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

Deepti Domingo

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Clinical Neuroradiology|May 13, 2022
Resting-state Networks in Tinnitus : A Scoping ReviewTori Elyssa Kok, Deepti Domingo, Joshua Hassan, et al.
Human Molecular Genetics|July 16, 2020
A synonymous UPF3B variant causing a speech disorder implicates NMD as a regulator of neurodevelopmental disorder gene networksDeepti Domingo, Urwah Nawaz, Mark Corbett, et al.
Scientific Reports|March 26, 2017
USP9X deubiquitylating enzyme maintains RAPTOR protein levels, mTORC1 signalling and proliferation in neural progenitorsCaitlin R Bridges, Men-Chee Tan, Susitha Premarathne, et al.
European Journal of Nutrition|January 24, 2022
Associations between intake of dietary flavonoids and the 10-year incidence of tinnitus in older adultsDiana Tang, Yvonne Tran, Joshua R Lewis, et al.
International Journal of Audiology|August 2, 2022
COVID-19 and tinnitus: an initiative to improve tinnitus careBoaz Mui, Natalie Leong, Brenton Keil, et al.
Human Molecular Genetics|March 6, 2015
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brainLachlan A Jolly, Lam Son Nguyen, Deepti Domingo, et al.
Nature Communications|January 22, 2026
Neural crest cell-derived DKK1 and NEDD4 modulate Wnt signalling in the second heart field to orchestrate outflow tract developmentSophie Wiszniak, Dimuthu Alankarage, Iman Lohraseb, et al.
Neuron|October 6, 2019
Inhibition of Upf2-Dependent Nonsense-Mediated Decay Leads to Behavioral and Neurophysiological Abnormalities by Activating the Immune ResponseJennifer L Johnson, Loredana Stoica, Yuwei Liu, et al.
American Journal of Human Genetics|February 3, 2016
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital MalformationsMargot R F Reijnders, Vasilios Zachariadis, Brooke Latour, et al.
American Journal of Human Genetics|April 17, 2018
Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital AnomaliesHanyin Cheng, Avinash V Dharmadhikari, Sylvia Varland, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Clinical Neuroradiology|May 13, 2022
Resting-state Networks in Tinnitus : A Scoping ReviewTori Elyssa Kok, Deepti Domingo, Joshua Hassan, et al.
Human Molecular Genetics|July 16, 2020
A synonymous UPF3B variant causing a speech disorder implicates NMD as a regulator of neurodevelopmental disorder gene networksDeepti Domingo, Urwah Nawaz, Mark Corbett, et al.
Scientific Reports|March 26, 2017
USP9X deubiquitylating enzyme maintains RAPTOR protein levels, mTORC1 signalling and proliferation in neural progenitorsCaitlin R Bridges, Men-Chee Tan, Susitha Premarathne, et al.
European Journal of Nutrition|January 24, 2022
Associations between intake of dietary flavonoids and the 10-year incidence of tinnitus in older adultsDiana Tang, Yvonne Tran, Joshua R Lewis, et al.
International Journal of Audiology|August 2, 2022
COVID-19 and tinnitus: an initiative to improve tinnitus careBoaz Mui, Natalie Leong, Brenton Keil, et al.
Human Molecular Genetics|March 6, 2015
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brainLachlan A Jolly, Lam Son Nguyen, Deepti Domingo, et al.
Nature Communications|January 22, 2026
Neural crest cell-derived DKK1 and NEDD4 modulate Wnt signalling in the second heart field to orchestrate outflow tract developmentSophie Wiszniak, Dimuthu Alankarage, Iman Lohraseb, et al.
Neuron|October 6, 2019
Inhibition of Upf2-Dependent Nonsense-Mediated Decay Leads to Behavioral and Neurophysiological Abnormalities by Activating the Immune ResponseJennifer L Johnson, Loredana Stoica, Yuwei Liu, et al.
American Journal of Human Genetics|February 3, 2016
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital MalformationsMargot R F Reijnders, Vasilios Zachariadis, Brooke Latour, et al.
American Journal of Human Genetics|April 17, 2018
Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital AnomaliesHanyin Cheng, Avinash V Dharmadhikari, Sylvia Varland, et al.
Pageof 2