Concepedia

Author

Harry Ford

National Cancer Institute

Also Known As

H Ford, H Ford Jr, H. FORD, H. Ford, H. Ford Junior, H. JUN. FORD, Harry Ford, Harry Ford Jr., Harry Ford,, Harry Ford, Jr

73

Publications

2.1K

Citations

26

H-Index

72

Concepts

All Affiliations

National Cancer InstituteNational Institutes of HealthUnited States Naval Research LaboratoryNational Institute of Allergy and Infectious Diseases
HF

About

Harry Ford is an author at National Cancer Institute specializing in biochemistry, medicine, and natural sciences.

Top Concepts

#ConceptH-IndexPublicationsCitations

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Medicine

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Biochemistry

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Natural Sciences

18

23

1.3K

4

Engineering

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3

159

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Health Sciences

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Harry Ford

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42

Publications

2.1K

Citations

26

H-Index

YearCitations

Acid-stable 2'-fluoro purine dideoxynucleosides as active agents against HIV

Víctor E. Márquez, Christopher K. H. Tseng, Hiroaki Mitsuya,

Journal of Medicinal Chemistry

1990

211

Adenoviral vectors capable of replication improve the efficacy of HSVtk/GCV suicide gene therapy of cancer

Oliver Wildner, John C. Morris, Nicholas N. Vahanian,

Gene Therapy

1999

170

HIV-1 Reverse Transcriptase Can Discriminate between Two Conformationally Locked Carbocyclic AZT Triphosphate Analogues

Víctor E. Márquez, Abdallah Ezzitouni, Pamela Russ,

Journal of the American Chemical Society

1998

161

A general method for the preparation of benzylic α,α-difluorophosphonic acids; non-hydrolyzable mimemtics of phosphotyrosine

Mark S. Smyth, Harry Ford, Terrence R. Burke

Tetrahedron Letters

1992

129

In vitro anti-human immunodeficiency virus (HIV) activities of transition state mimetic HIV protease inhibitors containing allophenylnorstatine

Seiji Kageyama, Tsutomu Mimoto, Yasuhiko Murakawa,

Antimicrobial Agents and Chemotherapy

1993

111

4‘-<i>O</i>-[2-(2-Fluoromalonyl)]-<scp>l</scp>-tyrosine:  A Phosphotyrosyl Mimic for the Preparation of Signal Transduction Inhibitory Peptides

Terrence R. Burke, Bin Ye, Miki Akamatsu,

Journal of Medicinal Chemistry

1996

96

Mechanism of inhibition of DNA (cytosine C5)-methyltransferases by oligodeoxyribonucleotides containing 5,6-dihydro-5-azacytosine 1 1Edited by R. Huber

Gholamreza Sheikhnejad, Adam S. Brank, Judith K. Christman,

Journal of Molecular Biology

1999

80

Synthesis, Conformational Analysis, and Biological Activity of a Rigid Carbocyclic Analogue of 2′-Deoxy Aristeromycin Built on a Bicyclo[3.1.0]hexane Template

M. Arshad Siddiqui, Harry Ford, Clifford George,

Nucleosides and Nucleotides

1996

76

Synthesis of Conformationally Restricted Carbocyclic Nucleosides: The Role of the O(4′)-Atom in the Key Hydration Step of Adenosine Deaminase

Víctor E. Márquez, Pamela Russ, Randolph Alonso,

Helvetica Chimica Acta

1999

75

Adenosine Deaminase Prefers a Distinct Sugar Ring Conformation for Binding and Catalysis:  Kinetic and Structural Studies

Harry Ford, Fang Dai, Lan Mu,

Biochemistry

2000

73

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