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L Mitchell

Showing results (1491-1500 of 2,003) with videos related to

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JAMA Surgery|November 3, 2016
Patterns of Care in Hospitalized Vascular Surgery Patients at End of LifeDale G Wilson, Sheena K Harris, Heidi Peck, et al.
Annals of Clinical Biochemistry|November 1, 1983
Stability of four steroids in lyophilised human serumR E Das, D H Calam, F L Mitchell, et al.
British Journal of Cancer|July 2, 1998
Chromosome instability is a predominant trait of fibroblasts from Li-Fraumeni familiesJ M Boyle, E L Mitchell, M J Greaves, et al.
Spine Deformity|December 9, 2025
Activity capacity in children with early onset scoliosis compared to pulmonary function (spirometry) and patient-reported outcomesMalvika Choudhari, Mark Belio, Di Hu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2012
Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationshipsKristen Lipscomb Sund, Sarah L Zimmerman, Cameron Thomas, et al.
Journal of Vascular Surgery|January 8, 2014
A modern series of acute aortic occlusionJeffrey D Crawford, Kenneth H Perrone, Victor W Wong, et al.
Journal of Healthcare Management / American College of Healthcare Executives|November 13, 2025
Disaster Preparedness Training Relevance for Organizational Response Effectiveness: A Healthcare Executive PerspectiveAttila J Hertelendy, John G Richmond, Walfried M Lassar, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Neuroprotective Parkinson's Disease Therapeutic: Transition Metal Dichalcogenide Nanoflower Treatments Alleviate Pathological Cell StressCharles L Mitchell, Mikhail Matveyenka, Harris C Brown, et al.
Mutagenesis|March 1, 1989
CHO mutant UV61 removes (6-4) photoproducts but not cyclobutane dimersL H Thompson, D L Mitchell, J D Regan, et al.
Epilepsia|November 26, 2003
An Xp; Yq translocation causing a novel contiguous gene syndrome in brothers with generalized epilepsy, ichthyosis, and attention deficitsMichael J Doherty, Ian A Glass, Craig L Bennett, et al.
Pageof 201

Showing results (1491-1500 of 2,003) with videos related to

Sort By:
Pageof 201
JAMA Surgery|November 3, 2016
Patterns of Care in Hospitalized Vascular Surgery Patients at End of LifeDale G Wilson, Sheena K Harris, Heidi Peck, et al.
Annals of Clinical Biochemistry|November 1, 1983
Stability of four steroids in lyophilised human serumR E Das, D H Calam, F L Mitchell, et al.
British Journal of Cancer|July 2, 1998
Chromosome instability is a predominant trait of fibroblasts from Li-Fraumeni familiesJ M Boyle, E L Mitchell, M J Greaves, et al.
Spine Deformity|December 9, 2025
Activity capacity in children with early onset scoliosis compared to pulmonary function (spirometry) and patient-reported outcomesMalvika Choudhari, Mark Belio, Di Hu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2012
Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationshipsKristen Lipscomb Sund, Sarah L Zimmerman, Cameron Thomas, et al.
Journal of Vascular Surgery|January 8, 2014
A modern series of acute aortic occlusionJeffrey D Crawford, Kenneth H Perrone, Victor W Wong, et al.
Journal of Healthcare Management / American College of Healthcare Executives|November 13, 2025
Disaster Preparedness Training Relevance for Organizational Response Effectiveness: A Healthcare Executive PerspectiveAttila J Hertelendy, John G Richmond, Walfried M Lassar, et al.
Biorxiv : the Preprint Server for Biology|November 19, 2025
Neuroprotective Parkinson's Disease Therapeutic: Transition Metal Dichalcogenide Nanoflower Treatments Alleviate Pathological Cell StressCharles L Mitchell, Mikhail Matveyenka, Harris C Brown, et al.
Mutagenesis|March 1, 1989
CHO mutant UV61 removes (6-4) photoproducts but not cyclobutane dimersL H Thompson, D L Mitchell, J D Regan, et al.
Epilepsia|November 26, 2003
An Xp; Yq translocation causing a novel contiguous gene syndrome in brothers with generalized epilepsy, ichthyosis, and attention deficitsMichael J Doherty, Ian A Glass, Craig L Bennett, et al.
Pageof 201