(Q77220547)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9731541%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

title

Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy (English)

1 reference

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3 December 2019

1 reference

Rust S

1

1 reference

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3 December 2019

Walter M

2

1 reference

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3 December 2019

Funke H

3

1 reference

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3 December 2019

von Eckardstein A

4

1 reference

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3 December 2019

Cullen P

5

1 reference

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3 December 2019

Kroes HY

6

1 reference

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3 December 2019

Hordijk R

7

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3 December 2019

Geisel J

8

1 reference

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3 December 2019

Kastelein J

9

1 reference

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3 December 2019

Molhuizen HO

10

1 reference

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3 December 2019

Schreiner M

11

1 reference

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3 December 2019

Mischke A

12

1 reference

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3 December 2019

Hahmann HW

13

1 reference

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3 December 2019

Assmann G

14

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3 December 2019

publication date

1 September 1998

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3 December 2019

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3 December 2019

volume

20

1 reference

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3 December 2019

issue

1

1 reference

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3 December 2019

page(s)

96-98

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https://scigraph.springernature.com/pub.10.1038/1770

3 December 2019

exact match

0 references

cites work

The Tromsø heart-study. High-density lipoprotein and coronary heart-disease: a prospective case-control study

1 reference

7 January 2021

Lipoproteins, cardiovascular disease, and death. The Framingham study

1 reference

7 January 2021

Homozygous Tangier disease and cardiovascular disease

1 reference

7 January 2021

DNA inversion within the apolipoproteins AI/CIII/AIV-encoding gene cluster of certain patients with premature atherosclerosis

1 reference

7 January 2021

A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities

1 reference

7 January 2021

A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity

1 reference

7 January 2021

Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease

1 reference

7 January 2021

The high density lipoprotein- and apolipoprotein A-I-induced mobilization of cellular cholesterol is impaired in fibroblasts from Tangier disease subjects

1 reference

7 January 2021

Defective removal of cellular cholesterol and phospholipids by apolipoprotein A-I in Tangier Disease

1 reference

7 January 2021

HDL-mediated efflux of intracellular cholesterol is impaired in fibroblasts from Tangier disease patients

1 reference

7 January 2021

Defective regulation of phosphatidylcholine-specific phospholipases C and D in a kindred with Tangier disease. Evidence for the involvement of phosphatidylcholine breakdown in HDL-mediated cholesterol efflux mechanisms

1 reference

7 January 2021

Characterization of high density lipoproteins in patients heterozygous for Tangier disease

1 reference

7 January 2021

Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22

1 reference

7 January 2021

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

1 reference

7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

7 January 2021

Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32).

1 reference

7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

7 January 2021

Genetic dissection of complex traits

1 reference

7 January 2021

Identifiers

DOI

10.1038/1770

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9731541%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

1 reference