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Veterinary Ophthalmology
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October 8, 2024
Replication kinetics and cytopathic effect of feline calicivirus in feline corneal epithelial cells
Daniela I Saade, Chin-Chi Liu, Erinn P Mills, et al.
Translational Oncology
|
August 3, 2013
Altered RECQ Helicase Expression in Sporadic Primary Colorectal Cancers
Victoria 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 registries
Kathleen 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 patients
Lucas R Sass, Mohammadreza Khani, Jacob Romm, et al.
CBE Life Sciences Education
|
May 21, 2024
Development of the Mentoring in Undergraduate Research Survey
Lisa 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 employees
Benjamin 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 ataxia
Lijia 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 study
Kathleen 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 study
Gregory 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 ataxia
Lijia Huang, Jodi Warman-Chardon, Melissa T Carter, et al.
Page
of 89
Search research articles
Search
Showing results (741-750 of 884) with videos related to
Sort By:
Page
of 89
Veterinary Ophthalmology
|
October 8, 2024
Replication kinetics and cytopathic effect of feline calicivirus in feline corneal epithelial cells
Daniela I Saade, Chin-Chi Liu, Erinn P Mills, et al.
Translational Oncology
|
August 3, 2013
Altered RECQ Helicase Expression in Sporadic Primary Colorectal Cancers
Victoria 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 registries
Kathleen 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 patients
Lucas R Sass, Mohammadreza Khani, Jacob Romm, et al.
CBE Life Sciences Education
|
May 21, 2024
Development of the Mentoring in Undergraduate Research Survey
Lisa 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 employees
Benjamin 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 ataxia
Lijia 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 study
Kathleen 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 study
Gregory 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 ataxia
Lijia Huang, Jodi Warman-Chardon, Melissa T Carter, et al.
Page
of 89