(Q82125863)

English

An intronic MYLK variant associated with inflammatory lung disease regulates promoter activity of the smooth muscle myosin light chain kinase isoform

scientific article published on 21 October 2011

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22015949%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

An intronic MYLK variant associated with inflammatory lung disease regulates promoter activity of the smooth muscle myosin light chain kinase isoform (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22015949%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

1 reference

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author name string

Yoo Jeong Han

1

1 reference

Europe PubMed Central

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15 January 2020

Shwu-Fan Ma

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22015949%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Michael S Wade

3

1 reference

Europe PubMed Central

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15 January 2020

Carlos Flores

4

1 reference

Europe PubMed Central

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15 January 2020

Joe G N Garcia

5

1 reference

Europe PubMed Central

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15 January 2020

publication date

21 October 2011

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15 January 2020

Journal of Molecular Medicine

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Europe PubMed Central

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15 January 2020

90

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15 January 2020

3

1 reference

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15 January 2020

299-308

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15 January 2020

https://scigraph.springernature.com/pub.10.1007/s00109-011-0820-9

0 references

A variant of the myosin light chain kinase gene is associated with severe asthma in African Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide transcription and the implications for genomic organization

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation in the myosin light chain kinase gene is associated with development of acute lung injury after major trauma

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of cis- and trans-acting elements in the imprinted human SNURF-SNRPN locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systematic discovery of regulatory motifs in human promoters and 3' UTRs by comparison of several mammals

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nested genes in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The carboxyl terminus of the smooth muscle myosin light chain kinase is expressed as an independent protein, telokin

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A single human myosin light chain kinase gene (MLCK; MYLK).

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alternative splicing attenuates transgenic expression directed by the apolipoprotein E promoter-enhancer based expression vector pLIV11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of an enhancer and an alternative promoter in the first intron of the alpha-fetoprotein gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of endothelial cell gap formation and barrier dysfunction: role of myosin light chain phosphorylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomics of long-range regulatory elements

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe asthma: an overview

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RNA editing by adenosine deaminases that act on RNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanisms regulating endothelial cell barrier function

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ADAR gene family and A-to-I RNA editing: diverse roles in posttranscriptional gene regulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An overview of nested genes in eukaryotic genomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ACTN3 and MLCK genotype associations with exertional muscle damage

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of phenotypes: genes and transcripts

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intronic mutations outside of Alu-repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcription regulation and animal diversity

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of endothelial cell gap formation and paracellular permeability.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MYLK polymorphism associated with blood eosinophil level among asthmatic patients in a Korean population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sphingosine 1-phosphate promotes endothelial cell barrier integrity by Edg-dependent cytoskeletal rearrangement

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Forkhead-box transcription factors and their role in the immune system

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased myosin light chain kinase expression in hypertension: Regulation by serum response factor via an insertion mutation in the promoter

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cis- and trans-acting elements regulate the mouse Psmb9 meiotic recombination hotspot

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myosin light chain kinase in endothelium: molecular cloning and regulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CAGE Basic/Analysis Databases: the CAGE resource for comprehensive promoter analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcription of the nude gene (WHN) in human normal organs and mediastinal and pulmonary tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in the myosin light chain kinase gene that confer risk of severe sepsis are associated with a lower risk of asthma

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of endothelial junctional permeability

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Why genes in pieces?

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation in MYLK and lung injury in children and adults with community-acquired pneumonia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel polymorphisms in the myosin light chain kinase gene confer risk for acute lung injury.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22015949

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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