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 Lynch

Showing results (631-640 of 1,234) with videos related to

Pageof 124
Sort By:
The Nebraska Medical Journal|May 1, 1989
Familial pancreatic cancer (Part 1): Genetic pathology reviewH T Lynch, S J Lanspa, R J Fitzgibbons, et al.
Cancer Research|June 1, 1995
Malignant breast epithelium selects for insulin-like growth factor II expression in breast stroma: evidence for paracrine functionC Singer, A Rasmussen, H S Smith, et al.
Cell Death & Disease|April 6, 2013
TTC5 is required to prevent apoptosis of acute myeloid leukemia stem cellsJ T Lynch, T D D Somerville, G J Spencer, et al.
Organic Letters|February 4, 2025
The Synthesis of Glycosyl Amides from Unprotected Carbohydrates and AcylsilanesEmma M Dangerfield, Amy J Foster, Amy T Lynch, et al.
Osteoarthritis and Cartilage|July 10, 2024
Sex differences in patellar facet shape among healthy and osteoarthritic cohortsLaura A B Wilson, Joseph T Lynch, Jo M Ménard, et al.
Journal of Child and Adolescent Psychopharmacology|June 9, 2026
Context Matters: Variation in Pharmacologic Management of Pediatric Agitation Across Emergency and Inpatient Psychiatric SettingsSean T Lynch, Angelo I Chaia, Ricky Burns, et al.
Familial Cancer|March 11, 2006
BRCA1 and BRCA2 mutations in breast and ovarian cancer syndrome: reflection on the Creighton University historical series of high risk familiesOlga M Sinilnikova, Sylvie Mazoyer, Colette Bonnardel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 16, 1999
Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob diseaseB B Worrall, S T Herman, S Capellari, et al.
Annals of Neurology|November 18, 2000
A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathyD Thyagarajan, S Bressman, C Bruno, et al.
Cancer Genetics and Cytogenetics|December 5, 2000
E-cadherin mutation-based genetic counseling and hereditary diffuse gastric carcinomaH T Lynch, W Grady, J F Lynch, et al.
Pageof 124

Showing results (631-640 of 1,234) with videos related to

Sort By:
Pageof 124
The Nebraska Medical Journal|May 1, 1989
Familial pancreatic cancer (Part 1): Genetic pathology reviewH T Lynch, S J Lanspa, R J Fitzgibbons, et al.
Cancer Research|June 1, 1995
Malignant breast epithelium selects for insulin-like growth factor II expression in breast stroma: evidence for paracrine functionC Singer, A Rasmussen, H S Smith, et al.
Cell Death & Disease|April 6, 2013
TTC5 is required to prevent apoptosis of acute myeloid leukemia stem cellsJ T Lynch, T D D Somerville, G J Spencer, et al.
Organic Letters|February 4, 2025
The Synthesis of Glycosyl Amides from Unprotected Carbohydrates and AcylsilanesEmma M Dangerfield, Amy J Foster, Amy T Lynch, et al.
Osteoarthritis and Cartilage|July 10, 2024
Sex differences in patellar facet shape among healthy and osteoarthritic cohortsLaura A B Wilson, Joseph T Lynch, Jo M Ménard, et al.
Journal of Child and Adolescent Psychopharmacology|June 9, 2026
Context Matters: Variation in Pharmacologic Management of Pediatric Agitation Across Emergency and Inpatient Psychiatric SettingsSean T Lynch, Angelo I Chaia, Ricky Burns, et al.
Familial Cancer|March 11, 2006
BRCA1 and BRCA2 mutations in breast and ovarian cancer syndrome: reflection on the Creighton University historical series of high risk familiesOlga M Sinilnikova, Sylvie Mazoyer, Colette Bonnardel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 16, 1999
Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob diseaseB B Worrall, S T Herman, S Capellari, et al.
Annals of Neurology|November 18, 2000
A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathyD Thyagarajan, S Bressman, C Bruno, et al.
Cancer Genetics and Cytogenetics|December 5, 2000
E-cadherin mutation-based genetic counseling and hereditary diffuse gastric carcinomaH T Lynch, W Grady, J F Lynch, et al.
Pageof 124