A high-resolution genetic map of mouse chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdf-ocd) region (Q74450796)

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10 November 2019

title

A high-resolution genetic map of mouse chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdf-ocd) region (English)

1 reference

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10 November 2019

2

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10 November 2019

Georges F. Carle

4

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10 November 2019

author name string

C Poirier

1

1 reference

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10 November 2019

M Fernandes

3

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10 November 2019

V Stanescu

5

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10 November 2019

R Stanescu

6

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10 November 2019

J L Guénet

7

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10 November 2019

publication date

1 May 1998

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10 November 2019

number of pages

2

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based on heuristic

inferred from page(s)

published in

Mammalian Genome

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10 November 2019

volume

9

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10 November 2019

issue

5

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10 November 2019

page(s)

390-391

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https://scigraph.springernature.com/pub.10.1007/s003359900777

10 November 2019

exact match

0 references

cites work

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The mouse homologs of RELA and MLK3 are located within a 120-kb fragment on chromosome 19

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Chromosomal localization of the human ciliary neurotrophic factor gene (CNTF) to 11q12 by fluorescence in situ hybridization

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Assignment of the human FAU gene to a subregion of chromosome 11q13.

21 January 2018

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MAPMAKER: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations

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Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

21 January 2018

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Structure and chromosomal assignment of the mouse fra-1 gene, and its exclusion as a candidate gene for oc (osteosclerosis)

21 January 2018

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Ciliary neurotrophic factor prevents degeneration of motor neurons in mouse mutant progressive motor neuronopathy

21 January 2018

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Reverse mapping of the gene encoding the human fos-related antigen-1 (fra-1) within chromosome band 11q13

21 January 2018

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Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse

21 January 2018

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Chromosomal localization of genes encoding the transcription factors, c-rel, NF-kappa Bp50, NF-kappa Bp65, and lyt-10 by fluorescence in situ hybridization

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/9545499

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The mouse mutation muscle deficient (mdf) is characterized by a progressive motoneuron disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9545499

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S003359900777

1 reference

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10 November 2019

1 reference