filaments

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287099

Lewy Bodies of Parkinson's Disease Contain Neurofilament Antigens

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287099

Hereditary motor sensory neuropathy type II with neurofilament accumulation: new finding or new disorder?

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287099

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287099

Genetic and clinical aspects of Charcot-Marie-Tooth's disease

29 November 2018

1 reference

12 December 2020

The clinical features of hereditary motor and sensory neuropathy types I and II

1 reference

12 December 2020

Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

1 reference

12 December 2020

Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis

1 reference

12 December 2020

Involvement of neurofilaments in motor neuron disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

1 reference

12 December 2020

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

1 reference

12 December 2020

Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13

1 reference

12 December 2020

Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage

1 reference

12 December 2020

A new type of hereditary motor and sensory neuropathy linked to chromosome 3

1 reference

12 December 2020

2nd Workshop of the European CMT Consortium: 53rd ENMC International Workshop on Classification and Diagnostic Guidelines for Charcot-Marie-Tooth Type 2 (CMT2-HMSN II) and Distal Hereditary Motor Neuropathy (distal HMN-Spinal CMT) 26-28 September 19

1 reference

12 December 2020

Novel insertion in the KSP region of the neurofilament heavy gene in amyotrophic lateral sclerosis (ALS)

1 reference

12 December 2020

Effects of PMP22 duplication and deletions on the axonal cytoskeleton

1 reference

12 December 2020

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

12 December 2020

Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1086/302962

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5 July 2017

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5 July 2017

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