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Journal of Molecular Biology
|
June 29, 2026
UPF3A and UPF3B shape the transcriptome cooperatively yet oppose cell function
Urwah Nawaz, Emmylou Nicolas-Martinez, Saba Montazaribarforoushi, et al.
Pediatric Blood & Cancer
|
April 1, 2024
Proteomic insights into paediatric cancer: Unravelling molecular signatures and therapeutic opportunities
Bhavna D Padhye, Urwah Nawaz, Peter G Hains, et al.
Nature Communications
|
March 16, 2022
Comprehensive evaluation of deconvolution methods for human brain gene expression
Gavin J Sutton, Daniel Poppe, Rebecca K Simmons, et al.
NPJ Precision Oncology
|
February 12, 2026
OnCorr: A pan-cancer mRNA-protein correlation tool for precision oncology
Urwah Nawaz, Niantao Deng, Ori Livson, 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.
Genes & Development
|
November 20, 2025
Potent synthetic lethality between PLK1 and EYA family inhibitors in tumors of the central and peripheral nervous systems
Christopher B Nelson, Jadon K Wells, Ekaagra Kesarwani, et al.
American Journal of Human Genetics
|
November 7, 2020
RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial Features
Elizabeth E Palmer, Renee Carroll, Marie Shaw, 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 Medical Genetics. Part A
|
February 29, 2024
De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delay
Thoa Ha, Angela Morgan, Meghan N Bartos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 2, 2022
De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations
Kerith-Rae Dias, Colleen M Carlston, Laura E R Blok, et al.
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Search research articles
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Journal of Molecular Biology
|
June 29, 2026
UPF3A and UPF3B shape the transcriptome cooperatively yet oppose cell function
Urwah Nawaz, Emmylou Nicolas-Martinez, Saba Montazaribarforoushi, et al.
Pediatric Blood & Cancer
|
April 1, 2024
Proteomic insights into paediatric cancer: Unravelling molecular signatures and therapeutic opportunities
Bhavna D Padhye, Urwah Nawaz, Peter G Hains, et al.
Nature Communications
|
March 16, 2022
Comprehensive evaluation of deconvolution methods for human brain gene expression
Gavin J Sutton, Daniel Poppe, Rebecca K Simmons, et al.
NPJ Precision Oncology
|
February 12, 2026
OnCorr: A pan-cancer mRNA-protein correlation tool for precision oncology
Urwah Nawaz, Niantao Deng, Ori Livson, 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.
Genes & Development
|
November 20, 2025
Potent synthetic lethality between PLK1 and EYA family inhibitors in tumors of the central and peripheral nervous systems
Christopher B Nelson, Jadon K Wells, Ekaagra Kesarwani, et al.
American Journal of Human Genetics
|
November 7, 2020
RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial Features
Elizabeth E Palmer, Renee Carroll, Marie Shaw, 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 Medical Genetics. Part A
|
February 29, 2024
De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delay
Thoa Ha, Angela Morgan, Meghan N Bartos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 2, 2022
De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations
Kerith-Rae Dias, Colleen M Carlston, Laura E R Blok, et al.
Page
of 1