(Q35012989)

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An approximately 140-kb deletion associated with feline spinal muscular atrophy implies an essential LIX1 function for motor neuron survival

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scholarly article

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Europe PubMed Central

PubMed publication ID

5 August 2017

An approximately 140-kb deletion associated with feline spinal muscular atrophy implies an essential LIX1 function for motor neuron survival (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

spinal muscular atrophy

1 reference

based on heuristic

inferred from title

muscular atrophy

1 reference

based on heuristic

inferred from title

William J Murphy

7

object named as

William J Murphy

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Stephen J. O'Brien

13

object named as

Stephen J O'Brien

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Europe PubMed Central

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5 August 2017

Marilyn Menotti-Raymond

2

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Marilyn Menotti-Raymond

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Europe PubMed Central

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5 August 2017

author name string

John C Fyfe

1

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Europe PubMed Central

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5 August 2017

Victor A David

3

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Europe PubMed Central

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5 August 2017

Lars Brichta

4

1 reference

Europe PubMed Central

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5 August 2017

Alejandro A Schäffer

5

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Europe PubMed Central

PubMed publication ID

5 August 2017

Richa Agarwala

6

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Europe PubMed Central

PubMed publication ID

5 August 2017

William J Wedemeyer

8

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Europe PubMed Central

PubMed publication ID

5 August 2017

Brittany L Gregory

9

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Europe PubMed Central

PubMed publication ID

5 August 2017

Bethany G Buzzell

10

1 reference

Europe PubMed Central

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5 August 2017

Meghan C Drummond

11

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Europe PubMed Central

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5 August 2017

Brunhilde Wirth

12

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Europe PubMed Central

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5 August 2017

publication date

9 August 2006

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Europe PubMed Central

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5 August 2017

Genome Research

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Europe PubMed Central

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5 August 2017

16

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5 August 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

1084-1090

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Application of assisted reproduction for population management in felids: the potential and reality for conservation of small cats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

Mildly affected patients with spinal muscular atrophy are partially protected by an increased SMN2 copy number

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

Binding proteins for mRNA localization and local translation, and their dysfunction in genetic neurological disease

1 reference

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8 July 2018

Mfold web server for nucleic acid folding and hybridization prediction

1 reference

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8 July 2018

EVA: Evaluation of protein structure prediction servers.

1 reference

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8 July 2018

The dsRNA binding protein family: critical roles, diverse cellular functions

1 reference

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8 July 2018

Second-Generation Integrated Genetic Linkage/Radiation Hybrid Maps of the Domestic Cat (Felis catus)

1 reference

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8 July 2018

SMN-mediated assembly of RNPs: a complex story

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

Genetic testing and risk assessment for spinal muscular atrophy (SMA).

1 reference

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8 July 2018

The Feline Genome Project

1 reference

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8 July 2018

Mice deficient in the insulin-regulated membrane aminopeptidase show substantial decreases in glucose transporter GLUT4 levels but maintain normal glucose homeostasis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

When the message goes awry: disease-producing mutations that influence mRNA content and performance.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

Animal models of spinal muscular atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

A greedy algorithm for aligning DNA sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

A radiation hybrid map of the cat genome: implications for comparative mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

A fast and scalable radiation hybrid map construction and integration strategy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

Quantitative analysis of survival motor neuron copies: identification of subtle SMN1 mutations in patients with spinal muscular atrophy, genotype-phenotype correlation, and implications for genetic counseling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

Development of a feline whole genome radiation hybrid panel and comparative mapping of human chromosome 12 and 22 loci.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

On constructing radiation hybrid maps.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

De novo rearrangements found in 2% of index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate, and implications for genetic counseling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

The survival motor neuron protein in spinal muscular atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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8 July 2018

Correlation between severity and SMN protein level in spinal muscular atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

The complete amino acid sequence of human placental oxytocinase

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8 July 2018

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=1557767

8 July 2018

Nonhomologous recombination in the human genome: deletions in the human factor VIII gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

8 July 2018

Poly(A) signals.

1 reference

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8 July 2018

Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy

1 reference

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8 July 2018

Inherited motor neuron disease in domestic cats: a model of spinal muscular atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

25 October 2018

Optimizing exact genetic linkage computations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

25 October 2018

Radiation hybrid mapping of 304 novel microsatellites in the domestic cat genome

1 reference

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25 October 2018

Cloning and expression analysis of chicken Lix1, a founding member of a novel gene family.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1557767

25 October 2018

Different molecular basis for spinal muscular atrophy in South African black patients

1 reference

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25 October 2018

Spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16899656

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Murine Lix1, a novel marker for substantia nigra, cortical layer 5, and hindbrain structures

1 reference

https://pubmed.ncbi.nlm.nih.gov/16899656

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

International SMA consortium meeting. (26-28 June 1992, Bonn, Germany)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16899656

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1101/GR.5268806

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

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