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Showing results (761-770 of 776) with videos related to

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Nature Communications|September 27, 2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disordersArthur S Lee, Lauren J Ayers, Michael Kosicki, et al.
Science (New York, N.Y.)|October 20, 2000
Control of viremia and prevention of clinical AIDS in rhesus monkeys by cytokine-augmented DNA vaccinationD H Barouch, S Santra, J E Schmitz, et al.
The British Journal of Dermatology|November 6, 2021
Aetiology of tinea capitis in China: a multicentre prospective studyX-Q Chen, D-Y Zheng, Y-Y Xiao, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 29, 2026
Izalontamab brengitecan (Iza-bren; BL-B01D1), a first-in-class EGFR-HER3 bispecific antibody-drug conjugate, for patients with EGFR-mutated NSCLC: Pooled analysis of phase 1 and phase 2 trialsS-D Hong, Y-S Wang, H-Y Zhao, et al.
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Common and rare variant genetic contributions in African Americans with autismMatilde Cirnigliaro, Jennifer K Lowe, Alexander O Flynn-Carroll, et al.
JAMA Dermatology|November 20, 2024
Low-Dose Oral Minoxidil Initiation for Patients With Hair Loss: An International Modified Delphi Consensus StatementYagiz Matthew Akiska, Paradi Mirmirani, Ingrid Roseborough, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2024
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disordersJulie A Jurgens, Brenda J Barry, Wai-Man Chan, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disordersJulie A Jurgens, Brenda J Barry, Wai-Man Chan, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
NeuroDev: etiology and experience of neurodevelopmental disorders in Kenya and South AfricaPatricia Kipkemoi, Emily O'Heir, Mutaz Amin, et al.
Medrxiv : the Preprint Server for Health Sciences|January 20, 2025
Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populationsMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Pageof 78

Showing results (761-770 of 776) with videos related to

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Pageof 78
Nature Communications|September 27, 2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disordersArthur S Lee, Lauren J Ayers, Michael Kosicki, et al.
Science (New York, N.Y.)|October 20, 2000
Control of viremia and prevention of clinical AIDS in rhesus monkeys by cytokine-augmented DNA vaccinationD H Barouch, S Santra, J E Schmitz, et al.
The British Journal of Dermatology|November 6, 2021
Aetiology of tinea capitis in China: a multicentre prospective studyX-Q Chen, D-Y Zheng, Y-Y Xiao, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 29, 2026
Izalontamab brengitecan (Iza-bren; BL-B01D1), a first-in-class EGFR-HER3 bispecific antibody-drug conjugate, for patients with EGFR-mutated NSCLC: Pooled analysis of phase 1 and phase 2 trialsS-D Hong, Y-S Wang, H-Y Zhao, et al.
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Common and rare variant genetic contributions in African Americans with autismMatilde Cirnigliaro, Jennifer K Lowe, Alexander O Flynn-Carroll, et al.
JAMA Dermatology|November 20, 2024
Low-Dose Oral Minoxidil Initiation for Patients With Hair Loss: An International Modified Delphi Consensus StatementYagiz Matthew Akiska, Paradi Mirmirani, Ingrid Roseborough, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2024
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disordersJulie A Jurgens, Brenda J Barry, Wai-Man Chan, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disordersJulie A Jurgens, Brenda J Barry, Wai-Man Chan, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
NeuroDev: etiology and experience of neurodevelopmental disorders in Kenya and South AfricaPatricia Kipkemoi, Emily O'Heir, Mutaz Amin, et al.
Medrxiv : the Preprint Server for Health Sciences|January 20, 2025
Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populationsMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.
Pageof 78