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Nature|August 3, 2022
A non-canonical vitamin K cycle is a potent ferroptosis suppressorEikan Mishima, Junya Ito, Zijun Wu, et al.Scandinavian Journal of Work, Environment & Health|March 17, 2006
Residential radon and lung cancer--detailed results of a collaborative analysis of individual data on 7148 persons with lung cancer and 14,208 persons without lung cancer from 13 epidemiologic studies in EuropeSarah Darby, David Hill, Harz Deo, et al.Molecular and Cellular Endocrinology|November 1, 2011
Molecular bases of endometrial cancer: new roles for new actors in the diagnosis and the therapy of the diseaseMarta Llauradó, Anna Ruiz, Blanca Majem, et al.BMJ (Clinical Research Ed.)|December 23, 2004
Radon in homes and risk of lung cancer: collaborative analysis of individual data from 13 European case-control studiesS Darby, D Hill, A Auvinen, et al.The Journal of Investigative Dermatology|March 8, 2023
Gene Expression-Based Molecular Test as Diagnostic Aid for the Differential Diagnosis of Psoriasis and Eczema in Formalin-Fixed and Paraffin-Embedded Tissue, Microbiopsies, and Tape StripsFelix Fischer, Anais Doll, Deniz Uereyener, et al.Journal of Medicinal Chemistry|July 20, 1999
Identification of pharmacokinetically stable 3, 10-dibromo-8-chlorobenzocycloheptapyridine farnesyl protein transferase inhibitors with potent enzyme and cellular activitiesA G Taveras, J Deskus, J Chao, et al.Cancer Research|November 11, 1998
Antitumor activity of SCH 66336, an orally bioavailable tricyclic inhibitor of farnesyl protein transferase, in human tumor xenograft models and wap-ras transgenic miceM Liu, M S Bryant, J Chen, et al.ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of a Potent, Injectable Inhibitor of Aurora Kinases Based on the Imidazo-[1,2-a]-Pyrazine CoreTao Yu, Jayaram R Tagat, Angela D Kerekes, et al.Blood|December 6, 2024
A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutationsNatalia Borbaran Bravo, Ekaterina Deordieva, Larissa Doll, et al.Human Genetics|June 20, 2021
Unraveling the genetic complexities of combined retinal dystrophy and hearing impairmentPaulina Bahena, Narsis Daftarian, Reza Maroofian, et al.Pageof 273