(Q33909207)

29 July 2017

title

A canine model of Cohen syndrome: Trapped Neutrophil Syndrome (English)

1 reference

29 July 2017

1 reference

1 reference

Jeremy R Shearman

1

1 reference

29 July 2017

Alan N Wilton

series ordinal

2

1 reference

29 July 2017

language of work or name

English

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publication date

23 May 2011

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29 July 2017

1 reference

29 July 2017

volume

12

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29 July 2017

page(s)

258

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Creative Commons Attribution 2.0 Generic

29 July 2017

copyright license

start time

23 May 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

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mtDNA data indicate a single origin for dogs south of Yangtze River, less than 16,300 years ago, from numerous wolves

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Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1.

5 July 2018

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Breed relationships facilitate fine-mapping studies: a 7.8-kb deletion cosegregates with Collie eye anomaly across multiple dog breeds

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Elimination of neutrophil elastase and the genes for [corrected] adaptor protein complex 3 subunits [corrected] as the cause of trapped neutrophil syndrome in Border collies

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5 July 2018

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Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome

5 July 2018

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5 July 2018

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Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport

5 July 2018

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5 July 2018

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Cohen syndrome: essential features, natural history, and heterogeneity

5 July 2018

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5 July 2018

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A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies

5 July 2018

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A simple salting out procedure for extracting DNA from human nucleated cells

5 July 2018

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Structure and Functional Expression of a Human Interleukin-8 Receptor

5 July 2018

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Neutropenia with a probable hereditary basis in Border Collies.

5 July 2018

1 reference

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Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome

21 January 2018

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https://api.crossref.org/works/10.1186%2F1471-2164-12-258

Linkage analysis with multiplexed short tandem repeat polymorphisms using infrared fluorescence and M13 tailed primers.

21 January 2018

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Cohen syndrome resulting from a novel large intragenic COH1 deletion segregating in an isolated Greek island population.

21 January 2018

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Granulocytopenia in Cohen syndrome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21605373

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Exclusion of CXCR4 as the cause of trapped neutrophil syndrome in Border Collies using five microsatellites on canine chromosome 19

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21605373

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2164-12-258

1 reference

Dimensions Publication ID

29 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2164-12-258

release_oidtdururzbuxj6o2rwolikywe

9 September 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/oidtdururzbuxj6o2rwolikywe

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

3128065

1 reference

29 July 2017

1 reference