Inheritable biotin-treatable disorders and associated phenomena.
about
Functional characterization of sodium-dependent multivitamin transporter in MDCK-MDR1 cells and its utilization as a target for drug deliverySodium dependent multivitamin transporter (SMVT): a potential target for drug deliveryComparative analysis of ontogenic changes in renal and intestinal biotin transport in the ratMembrane targeting and intracellular trafficking of the human sodium-dependent multivitamin transporter in polarized epithelial cells.Molecular characterization of the 5' regulatory region of rat sodium-dependent multivitamin transporter gene.Intestinal absorption of water-soluble vitamins in health and diseaseThe impact of molecular genetics on oral health paradigms.Biotin uptake by human intestinal and liver epithelial cells: role of the SMVT system.Biotin uptake by human proximal tubular epithelial cells: cellular and molecular aspects.Molecular mechanisms involved in the adaptive regulation of human intestinal biotin uptake: A study of the hSMVT system.Regulation of the human biotin transporter hSMVT promoter by KLF-4 and AP-2: confirmation of promoter activity in vivo.Chronic alcohol exposure inhibits biotin uptake by pancreatic acinar cells: possible involvement of epigenetic mechanisms.Inhibition of intestinal biotin absorption by chronic alcohol feeding: cellular and molecular mechanismsChronic alcohol exposure negatively impacts the physiological and molecular parameters of the renal biotin reabsorption process.Biotinidase deficiency mimicking primary immune deficiencies.A biotinidase Km variant causing late onset bilateral optic neuropathy.Salmonella infection inhibits intestinal biotin transport: cellular and molecular mechanisms.Functional and molecular aspects of biotin uptake via SMVT in human corneal epithelial (HCEC) and retinal pigment epithelial (D407) cells.Conditional knockout of the Slc5a6 gene in mouse intestine impairs biotin absorption.Cell and molecular aspects of human intestinal biotin absorption.The sodium/multivitamin transporter: a multipotent system with therapeutic implications.Mutations in SLC5A6 associated with brain, immune, bone, and intestinal dysfunction in a young child.Organic acidurias and related abnormalities.Immunodeficiency as a component of recognizable syndromes.Uptake of biotin by human hepatoma cell line, Hep G2: a carrier-mediated process similar to that of normal liver.Biotin deficiency enhances the inflammatory response of human dendritic cells.A novel molecular mechanism to explain biotin-unresponsive holocarboxylase synthetase deficiency.Biotin uptake by rabbit corneal epithelial cells: role of sodium-dependent multivitamin transporter (SMVT).Biotin Deficiency Induces Th1- and Th17-Mediated Proinflammatory Responses in Human CD4+ T Lymphocytes via Activation of the mTOR Signaling Pathway.
P2860
Q24644494-FC6E5B7E-D8BF-45E8-8E6C-8178315D7AB0Q26863420-10AD0A00-3725-4957-93AE-C2602BFFB6BBQ28570364-47527657-107B-49A1-A833-AA852C981DDBQ30487118-192AA5EB-5B97-4F16-AD05-7ABDCF63C72BQ31919395-CC0DB778-6393-4BA0-9FF5-2EFC5D817BB9Q33725184-7A4AE460-EF2D-448E-B761-F854ED87D8F0Q33842939-67515639-A8FE-4C3D-B780-FC5A6CBCEA42Q34184789-980AAEC8-B745-4774-8FC1-3557EA7BAE75Q34370774-DF5E1D4E-872A-4F91-A670-750C4989530AQ34564505-EF33CB72-5174-44B1-B10F-7AEDBD7F4170Q34585806-8B2F6ACD-8613-47C0-9F1A-B9A9FAC28C3EQ34602245-160A24D6-D378-48F9-8AD8-6F216780BD11Q34719007-60330D41-5D8B-4FB4-ADB2-B8E32112B9DDQ34719183-5917A9FC-BDE4-4FA7-B9A0-824F77405CACQ35614886-935F2D57-C2C7-4430-9358-CFABEE00A7C3Q35627719-FB64D23E-7AE3-4B3F-BD5E-9ACDC3E27711Q35859253-CF3C0120-CB0B-4C4D-AC14-E750DEC4B538Q36331516-84095867-6963-4177-800D-B0180E42C020Q36527938-17A5BAF9-DB38-40DA-A89B-795833F60037Q37105800-C4CF6BC3-0B89-42B4-8220-53188D7C40F8Q38394090-23A9A21A-65AB-45A1-8637-A18FE559F8DFQ38728153-819E2209-CE3D-4A3F-AECF-69E55BAFF9E1Q40422979-ABF297D8-89EB-4195-94EA-92B545564E3BQ41300576-351ABB41-C591-450D-B318-C9BEC621E600Q41427128-CFAB05E8-B89A-45AA-B302-E9E967730ECDQ42361270-470BF99E-F74E-4189-A8FE-B61F937AC45AQ45345342-686AECA2-A5FD-48B4-A2CB-7239CA4ADA3FQ53594005-6570E81C-F8F1-4148-A4E7-E6092D1E5CCBQ55421717-790FDFB9-071D-4061-9349-34FB0CA281A1
P2860
Inheritable biotin-treatable disorders and associated phenomena.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Inheritable biotin-treatable disorders and associated phenomena.
@en
Inheritable biotin-treatable disorders and associated phenomena.
@nl
type
label
Inheritable biotin-treatable disorders and associated phenomena.
@en
Inheritable biotin-treatable disorders and associated phenomena.
@nl
prefLabel
Inheritable biotin-treatable disorders and associated phenomena.
@en
Inheritable biotin-treatable disorders and associated phenomena.
@nl
P1476
Inheritable biotin-treatable disorders and associated phenomena.
@en
P2093
P304
P356
10.1146/ANNUREV.NU.06.070186.001533
P407
P577
1986-01-01T00:00:00Z