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

Charis Eng

Showing results (341-350 of 555) with videos related to

Pageof 56
Sort By:
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 27, 2016
Von Hippel-Lindau Disease: Genetics and Role of Genetic Counseling in a Multiple Neoplasia SyndromeSarah M Nielsen, Lindsay Rhodes, Ignacio Blanco, et al.
Human Molecular Genetics|June 27, 2020
Germline PTEN mutations are associated with a skewed peripheral immune repertoire in humans and miceRitika Jaini, Matthew G Loya, Alexander T King, et al.
The American Journal of Gastroenterology|June 24, 2003
GI polyposis and glycogenic acanthosis of the esophagus associated with PTEN mutation positive Cowden syndrome in the absence of cutaneous manifestationsThomas J McGarrity, Maria J Wagner Baker, Francesca M Ruggiero, et al.
NPJ Genomic Medicine|November 29, 2022
Brain single cell transcriptomic profiles in episodic memory phenotypes associated with temporal lobe epilepsyRobyn M Busch, Lamis Yehia, Bo Hu, et al.
Epilepsia Open|June 9, 2018
Preliminary report: Late seizure recurrence years after epilepsy surgery may be associated with alterations in brain tissue transcriptomeLara Jehi, Lamis Yehia, Charissa Peterson, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paragangliomaSarah R McWhinney, Robert T Pilarski, Shawnia R Forrester, et al.
Assessment|December 31, 2009
Autism spectrum disorders as a qualitatively distinct category from typical behavior in a large, clinically ascertained sampleThomas W Frazier, Eric A Youngstrom, Leslie Sinclair, et al.
The New England Journal of Medicine|September 28, 2007
Evidence of MEN-2 in the original description of classic pheochromocytomaHartmut P H Neumann, Alexander Vortmeyer, Dieter Schmidt, et al.
International Journal of Cancer|March 29, 2002
Prevalence of germline mutations of MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer families from SpainTrinidad Caldes, Javier Godino, Miguel de la Hoya, et al.
Autism : the International Journal of Research and Practice|October 10, 2013
Demographic and clinical correlates of autism symptom domains and autism spectrum diagnosisThomas W Frazier, Eric A Youngstrom, Rebecca Embacher, et al.
Pageof 56

Showing results (341-350 of 555) with videos related to

Sort By:
Pageof 56
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 27, 2016
Von Hippel-Lindau Disease: Genetics and Role of Genetic Counseling in a Multiple Neoplasia SyndromeSarah M Nielsen, Lindsay Rhodes, Ignacio Blanco, et al.
Human Molecular Genetics|June 27, 2020
Germline PTEN mutations are associated with a skewed peripheral immune repertoire in humans and miceRitika Jaini, Matthew G Loya, Alexander T King, et al.
The American Journal of Gastroenterology|June 24, 2003
GI polyposis and glycogenic acanthosis of the esophagus associated with PTEN mutation positive Cowden syndrome in the absence of cutaneous manifestationsThomas J McGarrity, Maria J Wagner Baker, Francesca M Ruggiero, et al.
NPJ Genomic Medicine|November 29, 2022
Brain single cell transcriptomic profiles in episodic memory phenotypes associated with temporal lobe epilepsyRobyn M Busch, Lamis Yehia, Bo Hu, et al.
Epilepsia Open|June 9, 2018
Preliminary report: Late seizure recurrence years after epilepsy surgery may be associated with alterations in brain tissue transcriptomeLara Jehi, Lamis Yehia, Charissa Peterson, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paragangliomaSarah R McWhinney, Robert T Pilarski, Shawnia R Forrester, et al.
Assessment|December 31, 2009
Autism spectrum disorders as a qualitatively distinct category from typical behavior in a large, clinically ascertained sampleThomas W Frazier, Eric A Youngstrom, Leslie Sinclair, et al.
The New England Journal of Medicine|September 28, 2007
Evidence of MEN-2 in the original description of classic pheochromocytomaHartmut P H Neumann, Alexander Vortmeyer, Dieter Schmidt, et al.
International Journal of Cancer|March 29, 2002
Prevalence of germline mutations of MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer families from SpainTrinidad Caldes, Javier Godino, Miguel de la Hoya, et al.
Autism : the International Journal of Research and Practice|October 10, 2013
Demographic and clinical correlates of autism symptom domains and autism spectrum diagnosisThomas W Frazier, Eric A Youngstrom, Rebecca Embacher, et al.
Pageof 56