(Q24311566)

1

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P A Bolhuis

2

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R A Wolterman

3

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S te Nijenhuis

5

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L J Valentijn

6

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G W Hensels

7

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F G Jennekens

8

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M de Visser

9

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J E Hoogendijk

Isolation and sequence of a cDNA encoding the major structural protein of peripheral myelin

10

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language of work or name

English

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publication date

September 1993

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published in

Nature Genetics

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volume

5

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issue

1

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page(s)

35-9

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0993-35

Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A

20 April 2017

1 reference

Trembler mouse carries a point mutation in a myelin gene

21 January 2018

1 reference

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

21 January 2018

1 reference

Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.

21 January 2018

1 reference

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

21 January 2018

1 reference

Protein zero of peripheral nerve myelin: biosynthesis, membrane insertion, and evidence for homotypic interaction.

21 January 2018

1 reference

Role of myelin Po protein as a homophilic adhesion molecule

21 January 2018

1 reference

Three-Dimensional Structure of Immunoglobulins

21 January 2018

1 reference

Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.

21 January 2018

1 reference

Molecular basis for a polymorphism of human Fc gamma receptor II (CD32)

21 January 2018

1 reference

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

21 January 2018

1 reference

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

21 January 2018

1 reference

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

21 January 2018

1 reference

7 January 2021

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17

1 reference

7 January 2021

Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

1 reference

7 January 2021

The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2

1 reference

7 January 2021

Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group

1 reference

7 January 2021

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

1 reference

7 January 2021

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc? receptor gene region

1 reference

7 January 2021

Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17

1 reference

7 January 2021

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

1 reference

7 January 2021

The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A

1 reference

7 January 2021

The gene encoding peripheral myelin protein zero is located on mouse chromosome 1.

1 reference

7 January 2021

Construction of a physical map on mouse and human chromosome 1: comparison of 13 Mb of mouse and 11 Mb of human DNA

1 reference

7 January 2021

DNA Sequence, genomic organization, and chromosomal localization of the mouse peripheral myelin protein zero gene: Identification of polymorphic alleles

1 reference

7 January 2021

Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin

1 reference

7 January 2021

Isolation and analysis of the gene encoding peripheral myelin protein zero

1 reference

7 January 2021

Phosphorylation of P0Glycoprotein in Peripheral Nerve Myelin

1 reference

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

7 January 2021

The CEPH consortium linkage map of human chromosome 1

1 reference

7 January 2021

The genes for apolipoprotein all (APOA2) and the Duffy blood group (FY) are linked on chromosome 1 in man.

1 reference

7 January 2021

The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1.

1 reference

7 January 2021

The hypervariable gene locus PUM, which codes for the tumour associated epithelial mucins, is located on chromosome 1, within the region 1q21-24

1 reference

7 January 2021

The polymorphic Fc gamma receptor II gene maps to human chromosome 1q.

1 reference

7 January 2021