(Q34195373)

reason for preferred rank

31 July 2017

title

Screening of the early growth response 2 gene in Japanese patients with Charcot–Marie–Tooth disease type 1 (English)

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(03)00028-5

31 December 2023

Screening of the early growth response 2 gene in Japanese patients with Charcot-Marie-Tooth disease type 1 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12736090

31 December 2023

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(03)00028-5

31 December 2023

7

Kiyoshi Hayasaka

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12736090

31 December 2023

author name string

Chikahiko Numakura

1

1 reference

31 July 2017

Emi Shirahata

2

1 reference

31 July 2017

Sumimasa Yamashita

3

1 reference

31 July 2017

Masayo Kanai

4

1 reference

31 July 2017

Kazuki Kijima

5

1 reference

31 July 2017

Takasumi Matsuki

6

1 reference

31 July 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12736090

31 December 2023

publication date

1 June 2003

1 reference

31 July 2017

15 June 2003

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12736090

full work available at URL

31 December 2023

https://api.elsevier.com/content/article/PII:S0022510X03000285?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(03)00028-5

https://api.elsevier.com/content/article/PII:S0022510X03000285?httpAccept=text/plain

31 December 2023

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(03)00028-5

Journal of the Neurological Sciences

31 December 2023

published in

1 reference

31 July 2017

volume

210

1 reference

31 July 2017

issue

1-2

1 reference

31 July 2017

page(s)

61-64

1 reference

De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Connexin mutations in X-linked Charcot-Marie-Tooth disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Charcot-Marie-Tooth disease and related neuropathies: mutation distribution and genotype-phenotype correlation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Molecular analysis in Japanese patients with Charcot-Marie-Tooth disease: DGGE analysis for PMP22, MPZ, and Cx32/GJB1 mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

DYS19 marker in Japanese populations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Molecular cloning, sequencing, and mapping of EGR2, a human early growth response gene encoding a protein with "zinc-binding finger" structure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Identification of NAB1, a repressor of NGFI-A- and Krox20-mediated transcription

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

A Novel Mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

A novel missense mutation in the early growth response 2 gene associated with late-onset Charcot--Marie--Tooth disease type 1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Functional consequences of mutations in the early growth response 2 gene (EGR2) correlate with severity of human myelinopathies.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Disruption of Krox-20 results in alteration of rhombomeres 3 and 5 in the developing hindbrain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

WT1-mediated transcriptional activation is inhibited by dominant negative mutant proteins.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2803%2900028-5

NAB2, a corepressor of NGFI-A (Egr-1) and Krox20, is induced by proliferative and differentiative stimuli

7 January 2021

18

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(03)00028-5

31 December 2023

Identifiers

1 reference

31 July 2017

1 reference