Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Shagun

Showing results (681-690 of 700) with videos related to

Pageof 70
Sort By:
Nature Biotechnology|October 10, 2022
A comprehensive SARS-CoV-2-human protein-protein interactome reveals COVID-19 pathobiology and potential host therapeutic targetsYadi Zhou, Yuan Liu, Shagun Gupta, et al.
IMA Fungus|October 5, 2020
IMA Genome - F13: Draft genome sequences of <i>Ambrosiella cleistominuta</i>, <i>Cercospora brassicicola, C. citrullina, Physcia stellaris,</i> and <i>Teratosphaeria pseudoeucalypti</i>P Markus Wilken, Janneke Aylward, Ramesh Chand, et al.
American Journal of Medical Genetics. Part A|June 25, 2016
Spectrum of SMPD1 mutations in Asian-Indian patients with acid sphingomyelinase (ASM)-deficient Niemann-Pick diseasePrajnya Ranganath, Divya Matta, Gandham SriLakshmi Bhavani, et al.
Journal of Neurosurgery|October 31, 2025
Treatment outcomes for hypoglossal schwannomas: insights from a single-institution experience and literature reviewAhed H Kattaa, David J Park, Amit R Persad, et al.
IMA Fungus|February 24, 2022
IMA Genome - F16 : Draft genome assemblies of Fusarium marasasianum, Huntiella abstrusa, two Immersiporthe knoxdaviesiana isolates, Macrophomina pseudophaseolina, Macrophomina phaseolina, Naganishia randhawae, and Pseudocercospora cruentaBrenda D Wingfield, Lieschen De Vos, Andi M Wilson, et al.
Journal of Human Genetics|July 12, 2020
Identification and characterization of 30 novel pathogenic variations in 69 unrelated Indian patients with Mucolipidosis Type II and Type IIIDivya Pasumarthi, Neerja Gupta, Jayesh Sheth, et al.
Human Mutation|July 17, 2021
Functional characterization of novel variants in SMPD1 in Indian patients with acid sphingomyelinase deficiencyDipti Deshpande, Shailesh Kumar Gupta, Asodu Sandeep Sarma, et al.
American Journal of Medical Genetics. Part A|May 20, 2015
Novel and recurrent mutations in WISP3 and an atypical phenotypeGandham SriLakshmi Bhavani, Hitesh Shah, Ashwin B Dalal, et al.
Frontiers in Medicine|May 18, 2026
The interplay of maturity-onset diabetes of the young, obesity, uncontrolled hypertension, and cannabinoid hyperemesis in the progression to end-stage renal disease: a case reportNeguemadji Ngardig Ngaba, Victoria Lovallo, Anna ONeil, et al.
BMJ Open|May 19, 2026
Objective data-driven personalised approach to diagnosis of chronic tinnitus: the Tinnitus Detection (TIDE) project - protocol for the identification and validation of a biomarker for tinnitusSven Vanneste, Anusha Yasoda-Mohan, Feifan Chen, et al.
Pageof 70

Showing results (681-690 of 700) with videos related to

Sort By:
Pageof 70
Nature Biotechnology|October 10, 2022
A comprehensive SARS-CoV-2-human protein-protein interactome reveals COVID-19 pathobiology and potential host therapeutic targetsYadi Zhou, Yuan Liu, Shagun Gupta, et al.
IMA Fungus|October 5, 2020
IMA Genome - F13: Draft genome sequences of <i>Ambrosiella cleistominuta</i>, <i>Cercospora brassicicola, C. citrullina, Physcia stellaris,</i> and <i>Teratosphaeria pseudoeucalypti</i>P Markus Wilken, Janneke Aylward, Ramesh Chand, et al.
American Journal of Medical Genetics. Part A|June 25, 2016
Spectrum of SMPD1 mutations in Asian-Indian patients with acid sphingomyelinase (ASM)-deficient Niemann-Pick diseasePrajnya Ranganath, Divya Matta, Gandham SriLakshmi Bhavani, et al.
Journal of Neurosurgery|October 31, 2025
Treatment outcomes for hypoglossal schwannomas: insights from a single-institution experience and literature reviewAhed H Kattaa, David J Park, Amit R Persad, et al.
IMA Fungus|February 24, 2022
IMA Genome - F16 : Draft genome assemblies of Fusarium marasasianum, Huntiella abstrusa, two Immersiporthe knoxdaviesiana isolates, Macrophomina pseudophaseolina, Macrophomina phaseolina, Naganishia randhawae, and Pseudocercospora cruentaBrenda D Wingfield, Lieschen De Vos, Andi M Wilson, et al.
Journal of Human Genetics|July 12, 2020
Identification and characterization of 30 novel pathogenic variations in 69 unrelated Indian patients with Mucolipidosis Type II and Type IIIDivya Pasumarthi, Neerja Gupta, Jayesh Sheth, et al.
Human Mutation|July 17, 2021
Functional characterization of novel variants in SMPD1 in Indian patients with acid sphingomyelinase deficiencyDipti Deshpande, Shailesh Kumar Gupta, Asodu Sandeep Sarma, et al.
American Journal of Medical Genetics. Part A|May 20, 2015
Novel and recurrent mutations in WISP3 and an atypical phenotypeGandham SriLakshmi Bhavani, Hitesh Shah, Ashwin B Dalal, et al.
Frontiers in Medicine|May 18, 2026
The interplay of maturity-onset diabetes of the young, obesity, uncontrolled hypertension, and cannabinoid hyperemesis in the progression to end-stage renal disease: a case reportNeguemadji Ngardig Ngaba, Victoria Lovallo, Anna ONeil, et al.
BMJ Open|May 19, 2026
Objective data-driven personalised approach to diagnosis of chronic tinnitus: the Tinnitus Detection (TIDE) project - protocol for the identification and validation of a biomarker for tinnitusSven Vanneste, Anusha Yasoda-Mohan, Feifan Chen, et al.
Pageof 70