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Publisher : hal ccsd

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Academic Journal

Validation of Knock-Out Caco-2 TC7 Cells as Models of Enterocytes of Patients with Familial Genetic Hypobetalipoproteinemias

Authors : Bordat, Claire; Vairo, Donato; Cuerq, Charlotte ...

Subjects: abetalipoproteinemia; bioavailability; CRISPR

Source: ISSN: 2072-6643 ; Nutrients ; https://hal.inrae.fr/hal-04174914 ; Nutrients, 2023, 15 (3), pp.505. ⟨10.3390/nu15030505⟩.

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Dissertation/ Thesis

Characterization of vitamin E and carotenoid deficiency in patients with familial hypobetalipoproteinemias

Authors : Bordat, Claire;

Subjects: Chylomicron; Caroténoïdes; Hypobêtalipoprotéinémie familiale

Source: Biochimie [q-bio.BM]. Université Claude Bernard-Lyon I, 2022. Français. ⟨NNT : 2022LYO10194⟩

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Dissertation/ Thesis

Characterization of vitamin E and carotenoid deficiency in patients with familial hypobetalipoproteinemias ; Caractérisation du déficit en vitamine E et caroténoïdes chez les patients atteints d’hypobêtalipoprotéinémies familiales

Authors : Bordat, Claire;

Subjects: Carotenoids; Vitamin E; Α-Tocopherol

Source: https://theses.hal.science/tel-04341891 ; Biochimie [q-bio.BM]. Université Claude Bernard - Lyon I, 2022. Français. ⟨NNT : 2022LYO10194⟩.

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Academic Journal

Prevalence of Hypobetalipoproteinemia and Related Psychiatric Characteristics in a Psychiatric Population: Results from the Retrospective HYPOPSY Study

Authors : Cariou, Bertrand; Challet-Bouju, Gaëlle; Bernard, Céline ...

Subjects: Adult; ArtClinique; Autism spectrum disorders

Source: Lipids in Health and Disease ; https://hal.science/hal-03158601 ; Lipids in Health and Disease, 2018, 17 (1), pp.249. ⟨10.1186/s12944-018-0892-4⟩

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Academic Journal

Molecular analysis and intestinal expression of SAR1 genes and proteins in Anderson's disease (Chylomicron retention disease).

Authors : Georges, Amandine; Bonneau, Jessica; Bonnefont-Rousselot, Dominique ...

Subjects: MESH: Adolescent; MESH: Child; MESH: Monomeric GTP-Binding Proteins

Source: ISSN: 1750-1172 ; Orphanet Journal of Rare Diseases ; https://inserm.hal.science/inserm-00663694 ; Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.1. ⟨10.1186/1750-1172-6-1⟩.

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