287 results on '"Galluccio, Michele"'
Search Results
52. Chemical Targeting of Membrane Transporters: Insights into Structure/Function Relationships
53. Inactivation by Hg2+ and methylmercury of the glutamine/amino acid transporter (ASCT2) reconstituted in liposomes: Prediction of the involvement of a CXXC motif by homology modelling
54. Mutation of Aspartate 238 in FAD Synthase Isoform 6 Increases the Specific Activity by Weakening the FAD Binding
55. Discovery of Potent Inhibitors for the Large Neutral Amino Acid Transporter 1 (LAT1) by Structure-Based Methods
56. Supplemental_Material – Supplemental material for OCTN: A Small Transporter Subfamily with Great Relevance to Human Pathophysiology, Drug Discovery, and Diagnostics
57. Structure/function relationships of human mitochondrial ornithine/citrulline carrier by Cys mutagenesis. Relevance to mercury toxicity
58. Insights into the transport side of the human SLC38A9 transceptor
59. Regulatory Aspects of the Vacuolar CAT2 Arginine Transporter of S. lycopersicum: Role of Osmotic Pressure and Cations
60. Structure/function relationships of the human mitochondrial ornithine/citrulline carrier by Cys site-directed mutagenesis. Relevance to mercury toxicity
61. The LAT1 amino acid transporter: substrate binding site and drug discovery
62. MODULATING CELLULAR FLAVIN COFACTOR LEVELS IN HUMANS VIA THE BI-FUNCTIONAL AND MONOFUNCTIONAL FLAD1 GENE PRODUCTS
63. The Human SLC7A5 (LAT1): The Intriguing Histidine/Large Neutral Amino Acid Transporter and Its Relevance to Human Health
64. Bacterial Production, Characterization and Protein Modeling of a Novel Monofuctional Isoform of FAD Synthase in Humans: An Emergency Protein?
65. Glutamine Transport and Mitochondrial Metabolism in Cancer Cell Growth
66. Potent inhibitors of human LAT1 (SLC7A5) transporter based on dithiazole and dithiazine compounds for development of anticancer drugs
67. Studying Interactions of Drugs with Cell Membrane Nutrient Transporters: New Frontiers of Proteoliposome Nanotechnology
68. Novel insights into the transport mechanism of the human amino acid transporter LAT1 (SLC7A5). Probing critical residues for substrate translocation
69. Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder
70. Glutamine transport. From energy supply to sensing and beyond
71. Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency
72. LAT1 is the transport competent unit of the LAT1/CD98 heterodimeric amino acid transporter
73. Human FAD synthase is a bi-functional enzyme with a FAD hydrolase activity in the molybdopterin binding domain
74. Functional and Molecular Effects of Mercury Compounds on the Human OCTN1 Cation Transporter: C50 and C136 Are the Targets for Potent Inhibition
75. Membrane transporters for the special amino acid glutamine: structure/function relationships and relevance to human health
76. AMINO ACID TRANSPORTERS IN DRUG DISCOVERY
77. Large scale production of the active human ASCT2 (SLC1A5) transporter in Pichia pastoris — functional and kinetic asymmetry revealed in proteoliposomes
78. Biosynthesis of Flavin Cofactors in Man: Implications in Health and Disease
79. Bacterial Over-Expression and Purification of the 3'phosphoadenosine 5'phosphosulfate (PAPS) Reductase Domain of Human FAD Synthase: Functional Characterization and Homology Modeling
80. Strategies of Bacterial Over Expression of Membrane Transporters Relevant in Human Health: The Successful Case of the Three Members of OCTN Subfamily
81. Over-expression in Escherichia coli, purification and reconstitution in liposomes of the third member of the OCTN sub-family: The mouse carnitine transporter OCTN3
82. The human OCTN1 (SLC22A4) reconstituted in liposomes catalyzes acetylcholine transport which is defective in the mutant L503F associated to the Crohn's disease
83. Reconstitution in liposomes of the functionally active human OCTN1 (SLC22A4) transporter overexpressed in Escherichia coli
84. Over-Expression in E. coli and Purification of the Human OCTN2 Transport Protein
85. Mitochondrial localization of human FAD synthetase isoform 1
86. Over-expression in E. coli and purification of the human OCTN1 transport protein
87. Interaction of β-lactam antibiotics with the mitochondrial carnitine/acylcarnitine transporter
88. Over-expression in Escherichia coli, purification and characterization of isoform 2 of human FAD synthetase
89. The glutamine/amino acid transporter (ASCT2) reconstituted in liposomes: Transport mechanism, regulation by ATP and characterization of the glutamine/glutamate antiport
90. Over-expression in Escherichia coli and characterization of two recombinant isoforms of human FAD synthetase
91. Functional reconstitution into liposomes and characterization of the carnitine transporter from rat liver microsomes
92. Reconstitution into liposomes of the glutamine/amino acid transporter from renal cell plasma membrane: functional characterization, kinetics and activation by nucleotides
93. Inactivation by Hg2+ and methylmercury of the glutamine/amino acid transporter (ASCT2) reconstituted in liposomes: Prediction of the involvement of a CXXC motif by homology modelling
94. Mutational analysis of the mammalian mitochondrial Ca2+/H+ exchanger TMBIM5/MICS1.
95. Novel insights on the mitochondrial Ca2+/H+ exchanger TMBIM5.
96. Discovery of Potent Inhibitors for the Large Neutral Amino Acid Transporter 1 (LAT1) by Structure-Based Methods.
97. MONOSPECIFIC ANTIBODY AND METHOD OF PRODUCTION USING AS ANTIGEN AN ISOFORM OF THE HUMAN FAD SYNTHETASE
98. ATP dependence and antiport/uniport switch of the essential amino acid transporter SLC7A5 (LAT1): molecular basis and pathophysiology.
99. Flavin-sensitive variant FAD synthases underlying riboflavin responsive Multiple Acyl-CoA Dehydrogenation Deficiency.
100. Over-Production of the Human SLC7A10 in E. coli and Functional Assay in Proteoliposomes.
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