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Molecular Endocrinology (Baltimore, Md.)|April 1, 1991
In vitro binding of the purified hormone-binding subunit of the estrogen receptor to oligonucleotides containing natural or modified sequences of an estrogen-responsive elementN Medici, V Nigro, C Abbondanza, et al.Biochemical and Biophysical Research Communications|April 30, 1985
Particulate nature of the unoccupied uterine estrogen receptorA M Molinari, N Medici, I Armetta, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1986
Estradiol receptor has proteolytic activity that is responsible for its own transformationG A Puca, C Abbondanza, V Nigro, et al.Human Molecular Genetics|August 1, 1996
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoproteinV Nigro, G Piluso, A Belsito, et al.Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|October 1, 1995
[The treatment of benign laryngeal pathologies using CO2 laser in direct microlaryngoscopy with propofol-induced endovenous anesthesia in spontaneous respiration without intubation]A Macarone Palmieri, S Motta, D Testa, et al.La Radiologia Medica|November 19, 2011
The role of imaging in the pre- and postoperative evaluation of posterior occipito-cervical fusionA Leone, A Costantini, M Visocchi, et al.Annals of the New York Academy of Sciences|January 1, 1986
Interaction between estrogen receptor and subcellular structures of target cells: nuclear localization of unoccupied receptor and its modification induced by estradiolG A Puca, N Medici, I Armetta, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 21, 1999
[Diffuse axonal lesions in childhood]A Chiaretti, M Visocchi, L Viola, et al.Acta Neurochirurgica. Supplement|December 28, 2023
Emergency Treatment of Cervical Vertebromedullary Trauma: 10 Years of Experience and Outcome EvaluationM C Meluzio, M I Borruto, A Perna, et al.Human Molecular Genetics|October 1, 1992
Detection of a nonsense mutation in the dystrophin gene by multiple SSCPV Nigro, L Politano, G Nigro, et al.Pageof 51