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Journal of Medical Virology|October 20, 2012
Molecular study of human herpesvirus 6 and 8 involvement in coronary atherosclerosis and coronary instabilityMarco Magnoni, Mauro Malnati, Nicole Cristell, et al.
Cell Biology International Reports|November 6, 2012
Isolation and characterization of equine amnion mesenchymal stem cellsAlessandra Coli, Francesca Nocchi, Roberta Lamanna, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|October 15, 2013
Myeloid sarcoma with megakaryoblastic differentiation mimicking a sellar tumorMariangela Novello, Antonella Coli, Giuseppe Maria Della Pepa, et al.
European Journal of Endocrinology|December 2, 2015
Minichromosome maintenance protein 7 as prognostic marker of tumor aggressiveness in pituitary adenoma patientsAntonella Coli, Sylvia L Asa, Guido Fadda, et al.
Clinical Nuclear Medicine|January 29, 2019
Effect of Sentinel Node Biopsy in Clinically N0, BRAF V600E-Mutated, Small Papillary Thyroid Carcinoma: A Pilot StudyMarco Puccini, Gianpiero Manca, Carlo Maria Neri, et al.
The Quarterly Journal of Nuclear Medicine : Official Publication of the Italian Association of Nuclear Medicine (AIMN) [And] the International Association of Radiopharmacology (IAR)|December 1, 1995
How alternative are immunoassay systems employing non-radioisotopic labels? A comparative appraisal of their main analytical characteristicsD Pelizzola, E Bombardieri, A Brocchi, et al.
Future Science OA|June 11, 2025
Amniotic fluid MSCs for scaffold-free cartilage repair: spheroid fusion and chondrogenic microtissue developmentCarolina Coli Zuliani, Jéssica Bruna da Cunha, Victor Marchiori de Souza, et al.
Acta Histochemica|November 1, 2011
Glucagon-like peptide 1 (GLP-1) in the gastrointestinal tract of the pheasant (Phasianus colchicus)Andrea Pirone, Bao An Ding, Elisabetta Giannessi, et al.
Iscience|July 28, 2026
Optogenetics meets automated patch clampReetta Penttinen, Ariel Coli, Florian Hintermaier, et al.
American Journal of Human Genetics|February 17, 2001
Familial dysautonomia is caused by mutations of the IKAP geneS L Anderson, R Coli, I W Daly, et al.
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