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Clinical Neuroradiology
|
May 13, 2022
Resting-state Networks in Tinnitus : A Scoping Review
Tori 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 networks
Deepti 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 progenitors
Caitlin 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 adults
Diana Tang, Yvonne Tran, Joshua R Lewis, et al.
International Journal of Audiology
|
August 2, 2022
COVID-19 and tinnitus: an initiative to improve tinnitus care
Boaz 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 brain
Lachlan 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 development
Sophie 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 Response
Jennifer 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 Malformations
Margot 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 Anomalies
Hanyin Cheng, Avinash V Dharmadhikari, Sylvia Varland, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Clinical Neuroradiology
|
May 13, 2022
Resting-state Networks in Tinnitus : A Scoping Review
Tori 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 networks
Deepti 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 progenitors
Caitlin 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 adults
Diana Tang, Yvonne Tran, Joshua R Lewis, et al.
International Journal of Audiology
|
August 2, 2022
COVID-19 and tinnitus: an initiative to improve tinnitus care
Boaz 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 brain
Lachlan 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 development
Sophie 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 Response
Jennifer 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 Malformations
Margot 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 Anomalies
Hanyin Cheng, Avinash V Dharmadhikari, Sylvia Varland, et al.
Page
of 2