(Q46709463)

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Genetics: a gene of rare effect

scientific article published in April 2013

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23579660

Genetics: a gene of rare effect (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23579660

author name string

Stephen S Hall

1

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23579660

language of work or name

0 references

publication date

1 April 2013

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23579660

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23579660

496

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23579660

7444

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23579660

152-155

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23579660

Combined analysis of oligonucleotide microarray data from transgenic and knockout mice identifies direct SREBP target genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adenoviral-mediated expression of Pcsk9 in mice results in a low-density lipoprotein receptor knockout phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel putative SREBP and LXR target genes identified by microarray analysis in liver of cholesterol-fed mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Efficacy, safety, and tolerability of a monoclonal antibody to proprotein convertase subtilisin/kexin type 9 as monotherapy in patients with hypercholesterolaemia (MENDEL): a randomised, double-blind, placebo-controlled, phase 2 study

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atorvastatin with or without an antibody to PCSK9 in primary hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Implication of the proprotein convertase NARC-1/PCSK9 in the development of the nervous system

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of loss-of-function mutations in PCSK9 and identification of a compound heterozygote

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PCSK9: a convertase that coordinates LDL catabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The secretory proprotein convertase neural apoptosis-regulated convertase 1 (NARC-1): liver regeneration and neuronal differentiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Dallas Heart Study: a population-based probability sample for the multidisciplinary study of ethnic differences in cardiovascular health.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23579660

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/496152A

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23579660

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23579660

ResearchGate publication ID

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