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Journal of Agricultural and Food Chemistry|September 14, 2010
Food texture: pleasure and painGail Vance Civille
Physiology & Behavior|May 5, 2012
Sensory evaluation techniques - make "good for you" taste "good"Gail Vance Civille, Katherine Nolen Oftedal
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 1, 2004
Secondary leukemias in refractory germ cell tumor patients undergoing autologous stem-cell transplantation using high-dose etoposideWilliam Houck, Rafat Abonour, Gail Vance, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 2002
The embryonic stem cell transcription factors Oct-4 and FoxD3 interact to regulate endodermal-specific promoter expressionYing Guo, Robert Costa, Heather Ramsey, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|October 18, 2016
Prevalence of maternal cell contamination in amniotic fluid samplesJennifer Weida, Avinash S Patil, Frank P Schubert, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 24, 2013
Prognostic and predictive value of tumor vascular endothelial growth factor gene amplification in metastatic breast cancer treated with paclitaxel with and without bevacizumab; results from ECOG 2100 trialBryan P Schneider, Robert J Gray, Milan Radovich, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 4, 2015
Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199Bryan P Schneider, Lang Li, Milan Radovich, et al.
The New England Journal of Medicine|March 16, 2012
Prognostic relevance of integrated genetic profiling in acute myeloid leukemiaJay P Patel, Mithat Gönen, Maria E Figueroa, et al.
HGG Advances|April 8, 2025
Multiple molecular diagnoses identified through genome sequencing in individuals with suspected rare diseaseAlka Malhotra, Erin Thorpe, Alison J Coffey, et al.
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