(Q36578997)

English

Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos

scientific article published on September 1997

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos (English)

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

spinal muscular atrophy

1 reference

based on heuristic

inferred from title

muscular atrophy

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

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author name string

Schrank B

1

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Götz R

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Gunnersen JM

3

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Ure JM

4

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Toyka KV

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Smith AG

6

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Sendtner M

7

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

language of work or name

0 references

publication date

1 September 1997

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

number of pages

6

1 reference

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inferred from page(s)

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

94

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

18

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

9920-9925

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Molecular analysis of the SMN and NAIP genes in Spanish spinal muscular atrophy (SMA) families and correlation between number of copies of cBCD541 and SMA phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

9 September 2017

A novel nuclear structure containing the survival of motor neurons protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

9 September 2017

Suppression of apoptosis in mammalian cells by NAIP and a related family of IAP genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

9 September 2017

Two large insert vectors, lambda PS and lambda KO, facilitate rapid mapping and targeted disruption of mammalian genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

9 September 2017

Identification and characterization of a spinal muscular atrophy-determining gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

9 September 2017

Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

9 September 2017

A frame–shift deletion in the survival motor neuron gene in Spanish spinal muscular atrophy patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

9 September 2017

Use of a recombinant retrovirus to study post-implantation cell lineage in mouse embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

9 September 2017

Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

9 September 2017

A workbench for multiple alignment construction and analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

9 September 2017

Targeted replacement of the homeobox gene Hox-3.1 by the Escherichia coli lacZ in mouse chimeric embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

9 September 2017

From enigmatic to problematic: the new molecular genetics of childhood spinal muscular atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

30 September 2017

Genes for SMA: multum in parvo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

30 September 2017

Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classifications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

30 September 2017

Application of LacZ gene fusions to preimplantation development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

28 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

28 June 2018

Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

28 June 2018

Disruption of the CNTF gene results in motor neuron degeneration.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

20 September 2018

Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23295

20 September 2018

The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.18.9920

21 January 2018

Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.18.9920

21 January 2018

Genetic homogeneity between acute and chronic forms of spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.18.9920

21 January 2018

Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.18.9920

21 January 2018

Cell redundancy in the zona-intact preimplantation mouse blastocyst: a light and electron microscope study of dead cells and their fate

1 reference

https://pubmed.ncbi.nlm.nih.gov/9275227

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Classification of spinal muscular atrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/9275227

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SMA genes: deleted and duplicated

1 reference

https://pubmed.ncbi.nlm.nih.gov/9275227

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals

1 reference

https://pubmed.ncbi.nlm.nih.gov/9275227

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion analysis of SMN and NAIP genes in spinal muscular atrophy Italian families

1 reference

https://pubmed.ncbi.nlm.nih.gov/9275227

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9275227

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.94.18.9920

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

1997PNAS...94.9920S

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

0 references

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