Showing results (361-370 of 588) with videos related to

Sort By:
Pageof 59
Brain Communications|October 26, 2023
Molecular subtypes of epilepsy associated with post-surgical seizure recurrenceCourtney E Hershberger, Shreya Louis, Robyn M Busch, et al.
The Journal of Biological Chemistry|February 20, 2003
Peroxisome proliferator-activated receptor gamma-mediated differentiation: a mutation in colon cancer cells reveals divergent and cell type-specific mechanismsRajnish A Gupta, Pasha Sarraf, Elisabetta Mueller, et al.
Clinical and Translational Science|July 28, 2017
Patient Decisions to Receive Secondary Pharmacogenomic Findings and Development of a Multidisciplinary Practice Model to Integrate Results Into Patient CareJ Kevin Hicks, Amy Shealy, Allison Schreiber, et al.
The American Journal of Pathology|August 7, 2002
PTEN mutational spectra, expression levels, and subcellular localization in microsatellite stable and unstable colorectal cancersXiao-Ping Zhou, Anu Loukola, Reijo Salovaara, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|November 6, 2018
Development and Validation of Objective and Quantitative Eye Tracking-Based Measures of Autism Risk and Symptom LevelsThomas W Frazier, Eric W Klingemier, Sumit Parikh, et al.
Oncogene|January 16, 2004
PTEN mutations are common in sporadic microsatellite stable colorectal cancerNajah T Nassif, Glenn P Lobo, Xiaojuan Wu, et al.
Annual Review of Genomics and Human Genetics|August 31, 2022
Mosaicism in Tumor Suppressor Gene Syndromes: Prevalence, Diagnostic Strategies, and Transmission RiskJillian L Chen, David T Miller, Laura S Schmidt, et al.
BMC Medicine|July 16, 2020
New insights into genetic susceptibility of COVID-19: an ACE2 and TMPRSS2 polymorphism analysisYuan Hou, Junfei Zhao, William Martin, et al.
Nature Reviews. Endocrinology|November 27, 2025
An update on hypophysitisLea Miquel, Benoit Testud, Frederique Albarel, et al.
European Journal of Human Genetics : EJHG|September 29, 2018
Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiencyNicolas Jullien, Pauline Romanet, Mélanie Philippon, et al.
Pageof 59