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Polish Archives of Internal Medicine|August 23, 2022
Nephropathic cystinosis in Poland: a 40-year retrospective studyPrzemysław Sikora, Ryszard Grenda, Małgorzata Kowalczyk, et al.Journal of Inherited Metabolic Disease|February 14, 2025
C1GALT1C1-Associated Mosaic Disorder of Glycosylation in a FemaleRajindra P Aryal, Aditya Ramanujan, Camille Bucci, et al.The Journal of Experimental Medicine|June 6, 2000
Enhanced growth of primary tumors in cancer-prone mice after immunization against the mutant region of an inherited oncoproteinC T Siegel, K Schreiber, S C Meredith, et al.Pediatric Nephrology (Berlin, Germany)|April 2, 2017
Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutationsKathrin Ebner, Claudia Dafinger, Nadina Ortiz-Bruechle, et al.International Journal of Cardiology|March 27, 2012
Anabolic effects of exercise training in patients with advanced chronic heart failure (NYHA IIIb): impact on ubiquitin-protein ligases expression and skeletal muscle sizeRobert Höllriegel, Ephraim B Beck, Axel Linke, et al.Cold Spring Harbor Symposia on Quantitative Biology|April 20, 2011
Chromatin in the nuclear landscapeD B Beck, R Bonasio, S Kaneko, et al.The Journal of Experimental Medicine|August 8, 2001
Point mutation in essential genes with loss or mutation of the second allele: relevance to the retention of tumor-specific antigensG B Beck-Engeser, P A Monach, D Mumberg, et al.Autism in Adulthood : Challenges and Management|October 6, 2025
"The World's Really Not Set Up for the Neurodivergent Person": Understanding Emotion Dysregulation from the Perspective of Autistic AdultsKelly B Beck, Kristen T MacKenzie, Tanvi Kumar, et al.International Journal of Cardiology|June 12, 2012
Adiponectin promotes the migration of circulating angiogenic cells through p38-mediated induction of the CXCR4 receptorVolker Adams, John T Heiker, Robert Höllriegel, et al.Arthritis & Rheumatology (Hoboken, N.J.)|February 10, 2023
Novel Somatic UBA1 Variant in a Patient With VEXAS SyndromeBlanka Stiburkova, Katerina Pavelcova, Monika Belickova, et al.Pageof 61