(Q70670394)

English

Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction

scientific article published on 01 April 1993

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

myocardial infarction

1 reference

based on heuristic

inferred from title

author name string

Y Friedlander

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

E J Dann

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

E Leitersdorf

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

publication date

1 April 1993

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

91

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

299-300

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00218280

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Using mutagenic polymerase chain reaction primers to detect carriers of familial defective apolipoprotein B-100

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of biochemical genetic data on Jewish populations: II. Results and interpretations of heterogeneity indices and distance measures with respect to standards

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allele frequency estimation from data on relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype analysis of the human apolipoprotein B mutation associated with familial defective apolipoprotein B100

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypercholesterolaemia due to familial defective apolipoprotein B-100 in two Australian families

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of XbaI polymorphism of the apolipoprotein B gene in determining levels and covariability of lipid and lipoprotein variables in a sample of Israeli offspring with family history of myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apolipoprotein B gene mutations in Austrian subjects with heart disease and their kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of familial defective apolipoprotein B-100 in Finnish patients with elevated serum cholesterol

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diverse effect of ethnicity on plasma lipoprotein[a] levels in heterozygote patients with familial hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma Lp(a), apolipoprotein(a) isoforms and acute myocardial infarction in men and women: a case-control study in the Jerusalem population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA sequence of the human apolipoprotein B gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478017

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00218280

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8478017%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

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