نتائج البحث - Angelo Molinaro
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1
A mouse model for creatine transporter deficiency reveals early onset cognitive impairment and neuropathology associated with brain aging حسب Laura Baroncelli, Angelo Molinaro, Francesco Cacciante, M. Alessandri, Debora Napoli, Elena Putignano, Jonida Tola, Vincenzo Leuzzi, Giovanni Cioni, Tommaso Pizzorusso
منشور في 2016Artigo -
2
MicroRNA expression profile helps to distinguish benign nodules from papillary thyroid carcinomas starting from cells of fine-needle aspiration حسب Patrizia Agretti, Eleonora Ferrarini, Teresa Rago, Antonio Candelieri, Giuseppina De Marco, Antonio Dimida, Filippo Niccolai, Angelo Molinaro, G. Di Coscio, Aldo Pinchera, Paolo Vitti, Massimo Tonacchera
منشور في 2012Artigo -
3
Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (spor... حسب Rieko Takatani, Masanori Minagawa, Angelo Molinaro, Monica Reyes, Kaori Kinoshita, Tomozumi Takatani, Itsuro Kazukawa, Misako Nagatsuma, Kenichi Kashimada, Kenichi Sato, Kazuyuki Matsushita, Fumio Nomura, Naoki Shimojo, Harald Jüppner
منشور في 2015Artigo -
4
Identification and Functional Analysis of Novel Dual Oxidase 2 (DUOX2) Mutations in Children with Congenital or Subclinical Hypothyroidism حسب Giuseppina De Marco, Patrizia Agretti, Lucia Montanelli, Caterina Di Cosmo, Brunella Bagattini, Melissa De Servi, Eleonora Ferrarini, Antonio Dimida, Andrea Cláudia Freitas Ferreira, Angelo Molinaro, Claudia Ceccarelli, Federica Brozzi, Aldo Pinchera, Paolo Vitti, Massimo Tonacchera
منشور في 2011Artigo -
5
Chondroitin 6-sulphate is required for neuroplasticity and memory in ageing حسب Sujeong Yang, Sylvain Gigout, Angelo Molinaro, Yuko Naito‐Matsui, Sam Hilton, Simona Foscarin, Bart Nieuwenhuis, Chin Lik Tan, Joost Verhaagen, Tommaso Pizzorusso, Lisa M. Saksida, Timothy M. Bussey, Hiroshi Kitagawa, Jessica C. F. Kwok, James W. Fawcett
منشور في 2021Artigo -
6
iPSC-derived neurons profiling reveals GABAergic circuit disruption and acetylated α-tubulin defect which improves after iHDAC6 treatment in Rett syndrome حسب Elisa Landucci, Margherita Brindisi, Laura Bianciardi, Lorenza M. Catania, Sergio Daga, Susanna Croci, Elisa Frullanti, Chiara Fallerini, Stefania Butini, Simone Brogi, Simone Furini, Riccardo Melani, Angelo Molinaro, Flaminia Clelia Lorenzetti, Valentina Imperatore, Sonia Amabile, Jessica Mariani, Francesca Mari, Francesca Ariani, Tommaso Pizzorusso, Anna Maria Pinto, Flora M. Vaccarino, Alessandra Renieri, Giuseppe Campiani, Ilaria Meloni
منشور في 2018Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Internal medicine
Medicine
Gene
Genetics
Neuroscience
Biochemistry
Endocrinology
Thyroid
Ageing
Biopsy
Botany
Calcium
Cell biology
Chondroitin
Chondroitin sulphate
Chromosome
Chromosome 20
Cognition
Cognitive decline
Congenital hypothyroidism
Cytology
DNA methylation
Dementia
Differentially methylated regions
Disease
Dual (grammatical number)
Embryonic stem cell
Epilepsy
Exon