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S Ganesh

Showing results (271-280 of 315) with videos related to

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Scientific Reports|November 27, 2025
Development and validation of an integrated preclinical model mimicking cardiometabolic risk in postmenopausal female ratsP Sainath, Shakta Mani Satyam, Sanjay Bharati, et al.
Revista De Neurologia|October 22, 2002
[Juvenile myoclonic epilepsy in chromosome 6p12: clinical and genetic advances]A V Delgado-Escueta, D Bai, J Bailey, et al.
Scientific Reports|September 19, 2019
Quantification of wild-type and radiation attenuated Plasmodium falciparum sporozoite motility in human skinBéatrice M F Winkel, Clarize M de Korne, Matthias N van Oosterom, et al.
Iscience|June 13, 2024
<i>De novo</i> <i>TLK1</i> and <i>MDM1</i> mutations in a patient with a neurodevelopmental disorder and immunodeficiencyMarina Villamor-Payà, María Sanchiz-Calvo, Jordann Smak, et al.
Omics : a Journal of Integrative Biology|April 1, 2021
Proteomic Alterations Associated with Oral Cancer Patients with Tobacco Using HabitsFirdous Ahmad Bhat, Sonali V Mohan, Shankargouda Patil, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
Identification of a <i>de novo</i> mutation in <i>TLK1</i> associated with a neurodevelopmental disorder and immunodeficiencyMarina Villamor-Payà, María Sanchiz-Calvo, Jordann Smak, et al.
American Journal of Human Genetics|November 27, 2010
A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataractsGaneshwaran H Mochida, Vijay S Ganesh, Jillian M Felie, et al.
Frontiers in Immunology|November 16, 2018
Early Induction of Human Regulatory Dermal Antigen Presenting Cells by Skin-Penetrating <i>Schistosoma Mansoni</i> CercariaeBéatrice M F Winkel, Mirjam R Dalenberg, Clarize M de Korne, et al.
Annals of Clinical and Translational Neurology|August 3, 2024
Protein-extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregationJohanna Ranta-Aho, Kevin J Felice, Per Harald Jonson, et al.
Plos Pathogens|September 8, 2020
Plasmodium sporozoites induce regulatory macrophagesBéatrice M F Winkel, Leonard R Pelgrom, Roos van Schuijlenburg, et al.
Pageof 32

Showing results (271-280 of 315) with videos related to

Sort By:
Pageof 32
Scientific Reports|November 27, 2025
Development and validation of an integrated preclinical model mimicking cardiometabolic risk in postmenopausal female ratsP Sainath, Shakta Mani Satyam, Sanjay Bharati, et al.
Revista De Neurologia|October 22, 2002
[Juvenile myoclonic epilepsy in chromosome 6p12: clinical and genetic advances]A V Delgado-Escueta, D Bai, J Bailey, et al.
Scientific Reports|September 19, 2019
Quantification of wild-type and radiation attenuated Plasmodium falciparum sporozoite motility in human skinBéatrice M F Winkel, Clarize M de Korne, Matthias N van Oosterom, et al.
Iscience|June 13, 2024
<i>De novo</i> <i>TLK1</i> and <i>MDM1</i> mutations in a patient with a neurodevelopmental disorder and immunodeficiencyMarina Villamor-Payà, María Sanchiz-Calvo, Jordann Smak, et al.
Omics : a Journal of Integrative Biology|April 1, 2021
Proteomic Alterations Associated with Oral Cancer Patients with Tobacco Using HabitsFirdous Ahmad Bhat, Sonali V Mohan, Shankargouda Patil, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
Identification of a <i>de novo</i> mutation in <i>TLK1</i> associated with a neurodevelopmental disorder and immunodeficiencyMarina Villamor-Payà, María Sanchiz-Calvo, Jordann Smak, et al.
American Journal of Human Genetics|November 27, 2010
A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataractsGaneshwaran H Mochida, Vijay S Ganesh, Jillian M Felie, et al.
Frontiers in Immunology|November 16, 2018
Early Induction of Human Regulatory Dermal Antigen Presenting Cells by Skin-Penetrating <i>Schistosoma Mansoni</i> CercariaeBéatrice M F Winkel, Mirjam R Dalenberg, Clarize M de Korne, et al.
Annals of Clinical and Translational Neurology|August 3, 2024
Protein-extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregationJohanna Ranta-Aho, Kevin J Felice, Per Harald Jonson, et al.
Plos Pathogens|September 8, 2020
Plasmodium sporozoites induce regulatory macrophagesBéatrice M F Winkel, Leonard R Pelgrom, Roos van Schuijlenburg, et al.
Pageof 32