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Genetically based reduced MAOA and COMT functioning is associated with the cortisol stress response: a replication study

Molecular psychiatry, 2012-02, Vol.17 (2), p.119-121

2012

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The role of the microsomal triglygeride transfer protein in abetalipoproteinemia

Annual review of nutrition, 2000-01, Vol.20 (1), p.663-697

2000

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Prospective Evaluation of Quality of Life and Sexual Functioning After Laparoscopic Total Mesorectal Excision

Diseases of the colon & rectum, 2007-02, Vol.50 (2), p.147-155

2007

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Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities

Clinical genetics, 2008-12, Vol.74 (6), p.546-552

2008

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Evidence for plasticity genotypes in a gene–gene–environment interaction: the TRAILS study

Genes, brain and behavior, 2010-11, Vol.9 (8), p.968-973

2010

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Absence of Microsomal Triglyceride Transfer Protein in Individuals with Abetalipoproteinemia

Science (American Association for the Advancement of Science), 1992-11, Vol.258 (5084), p.999-1001

1992

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The UFM1 Pathway Impacts HCMV US2-Mediated Degradation of HLA Class I

Molecules (Basel, Switzerland), 2021-01, Vol.26 (2), p.287

2021

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Predicting mental disorders from hypothalamic-pituitary-adrenal axis functioning: a 3-year follow-up in the TRAILS study

Psychological medicine, 2015-08, Vol.45 (11), p.2403-2412

2015

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

Nature (London), 1993-09, Vol.365 (6441), p.65-69

1993

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Cat owners’ anthropomorphic perceptions of feline emotions and interpretation of photographs

Applied animal behaviour science, 2024-01, Vol.270, p.106150, Article 106150

2024

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

Arteriosclerosis, thrombosis, and vascular biology, 1999-10, Vol.19 (10), p.2494-2508

1999

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Apolipoprotein B production and very low density lipoprotein secretion by calf liver slices

Journal of biochemistry (Tokyo), 1999-07, Vol.126 (1), p.188-193

1999

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

Histochemistry and cell biology, 2007-08, Vol.128 (2), p.115-123

2007

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Alterations in lipoprotein density classes in infantile visceral Leishmaniasis: presence of apolipoprotein SAA

European journal of clinical investigation, 1992-03, Vol.22 (3), p.190-199

1992

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A novel abetalipoproteinemia genotype. Identification of a missense mutation in the 97-kDa subunit of the microsomal triglyceride transfer protein that prevents complex formation with protein disulfide isomerase

The Journal of biological chemistry, 1996-11, Vol.271 (47), p.29945-29952

1996

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Postprandial lipid absorption in seven heterozygous carriers of deleterious variants of MTTP in two abetalipoproteinemic families

Journal of clinical lipidology, 2019-01, Vol.13 (1), p.201-212

2019

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Apolipoprotein B48 glycosylation in abetalipoproteinemia and Anderson's disease

Gastroenterology (New York, N.Y. 1943), 2001-11, Vol.121 (5), p.1101-1108

2001

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Hypocholestérolémies génétiques : abêtalipoprotéinémie, hypobêtalipoprotéinémie familiale, maladie d'Anderson

EMC - Gastro-entérologie, 2009-01, Vol.4 (4), p.1-8

2009

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Description of two different patients with abetalipoproteinemia: synthesis of a normal-sized apolipoprotein B-48 in intestinal organ culture

Journal of lipid research, 1990-01, Vol.31 (1), p.1-15

1990

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

The Journal of clinical investigation, 1986-08, Vol.78 (2), p.398-410

1986

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Isolation, Culture and Characterization of Adult Human Hepatocytes from Surgical Liver Biopsies

Hepatology (Baltimore, Md.), 1984-09, Vol.4 (5), p.849-854

1984

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Effects of dietary coconut oil on apolipoprotein B synthesis and VLDL secretion by calf liver slices

British journal of nutrition, 2001-07, Vol.86 (1), p.13-19

2001

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Liver fibrosis in a patient with familial homozygous hypobetalipoproteinaemia: possible role of vitamin supplementation

Gut, 1992-03, Vol.33 (3), p.414-417

1992

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Immunoperoxidase Localization of Apolipoprotein D in Human Enterocytes and Hepatocytes

Scandinavian journal of gastroenterology, 1988, Vol.23 (4), p.477-483

1988

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Genetically based reduced MAOA and COMT functioning is associated with the cortisol stress response: a replication study

The role of the microsomal triglygeride transfer protein in abetalipoproteinemia

Prospective Evaluation of Quality of Life and Sexual Functioning After Laparoscopic Total Mesorectal Excision

Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities

Evidence for plasticity genotypes in a gene–gene–environment interaction: the TRAILS study

Absence of Microsomal Triglyceride Transfer Protein in Individuals with Abetalipoproteinemia

The UFM1 Pathway Impacts HCMV US2-Mediated Degradation of HLA Class I

Predicting mental disorders from hypothalamic-pituitary-adrenal axis functioning: a 3-year follow-up in the TRAILS study

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

Cat owners’ anthropomorphic perceptions of feline emotions and interpretation of photographs

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

Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia

Apolipoprotein B production and very low density lipoprotein secretion by calf liver slices

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

Alterations in lipoprotein density classes in infantile visceral Leishmaniasis: presence of apolipoprotein SAA

A novel abetalipoproteinemia genotype. Identification of a missense mutation in the 97-kDa subunit of the microsomal triglyceride transfer protein that prevents complex formation with protein disulfide isomerase

Postprandial lipid absorption in seven heterozygous carriers of deleterious variants of MTTP in two abetalipoproteinemic families

Apolipoprotein B48 glycosylation in abetalipoproteinemia and Anderson's disease

Hypocholestérolémies génétiques : abêtalipoprotéinémie, hypobêtalipoprotéinémie familiale, maladie d'Anderson

Description of two different patients with abetalipoproteinemia: synthesis of a normal-sized apolipoprotein B-48 in intestinal organ culture

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

Isolation, Culture and Characterization of Adult Human Hepatocytes from Surgical Liver Biopsies

Effects of dietary coconut oil on apolipoprotein B synthesis and VLDL secretion by calf liver slices

Liver fibrosis in a patient with familial homozygous hypobetalipoproteinaemia: possible role of vitamin supplementation

Immunoperoxidase Localization of Apolipoprotein D in Human Enterocytes and Hepatocytes

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