(Q46526322)

22 December 2017

title

Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia (English)

1 reference

22 December 2017

1 reference

7

Jerome I Rotter

1 reference

22 December 2017

10

Aldons J Lusis

1 reference

PubMed ID

11988495

22 December 2017

Leena Peltonen-Palotie

9

object named as

Leena Peltonen

1 reference

22 December 2017

Päivi Pajukanta

3

object named as

Päivi Pajukanta

1 reference

22 December 2017

Rita M. Cantor

4

object named as

Rita M Cantor

1 reference

22 December 2017

author name string

Hooman Allayee

1

1 reference

22 December 2017

Kelly L Krass

2

1 reference

22 December 2017

Carla J H van der Kallen

5

1 reference

22 December 2017

Rebecca Mar

6

1 reference

22 December 2017

Tjerk W A de Bruin

8

1 reference

22 December 2017

publication date

1 May 2002

1 reference

22 December 2017

number of pages

6

0 references

published in

Circulation Research

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22 December 2017

volume

90

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22 December 2017

page(s)

926-931

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22 December 2017

issue

8

1 reference

22 December 2017

Impaired fatty acid metabolism in familial combined hyperlipidemia. A mechanism associating hepatic apolipoprotein B overproduction and insulin resistance

cites work

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families

30 October 2021

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Leptin receptor gene variation and obesity: lack of association in a white British male population

30 October 2021

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https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

Novel genes for familial combined hyperlipidemia

30 October 2021

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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

Strategies for multilocus linkage analysis in humans

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

Comparison of the measurement of lipids and lipoproteins versus assay of apolipoprotein B for estimation of coronary heart disease risk: a study in familial combined hyperlipidemia

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

Genotype at a major locus with large effects on apolipoprotein B levels predicts familial combined hyperlipidemia

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

The role of the LDL receptor in apolipoprotein B secretion

30 October 2021

1 reference

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Avoiding recomputation in linkage analysis.

30 October 2021

1 reference

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Genomic structure of the human OB receptor and identification of two novel intronic microsatellites.

30 October 2021

1 reference

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Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

Familial combined hyperlipidaemia: Use of stable isotopes to demonstrate overproduction of very low‐density lipoprotein apolipoprotein B by the liver

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia

30 October 2021

1 reference

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Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A

30 October 2021

1 reference

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Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein

30 October 2021

1 reference

https://opencitations.net/index/coci/api/v1/references/10.1161/01.RES.0000015885.27134.F0

10.1161/01.RES.0000015885.27134.F0

30 October 2021

Identifiers

DOI

1 reference

22 December 2017

PubMed ID

11988495

1 reference

22 December 2017