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Genomics|August 1, 1991
Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysisE R Maher, E Bentley, J R Yates, et al.JAMA Cardiology|September 16, 2020
Risk of QT Interval Prolongation Associated With Use of Hydroxychloroquine With or Without Concomitant Azithromycin Among Hospitalized Patients Testing Positive for Coronavirus Disease 2019 (COVID-19)Nicholas J Mercuro, Christina F Yen, David J Shim, et al.JAMA|May 10, 2012
Probiotics for the prevention and treatment of antibiotic-associated diarrhea: a systematic review and meta-analysisSusanne Hempel, Sydne J Newberry, Alicia R Maher, et al.Epigenetics|March 21, 2012
KIBRA gene methylation is associated with unfavorable biological prognostic parameters in chronic lymphocytic leukemiaThoraia Shinawi, Victoria Hill, Antonis Dagklis, et al.Arthritis and Rheumatism|July 27, 2012
Mechanisms of bone fragility in a mouse model of glucocorticoid-treated rheumatoid arthritis: implications for insufficiency fracture riskMasahiko Takahata, Jason R Maher, Subhash C Juneja, et al.Journal of the American Chemical Society|October 28, 2010
Linear 6,6'-biazulenyl framework featuring isocyanide termini: synthesis, structure, redox behavior, complexation, and self-assembly on Au(111)Tiffany R Maher, Andrew D Spaeth, Brad M Neal, et al.Familial Cancer|July 12, 2014
Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatmentFred H Menko, Eamonn R Maher, Laura S Schmidt, et al.American Journal of Human Genetics|April 1, 1997
Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumorsA H Prowse, A R Webster, F M Richards, et al.The Turkish Journal of Pediatrics|June 2, 2009
Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 geneHakan Cangül, Ozlem Ozdemir, Tahsin Yakut, et al.Journal of Medical Genetics|May 1, 1997
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndromeD Catchpoole, W W Lam, D Valler, et al.Pageof 63