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L Bowers

Showing results (281-290 of 314) with videos related to

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Angewandte Chemie (International Ed. in English)|July 15, 2010
Directed evolution of DNA polymerases for next-generation sequencingAaron M Leconte, Maha P Patel, Lauryn E Sass, et al.
JSES Reviews, Reports, and Techniques|August 17, 2023
Pectoralis minor syndrome - review of pathoanatomy, diagnosis, and management of the primary cause of neurogenic thoracic outlet syndromeAdil S Ahmed, Alexander R Graf, Anthony L Karzon, et al.
JDS Communications|December 9, 2024
Supplementing Silicoglycidol for the reduction of aflatoxin M<sub>1</sub> in milk and biomarkers of liver dysfunction in dairy cowsE H Branstad-Spates, C S McCarthy, B C Dooley, et al.
Epidemiology and Psychiatric Sciences|October 21, 2016
Factors associated with use of psychiatric intensive care and seclusion in adult inpatient mental health servicesA E Cullen, L Bowers, M Khondoker, et al.
Molecular and Cellular Neurosciences|October 22, 2008
Sensorimotor enhancement in mouse mutants lacking the Purkinje cell-specific Gi/o modulator, Pcp2(L7)Emilia Iscru, Yelda Serinagaoglu, Karl Schilling, et al.
Oncogene|August 24, 2010
Rates of loss of heterozygosity and mitotic recombination in NF2 schwannomas, sporadic vestibular schwannomas and schwannomatosis schwannomasK D Hadfield, M J Smith, J E Urquhart, et al.
Journal of Psychiatric and Mental Health Nursing|January 28, 2014
Safewards: the empirical basis of the model and a critical appraisalL Bowers, J Alexander, H Bilgin, et al.
JB & JS Open Access|March 17, 2025
Arthroscopic Pectoralis Minor Release and Infraclavicular Brachial Plexus Decompression for Neurogenic Thoracic Outlet Syndrome: A Novel Treatment for an Old ProblemEric R Wagner, Thomas J McQuillan, Oluwakorede Omole, et al.
Human Mutation|June 20, 2022
Screening of potential novel candidate genes in schwannomatosis patientsCristina Perez-Becerril, Andrew J Wallace, Helene Schlecht, et al.
Human Mutation|December 1, 2015
The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing SyndromesMiriam J Smith, Jill E Urquhart, Elaine F Harkness, et al.
Pageof 32

Showing results (281-290 of 314) with videos related to

Sort By:
Pageof 32
Angewandte Chemie (International Ed. in English)|July 15, 2010
Directed evolution of DNA polymerases for next-generation sequencingAaron M Leconte, Maha P Patel, Lauryn E Sass, et al.
JSES Reviews, Reports, and Techniques|August 17, 2023
Pectoralis minor syndrome - review of pathoanatomy, diagnosis, and management of the primary cause of neurogenic thoracic outlet syndromeAdil S Ahmed, Alexander R Graf, Anthony L Karzon, et al.
JDS Communications|December 9, 2024
Supplementing Silicoglycidol for the reduction of aflatoxin M<sub>1</sub> in milk and biomarkers of liver dysfunction in dairy cowsE H Branstad-Spates, C S McCarthy, B C Dooley, et al.
Epidemiology and Psychiatric Sciences|October 21, 2016
Factors associated with use of psychiatric intensive care and seclusion in adult inpatient mental health servicesA E Cullen, L Bowers, M Khondoker, et al.
Molecular and Cellular Neurosciences|October 22, 2008
Sensorimotor enhancement in mouse mutants lacking the Purkinje cell-specific Gi/o modulator, Pcp2(L7)Emilia Iscru, Yelda Serinagaoglu, Karl Schilling, et al.
Oncogene|August 24, 2010
Rates of loss of heterozygosity and mitotic recombination in NF2 schwannomas, sporadic vestibular schwannomas and schwannomatosis schwannomasK D Hadfield, M J Smith, J E Urquhart, et al.
Journal of Psychiatric and Mental Health Nursing|January 28, 2014
Safewards: the empirical basis of the model and a critical appraisalL Bowers, J Alexander, H Bilgin, et al.
JB & JS Open Access|March 17, 2025
Arthroscopic Pectoralis Minor Release and Infraclavicular Brachial Plexus Decompression for Neurogenic Thoracic Outlet Syndrome: A Novel Treatment for an Old ProblemEric R Wagner, Thomas J McQuillan, Oluwakorede Omole, et al.
Human Mutation|June 20, 2022
Screening of potential novel candidate genes in schwannomatosis patientsCristina Perez-Becerril, Andrew J Wallace, Helene Schlecht, et al.
Human Mutation|December 1, 2015
The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing SyndromesMiriam J Smith, Jill E Urquhart, Elaine F Harkness, et al.
Pageof 32