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P RICHARD

Showing results (711-720 of 939) with videos related to

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The Journal of Clinical Investigation|April 21, 2015
Integrated compensatory network is activated in the absence of NCC phosphorylationP Richard Grimm, Yoskaly Lazo-Fernandez, Eric Delpire, et al.
Plos One|June 7, 2014
Limited evolution of inferred HIV-1 tropism while viremia is undetectable during standard HAART therapyGuinevere Q Lee, Winnie Dong, Theresa Mo, et al.
Plos Pathogens|April 9, 2024
Correction: An activator of G protein-coupled receptor and MEK1/2-ERK1/2 signaling inhibits HIV-1 replication by altering viral RNA processingRaymond W Wong, Ahalya Balachandran, Peter K Cheung, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 16, 1998
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathyJ Flavigny, P Richard, R Isnard, et al.
AIDS (London, England)|July 2, 2005
Rates of antiretroviral resistance among HIV-infected patients with and without a history of injection drug useEvan Wood, Robert S Hogg, Benita Yip, et al.
The Journal of Infectious Diseases|September 23, 2006
A simple, dynamic measure of antiretroviral therapy adherence predicts failure to maintain HIV-1 suppressionRobert Gross, Benita Yip, Vincent Lo Re, et al.
The Journal of Antimicrobial Chemotherapy|March 11, 2015
Highly frequent HIV-1 minority resistant variants at baseline of the ANRS 139 TRIO trial had a limited impact on virological responseCharlotte Charpentier, Guinevere Q Lee, Christophe Rodriguez, et al.
JCI Insight|September 2, 2021
Ghrelin cell-expressed insulin receptors mediate meal- and obesity-induced declines in plasma ghrelinKripa Shankar, Shota Takemi, Deepali Gupta, et al.
Journal of Medical Genetics|July 29, 1999
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathyP Richard, R Isnard, L Carrier, et al.
Circulation Research|February 19, 1999
Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndromeN Neyroud, P Richard, N Vignier, et al.
Pageof 94

Showing results (711-720 of 939) with videos related to

Sort By:
Pageof 94
The Journal of Clinical Investigation|April 21, 2015
Integrated compensatory network is activated in the absence of NCC phosphorylationP Richard Grimm, Yoskaly Lazo-Fernandez, Eric Delpire, et al.
Plos One|June 7, 2014
Limited evolution of inferred HIV-1 tropism while viremia is undetectable during standard HAART therapyGuinevere Q Lee, Winnie Dong, Theresa Mo, et al.
Plos Pathogens|April 9, 2024
Correction: An activator of G protein-coupled receptor and MEK1/2-ERK1/2 signaling inhibits HIV-1 replication by altering viral RNA processingRaymond W Wong, Ahalya Balachandran, Peter K Cheung, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 16, 1998
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathyJ Flavigny, P Richard, R Isnard, et al.
AIDS (London, England)|July 2, 2005
Rates of antiretroviral resistance among HIV-infected patients with and without a history of injection drug useEvan Wood, Robert S Hogg, Benita Yip, et al.
The Journal of Infectious Diseases|September 23, 2006
A simple, dynamic measure of antiretroviral therapy adherence predicts failure to maintain HIV-1 suppressionRobert Gross, Benita Yip, Vincent Lo Re, et al.
The Journal of Antimicrobial Chemotherapy|March 11, 2015
Highly frequent HIV-1 minority resistant variants at baseline of the ANRS 139 TRIO trial had a limited impact on virological responseCharlotte Charpentier, Guinevere Q Lee, Christophe Rodriguez, et al.
JCI Insight|September 2, 2021
Ghrelin cell-expressed insulin receptors mediate meal- and obesity-induced declines in plasma ghrelinKripa Shankar, Shota Takemi, Deepali Gupta, et al.
Journal of Medical Genetics|July 29, 1999
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathyP Richard, R Isnard, L Carrier, et al.
Circulation Research|February 19, 1999
Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndromeN Neyroud, P Richard, N Vignier, et al.
Pageof 94