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

R Gilbert

Showing results (1191-1200 of 1,457) with videos related to

Pageof 146
Sort By:
Frontiers in Oncology|August 2, 2021
Reversing Epigenetic Gene Silencing to Overcome Immune Evasion in CNS MalignanciesNivedita M Ratnam, Heather M Sonnemann, Stephen C Frederico, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 21, 2005
Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2Kristen L Deak, Margaret E Dickerson, Elwood Linney, et al.
JMIR AI|January 16, 2026
Treatment Recommendations for Clinical Deterioration on the Wards: Development and Validation of Machine Learning ModelsEric Pulick, Kyle A Carey, Tonela Qyli, et al.
Neuro-Oncology Advances|July 10, 2020
NCI-CONNECT: Comprehensive Oncology Network Evaluating Rare CNS Tumors-Histone Mutated Midline Glioma Workshop ProceedingsBrett J Theeler, Yamini Dalal, Michelle Monje, et al.
Molecular Psychiatry|October 14, 2005
Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locusX Liang, N Schnetz-Boutaud, S J Kenealy, et al.
Journal of Neurogenetics|July 3, 2002
Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorderM M Menold, Y Shao, C M Wolpert, et al.
Science (New York, N.Y.)|March 12, 2005
Complement factor H variant increases the risk of age-related macular degenerationJonathan L Haines, Michael A Hauser, Silke Schmidt, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21Holly N Cukier, Daria Salyakina, Sarah F Blankstein, et al.
Neuro-Oncology|August 30, 2024
cIMPACT-NOW update 8: Clarifications on molecular risk parameters and recommendations for WHO grading of meningiomasFelix Sahm, Kenneth D Aldape, Priscilla K Brastianos, et al.
Neuroscience Letters|July 24, 2003
The Q7R Saitohin gene polymorphism is not associated with Alzheimer diseaseSofia A Oliveira, Eden R Martin, William K Scott, et al.
Pageof 146

Showing results (1191-1200 of 1,457) with videos related to

Sort By:
Pageof 146
Frontiers in Oncology|August 2, 2021
Reversing Epigenetic Gene Silencing to Overcome Immune Evasion in CNS MalignanciesNivedita M Ratnam, Heather M Sonnemann, Stephen C Frederico, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 21, 2005
Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2Kristen L Deak, Margaret E Dickerson, Elwood Linney, et al.
JMIR AI|January 16, 2026
Treatment Recommendations for Clinical Deterioration on the Wards: Development and Validation of Machine Learning ModelsEric Pulick, Kyle A Carey, Tonela Qyli, et al.
Neuro-Oncology Advances|July 10, 2020
NCI-CONNECT: Comprehensive Oncology Network Evaluating Rare CNS Tumors-Histone Mutated Midline Glioma Workshop ProceedingsBrett J Theeler, Yamini Dalal, Michelle Monje, et al.
Molecular Psychiatry|October 14, 2005
Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locusX Liang, N Schnetz-Boutaud, S J Kenealy, et al.
Journal of Neurogenetics|July 3, 2002
Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorderM M Menold, Y Shao, C M Wolpert, et al.
Science (New York, N.Y.)|March 12, 2005
Complement factor H variant increases the risk of age-related macular degenerationJonathan L Haines, Michael A Hauser, Silke Schmidt, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2011
Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21Holly N Cukier, Daria Salyakina, Sarah F Blankstein, et al.
Neuro-Oncology|August 30, 2024
cIMPACT-NOW update 8: Clarifications on molecular risk parameters and recommendations for WHO grading of meningiomasFelix Sahm, Kenneth D Aldape, Priscilla K Brastianos, et al.
Neuroscience Letters|July 24, 2003
The Q7R Saitohin gene polymorphism is not associated with Alzheimer diseaseSofia A Oliveira, Eden R Martin, William K Scott, et al.
Pageof 146