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Siddharth Gupta

Showing results (71-80 of 77) with videos related to

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Journal of Neurochemistry|September 30, 2023
Dendrimer nanotherapy targeting of glial dysfunction improves inflammation and neurobehavioral phenotype in adult female Mecp2-heterozygous mouse model of Rett syndromeElizabeth Smith Khoury, Ruchit V Patel, Caroline O'Ferrall, et al.
European Journal of Human Genetics : EJHG|July 9, 2015
Loss-of-function variants in HIVEP2 are a cause of intellectual disabilitySiddharth Srivastava, Hartmut Engels, Ina Schanze, et al.
Children (Basel, Switzerland)|September 23, 2022
A Review of the Multi-Systemic Complications of a Ketogenic Diet in Children and Infants with EpilepsyKyra Newmaster, Zahra Zhu, Elizabeth Bolt, et al.
Computers in Biology and Medicine|May 5, 2026
Attention mechanisms in UNet variants for medical/non-medical image segmentation: A comprehensive and state-of-the-art narrative reviewSiddharth Gupta, Yogendra Chhetri, Amit Pandey, et al.
Diagnostics (Basel, Switzerland)|September 14, 2024
Cardiovascular Disease Risk Stratification Using Hybrid Deep Learning Paradigm: First of Its Kind on Canadian Trial DataMrinalini Bhagawati, Sudip Paul, Laura Mantella, et al.
Stem Cell Reports|October 22, 2021
CALR frameshift mutations in MPN patient-derived iPSCs accelerate maturation of megakaryocytesKathrin Olschok, Lijuan Han, Marcelo A S de Toledo, et al.
Stem Cell Reports|January 26, 2024
Proinflammatory phenotype of iPS cell-derived JAK2 V617F megakaryocytes induces fibrosis in 3D in vitro bone marrow nicheNiclas Flosdorf, Janik Böhnke, Marcelo A S de Toledo, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
Journal of Neurochemistry|September 30, 2023
Dendrimer nanotherapy targeting of glial dysfunction improves inflammation and neurobehavioral phenotype in adult female Mecp2-heterozygous mouse model of Rett syndromeElizabeth Smith Khoury, Ruchit V Patel, Caroline O'Ferrall, et al.
European Journal of Human Genetics : EJHG|July 9, 2015
Loss-of-function variants in HIVEP2 are a cause of intellectual disabilitySiddharth Srivastava, Hartmut Engels, Ina Schanze, et al.
Children (Basel, Switzerland)|September 23, 2022
A Review of the Multi-Systemic Complications of a Ketogenic Diet in Children and Infants with EpilepsyKyra Newmaster, Zahra Zhu, Elizabeth Bolt, et al.
Computers in Biology and Medicine|May 5, 2026
Attention mechanisms in UNet variants for medical/non-medical image segmentation: A comprehensive and state-of-the-art narrative reviewSiddharth Gupta, Yogendra Chhetri, Amit Pandey, et al.
Diagnostics (Basel, Switzerland)|September 14, 2024
Cardiovascular Disease Risk Stratification Using Hybrid Deep Learning Paradigm: First of Its Kind on Canadian Trial DataMrinalini Bhagawati, Sudip Paul, Laura Mantella, et al.
Stem Cell Reports|October 22, 2021
CALR frameshift mutations in MPN patient-derived iPSCs accelerate maturation of megakaryocytesKathrin Olschok, Lijuan Han, Marcelo A S de Toledo, et al.
Stem Cell Reports|January 26, 2024
Proinflammatory phenotype of iPS cell-derived JAK2 V617F megakaryocytes induces fibrosis in 3D in vitro bone marrow nicheNiclas Flosdorf, Janik Böhnke, Marcelo A S de Toledo, et al.
Pageof 8