Science, medicine, and the future: Genetics and cardiovascular risk. (Q28366460)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11744567%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

review article

1 reference

title

Science, medicine, and the future: Genetics and cardiovascular risk (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11744567%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

1 reference

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4 December 2019

I N Day

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11744567%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

language of work or name

English

0 references

publication date

1 December 2001

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4 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11744567%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

volume

323

1 reference

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4 December 2019

issue

7326

1 reference

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4 December 2019

page(s)

1409-1412

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Congenital heart disease caused by mutations in the transcription factor NKX2-5

4 December 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

A pilot study of ex vivo gene therapy for homozygous familial hypercholesterolaemia

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

Molecular and cellular mechanisms of cardiac arrhythmias

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

Gene therapy for restenosis after balloon angioplasty and stenting.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

Outcome of case finding among relatives of patients with known heterozygous familial hypercholesterolaemia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

The 22q11 deletion syndromes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosis

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

Familial risks of congenital heart defect assessed in a population-based epidemiologic study.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

Association of mutations in the apolipoprotein B gene with hypercholesterolemia and the risk of ischemic heart disease

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemia.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

Differences in the Phenotypic Characteristics of Subjects With Familial Defective Apolipoprotein B-100 and Familial Hypercholesterolemia

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1121864

Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindred

27 November 2018

1 reference

12 December 2020

The use of long PCR to confirm three common alleles at the CYP2A6 locus and the relationship between genotype and smoking habit

1 reference

12 December 2020

Genetic and environmental factors affecting the incidence of coronary artery disease in heterozygous familial hypercholesterolemia

1 reference

12 December 2020

Phenotypic variation in heterozygous familial hypercholesterolemia: a comparison of Chinese patients with the same or similar mutations in the LDL receptor gene in China or Canada

1 reference

12 December 2020

Cholesterol reduction yields clinical benefit: impact of statin trials

1 reference

12 December 2020

10.1136/BMJ.323.7326.1409

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11744567%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11744567%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

PubMed publication ID

11744567

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11744567%20AND%20SRC:MED&resulttype=core&format=json