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J Mahoney

Showing results (761-770 of 775) with videos related to

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Nature|July 1, 2026
Dual tumour-myeloid targeting of glioblastoma with GPNMB CAR-T cellsNeil Savage, Shan Grewal, Muhammad Vaseem Shaikh, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|November 19, 2024
Lung allograft dysbiosis associates with immune response and primary graft dysfunctionNathaniel C Nelson, Kendrew K Wong, Ian J Mahoney, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Genetic variants disrupting activity-dependent CELF2 shuttling cause neuronal hyperexcitability, learning deficits, and seizuresMichelle Hua, Mohamad-Reza Aghanoori, Melissa MacPherson, et al.
American Journal of Respiratory and Critical Care Medicine|February 15, 2024
Longitudinal Lower Airway Microbial Signatures of Acute Cellular Rejection in Lung TransplantationJake G Natalini, Kendrew K Wong, Nathaniel C Nelson, et al.
Nature Communications|February 7, 2024
ASPSCR1-TFE3 reprograms transcription by organizing enhancer loops around hexameric VCP/p97Amir Pozner, Li Li, Shiv Prakash Verma, et al.
Biorxiv : the Preprint Server for Biology|October 24, 2023
ASPSCR1-TFE3 reprograms transcription by organizing enhancer loops around hexameric VCP/p97Amir Pozner, Shiv Prakash Verma, Li Li, et al.
Plos One|September 7, 2012
Creation of an open-access, mutation-defined fibroblast resource for neurological disease researchSelina Wray, Matthew Self, , et al.
The Journal of Clinical Investigation|June 11, 2026
Pathological disruption of CELF2 shuttling causes neuronal hyperactivity, learning deficits, and seizuresMichelle Hua, Mohamad-Reza Aghanoori, Melissa J MacPherson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 3, 2018
Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlationMagdalena Koczkowska, Tom Callens, Alicia Gomes, et al.
Human Mutation|March 8, 2012
Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathyJohann Böhm, Valérie Biancalana, Elizabeth T Dechene, et al.
Pageof 78

Showing results (761-770 of 775) with videos related to

Sort By:
Pageof 78
Nature|July 1, 2026
Dual tumour-myeloid targeting of glioblastoma with GPNMB CAR-T cellsNeil Savage, Shan Grewal, Muhammad Vaseem Shaikh, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|November 19, 2024
Lung allograft dysbiosis associates with immune response and primary graft dysfunctionNathaniel C Nelson, Kendrew K Wong, Ian J Mahoney, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Genetic variants disrupting activity-dependent CELF2 shuttling cause neuronal hyperexcitability, learning deficits, and seizuresMichelle Hua, Mohamad-Reza Aghanoori, Melissa MacPherson, et al.
American Journal of Respiratory and Critical Care Medicine|February 15, 2024
Longitudinal Lower Airway Microbial Signatures of Acute Cellular Rejection in Lung TransplantationJake G Natalini, Kendrew K Wong, Nathaniel C Nelson, et al.
Nature Communications|February 7, 2024
ASPSCR1-TFE3 reprograms transcription by organizing enhancer loops around hexameric VCP/p97Amir Pozner, Li Li, Shiv Prakash Verma, et al.
Biorxiv : the Preprint Server for Biology|October 24, 2023
ASPSCR1-TFE3 reprograms transcription by organizing enhancer loops around hexameric VCP/p97Amir Pozner, Shiv Prakash Verma, Li Li, et al.
Plos One|September 7, 2012
Creation of an open-access, mutation-defined fibroblast resource for neurological disease researchSelina Wray, Matthew Self, , et al.
The Journal of Clinical Investigation|June 11, 2026
Pathological disruption of CELF2 shuttling causes neuronal hyperactivity, learning deficits, and seizuresMichelle Hua, Mohamad-Reza Aghanoori, Melissa J MacPherson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 3, 2018
Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlationMagdalena Koczkowska, Tom Callens, Alicia Gomes, et al.
Human Mutation|March 8, 2012
Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathyJohann Böhm, Valérie Biancalana, Elizabeth T Dechene, et al.
Pageof 78