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Genetics research

Showing results (21-30 of 499) with videos related to

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Genetics Research|October 27, 2022
Molecular Characterization of Wild and Cultivated Strawberry (<i>Fragaria</i> × <i>ananassa</i>) through DNA Barcode MarkersAwais Qarni, Khushi Muhammad, Abdul Wahab, et al.
Genetics Research|October 27, 2022
Associations between Extracellular Matrix Protein 1 Gene Polymorphism and Progression of Liver DiseaseXiuting He, Ting Liu, Rui Zhang, et al.
Genetics Research|October 27, 2022
Bioinformatics Analysis Identifies TNFRSF1A as a Biomarker of Liver Injury in Sepsis TNFRSF1A is a Biomarker for Septic Liver InjuryShangxun Zhou, Wei Zhao, Junjie Li, et al.
Genetics Research|September 26, 2022
Molecular, Biochemical, and Clinical Characterization of Thirteen Patients with Glycogen Storage Disease 1a in MalaysiaSiti Aishah Abdul Wahab, Yusnita Yakob, Mohd Khairul Nizam Mohd Khalid, et al.
Genetics Research|July 20, 2011
How to deal with genotype uncertainty in variance component quantitative trait loci analysesXia Shen, Lars Rönnegård, Orjan Carlborg
Genetics Research|December 29, 2015
A refined high carbohydrate diet is associated with changes in the serotonin pathway and visceral obesityPaola A Spadaro, Helen L Naug, Eugene F DU Toit, et al.
Genetics Research|December 23, 2015
Multiomic analysis of mice epilepsy models suggest that miR-21a expression modulates mRNA and protein levels related to seizure deteriorationXiaoxiao Hu, Xin Fu, A O Jiang, et al.
Genetics Research|September 15, 2015
Determination of obesity associated gene variants related to TMEM18 through ultra-deep targeted re-sequencing in a case-control cohort for pediatric obesityMathias Rask-Andersen, Markus Sällman Almén, Josefin A Jacobsson, et al.
Genetics Research|April 30, 2019
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutationHager Jaouadi, Amel Ben Chehida, Lilia Kraoua, et al.
Genetics Research|August 9, 2018
Comprehensive review on the molecular genetics of autosomal recessive primary microcephaly (MCPH)Muhammad Naveed, Syeda Khushbakht Kazmi, Mariyam Amin, et al.
Pageof 50

Showing results (21-30 of 499) with videos related to

Sort By:
Pageof 50
Genetics Research|October 27, 2022
Molecular Characterization of Wild and Cultivated Strawberry (<i>Fragaria</i> × <i>ananassa</i>) through DNA Barcode MarkersAwais Qarni, Khushi Muhammad, Abdul Wahab, et al.
Genetics Research|October 27, 2022
Associations between Extracellular Matrix Protein 1 Gene Polymorphism and Progression of Liver DiseaseXiuting He, Ting Liu, Rui Zhang, et al.
Genetics Research|October 27, 2022
Bioinformatics Analysis Identifies TNFRSF1A as a Biomarker of Liver Injury in Sepsis TNFRSF1A is a Biomarker for Septic Liver InjuryShangxun Zhou, Wei Zhao, Junjie Li, et al.
Genetics Research|September 26, 2022
Molecular, Biochemical, and Clinical Characterization of Thirteen Patients with Glycogen Storage Disease 1a in MalaysiaSiti Aishah Abdul Wahab, Yusnita Yakob, Mohd Khairul Nizam Mohd Khalid, et al.
Genetics Research|July 20, 2011
How to deal with genotype uncertainty in variance component quantitative trait loci analysesXia Shen, Lars Rönnegård, Orjan Carlborg
Genetics Research|December 29, 2015
A refined high carbohydrate diet is associated with changes in the serotonin pathway and visceral obesityPaola A Spadaro, Helen L Naug, Eugene F DU Toit, et al.
Genetics Research|December 23, 2015
Multiomic analysis of mice epilepsy models suggest that miR-21a expression modulates mRNA and protein levels related to seizure deteriorationXiaoxiao Hu, Xin Fu, A O Jiang, et al.
Genetics Research|September 15, 2015
Determination of obesity associated gene variants related to TMEM18 through ultra-deep targeted re-sequencing in a case-control cohort for pediatric obesityMathias Rask-Andersen, Markus Sällman Almén, Josefin A Jacobsson, et al.
Genetics Research|April 30, 2019
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutationHager Jaouadi, Amel Ben Chehida, Lilia Kraoua, et al.
Genetics Research|August 9, 2018
Comprehensive review on the molecular genetics of autosomal recessive primary microcephaly (MCPH)Muhammad Naveed, Syeda Khushbakht Kazmi, Mariyam Amin, et al.
Pageof 50