(Q46812710)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

title

Variants in the NOTCH1 gene in patients with aortic coarctation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

author

Tatiana V. Tatarinova

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

Natalia A Smolina

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

Artem Kiselev

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

Olga Moiseeva

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

Anna Malashicheva

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

Anna Kostareva

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

author name string

Olga Freylikhman

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

Sergey Zhuk

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

Alexandra Klyushina

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

Gunnar Sjoberg

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

publication date

12 January 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

published in

Congenital Heart Disease

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

volume

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

5 March 2020

page(s)

391-396

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24418111%20AND%20SRC:MED&resulttype=core&format=json

Genetic factors in congenital heart malformation

5 March 2020

cites work

1 reference

Mutation in myosin heavy chain 6 causes atrial septal defect

21 January 2018

1 reference

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

21 January 2018

1 reference

TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts

21 January 2018

1 reference

Mutations in sarcomeric protein genes not only lead to cardiomyopathy but also to congenital cardiovascular malformations

21 January 2018

1 reference

Genetics of congenital heart disease: the glass half empty

21 January 2018

1 reference

Bicuspid aortic valve is heritable

21 January 2018

1 reference

A prospective study to assess the frequency of familial clustering of congenital bicuspid aortic valve

21 January 2018

1 reference

The epidemiology of cardiovascular defects, part I: a study based on data from three large registries of congenital malformations

21 January 2018

1 reference

Echocardiographic evaluation of asymptomatic parental and sibling cardiovascular anomalies associated with congenital left ventricular outflow tract lesions

21 January 2018

1 reference

Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability.

21 January 2018

1 reference

Mutations in NOTCH1 cause aortic valve disease

21 January 2018

1 reference

Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysms

21 January 2018

1 reference

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling

21 January 2018

1 reference

Notch signaling is essential for ventricular chamber development

21 January 2018

1 reference

The multifaceted role of Notch in cardiac development and disease

21 January 2018

1 reference

An essential role for Notch in neural crest during cardiovascular development and smooth muscle differentiation.

21 January 2018

1 reference

Notch signaling in cardiac development

21 January 2018

1 reference

Notch signaling in vascular development

21 January 2018

1 reference

Synergy and antagonism between Notch and BMP receptor signaling pathways in endothelial cells.

21 January 2018

1 reference

Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

21 January 2018

1 reference

Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation

21 January 2018

1 reference

Notch activation results in phenotypic and functional changes consistent with endothelial-to-mesenchymal transformation

21 January 2018

1 reference

NOTCH1 missense alleles associated with left ventricular outflow tract defects exhibit impaired receptor processing and defective EMT.

21 January 2018

1 reference

Notch promotes epithelial-mesenchymal transition during cardiac development and oncogenic transformation

21 January 2018

1 reference