M. J. ROBINS - Concepedia

Author

M. J. ROBINS

University of Alberta

Also Known As

M J Robins, M. J. ROBINS, M. J. Robins, M.J. Robins, Moms J. Robins, Moms Robins, Morris J. Robins, Robins, M.J.

Publications

761

Citations

H-Index

Concepts

All Affiliations

University of Alberta Brigham Young University Austin Hospital Massachusetts Institute of Technology

About

M. J. ROBINS is an author at University of Alberta specializing in medicine, pharmacology, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	215
2	Natural Sciences	3	3	69
3	Biochemistry	3	3	69
4	Cell Biology	1	1	25
5	Cell Systems	1	1	25

M. J. ROBINS

Publications

692

Citations

H-Index

Page 1

	Year	Citations
2'-Deoxy-2'-methylenecytidine and 2'-deoxy-2',2'-difluorocytidine 5'-diphosphates: potent mechanism-based inhibitors of ribonucleotide reductase C. H. Baker, Jennifer A. Banzon, J. Martin Bollinger, Journal of Medicinal Chemistry	1991	252
In vitro and in vivo comparison of the abilities of purine and pyrimidine 2',3'-dideoxynucleosides to inhibit duck hepadnavirus Bernice Lee, Wenxin Luo, Satoru Suzuki, Antimicrobial Agents and Chemotherapy Duck Hepadnavirus ReplicationViral ReplicationHepadnavirus DnaPyrimidine 2',3'-DideoxynucleosidesMedicine	1989	89
Photoaffinity labeling of the human erythrocyte nucleoside transporter by N6-(p-Azidobenzyl)adenosine and nitrobenzylthioinosine. Evidence that the transporter is a band 4.5 polypeptide. James D. Young, Simon M. Jarvis, M. J. ROBINS, Journal of Biological Chemistry	1983	83
Alternative model for mechanism-based inhibition of Escherichia coli ribonucleotide reductase by 2'-azido-2'-deoxyuridine 5'-diphosphate Scott P. Salowe, J. Martin Bollinger, Mark A. Ator, Biochemistry	1993	57
Antirhinovirus activity of purine nucleoside analogs Erik De Clercq, R Bernaerts, D. E. BERGSTROM, Antimicrobial Agents and Chemotherapy Viral ReplicationMedicineImmunologySelectivity IndexVirology	1986	37
Nucleobase transporter-mediated permeation of 2‘,3‘-dideoxyguanosine in human erythrocytes and human T-lymphoblastoid CCRF-CEM cells. W P Gati, A.R. Paterson, D. Lorne Tyrrell, Journal of Biological Chemistry	1992	28
Conjugates of Fluorescein and Saenta (5′-<i>S</i>-(2-Aminoethyl)-<i>N</i><sup>6</sup>-(4-nitrobenzyl)-5′-thioadenosine): Flow Cytometry Probes for the<i>ES</i>Nucleoside Transporter Elements of the Plasma Membrane John K. Buolamwini, James D. Craik, James S. Wiley, Nucleosides and Nucleotides Proteinlipid InteractionFlow Cytometry ProbesMolecular BiologyAbstract SaentaAnalytical Ultracentrifugation	1994	25
5′-<i>S</i>-(2-aminoethyl)-<i>N</i>6-(4-nitrobenzyl)-5′-thioadenosine (SAENTA), a novel ligand with high affinity for polypeptides associated with nucleoside transport. Partial purification of the nitrobenzylthioinosine-binding protein of pig erythrocytes by affinity chromatography F R Agbanyo, D Vijayalakshmi, James D. Craik, Biochemical Journal	1990	24
Synthesis, Transformation Chemistry, and Biological Activity of Guanine Nucleosides and Analoges M. J. ROBINS, Ruiming Zou, Fritz Hansske, Nucleosides Nucleotides & Nucleic Acids Organic ChemistryChemistryChemical BiologyPharmaceutical ChemistryMedicinal Chemistry	1989	23
A new fluorescent probe for the equilibrative inhibitor-sensitive nucleoside transporter. 5′-<i>S</i>-(2-aminoethyl)-<i>N</i>6-(4-nitrobenzyl)-5′-thioadenosine (SAENTA)-<i>x</i>2-fluorescein James S. Wiley, Anne M. Brocklebank, Marie B. Snook, Biochemical Journal Molecular BiologyCellular PharmacologyChemical BiologyExperimental PharmacologyPharmaceutical Chemistry	1991	21

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