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English
Genetics. Simple genetics for a complex disease
scientific article published on May 2013
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
title
Genetics. Simple genetics for a complex disease
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
author
Helen Hobbs
series ordinal
2
object named as
Helen H Hobbs
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
Jonathan C. Cohen
series ordinal
1
object named as
Jonathan C Cohen
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
language of work or name
English
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publication date
1 May 2013
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
published in
Science
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
volume
340
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
issue
6133
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
page(s)
689-690
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
cites work
SEC24A deficiency lowers plasma cholesterol through reduced PCSK9 secretion
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839083
retrieved
6 September 2017
Potential of proprotein convertase subtilisin/kexin type 9 based therapeutics
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839083
retrieved
6 September 2017
Molecular characterization of proprotein convertase subtilisin/kexin type 9-mediated degradation of the LDLR.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839083
retrieved
6 September 2017
PCSK9: a convertase that coordinates LDL catabolism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839083
retrieved
6 September 2017
Molecular characterization of loss-of-function mutations in PCSK9 and identification of a compound heterozygote
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839083
retrieved
6 September 2017
Sequence variations in PCSK9, low LDL, and protection against coronary heart disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839083
retrieved
6 September 2017
Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839083
retrieved
6 September 2017
Are rare variants responsible for susceptibility to complex diseases?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839083
retrieved
6 September 2017
A receptor-mediated pathway for cholesterol homeostasis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839083
retrieved
6 September 2017
The C679X mutation in PCSK9 is present and lowers blood cholesterol in a Southern African population
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839083
retrieved
2 September 2018
Identifiers
DOI
10.1126/SCIENCE.1239101
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
PMCID
3839083
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
PubMed ID
23661745
1 reference
stated in
Europe PubMed Central
PMCID
3839083
retrieved
19 August 2017
ResearchGate publication ID
236675836
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