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Kishore R

Showing results (161-170 of 267) with videos related to

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Congenital Heart Disease|July 24, 2018
Incidence and factors influencing the spontaneous closure of Fontan fenestrationSudheer R Gorla, Nataley K Jhingoeri, Abhishek Chakraborty, et al.
Transplantation|January 13, 2018
Deceased Donor Organ Transplantation Performed in the United States for Noncitizens and NonresidentsFrancis L Delmonico, Susan Gunderson, Kishore R Iyer, et al.
International Review of Cell and Molecular Biology|September 26, 2015
Science and Art of Cell-Based Ocular Surface RegenerationVivek Singh, Sachin Shukla, Charanya Ramachandran, et al.
Journal of Refractive Surgery (Thorofare, N.J. : 1995)|June 7, 2017
Small Incision Lenticule Extraction (SMILE) for Hyperopia: Optical Zone Diameter and Spherical Aberration InductionDan Z Reinstein, Kishore R Pradhan, Glenn I Carp, et al.
Journal of Biochemical and Biophysical Methods|November 23, 2006
Preparation of a monolithic capillary column with immobilized alpha-mannose for affinity chromatography of lectinsK Kishore R Tetala, Bo Chen, Gerben M Visser, et al.
American Journal of Medical Genetics. Part A|April 8, 2022
Decompensation of cardiorespiratory function and emergence of anemia during pregnancy in a case of mitochondrial myopathy, lactic acidosis, and sideroblastic anemia 2 with compound heterozygous YARS2 pathogenic variantsLaura I Rudaks, Eloise Watson, Carly Oboudiyat, et al.
Scientific Reports|January 11, 2022
A novel deep learning-based 3D cell segmentation framework for future image-based disease detectionAndong Wang, Qi Zhang, Yang Han, et al.
Neurology. Genetics|April 30, 2024
Two Novel Variants in <i>PI4KA</i> in a Family Presenting With Hereditary Spastic Paraparesis: A Case ReportJevin M Parmar, Elyshia L McNamara, Phillipa J Lamont, et al.
Internal Medicine Journal|April 24, 2023
Informing a value care model: lessons from an integrated adult neurogenomics clinicAlison McLean, Michel Tchan, Sophie Devery, et al.
European Journal of Human Genetics : EJHG|February 16, 2023
A biallelic variant of DCAF13 implicated in a neuromuscular disorder in humansHumera Manzoor, Hafsa Zahid, Christopher A Emerling, et al.
Pageof 27

Showing results (161-170 of 267) with videos related to

Sort By:
Pageof 27
Congenital Heart Disease|July 24, 2018
Incidence and factors influencing the spontaneous closure of Fontan fenestrationSudheer R Gorla, Nataley K Jhingoeri, Abhishek Chakraborty, et al.
Transplantation|January 13, 2018
Deceased Donor Organ Transplantation Performed in the United States for Noncitizens and NonresidentsFrancis L Delmonico, Susan Gunderson, Kishore R Iyer, et al.
International Review of Cell and Molecular Biology|September 26, 2015
Science and Art of Cell-Based Ocular Surface RegenerationVivek Singh, Sachin Shukla, Charanya Ramachandran, et al.
Journal of Refractive Surgery (Thorofare, N.J. : 1995)|June 7, 2017
Small Incision Lenticule Extraction (SMILE) for Hyperopia: Optical Zone Diameter and Spherical Aberration InductionDan Z Reinstein, Kishore R Pradhan, Glenn I Carp, et al.
Journal of Biochemical and Biophysical Methods|November 23, 2006
Preparation of a monolithic capillary column with immobilized alpha-mannose for affinity chromatography of lectinsK Kishore R Tetala, Bo Chen, Gerben M Visser, et al.
American Journal of Medical Genetics. Part A|April 8, 2022
Decompensation of cardiorespiratory function and emergence of anemia during pregnancy in a case of mitochondrial myopathy, lactic acidosis, and sideroblastic anemia 2 with compound heterozygous YARS2 pathogenic variantsLaura I Rudaks, Eloise Watson, Carly Oboudiyat, et al.
Scientific Reports|January 11, 2022
A novel deep learning-based 3D cell segmentation framework for future image-based disease detectionAndong Wang, Qi Zhang, Yang Han, et al.
Neurology. Genetics|April 30, 2024
Two Novel Variants in <i>PI4KA</i> in a Family Presenting With Hereditary Spastic Paraparesis: A Case ReportJevin M Parmar, Elyshia L McNamara, Phillipa J Lamont, et al.
Internal Medicine Journal|April 24, 2023
Informing a value care model: lessons from an integrated adult neurogenomics clinicAlison McLean, Michel Tchan, Sophie Devery, et al.
European Journal of Human Genetics : EJHG|February 16, 2023
A biallelic variant of DCAF13 implicated in a neuromuscular disorder in humansHumera Manzoor, Hafsa Zahid, Christopher A Emerling, et al.
Pageof 27