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Christopher Campbell

Showing results (61-70 of 86) with videos related to

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Clinical Chemistry and Laboratory Medicine|April 27, 2022
Patients with severe COVID-19 do not have elevated autoantibodies against common diagnostic autoantigensAntigona Ulndreaj, Mingyue Wang, Salvia Misaghian, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 6, 2024
Developing and applying potentially scalable recruitment strategies to accelerate ADRD research participation of Black adultsRalph Richards, Mollie Richards, Jane Musema, et al.
Journal of Neurotrauma|April 6, 2023
Associations of Microvascular Injury-Related Biomarkers With Traumatic Brain Injury Severity and Outcomes: A Transforming Research and Clinical Knowledge in Traumatic Brain Injury (TRACK-TBI) Pilot StudyAndrea L C Schneider, J Russell Huie, Sonia Jain, et al.
Alzheimer'S & Dementia (New York, N. Y.)|May 31, 2023
Accelerating diversity in Alzheimer's disease research by partnering with a community advisory boardAlex Pena-Garcia, Ralph Richards, Mollie Richards, et al.
Elife|February 23, 2022
Hydrop enables droplet-based single-cell ATAC-seq and single-cell RNA-seq using dissolvable hydrogel beadsFlorian V De Rop, Joy N Ismail, Carmen Bravo González-Blas, et al.
Diagnostics (Basel, Switzerland)|June 24, 2022
Acute and Chronic Cardiopulmonary Effects of High Dose Interleukin-2 Therapy: An Observational Magnetic Resonance Imaging StudyJakub Lagan, Josephine H Naish, Christien Fortune, et al.
BMJ Open|February 2, 2022
Relationship between sociodemographics, healthcare providers' competence and healthcare access among two-spirit, gay, bisexual, queer and other men who have sex with men in Manitoba: results from a community-based cross-sectional studyRusty Souleymanov, Jared Star, Albert McLeod, et al.
European Journal of Human Genetics : EJHG|December 15, 2019
Diagnostic yield of panel-based genetic testing in syndromic inherited retinal diseaseOmamah A Jiman, Rachel L Taylor, Eva Lenassi, et al.
Investigative Ophthalmology & Visual Science|January 28, 2017
Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early FeatureRachel L Taylor, Mark T Handley, Sarah Waller, et al.
European Journal of Human Genetics : EJHG|April 6, 2017
Validation of copy number variation analysis for next-generation sequencing diagnosticsJamie M Ellingford, Christopher Campbell, Stephanie Barton, et al.
Pageof 9

Showing results (61-70 of 86) with videos related to

Sort By:
Pageof 9
Clinical Chemistry and Laboratory Medicine|April 27, 2022
Patients with severe COVID-19 do not have elevated autoantibodies against common diagnostic autoantigensAntigona Ulndreaj, Mingyue Wang, Salvia Misaghian, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 6, 2024
Developing and applying potentially scalable recruitment strategies to accelerate ADRD research participation of Black adultsRalph Richards, Mollie Richards, Jane Musema, et al.
Journal of Neurotrauma|April 6, 2023
Associations of Microvascular Injury-Related Biomarkers With Traumatic Brain Injury Severity and Outcomes: A Transforming Research and Clinical Knowledge in Traumatic Brain Injury (TRACK-TBI) Pilot StudyAndrea L C Schneider, J Russell Huie, Sonia Jain, et al.
Alzheimer'S & Dementia (New York, N. Y.)|May 31, 2023
Accelerating diversity in Alzheimer's disease research by partnering with a community advisory boardAlex Pena-Garcia, Ralph Richards, Mollie Richards, et al.
Elife|February 23, 2022
Hydrop enables droplet-based single-cell ATAC-seq and single-cell RNA-seq using dissolvable hydrogel beadsFlorian V De Rop, Joy N Ismail, Carmen Bravo González-Blas, et al.
Diagnostics (Basel, Switzerland)|June 24, 2022
Acute and Chronic Cardiopulmonary Effects of High Dose Interleukin-2 Therapy: An Observational Magnetic Resonance Imaging StudyJakub Lagan, Josephine H Naish, Christien Fortune, et al.
BMJ Open|February 2, 2022
Relationship between sociodemographics, healthcare providers' competence and healthcare access among two-spirit, gay, bisexual, queer and other men who have sex with men in Manitoba: results from a community-based cross-sectional studyRusty Souleymanov, Jared Star, Albert McLeod, et al.
European Journal of Human Genetics : EJHG|December 15, 2019
Diagnostic yield of panel-based genetic testing in syndromic inherited retinal diseaseOmamah A Jiman, Rachel L Taylor, Eva Lenassi, et al.
Investigative Ophthalmology & Visual Science|January 28, 2017
Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early FeatureRachel L Taylor, Mark T Handley, Sarah Waller, et al.
European Journal of Human Genetics : EJHG|April 6, 2017
Validation of copy number variation analysis for next-generation sequencing diagnosticsJamie M Ellingford, Christopher Campbell, Stephanie Barton, et al.
Pageof 9