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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 15, 2013
The alternative lengthening of telomere phenotype is significantly associated with loss of ATRX expression in high-grade pediatric and adult astrocytomas: a multi-institutional study of 214 astrocytomasMalak Abedalthagafi, Joanna J Phillips, Grace E Kim, et al.
Archives of Biochemistry and Biophysics|March 23, 2016
Mechanistic insights into the first Lygus-active β-pore forming proteinAgoston Jerga, Danqi Chen, Chunfen Zhang, et al.
American Journal of Human Genetics|May 10, 2011
Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairmentMargit Schraders, Stefan A Haas, Nicole J D Weegerink, et al.
Cell Reports|April 21, 2021
Airway basal stem cells generate distinct subpopulations of PNECsHongmei Mou, Ying Yang, Molly A Riehs, et al.
Journal of Pediatric Hematology/Oncology|December 10, 2019
Germline MUTYH Mutation in a Pediatric Cancer Survivor Developing a Secondary MalignancyVincent Lavergne, Amit Sabnis, Asmin Tupule, et al.
Molecular Cell|January 31, 2017
Phosphorylation-Dependent Feedback Inhibition of RIG-I by DAPK1 Identified by Kinome-wide siRNA ScreeningJoschka Willemsen, Oliver Wicht, Julia C Wolanski, et al.
Advanced Genetics (Hoboken, N.J.)|March 13, 2023
Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of AgeCatherine A Brownstein, Elise Douard, Robin L Haynes, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 21, 2019
Phase I Clinical Trial of the Wee1 Inhibitor Adavosertib (AZD1775) with Irinotecan in Children with Relapsed Solid Tumors: A COG Phase I Consortium Report (ADVL1312)Kristina A Cole, Sharmistha Pal, Rachel A Kudgus, et al.
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