Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

John Dean

Showing results (101-110 of 143) with videos related to

Pageof 15
Sort By:
Journal of Periodontology|October 1, 2004
Subantimicrobial dose doxycycline enhances the efficacy of scaling and root planing in chronic periodontitis: a multicenter trialPhilip M Preshaw, Arthur F Hefti, M John Novak, et al.
Journal of Vascular and Interventional Radiology : JVIR|October 6, 2009
Research reporting standards for percutaneous vertebral augmentationMartin G Radvany, Kieran J Murphy, Steven F Millward, et al.
BMJ Open|January 20, 2021
Systems approach to health service design, delivery and improvement: a systematic review and meta-analysisAlexander Komashie, James Ward, Tom Bashford, et al.
Human Molecular Genetics|May 22, 2024
PSMC5 insufficiency and P320R mutation impair proteasome functionZhong-Qiu Yu, Jenny Carmichael, Galen A Collins, et al.
ACS Applied Bio Materials|January 12, 2022
Amino/Amido Conjugates Form to Nanoscale Cobalt Physiometacomposite (PMC) Materials Functionally Delivering Nucleic Acid Therapeutic to Nucleus Enhancing Anticancer Activity via Ras-Targeted Protein InterferenceRobert K DeLong, John Dean, Garry Glaspell, et al.
American Journal of Medical Genetics. Part A|February 1, 2018
Extending the phenotype associated with the CSNK2A1-related Okur-Chung syndrome-A clinical study of 11 individualsCeris I Owen, Ramsay Bowden, Michael J Parker, et al.
American Journal of Human Genetics|March 16, 2007
Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndromeGillian Rice, William G Newman, John Dean, et al.
Clinical Radiology|December 23, 2022
Alerts and notification of imaging reports recommendationsTeik Choon See, , Mark Callaway, et al.
American Journal of Human Genetics|March 15, 2025
Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of resultsShona M Kerr, Lucija Klaric, Marisa D Muckian, et al.
Scientific Reports|July 31, 2019
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohortShona M Kerr, Lucija Klaric, Mihail Halachev, et al.
Pageof 15

Showing results (101-110 of 143) with videos related to

Sort By:
Pageof 15
Journal of Periodontology|October 1, 2004
Subantimicrobial dose doxycycline enhances the efficacy of scaling and root planing in chronic periodontitis: a multicenter trialPhilip M Preshaw, Arthur F Hefti, M John Novak, et al.
Journal of Vascular and Interventional Radiology : JVIR|October 6, 2009
Research reporting standards for percutaneous vertebral augmentationMartin G Radvany, Kieran J Murphy, Steven F Millward, et al.
BMJ Open|January 20, 2021
Systems approach to health service design, delivery and improvement: a systematic review and meta-analysisAlexander Komashie, James Ward, Tom Bashford, et al.
Human Molecular Genetics|May 22, 2024
PSMC5 insufficiency and P320R mutation impair proteasome functionZhong-Qiu Yu, Jenny Carmichael, Galen A Collins, et al.
ACS Applied Bio Materials|January 12, 2022
Amino/Amido Conjugates Form to Nanoscale Cobalt Physiometacomposite (PMC) Materials Functionally Delivering Nucleic Acid Therapeutic to Nucleus Enhancing Anticancer Activity via Ras-Targeted Protein InterferenceRobert K DeLong, John Dean, Garry Glaspell, et al.
American Journal of Medical Genetics. Part A|February 1, 2018
Extending the phenotype associated with the CSNK2A1-related Okur-Chung syndrome-A clinical study of 11 individualsCeris I Owen, Ramsay Bowden, Michael J Parker, et al.
American Journal of Human Genetics|March 16, 2007
Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndromeGillian Rice, William G Newman, John Dean, et al.
Clinical Radiology|December 23, 2022
Alerts and notification of imaging reports recommendationsTeik Choon See, , Mark Callaway, et al.
American Journal of Human Genetics|March 15, 2025
Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of resultsShona M Kerr, Lucija Klaric, Marisa D Muckian, et al.
Scientific Reports|July 31, 2019
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohortShona M Kerr, Lucija Klaric, Mihail Halachev, et al.
Pageof 15