Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta (Q28199148)

GOA release 2020-03-11

author name string

C Zhao

1

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J Takita

2

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Y Tanaka

3

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M Setou

4

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T Nakagawa

5

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S Takeda

6

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H W Yang

7

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S Terada

8

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T Nakata

9

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Y Takei

10

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M Saito

11

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S Tsuji

12

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Y Hayashi

13

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N Hirokawa

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

14

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language of work or name

English

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publication date

1 June 2001

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published in

Cell

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volume

105

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issue

5

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page(s)

587-97

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900363-4

7 January 2021

The major brain isoform of kif1b lacks the putative mitochondria-binding domain

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The novel gene D4Mil1e maps to mouse chromosome 4 and human chromosome 1p36

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A novel mouse kinesin of the UNC-104/KIF1 subfamily encoded by the Kif1b gene

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Altered microtubule organization in small-calibre axons of mice lacking tau protein

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Genetic aspects of hereditary motor and sensory neuropathy (types I and II)

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Kinesin and dynein superfamily proteins and the mechanism of organelle transport

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Brain dynein (MAP1C) localizes on both anterogradely and retrogradely transported membranous organelles in vivo.

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The quantiative measurement of motor inco-ordination in naive mice using an acelerating rotarod

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Motor discoordination results from combined gene disruption of the NMDA receptor NR2A and NR2C subunits, but not from single disruption of the NR2A or NR2C subunit

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SSCP analysis of long DNA fragments in low pH gel

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Interaction of dynamin with microtubules: its structure and GTPase activity investigated by using highly purified dynamin

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Identification and classification of 16 new kinesin superfamily (KIF) proteins in mouse genome

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Visualization of the dynamics of synaptic vesicle and plasma membrane proteins in living axons

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KIF1B, a novel microtubule plus end-directed monomeric motor protein for transport of mitochondria

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Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

1 reference

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7 January 2021

The neuron-specific kinesin superfamily protein KIF1A is a unique monomeric motor for anterograde axonal transport of synaptic vesicle precursors

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The neuropathy of elderly mice

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Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2A

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Kinesin superfamily motor protein KIF17 and mLin-10 in NMDA receptor-containing vesicle transport

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Introduction to the Third International Symposium on Charcot-Marie-Tooth disorders.

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Left-right asymmetry and kinesin superfamily protein KIF3A: new insights in determination of laterality and mesoderm induction by kif3A-/- mice analysis

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Kinesin superfamily protein 3 (KIF3) motor transports fodrin-associating vesicles important for neurite building

1 reference

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7 January 2021

Targeted disruption of mouse conventional kinesin heavy chain, kif5B, results in abnormal perinuclear clustering of mitochondria

1 reference

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Defect in synaptic vesicle precursor transport and neuronal cell death in KIF1A motor protein-deficient mice.

1 reference

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7 January 2021

10.1016/S0092-8674(01)00363-4

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1494467

1494467

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference