نتایج جستجو برای: nucleoside analogue

تعداد نتایج: 55760  

2014
Hila Haskelberg Nicholas Pocock Janaki Amin Peter Robert Ebeling Sean Emery Andrew Carr Anthony Allworth Jonathan Anderson David Baker Mark Bloch Mark Boyd John Chuah David Cooper Stephen Davies Linda Dayan William Donohue Nicholas Doong Dominic Dwyer John Dyer Robert Finlayson Michelle Giles David Gordon Mark Kelly Nicholas Medland Richard Moore David Nolan David Orth Jeffrey Post John Quin Tim Read Norman Roth Darren Russell David Shaw David Smith Don Smith Alan Street Ban Kiem Tee Ian Woolley

BACKGROUND Therapy with tenofovir is associated with lower bone mineral density (BMD), higher markers of bone turnover and increased fracture risk in HIV-infected adults. Bone structural parameters generated by hip structural analysis may represent a separate measure of bone strength, but have not been assessed in HIV. METHODS Dual-energy X-ray absorptiometry (DXA) scans from 254 HIV-infected...

Journal: :Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2003
Joel E Gallant Stanley Deresinski

Tenofovir disoproxil fumarate (tenofovir DF) is a bioavailable prodrug of tenofovir, a potent nucleotide analogue reverse-transcriptase inhibitor with activity against human immunodeficiency virus (HIV) and hepatitis B virus. It is administered as a single 300-mg tablet once daily. It was approved for the treatment of HIV infection on the basis of data from clinical trials demonstrating activit...

2015
Sakilam Satishkumar Prasanna K. Vuram Siva Subrahmanyam Relangi Venkateshwarlu Gurram Hong Zhou Robert J. Kreitman Michelle M. Martínez Montemayor Lijia Yang Muralidharan Kaliyaperumal Somesh Sharma Narender Pottabathini Mahesh K. Lakshman

Cladribine, 2-chloro-2'-deoxyadenosine, is a highly efficacious, clinically used nucleoside for the treatment of hairy cell leukemia. It is also being evaluated against other lymphoid malignancies and has been a molecule of interest for well over half a century. In continuation of our interest in the amide bond-activation in purine nucleosides via the use of (benzotriazol-1yl-oxy)tris(dimethyla...

2010
Rubén Agudo Cristina Ferrer-Orta Armando Arias Ignacio de la Higuera Celia Perales Rosa Pérez-Luque Nuria Verdaguer Esteban Domingo

Resistance of viruses to mutagenic agents is an important problem for the development of lethal mutagenesis as an antiviral strategy. Previous studies with RNA viruses have documented that resistance to the mutagenic nucleoside analogue ribavirin (1-β-D-ribofuranosyl-1-H-1,2,4-triazole-3-carboxamide) is mediated by amino acid substitutions in the viral polymerase that either increase the genera...

Journal: :Journal of virology 2006
Valentina Svicher Tobias Sing Maria Mercedes Santoro Federica Forbici Fátima Rodríguez-Barrios Ada Bertoli Niko Beerenwinkel Maria Concetta Bellocchi Federigo Gago Antonella d'Arminio Monforte Andrea Antinori Thomas Lengauer Francesca Ceccherini-Silberstein Carlo Federico Perno

We characterized 16 additional mutations in human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) whose role in drug resistance is still unknown by analyzing 1,906 plasma-derived HIV-1 subtype B pol sequences from 551 drug-naïve patients and 1,355 nucleoside RT inhibitor (NRTI)-treated patients. Twelve mutations positively associated with NRTI treatment strongly correlated both...

Journal: :Antiviral therapy 2012
Young-Suk Lim Tae Hoon Lee Nae-Yun Heo Ju Hyun Shim Han Chu Lee Dong Jin Suh

BACKGROUND The combination of entecavir, a nucleoside analogue, and adefovir, a nucleotide analogue, would be a promising salvage treatment for chronic hepatitis B (CHB) patients who fail nucleoside/nucleotide analogue (NA) regimens. METHODS A total of 89 CHB patients who had failed NA regimens and were treated with entecavir plus adefovir combination for at least 12 months were included. R...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Zengmin Li Xiaopeng Bai Hameer Ruparel Sobin Kim Nicholas J Turro Jingyue Ju

DNA sequencing by synthesis during a polymerase reaction using laser-induced fluorescence detection is an approach that has a great potential to increase the throughput and data quality of DNA sequencing. We report the design and synthesis of a photocleavable fluorescent nucleoside triphosphate, one of the essential molecules required for the sequencing-by-synthesis approach. We synthesized thi...

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