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A Pandya

Showing results (151-160 of 217) with videos related to

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Electrophoresis|August 1, 1997
Applications of microsatellite-based Y chromosome haplotypingM Kayser, P de Knijff, P Dieltjes, et al.
Journal of Biomolecular Structure & Dynamics|January 31, 2022
Excavating phytochemicals from plants possessing antiviral activities for identifying SARS-CoV hemagglutinin-esterase inhibitors by diligent computational workflowChirag N Patel, Dweipayan Goswami, Dharmesh G Jaiswal, et al.
Journal of Pharmacy & Bioallied Sciences|July 14, 2025
<i>In Vitro</i> Evaluation of Different Surface Treatments on Osseointegration of Dental ImplantsRajnee Yadav, Bharani K Bhattu, Bhavini B Solanki, et al.
Journal of Biomolecular Structure & Dynamics|December 29, 2017
Pharmacophore-based virtual screening of catechol-o-methyltransferase (COMT) inhibitors to combat Alzheimer's diseaseChirag N Patel, John J Georrge, Krunal M Modi, et al.
ISRN Bioinformatics|May 5, 2015
A Computational Approach towards the Understanding of Plasmodium falciparum Multidrug Resistance Protein 1Saumya K Patel, Linz-Buoy George, Sivakumar Prasanth Kumar, et al.
Frontiers in Genetics|February 4, 2012
Epitope-based immunoinformatics and molecular docking studies of nucleocapsid protein and ovarian tumor domain of crimean-congo hemorrhagic Fever virusPappu Srinivasan, Sivakumar Prasanth Kumar, Muthusamy Karthikeyan, et al.
The Journal of Biological Chemistry|November 4, 1994
UVM, an ultraviolet-inducible RecA-independent mutagenic phenomenon in Escherichia coliV A Palejwala, G A Pandya, O S Bhanot, et al.
Journal of Medical Genetics|June 17, 2005
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12D Yan, X Ke, S H Blanton, et al.
American Journal of Medical Genetics|April 20, 1999
Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: growth, development, and profilesG S Fisch, N J Carpenter, J J Holden, et al.
American Journal of Human Genetics|December 1, 1999
Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from MongoliaA Pandya, X J Xia, R Erdenetungalag, et al.
Pageof 22

Showing results (151-160 of 217) with videos related to

Sort By:
Pageof 22
Electrophoresis|August 1, 1997
Applications of microsatellite-based Y chromosome haplotypingM Kayser, P de Knijff, P Dieltjes, et al.
Journal of Biomolecular Structure & Dynamics|January 31, 2022
Excavating phytochemicals from plants possessing antiviral activities for identifying SARS-CoV hemagglutinin-esterase inhibitors by diligent computational workflowChirag N Patel, Dweipayan Goswami, Dharmesh G Jaiswal, et al.
Journal of Pharmacy & Bioallied Sciences|July 14, 2025
<i>In Vitro</i> Evaluation of Different Surface Treatments on Osseointegration of Dental ImplantsRajnee Yadav, Bharani K Bhattu, Bhavini B Solanki, et al.
Journal of Biomolecular Structure & Dynamics|December 29, 2017
Pharmacophore-based virtual screening of catechol-o-methyltransferase (COMT) inhibitors to combat Alzheimer's diseaseChirag N Patel, John J Georrge, Krunal M Modi, et al.
ISRN Bioinformatics|May 5, 2015
A Computational Approach towards the Understanding of Plasmodium falciparum Multidrug Resistance Protein 1Saumya K Patel, Linz-Buoy George, Sivakumar Prasanth Kumar, et al.
Frontiers in Genetics|February 4, 2012
Epitope-based immunoinformatics and molecular docking studies of nucleocapsid protein and ovarian tumor domain of crimean-congo hemorrhagic Fever virusPappu Srinivasan, Sivakumar Prasanth Kumar, Muthusamy Karthikeyan, et al.
The Journal of Biological Chemistry|November 4, 1994
UVM, an ultraviolet-inducible RecA-independent mutagenic phenomenon in Escherichia coliV A Palejwala, G A Pandya, O S Bhanot, et al.
Journal of Medical Genetics|June 17, 2005
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12D Yan, X Ke, S H Blanton, et al.
American Journal of Medical Genetics|April 20, 1999
Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: growth, development, and profilesG S Fisch, N J Carpenter, J J Holden, et al.
American Journal of Human Genetics|December 1, 1999
Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from MongoliaA Pandya, X J Xia, R Erdenetungalag, et al.
Pageof 22