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T Carter

Showing results (741-750 of 884) with videos related to

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Veterinary Ophthalmology|October 8, 2024
Replication kinetics and cytopathic effect of feline calicivirus in feline corneal epithelial cellsDaniela I Saade, Chin-Chi Liu, Erinn P Mills, et al.
Translational Oncology|August 3, 2013
Altered RECQ Helicase Expression in Sporadic Primary Colorectal CancersVictoria Valinluck Lao, Piri Welcsh, Yanxin Luo, et al.
American Journal of Epidemiology|November 13, 2025
Enhancing COVID-19 vaccine effectiveness evidence generation using tokenized immunization registriesKathleen M Andersen, Leah J McGrath, Kristen E Allen, et al.
Fluids and Barriers of the CNS|January 22, 2020
Non-invasive MRI quantification of cerebrospinal fluid dynamics in amyotrophic lateral sclerosis patientsLucas R Sass, Mohammadreza Khani, Jacob Romm, et al.
CBE Life Sciences Education|May 21, 2024
Development of the Mentoring in Undergraduate Research SurveyLisa B Limeri, Nathan T Carter, Riley A Hess, et al.
Journal of the American Veterinary Medical Association|July 2, 2009
Euthanasia-related strain and coping strategies in animal shelter employeesBenjamin E Baran, Joseph A Allen, Steven G Rogelberg, et al.
Orphanet Journal of Rare Diseases|September 19, 2012
Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxiaLijia Huang, Jodi Warman Chardon, Melissa T Carter, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|April 30, 2025
Inpatient burden of COVID-19 in Japan: A retrospective cohort studyKathleen M Andersen, Matthew A Brouillette, Kanae Togo, et al.
The American Journal of Hospice & Palliative Care|March 2, 2005
Modafinil to treat fatigue in amyotrophic lateral sclerosis: an open label pilot studyGregory T Carter, Michael D Weiss, Jau-Shin Lou, et al.
Orphanet Journal of Rare Diseases|March 30, 2022
Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxiaLijia Huang, Jodi Warman-Chardon, Melissa T Carter, et al.
Pageof 89

Showing results (741-750 of 884) with videos related to

Sort By:
Pageof 89
Veterinary Ophthalmology|October 8, 2024
Replication kinetics and cytopathic effect of feline calicivirus in feline corneal epithelial cellsDaniela I Saade, Chin-Chi Liu, Erinn P Mills, et al.
Translational Oncology|August 3, 2013
Altered RECQ Helicase Expression in Sporadic Primary Colorectal CancersVictoria Valinluck Lao, Piri Welcsh, Yanxin Luo, et al.
American Journal of Epidemiology|November 13, 2025
Enhancing COVID-19 vaccine effectiveness evidence generation using tokenized immunization registriesKathleen M Andersen, Leah J McGrath, Kristen E Allen, et al.
Fluids and Barriers of the CNS|January 22, 2020
Non-invasive MRI quantification of cerebrospinal fluid dynamics in amyotrophic lateral sclerosis patientsLucas R Sass, Mohammadreza Khani, Jacob Romm, et al.
CBE Life Sciences Education|May 21, 2024
Development of the Mentoring in Undergraduate Research SurveyLisa B Limeri, Nathan T Carter, Riley A Hess, et al.
Journal of the American Veterinary Medical Association|July 2, 2009
Euthanasia-related strain and coping strategies in animal shelter employeesBenjamin E Baran, Joseph A Allen, Steven G Rogelberg, et al.
Orphanet Journal of Rare Diseases|September 19, 2012
Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxiaLijia Huang, Jodi Warman Chardon, Melissa T Carter, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|April 30, 2025
Inpatient burden of COVID-19 in Japan: A retrospective cohort studyKathleen M Andersen, Matthew A Brouillette, Kanae Togo, et al.
The American Journal of Hospice & Palliative Care|March 2, 2005
Modafinil to treat fatigue in amyotrophic lateral sclerosis: an open label pilot studyGregory T Carter, Michael D Weiss, Jau-Shin Lou, et al.
Orphanet Journal of Rare Diseases|March 30, 2022
Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxiaLijia Huang, Jodi Warman-Chardon, Melissa T Carter, et al.
Pageof 89