Concepedia

Carnitine transport into muscular cells. inhibition of transport and cell growth by mildronate

Béatrice Georges, Françoise Le Borgne, Stéphane Galland, Muriel Isoir, David Ecosse, Florence Grand-Jean, Jean Demarquoy

Biochemical Pharmacology · 2000 · 36 citations · 14 references

DOI

Concepts

References

14

Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter

Jun‐ichi Nezu, Ikumi Tamai, Asuka Oku et al. · Nature Genetics · 1999 · 559 citations

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Tissue distribution of carnitine biosynthetic enzymes in man

Charles J. Rebouche, Andrew G. Engel · Biochimica et Biophysica Acta (BBA) - General Subjects · 1980 · 236 citations

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Mutations of OCTN2, an Organic Cation/Carnitine Transporter, Lead to Deficient Cellular Carnitine Uptake in Primary Carnitine Deficiency

Nelson L.S. Tang, Vadivel Ganapathy, Xiang Wu et al. · Human Molecular Genetics · 1999 · 155 citations · Full text

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3-(2,2,2-Trimethylhydrazinium)propionate(thp)-a novel γ-butyrobetaine hydroxylase inhibitor with cardioprotective properties

Boris Z. Simkhovich, Zhanna V. Shutenko, Dainuvīte V. Meirēna et al. · Biochemical Pharmacology · 1988 · 110 citations

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Sodium gradient-stimulated transport of l-carnitine into renal brush border membrane vesicles: Kinetics, specificity, and regulation by dietary carnitine

Charles J. Rebouche, Diane L. Mack · Archives of Biochemistry and Biophysics · 1984 · 110 citations

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