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Blood|December 16, 2006
Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)Takashi Akasaka, Theodore Balasas, Lisa J Russell, et al.British Journal of Pharmacology|November 11, 2025
Transcriptional and functional effects of mavacamten in multiple porcine and human models with hypertrophic cardiomyopathyElisa Kiselev, Wilson Agyapong, Bjarne Jürgens, et al.Neuro-Oncology|October 6, 2025
Intracranial metastases from solid tumors: Call to Action and Consensus from the Society for Neuro-Oncology and American Society of Clinical Oncology CollaborativeAkanksha Sharma, Lucy Boyce Kennedy, Amanda E D Van Swearingen, et al.Physical Review Letters|October 5, 2025
Search for Millicharged Particles in Proton-Proton Collisions at sqrt[s]=13.6 TeVS Alcott, Z Bhatti, J Brooke, et al.Human Molecular Genetics|October 8, 2015
Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problemsRaman Kumar, Mark A Corbett, Bregje W M Van Bon, et al.Brain : a Journal of Neurology|October 21, 2017
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic featuresCristina Elena Niturad, Dorit Lev, Vera M Kalscheuer, et al.European Heart Journal|October 24, 2023
Outcomes of transcatheter pulmonary SAPIEN 3 valve implantation: an international registrySebastien Hascoët, James R Bentham, Luca Giugno, et al.Cell Host & Microbe|March 4, 2026
Microbial metabolism of food allergens determines the severity of IgE-mediated anaphylaxisElisa Sánchez-Martínez, Liam E Rondeau, Manuel Garrido-Romero, et al.American Journal of Human Genetics|December 1, 2014
Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathologyGabrielle R Wilson, Joe C H Sim, Catriona McLean, et al.Pageof 184