(Q72234260)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

title

Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

author name string

S A Cook

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

K R Johnson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

R T Bronson

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

M T Davisson

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

publication date

1 March 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

number of pages

5

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

page(s)

187-191

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00293010

25 October 2019

exact match

0 references

cites work

The structures and related functions of phosphorylase a.

1 reference

12 December 2020

A Macintosh program for storage and analysis of experimental genetic mapping data

1 reference

12 December 2020

mnd2: a new mouse model of inherited motor neuron disease

1 reference

12 December 2020

A genetic map of the mouse suitable for typing intraspecific crosses

1 reference

12 December 2020

Survival effect of ciliary neurotrophic factor (CNTF) on chick embryonic motoneurons in culture: comparison with other neurotrophic factors and cytokines.

1 reference

12 December 2020

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

1 reference

12 December 2020

A new mouse mutant with progressive motor neuronopathy.

1 reference

12 December 2020

The Fine Structure of the Cervical Spinal Cord, Ventral Root and Brachial Nerves in the Wobbler (WR) Mouse

1 reference

12 December 2020

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

1 reference

12 December 2020

An hereditary motor neurone disease with progressive denervation of muscle in the mouse: the mutant 'wobbler'.

1 reference

12 December 2020

Ultrastructure of chromatolytic motoneurons and anterior spinal roots in a case of Werdnig-Hoffmann disease.

1 reference

12 December 2020

Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studies

1 reference

12 December 2020

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity

1 reference

12 December 2020

Ciliary neurotrophic factor prevents the degeneration of motor neurons after axotomy.

1 reference

12 December 2020

Chromosomal localization of the murine gene and two related sequences encoding high-mobility-group I and Y proteins

1 reference

12 December 2020

Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease)

1 reference

12 December 2020

Localization of the muscle, liver, and brain glycogen phosphorylase genes on linkage maps of mouse chromosomes 19, 12, and 2, respectively

1 reference

12 December 2020

The Gene for Ciliary Neurotrophic Factor (CNTF) Maps to Murine Chromosome 19 and its Expression is Not Affected in the Hereditary Motoneuron Disease 'Wobbler' of the Mouse.

1 reference

12 December 2020

Glutamate oxalate transaminase (GOT) genetics in Mus musculus: linkage, polymorphism, and phenotypes of the Got-2 and Got-1 loci

1 reference

12 December 2020

Ultrastructural, morphometric, and immunocytochemical study of anterior horn cells in mice with "wasted" mutation

1 reference

12 December 2020

Characterization of immunologic and neuropathologic abnormalities in wasted mice

1 reference

12 December 2020

Regulation of myogenesis in paralyzed muscles in the mouse mutants peroneal muscular atrophy and muscular dysgenesis

1 reference

12 December 2020

Disruption of the CNTF gene results in motor neuron degeneration.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00293010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7749225%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference