Literature DB >> 1639406

Mapping of the motor neuron degeneration (Mnd) gene, a mouse model of amyotrophic lateral sclerosis (ALS).

A Messer1, J Plummer, P Maskin, J M Coffin, W N Frankel.   

Abstract

The motor neuron degeneration mutation (Mnd) causes a late-onset, progressive degeneration of upper and lower motor neurons in mice. After establishing genetic and environmental conditions that distinguish the phenotypes of Mnd/Mnd from +/Mnd mice, Mnd was mapped to proximal Chr 8, using endogenous retroviruses as markers. The map location was confirmed with additional linked polymorphic markers. The outcross/intercross matings to the strain AKR/J, which were used to follow the segregation of the retroviral markers with respect to Mnd, also revealed the existence of a timing effect. Approximately one-fourth of the affected Mnd/Mnd F2 progeny showed accelerated disease. The Mnd mouse model should allow study of mechanisms affecting onset and progression of specific neuronal degeneration in both animal and human neurological disease.

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Year:  1992        PMID: 1639406     DOI: 10.1016/0888-7543(92)90155-l

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  9 in total

1.  Alteration of enzymatic activities implicating neuronal degeneration in the spinal cord of the motor neuron degeneration mouse during postnatal development.

Authors:  K Fujita; K Shibayama; M Yamauchi; T Kato; M Ando; H Takahashi; K Iritani; N Yoshimoto; Y Nagata
Journal:  Neurochem Res       Date:  1998-04       Impact factor: 3.996

2.  Maps from two interspecific backcross DNA panels available as a community genetic mapping resource.

Authors:  L B Rowe; J H Nadeau; R Turner; W N Frankel; V A Letts; J T Eppig; M S Ko; S J Thurston; E H Birkenmeier
Journal:  Mamm Genome       Date:  1994-05       Impact factor: 2.957

3.  Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse.

Authors:  Hanlin Gao; Rose-Mary N Boustany; Janice A Espinola; Susan L Cotman; Lakshmi Srinidhi; Kristen Auger Antonellis; Tammy Gillis; Xuebin Qin; Shumei Liu; Leah R Donahue; Roderick T Bronson; Jerry R Faust; Derek Stout; Jonathan L Haines; Terry J Lerner; Marcy E MacDonald
Journal:  Am J Hum Genet       Date:  2001-12-21       Impact factor: 11.025

4.  Apparent loss and hypertrophy of interneurons in a mouse model of neuronal ceroid lipofuscinosis: evidence for partial response to insulin-like growth factor-1 treatment.

Authors:  J D Cooper; A Messer; A K Feng; J Chua-Couzens; W C Mobley
Journal:  J Neurosci       Date:  1999-04-01       Impact factor: 6.167

5.  Intracisternal A-type particle elements as genetic markers: detection by repeat element viral element amplified locus-PCR.

Authors:  N Kaushik; J P Stoye
Journal:  Mamm Genome       Date:  1994-11       Impact factor: 2.957

6.  The AXB and BXA set of recombinant inbred mouse strains.

Authors:  J D Marshall; J L Mu; Y C Cheah; M N Nesbitt; W N Frankel; B Paigen
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

7.  Sulfated glycoprotein-2 (Sgp-2) maps to mouse chromosome 14.

Authors:  E H Birkenmeier; V A Letts; W N Frankel; B S Magenheimer; J P Calvet
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

8.  A new strain congenic for the Mtv-7/Mls-1 locus of mouse chromosome 1.

Authors:  B A Taylor; W N Frankel
Journal:  Immunogenetics       Date:  1993       Impact factor: 2.846

9.  Endogenous nonecotropic proviruses mapped with oligonucleotide probes from the long terminal repeat region.

Authors:  W N Frankel; J M Coffin
Journal:  Mamm Genome       Date:  1994-05       Impact factor: 2.957

  9 in total

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