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Simranpreet Kaur

Showing results (41-50 of 72) with videos related to

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Neuromuscular Disorders : NMD|January 25, 2015
ResponseManoj P Menezes, Leigh Waddell, Guy M Lenk, et al.
Foodborne Pathogens and Disease|April 23, 2025
Antimicrobial Resistance and Genomic Insights into <i>Enterococcus faecalis</i> Isolates from Broilers and Their Handlers in Punjab, IndiaNeha Parmar, Randhir Singh, Anuj Tyagi, et al.
Clinical Case Reports|January 2, 2020
Whole exome sequencing reveals a de novo missense variant in <i>EEF1A2</i> in a Rett syndrome-like patientSimranpreet Kaur, Nicole J Van Bergen, Wendy Anne Gold, et al.
Human Mutation|June 11, 2025
<i>CHD8</i> Variant and Rett Syndrome: Overlapping Phenotypes, Molecular Convergence, and Expanding the Genetic SpectrumElaine Zhang, Teresa Zhao, Tim Sikora, et al.
Neuromuscular Disorders : NMD|June 26, 2016
TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophyRoula Ghaoui, Tatiana Benavides, Monkol Lek, et al.
Journal of Medical Genetics|June 20, 2025
Biallelic <i>SIDT2</i> loss-of-function in a child with cerebellar ataxia and lysosomal dysfunction mimics impairment of <i>SIDT2</i> in miceTan Nguyen, Grace Yoon, Blake R C Smith, et al.
3 Biotech|April 27, 2017
Antibiotic sensitivity pattern of indigenous lactobacilli isolated from curd and human milk samplesChetan Sharma, Sachin Gulati, Nishchal Thakur, et al.
Experimental Hematology|April 12, 2014
Mobilization with granulocyte colony-stimulating factor blocks medullar erythropoiesis by depleting F4/80(+)VCAM1(+)CD169(+)ER-HR3(+)Ly6G(+) erythroid island macrophages in the mouseRebecca N Jacobsen, Catherine E Forristal, Liza J Raggatt, et al.
Genomics|December 29, 2023
Genome-wide transcriptomic and biochemical profiling of major depressive disorder: Unravelling association with susceptibility, severity, and antidepressant responsePriyanka Singh, Ankit Srivastava, Lini Philip, et al.
European Journal of Human Genetics : EJHG|May 16, 2025
Understanding speech and language in KIF1A-associated neurological disorderLottie D Morison, Adam P Vogel, John Christodoulou, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
Neuromuscular Disorders : NMD|January 25, 2015
ResponseManoj P Menezes, Leigh Waddell, Guy M Lenk, et al.
Foodborne Pathogens and Disease|April 23, 2025
Antimicrobial Resistance and Genomic Insights into <i>Enterococcus faecalis</i> Isolates from Broilers and Their Handlers in Punjab, IndiaNeha Parmar, Randhir Singh, Anuj Tyagi, et al.
Clinical Case Reports|January 2, 2020
Whole exome sequencing reveals a de novo missense variant in <i>EEF1A2</i> in a Rett syndrome-like patientSimranpreet Kaur, Nicole J Van Bergen, Wendy Anne Gold, et al.
Human Mutation|June 11, 2025
<i>CHD8</i> Variant and Rett Syndrome: Overlapping Phenotypes, Molecular Convergence, and Expanding the Genetic SpectrumElaine Zhang, Teresa Zhao, Tim Sikora, et al.
Neuromuscular Disorders : NMD|June 26, 2016
TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophyRoula Ghaoui, Tatiana Benavides, Monkol Lek, et al.
Journal of Medical Genetics|June 20, 2025
Biallelic <i>SIDT2</i> loss-of-function in a child with cerebellar ataxia and lysosomal dysfunction mimics impairment of <i>SIDT2</i> in miceTan Nguyen, Grace Yoon, Blake R C Smith, et al.
3 Biotech|April 27, 2017
Antibiotic sensitivity pattern of indigenous lactobacilli isolated from curd and human milk samplesChetan Sharma, Sachin Gulati, Nishchal Thakur, et al.
Experimental Hematology|April 12, 2014
Mobilization with granulocyte colony-stimulating factor blocks medullar erythropoiesis by depleting F4/80(+)VCAM1(+)CD169(+)ER-HR3(+)Ly6G(+) erythroid island macrophages in the mouseRebecca N Jacobsen, Catherine E Forristal, Liza J Raggatt, et al.
Genomics|December 29, 2023
Genome-wide transcriptomic and biochemical profiling of major depressive disorder: Unravelling association with susceptibility, severity, and antidepressant responsePriyanka Singh, Ankit Srivastava, Lini Philip, et al.
European Journal of Human Genetics : EJHG|May 16, 2025
Understanding speech and language in KIF1A-associated neurological disorderLottie D Morison, Adam P Vogel, John Christodoulou, et al.
Pageof 8