A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective protein (Q50560640)

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scientific article published in May 1997

Language	Label	Description	Also known as
English	A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective protein	scientific article published in May 1997

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective protein (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

hypercholesterolemia

0 references

familial hypercholesterolemia

1 reference

based on heuristic

inferred from title

Brage Storstein Andresen

7

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

author name string

Jensen HK

1

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Holst H

2

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Jensen LG

3

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Jørgensen MM

4

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Andreasen PH

5

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Jensen TG

6

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Heath F

8

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Hansen PS

9

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Neve S

10

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Kristiansen K

11

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Faergeman O

12

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Kølvraa S

13

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Bolund L

14

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Gregersen N

15

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

publication date

1 May 1997

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

Atherosclerosis

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

131

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

1

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

67-72

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

The molecular basis and diagnosis of familial hypercholesterolaemia in South African Afrikaners

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2896%2906059-5

7 January 2021

Common low-density lipoprotein receptor mutations in the French Canadian population

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2896%2906059-5

7 January 2021

Two founder mutations in the LDL receptor gene in Norwegian familial hypercholesterolemia subjects

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2896%2906059-5

7 January 2021

The Trp23-Stop and Trp66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2896%2906059-5

7 January 2021

Allele-specific measurement of low-density lipoprotein receptor transcript levels

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2896%2906059-5

7 January 2021

Synthesis and sequence-specific proteolysis of hybrid proteins produced in Escherichia coli

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2896%2906059-5

7 January 2021

A new technique for the assay of infectivity of human adenovirus 5 DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2896%2906059-5

7 January 2021

Characterization of a disease-causing Glu119-Lys mutation in the low-density lipoprotein receptor gene in two Danish families with heterozygous familial hypercholesterolemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2896%2906059-5

7 January 2021

Detection of a novel mutation (stop 468) in exon 10 of the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2896%2906059-5

7 January 2021

The molecular chaperone calnexin binds Glc1Man9GlcNAc2 oligosaccharide as an initial step in recognizing unfolded glycoproteins

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2896%2906059-5

7 January 2021

Identifiers

10.1016/S0021-9150(96)06059-5

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/9180246

ResearchGate publication ID

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