Showing results (71-80 of 112) with videos related to

Sort By:
Pageof 12
Journal of Immunology (Baltimore, Md. : 1950)|May 21, 2009
Myosin IIA associates with NK cell lytic granules to enable their interaction with F-actin and function at the immunological synapseKeri B Sanborn, Gregory D Rak, Saumya Y Maru, et al.
Cold Spring Harbor Molecular Case Studies|October 17, 2023
Deep molecular tracking over the 12-yr development of endometrial cancer from hyperplasia in a single patientKatherine Reid, Olga Camacho-Vanegas, Deep Pandya, et al.
Hepatology (Baltimore, Md.)|October 16, 2004
Frequent inactivation of the tumor suppressor Kruppel-like factor 6 (KLF6) in hepatocellular carcinomaSigal Kremer-Tal, Helen L Reeves, Goutham Narla, et al.
Journal of Ovarian Research|January 26, 2012
Application of RNA-Seq transcriptome analysis: CD151 is an Invasion/Migration target in all stages of epithelial ovarian cancerRebecca A Mosig, Li Lin, Emir Senturk, et al.
The Journal of Biological Chemistry|September 2, 2000
The neuropeptide processing enzyme EC 3.4.24.15 is modulated by protein kinase A phosphorylationJ W Tullai, P M Cummins, A Pabon, et al.
Cold Spring Harbor Molecular Case Studies|October 20, 2019
Rapid development and use of patient-specific ctDNA biomarkers to avoid a "rash decision" in an ovarian cancer patientDeep Pandya, Sandra Catalina Camacho, Maria M Padron, et al.
Cancer Research|July 5, 2005
Targeted inhibition of the KLF6 splice variant, KLF6 SV1, suppresses prostate cancer cell growth and spreadGoutham Narla, Analisa DiFeo, Shen Yao, et al.
EMBO Molecular Medicine|February 18, 2011
Hyaline fibromatosis syndrome inducing mutations in the ectodomain of anthrax toxin receptor 2 can be rescued by proteasome inhibitorsJulie Deuquet, Ekkehart Lausch, Nicolas Guex, et al.
Digestive Diseases and Sciences|June 22, 2010
Loss of matrix metalloproteinase-2 amplifies murine toxin-induced liver fibrosis by upregulating collagen I expressionBrian D Radbill, Ritu Gupta, Maria Celeste M Ramirez, et al.
Pediatrics|October 18, 2006
Systemic hyalinosis: a distinctive early childhood-onset disorder characterized by mutations in the anthrax toxin receptor 2 gene (ANTRX2)Joseph T C Shieh, Petra Swidler, John A Martignetti, et al.
Pageof 12