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T Booth

Showing results (231-240 of 265) with videos related to

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Journal of Medical Radiation Sciences|August 13, 2021
Comprehensive nodal breast VMAT: solving the low-dose wash dilemma using an iterative knowledge-based radiotherapy planning solutionCameron Stanton, Linda J Bell, Andrew Le, et al.
The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing lossNaoko Sakuma, Hideaki Moteki, Hela Azaiez, et al.
Physics and Imaging in Radiation Oncology|June 30, 2025
Patient-specific deep learning tracking for real-time 2D pancreas localisation in kV-guided radiotherapyAbdella M Ahmed, Levi Madden, Maegan Stewart, et al.
Clinical Genetics|June 2, 2016
Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian familiesK Lebeko, C M Sloan-Heggen, J J N Noubiap, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2018
Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37Kevin T Booth, James W Askew, Zohreh Talebizadeh, et al.
Medical Physics|November 10, 2022
The dosimetric error due to uncorrected tumor rotation during real-time adaptive prostate stereotactic body radiation therapyChandrima Sengupta, Simon Skouboe, Thomas Ravkilde, et al.
American Journal of Human Genetics|September 25, 2018
Genomic Landscape and Mutational Signatures of Deafness-Associated GenesHela Azaiez, Kevin T Booth, Sean S Ephraim, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 2004
Synthesis of the thapsigarginsSteven V Ley, Alessandra Antonello, Emily P Balskus, et al.
Nature Communications|April 26, 2023
Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1FMaryna V Ivanchenko, Daniel M Hathaway, Alex J Klein, et al.
Ophthalmic Genetics|April 14, 2020
Is it Usher syndrome? Collaborative diagnosis and molecular genetics of patients with visual impairment and hearing lossHeather A Stiff, Christina M Sloan-Heggen, Ashley Ko, et al.
Pageof 27

Showing results (231-240 of 265) with videos related to

Sort By:
Pageof 27
Journal of Medical Radiation Sciences|August 13, 2021
Comprehensive nodal breast VMAT: solving the low-dose wash dilemma using an iterative knowledge-based radiotherapy planning solutionCameron Stanton, Linda J Bell, Andrew Le, et al.
The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing lossNaoko Sakuma, Hideaki Moteki, Hela Azaiez, et al.
Physics and Imaging in Radiation Oncology|June 30, 2025
Patient-specific deep learning tracking for real-time 2D pancreas localisation in kV-guided radiotherapyAbdella M Ahmed, Levi Madden, Maegan Stewart, et al.
Clinical Genetics|June 2, 2016
Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian familiesK Lebeko, C M Sloan-Heggen, J J N Noubiap, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2018
Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37Kevin T Booth, James W Askew, Zohreh Talebizadeh, et al.
Medical Physics|November 10, 2022
The dosimetric error due to uncorrected tumor rotation during real-time adaptive prostate stereotactic body radiation therapyChandrima Sengupta, Simon Skouboe, Thomas Ravkilde, et al.
American Journal of Human Genetics|September 25, 2018
Genomic Landscape and Mutational Signatures of Deafness-Associated GenesHela Azaiez, Kevin T Booth, Sean S Ephraim, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 2004
Synthesis of the thapsigarginsSteven V Ley, Alessandra Antonello, Emily P Balskus, et al.
Nature Communications|April 26, 2023
Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1FMaryna V Ivanchenko, Daniel M Hathaway, Alex J Klein, et al.
Ophthalmic Genetics|April 14, 2020
Is it Usher syndrome? Collaborative diagnosis and molecular genetics of patients with visual impairment and hearing lossHeather A Stiff, Christina M Sloan-Heggen, Ashley Ko, et al.
Pageof 27