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International Journal of Molecular Sciences|October 28, 2023
The Significance of Microenvironmental and Circulating Lactate in Breast CancerVincenza Frisardi, Simone Canovi, Salvatore Vaccaro, et al.
American Journal of Hypertension|April 29, 2011
A clinical phenotype mimicking essential hypertension in a newly discovered family with Liddle's syndromeErmanno Rossi, Enrico Farnetti, Davide Nicoli, et al.
Arthritis and Rheumatism|October 2, 2007
PlA1/A2 polymorphism of the platelet glycoprotein receptor IIIA and risk of cranial ischemic complications in giant cell arteritisCarlo Salvarani, Bruno Casali, Enrico Farnetti, et al.
Biochimica Et Biophysica Acta. Reviews on Cancer|October 4, 2022
Spartin: At the crossroad between ubiquitination and metabolism in cancerVincenza Ylenia Cusenza, Elena Bonora, Nicola Amodio, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|April 23, 2015
Polymorphisms in cyclooxygenase-2 gene in endometrial cancer patientsFederica Torricelli, Vincenzo Dario Mandato, Enrico Farnetti, et al.
BMC Cancer|April 18, 2015
HNF1B polymorphism influences the prognosis of endometrial cancer patients: a cohort studyVincenzo Dario Mandato, Enrico Farnetti, Federica Torricelli, et al.
Fetal and Pediatric Pathology|April 24, 2025
Thoracic Giant Venous Malformation in a Stillbirth with Pik3ca Somatic MutationNunzio Cosimo Mario Salfi, Sabrina Gismondi, Anna Martinelli, et al.
International Reviews of Immunology|July 5, 2006
Ex vivo programming of antigen-presenting B lymphocytes: considerations on DNA uptake and cell activationMatthew Wheeler, Xotchil Cortez-Gonzalez, Raffaele Frazzi, et al.
Frontiers in Oncology|March 27, 2023
The lncRNA epigenetics: The significance of m6A and m5C lncRNA modifications in cancerVincenza Ylenia Cusenza, Annalisa Tameni, Antonino Neri, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|December 19, 2022
Mother-newborn ABO group discrepancy caused by a rare BW.17 variantChiara Marraccini, Barbara Iotti, Petronilla Vanzanelli, et al.
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