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Nature|March 5, 2013
Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALSHong Joo Kim, Nam Chul Kim, Yong-Dong Wang, et al.
Current Biology : CB|March 24, 2009
Recent region-wide declines in Caribbean reef fish abundanceMichelle J Paddack, John D Reynolds, Consuelo Aguilar, et al.
Journal of Personalized Medicine|November 27, 2021
Association between Genetic Variants and Cisplatin-Induced Nephrotoxicity: A Genome-Wide Approach and Validation StudyZulfan Zazuli, Corine de Jong, Wei Xu, et al.
Pediatric Blood & Cancer|March 27, 2026
Novel Genetic Risk Factor Identified for L-Asparaginase-Induced Pancreatitis in Pediatric Patients With CancerEdward J Raack, Wan-Chun Chang, Miguel Cordova-Delgado, et al.
Elife|April 26, 2016
Determination of ubiquitin fitness landscapes under different chemical stresses in a classroom settingDavid Mavor, Kyle Barlow, Samuel Thompson, et al.
Orphanet Journal of Rare Diseases|September 25, 2012
Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia?Marie Morimoto, Zhongxin Yu, Peter Stenzel, et al.
The Journal of Experimental Medicine|July 31, 2025
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphomaMaggie P Fu, Mehul Sharma, Pariya Yousefi, et al.
American Journal of Respiratory and Critical Care Medicine|January 26, 2016
Association between Functional Small Airway Disease and FEV1 Decline in Chronic Obstructive Pulmonary DiseaseSurya P Bhatt, Xavier Soler, Xin Wang, et al.
Cell Reports. Medicine|May 7, 2025
Genetic biomarker study of sunvozertinib for clinical prognosis and prediction in NSCLC with EGFR exon 20 insertion mutationYan Xu, James Chih-Hsin Yang, Yanqiu Zhao, et al.
Neurology|December 31, 2017
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patientsMark McCormack, Hongsheng Gui, Andrés Ingason, et al.
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