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

Shiwani Sharma

Showing results (41-50 of 71) with videos related to

Pageof 8
Sort By:
Plos One|September 10, 2013
Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern AustraliaAlpana Dave, Kate Laurie, Sandra E Staffieri, et al.
Experimental Cell Research|May 19, 2009
NHS-A isoform of the NHS gene is a novel interactor of ZO-1Shiwani Sharma, Katrina S Y Koh, Caitlin Collin, et al.
Scientific Reports|July 7, 2023
Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouseMark M Hassall, Shari Javadiyan, Sonja Klebe, et al.
Human Molecular Genetics|November 27, 2007
Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic peopleAlex W Hewitt, Shiwani Sharma, Kathryn P Burdon, et al.
Experimental Eye Research|September 21, 2019
Epha2 genotype influences ultraviolet radiation induced cataract in miceAlpana Dave, Jamie E Craig, Karina Skrzypiec, et al.
Plos One|October 27, 2015
Measurement of Systemic Mitochondrial Function in Advanced Primary Open-Angle Glaucoma and Leber Hereditary Optic NeuropathyNicole J Van Bergen, Jonathan G Crowston, Jamie E Craig, et al.
Molecular Vision|February 5, 2019
Novel protein constituents of pathological ocular pseudoexfoliation syndrome deposits identified with mass spectrometryShiwani Sharma, Tim Chataway, Sonja Klebe, et al.
Clinical Lymphoma, Myeloma & Leukemia|August 2, 2024
Survival Outcomes and Prognostic Factors in Therapy-Related Acute Myeloid Leukemia: A SEER Database Study, 2000-2020Utsav Joshi, Uttam Bhetuwal, Sumeet K Yadav, et al.
European Journal of Human Genetics : EJHG|March 9, 2017
Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataractOwen M Siggs, Shari Javadiyan, Shiwani Sharma, et al.
Human Mutation|December 21, 2012
Identification of a novel oligomerization disrupting mutation in CRYΑA associated with congenital cataract in a South Australian familyKate J Laurie, Alpana Dave, Tania Straga, et al.
Pageof 8

Showing results (41-50 of 71) with videos related to

Sort By:
Pageof 8
Plos One|September 10, 2013
Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern AustraliaAlpana Dave, Kate Laurie, Sandra E Staffieri, et al.
Experimental Cell Research|May 19, 2009
NHS-A isoform of the NHS gene is a novel interactor of ZO-1Shiwani Sharma, Katrina S Y Koh, Caitlin Collin, et al.
Scientific Reports|July 7, 2023
Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouseMark M Hassall, Shari Javadiyan, Sonja Klebe, et al.
Human Molecular Genetics|November 27, 2007
Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic peopleAlex W Hewitt, Shiwani Sharma, Kathryn P Burdon, et al.
Experimental Eye Research|September 21, 2019
Epha2 genotype influences ultraviolet radiation induced cataract in miceAlpana Dave, Jamie E Craig, Karina Skrzypiec, et al.
Plos One|October 27, 2015
Measurement of Systemic Mitochondrial Function in Advanced Primary Open-Angle Glaucoma and Leber Hereditary Optic NeuropathyNicole J Van Bergen, Jonathan G Crowston, Jamie E Craig, et al.
Molecular Vision|February 5, 2019
Novel protein constituents of pathological ocular pseudoexfoliation syndrome deposits identified with mass spectrometryShiwani Sharma, Tim Chataway, Sonja Klebe, et al.
Clinical Lymphoma, Myeloma & Leukemia|August 2, 2024
Survival Outcomes and Prognostic Factors in Therapy-Related Acute Myeloid Leukemia: A SEER Database Study, 2000-2020Utsav Joshi, Uttam Bhetuwal, Sumeet K Yadav, et al.
European Journal of Human Genetics : EJHG|March 9, 2017
Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataractOwen M Siggs, Shari Javadiyan, Shiwani Sharma, et al.
Human Mutation|December 21, 2012
Identification of a novel oligomerization disrupting mutation in CRYΑA associated with congenital cataract in a South Australian familyKate J Laurie, Alpana Dave, Tania Straga, et al.
Pageof 8