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Acta Neuropathologica|March 14, 2016
Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat dietAnna Rocchi, Carmelo Milioto, Sara Parodi, et al.Frontiers in Oncology|October 24, 2022
The ALLgorithMM: How to define the hemodilution of bone marrow samples in lymphoproliferative diseasesIlaria Vigliotta, Silvia Armuzzi, Martina Barone, et al.European Journal of Clinical Investigation|November 16, 2022
Early administration of tofacitinib in COVID-19 pneumonitis: An open randomised controlled trialAlessia Ferrarini, Angelo Vacca, Antonio Giovanni Solimando, et al.Experimental Hematology & Oncology|April 1, 2026
Dual targeting of GPX4 and TXNRD1 triggers eradication of AML cells through induction of apoptosis and ferroptosisCécile Favreau, Maxence Bourgoin, Coline Savy, et al.Autophagy|June 2, 2015
The PRKAA1/AMPKα1 pathway triggers autophagy during CSF1-induced human monocyte differentiation and is a potential target in CMMLSandrine Obba, Zoheir Hizir, Laurent Boyer, et al.Science Immunology|November 3, 2023
CSF1R-dependent macrophages in the salivary gland are essential for epithelial regeneration after radiation-induced injuryJohn G McKendrick, Gareth-Rhys Jones, Sonia S Elder, et al.Revista De Neurologia|February 12, 2020
[Argentinean consensus guidelines on the use of monoclonal antibodies in patients with migraine]E D Doctorovich, F Martín-Bertuzzi, M T Goicochea, et al.La Radiologia Medica|November 8, 2025
Impact of whole-brain radiation therapy on neurocognitive functions, alopecia and hearing loss: a systematic review and meta-analysis endorsed by the Palliative Care and Neuro-Oncology Study Groups of the Italian Association of Radiotherapy and Clinical Oncology (AIRO)Rossella Di Franco, Donato Pezzulla, Silvia Chiesa, et al.Science Translational Medicine|May 31, 2023
Constitutive IL-1RA production by modified immune cells protects against IL-1-mediated inflammatory disordersMariasilvia Colantuoni, Raisa Jofra Hernandez, Emanuela Pettinato, et al.Nature Genetics|February 15, 2001
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndromeL Crisponi, M Deiana, A Loi, et al.Pageof 232