(Q47995278)

7 February 2018

title

Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele (English)

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7 February 2018

author name string

Cox GA

series ordinal

1

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7 February 2018

Mahaffey CL

series ordinal

2

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7 February 2018

Frankel WN

series ordinal

3

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7 February 2018

language of work or name

English

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publication date

1 December 1998

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7 February 2018

published in

Neuron

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7 February 2018

volume

21

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7 February 2018

issue

6

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7 February 2018

page(s)

1327-1337

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7 February 2018

Intrafamilial heterogeneity in hereditary motor neuron disease

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Purification and characterization of DNA polymerase alpha-associated replication protein A-dependent yeast DNA helicase A.

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7 January 2021

Yeast DNA helicase A: cloning, expression, purification, and enzymatic characterization

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Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.

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

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New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin.

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A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy

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7 January 2021

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

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7 January 2021

Structure and function of simian virus 40 large tumor antigen

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7 January 2021

The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis

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7 January 2021

The stumbler mutation maps to proximal mouse chromosome 2

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New seizure frequency QTL and the complex genetics of epilepsy in EL mice.

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7 January 2021

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

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Synergistic anti-apoptotic activity between Bcl-2 and SMN implicated in spinal muscular atrophy

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No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers

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7 January 2021

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

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7 January 2021

Identification and characterization of a spinal muscular atrophy-determining gene

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7 January 2021

Genetic and physical maps of the stargazer locus on mouse chromosome 15

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7 January 2021

Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis

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7 January 2021

The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

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7 January 2021

Direct selection: a method for the isolation of cDNAs encoded by large genomic regions

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7 January 2021

fos/jun repression of cardiac-specific transcription in quiescent and growth-stimulated myocytes is targeted at a tissue-specific cis element

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7 January 2021

An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy

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7 January 2021

Isolation of cDNA encoding a binding protein specific to 5'-phosphorylated single-stranded DNA with G-rich sequences

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7 January 2021

The selective isolation of novel cDNAs encoded by the regions surrounding the human interleukin 4 and 5 genes

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7 January 2021

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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7 January 2021

Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics

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7 January 2021

A new mouse mutant with progressive motor neuronopathy.

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7 January 2021

A yeast artificial chromosome contig spanning the mouse immunoglobulin kappa light chain locus

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7 January 2021

Localization of the Catf1 transcription factor gene to mouse chromosome 19

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7 January 2021

Positional cloning of the nude locus: genetic, physical, and transcription maps of the region and mutations in the mouse and rat

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7 January 2021

Molecular characterization of the rat insulin enhancer-binding complex 3b2. Cloning of a binding factor with putative helicase motifs

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7 January 2021

Genetics of amyotrophic lateral sclerosis

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7 January 2021

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

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7 January 2021

The multiple roles of transcription/repair factor TFIIH

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7 January 2021

The MEV mouse linkage testing stock: mapping 30 novel proviral insertions and establishment of an improved stock

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7 January 2021

A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients

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7 January 2021

Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree

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7 January 2021

A new twist to the tale? Apoptosis

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7 January 2021

Spinal muscular atrophy--clinical and genetic correlations

1 reference

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7 January 2021

10.1016/S0896-6273(00)80652-2

Identifiers

DOI

1 reference

7 February 2018

release_kbrzlmb2vreldc5huxr3fu2gzq

Fatcat ID

0 references

1 reference

7 February 2018