Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population. (Q44750279)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23229290%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

title

Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23229290%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

main subject

congenital heart disease

1 reference

4

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20 February 2020

Maria Grazia Andreassi

6

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20 February 2020

author name string

Monica Cresci

1

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20 February 2020

Cecilia Vecoli

2

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20 February 2020

Ilenia Foffa

3

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20 February 2020

Lamia Ait-Ali

5

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20 February 2020

language of work or name

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15 November 2012

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20 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23229290%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

volume

34

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20 February 2020

issue

4

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20 February 2020

page(s)

938-941

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Independent requirement for ISL1 in formation of pancreatic mesenchyme and islet cells

20 February 2020

cites work

1 reference

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The amphibian second heart field: Xenopus islet-1 is required for cardiovascular development

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21 January 2018

1 reference

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Human ISL1 heart progenitors generate diverse multipotent cardiovascular cell lineages

21 January 2018

1 reference

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Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart

21 January 2018

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Maternal and paternal environmental risk factors, metabolizing GSTM1 and GSTT1 polymorphisms, and congenital heart disease.

21 January 2018

1 reference

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ISL1 directly regulates FGF10 transcription during human cardiac outflow formation

21 January 2018

1 reference

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Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.

21 January 2018

1 reference

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Isl1 is a direct transcriptional target of Forkhead transcription factors in second-heart-field-derived mesoderm.

21 January 2018

1 reference

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Identification of regulatory elements in the Isl1 gene locus

21 January 2018

1 reference

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The anterior heart-forming field: voyage to the arterial pole of the heart

21 January 2018

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Islet1 cardiovascular progenitors: a single source for heart lineages?

21 January 2018

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Isl1 is upstream of sonic hedgehog in a pathway required for cardiac morphogenesis

21 January 2018

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Multipotent embryonic isl1+ progenitor cells lead to cardiac, smooth muscle, and endothelial cell diversification

21 January 2018

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Genetic insights into normal and abnormal heart development

21 January 2018

1 reference

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Gene regulatory networks in the evolution and development of the heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0578-Z

Common variation in ISL1 confers genetic susceptibility for human congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0578-Z

ISL1 common variant rs1017 is not associated with susceptibility to congenital heart disease in a Chinese population

21 January 2018

1 reference

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10.1007/S00246-012-0578-Z

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23229290%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference