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Gynecologic Oncology|March 7, 2024
Mutations in cancer-relevant genes are ubiquitous in histologically normal endometrial tissueDeep Pandya, Shannon Tomita, Maria Padron Rhenals, et al.Human Molecular Genetics|April 3, 2007
Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast growthRebecca A Mosig, Oonagh Dowling, Analisa DiFeo, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|June 13, 2018
Palbociclib as single agent or in combination with the endocrine therapy received before disease progression for estrogen receptor-positive, HER2-negative metastatic breast cancer: TREnd trialL Malorni, G Curigliano, A M Minisini, et al.Tumori|January 1, 1997
[Evaluation of quality of life in oncology. Rationale and objectives of the first phase of the Quality of Life in Oncology project]M Costantini, E Mencaglia, P Di Giulio, et al.Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|September 13, 2000
Cancer patients as 'experts' in defining quality of life domains. A multicentre survey by the Italian Group for the Evaluation of Outcomes in Oncology (IGEO)M Costantini, E Mencaglia, P D Giulio, et al.American Journal of Human Genetics|November 26, 2013
Morbid obesity resulting from inactivation of the ciliary protein CEP19 in humans and miceAdel Shalata, Maria C Ramirez, Robert J Desnick, et al.Nature Genetics|September 6, 2000
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome ConsortiumM Seri, R Cusano, S Gangarossa, et al.Gastroenterology|October 22, 2008
Pivotal role of mTOR signaling in hepatocellular carcinomaAugusto Villanueva, Derek Y Chiang, Pippa Newell, et al.Cancer Research|March 1, 2005
A germline DNA polymorphism enhances alternative splicing of the KLF6 tumor suppressor gene and is associated with increased prostate cancer riskGoutham Narla, Analisa Difeo, Helen L Reeves, et al.American Journal of Human Genetics|June 5, 2013
Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosisJohn A Martignetti, Lifeng Tian, Dong Li, et al.Pageof 12