Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies (Q24323150)

peripheral nervous system development

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

L E Warner

1

0 references

P Mancias

2

0 references

I J Butler

3

0 references

C M McDonald

4

0 references

L Keppen

5

0 references

K G Koob

6

0 references

J R Lupski

https://scigraph.springernature.com/pub.10.1038/ng0498-382

7

0 references

language of work or name

English

0 references

publication date

April 1998

0 references

published in

Nature Genetics

0 references

volume

18

0 references

page(s)

382-4

0 references

issue

4

0 references

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038/NG0498-382

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

The serum and TPA responsive promoter and intron-exon structure of EGR2, a human early growth response gene encoding a zinc finger protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

Structure, chromosome location, and expression of the mouse zinc finger gene Krox-20: multiple gene products and coregulation with the proto-oncogene c-fos

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

Base sequence discrimination by zinc-finger DNA-binding domains.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

Mapping functional regions of the segment-specific transcription factor Krox-20.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

The Transcription Factors SCIP and Krox-20 Mark Distinct Stages and Cell Fates in Schwann Cell Differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

Krox-20 controls myelination in the peripheral nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

Congenital hypomyelinating neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

Transcriptional activity of the zinc finger protein NGFI-A is influenced by its interaction with a cellular factor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

Charcot-Marie-Tooth disease: a gene-dosage effect

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

DNA-binding specificity of NGFI-A and related zinc finger transcription factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

Three-dimensional solution structure of a single zinc finger DNA-binding domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

Proposed structure for the zinc-binding domains from transcription factor IIIA and related proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

Zinc finger-DNA recognition: crystal structure of a Zif268-DNA complex at 2.1 A

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

inferred from DOI database lookup

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382

inferred from DOI database lookup

7 January 2021

based on heuristic

A model for the tertiary structure of the 28 residue DNA-binding motif ('zinc finger') common to many eukaryotic transcriptional regulatory proteins

1 reference

https://api.crossref.org/works/10.1038%2FNG0498-382