Chylomicron retention disease: a long term study of two cohorts (Q46088828)

19 December 2017

title

Chylomicron retention disease: a long term study of two cohorts (English)

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19 December 2017

chylomicron retention disease

main subject

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Marie-Claude Vohl

9

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Andrée Rasquin

6

object named as

Andrée Rasquin

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19 December 2017

author name string

Noel Peretti

1

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Claude C Roy

2

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Agnès Sassolas

3

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Colette Deslandres

4

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Eric Drouin

5

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Ernest Seidman

7

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Pierre Brochu

8

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Sylvie Labarge

10

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Raymonde Bouvier

11

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Marie-Elizabeth Samson-Bouma

12

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Mathilde Charcosset

13

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Alain Lachaux

14

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Emile Levy

15

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publication date

20 February 2009

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Molecular Genetics and Metabolism

published in

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19 December 2017

volume

97

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page(s)

136-142

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issue

2

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Intestinal lipoprotein assembly

cites work

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Use of immunoelectron microscopy and intestinal models to explore the elaboration of apolipoproteins required for intraenterocyte lipid transport

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Mechanisms of lipid malabsorption in Cystic Fibrosis: the impact of essential fatty acids deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Familial hypobetalipoproteinemia associated with a mutant species of apolipoprotein B (B-46)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Familial hypobetalipoproteinemia: genetics and metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Cloning and gene defects in microsomal triglyceride transfer protein associated with abetalipoproteinaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Hypobetalipoproteinemia with accumulation of an apoprotein B-like protein in intestinal cells. Immunoenzymatic and biochemical characterization of seven cases of Anderson's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Anderson's disease: exclusion of apolipoprotein and intracellular lipid transport genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

COPII proteins are required for Golgi fusion but not for endoplasmic reticulum budding of the pre-chylomicron transport vesicle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

COPII: a membrane coat formed by Sec proteins that drive vesicle budding from the endoplasmic reticulum

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

SEC12 encodes a guanine-nucleotide-exchange factor essential for transport vesicle budding from the ER.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Anderson or chylomicron retention disease: molecular impact of five mutations in the SAR1B gene on the structure and the functionality of Sar1b protein.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Altered lipid profile, lipoprotein composition, and oxidant and antioxidant status in pediatric Crohn disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Reference data for bone density and body composition measured with dual energy x ray absorptiometry in white children and young adults

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Chylomicron retention disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Apolipoprotein B48 glycosylation in abetalipoproteinemia and Anderson's disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Structural basis for cargo regulation of COPII coat assembly

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Modifier genes convert "simple" Mendelian disorders to complex traits

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Exit of major histocompatibility complex class II-invariant chain p35 complexes from the endoplasmic reticulum is modulated by phosphorylation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

The intracellular transport of chylomicrons requires the small GTPase, Sar1b

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Cholesterol is required for efficient endoplasmic reticulum-to-Golgi transport of secretory membrane proteins

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Apolipoprotein B100 exit from the endoplasmic reticulum (ER) is COPII-dependent, and its lipidation to very low density lipoprotein occurs post-ER.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Monogenic traits are not simple: lessons from phenylketonuria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathways

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Decreased expression of Intestinal I- and L-FABP levels in rare human genetic lipid malabsorption syndromes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Dietary (n-3) fatty acids and brain development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

Malabsorption, hypocholesterolemia, and fat-filled enterocytes with increased intestinal apoprotein B. Chylomicron retention disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2009.02.003

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.YMGME.2009.02.003

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19 December 2017

PubMed ID

19285442

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19 December 2017