Familial defective apolipoprotein B-100: detection and haplotype analysis of the Arg(3500)-->Gln mutation in hyperlipidemic Chinese (Q74348166)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

title

Familial defective apolipoprotein B-100: detection and haplotype analysis of the Arg(3500)-->Gln mutation in hyperlipidemic Chinese (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

author name string

J P Pan

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

S C Chou

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

D Y Tai

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

G J Lee-Chen

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

publication date

1 October 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

152

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

385-390

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

Familial defective apolipoprotein B-100: a single mutation that causes hypercholesterolemia and premature coronary artery disease

10 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

A receptor-mediated pathway for cholesterol homeostasis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

Familial defective apolipoprotein B-100: haplotype analysis of the arginine(3500)----glutamine mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

Identification of the apo B-3500 mutation in the Norwegian population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

Familial defective apolipoprotein B-100: a study of patients from lipid clinics in Scotland and Wales

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 allele

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

Report of the National Cholesterol Education Program Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. The Expert Panel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

DNA sequence of the human apolipoprotein B gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

DNA sequencing with chain-terminating inhibitors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

The CpG dinucleotide and human genetic disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900481-5

10.1016/S0021-9150(99)00481-5

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998466%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference