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

T Rogers

Showing results (611-620 of 652) with videos related to

Pageof 66
Sort By:
Frontiers in Molecular Biosciences|August 14, 2023
Fibroblast activation in response to TGFβ1 is modulated by co-culture with endothelial cells in a vascular organ-on-chip platformRebeccah J Luu, B Christopher Hoefler, Ashley L Gard, et al.
American Journal of Respiratory and Critical Care Medicine|October 31, 2002
Prevalence and clinical course of pleural effusions at 30 days after coronary artery and cardiac surgeryRichard W Light, Jeffrey T Rogers, J Phillip Moyers, et al.
Bioinformatics (Oxford, England)|June 9, 2023
MASH Native: a unified solution for native top-down proteomics data processingEli J Larson, Melissa R Pergande, Michelle E Moss, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
MASH Native: A Unified Solution for Native Top-Down Proteomics Data ProcessingEli J Larson, Melissa R Pergande, Michelle E Moss, et al.
Frontiers in Oncology|May 14, 2025
Longitudinal genomic profiling of chemotherapy-related CHIP variants in patients with ovarian cancerSara Corvigno, Jun Yao, Amma Asare, et al.
Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (Optometrists)|June 17, 2024
Strategies to address inequity of uncorrected refractive error in the Western Pacific: A modified Delphi processIan McCormick, Kelvin Tong, Nurliyana Abdullah, et al.
Cell|September 7, 2010
Iron-export ferroxidase activity of β-amyloid precursor protein is inhibited by zinc in Alzheimer's diseaseJames A Duce, Andrew Tsatsanis, Michael A Cater, et al.
American Journal of Human Genetics|September 13, 2003
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effectLinda L Bachinski, Bjarne Udd, Giovanni Meola, et al.
The Journal of Clinical Investigation|January 11, 2012
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12Gladys Montenegro, Adriana P Rebelo, James Connell, et al.
Journal of Medical Genetics|December 12, 2018
Breast cancer risk in neurofibromatosis type 1 is a function of the type of <i>NF1</i> gene mutation: a new genotype-phenotype correlationIan M Frayling, Victor-Felix Mautner, Rick van Minkelen, et al.
Pageof 66

Showing results (611-620 of 652) with videos related to

Sort By:
Pageof 66
Frontiers in Molecular Biosciences|August 14, 2023
Fibroblast activation in response to TGFβ1 is modulated by co-culture with endothelial cells in a vascular organ-on-chip platformRebeccah J Luu, B Christopher Hoefler, Ashley L Gard, et al.
American Journal of Respiratory and Critical Care Medicine|October 31, 2002
Prevalence and clinical course of pleural effusions at 30 days after coronary artery and cardiac surgeryRichard W Light, Jeffrey T Rogers, J Phillip Moyers, et al.
Bioinformatics (Oxford, England)|June 9, 2023
MASH Native: a unified solution for native top-down proteomics data processingEli J Larson, Melissa R Pergande, Michelle E Moss, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
MASH Native: A Unified Solution for Native Top-Down Proteomics Data ProcessingEli J Larson, Melissa R Pergande, Michelle E Moss, et al.
Frontiers in Oncology|May 14, 2025
Longitudinal genomic profiling of chemotherapy-related CHIP variants in patients with ovarian cancerSara Corvigno, Jun Yao, Amma Asare, et al.
Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (Optometrists)|June 17, 2024
Strategies to address inequity of uncorrected refractive error in the Western Pacific: A modified Delphi processIan McCormick, Kelvin Tong, Nurliyana Abdullah, et al.
Cell|September 7, 2010
Iron-export ferroxidase activity of β-amyloid precursor protein is inhibited by zinc in Alzheimer's diseaseJames A Duce, Andrew Tsatsanis, Michael A Cater, et al.
American Journal of Human Genetics|September 13, 2003
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effectLinda L Bachinski, Bjarne Udd, Giovanni Meola, et al.
The Journal of Clinical Investigation|January 11, 2012
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12Gladys Montenegro, Adriana P Rebelo, James Connell, et al.
Journal of Medical Genetics|December 12, 2018
Breast cancer risk in neurofibromatosis type 1 is a function of the type of <i>NF1</i> gene mutation: a new genotype-phenotype correlationIan M Frayling, Victor-Felix Mautner, Rick van Minkelen, et al.
Pageof 66