Showing results (81-90 of 169) with videos related to

Sort By:
Pageof 17
Blood|June 23, 2012
Anti-CD3ε mAb improves thymic architecture and prevents autoimmune manifestations in a mouse model of Omenn syndrome: therapeutic implicationsVeronica Marrella, Pietro L Poliani, Elena Fontana, et al.
The Journal of Allergy and Clinical Immunology|September 20, 2024
European Society for Immunodeficiencies guidelines for the management of patients with congenital athymiaAlexandra Y Kreins, Fatima Dhalla, Aisling M Flinn, et al.
The Journal of Clinical Investigation|September 15, 2015
Lentiviral-mediated gene therapy restores B cell tolerance in Wiskott-Aldrich syndrome patientsFrancesca Pala, Henner Morbach, Maria Carmina Castiello, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 11, 2016
Therapeutic Potential of Immunoproteasome Inhibition in Duchenne Muscular DystrophyAndrea Farini, Clementina Sitzia, Barbara Cassani, et al.
Bone|November 26, 2013
Exome sequencing identifies CTSK mutations in patients originally diagnosed as intermediate osteopetrosisAlessandra Pangrazio, Alessandro Puddu, Manuela Oppo, et al.
Bone|August 3, 2013
Lentiviral gene transfer of TCIRG1 into peripheral blood CD34(+) cells restores osteoclast function in infantile malignant osteopetrosisIlana Moscatelli, Christian Schneider Thudium, Carmen Flores, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 4, 2006
Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvementAlessandra Pangrazio, Pietro Luigi Poliani, André Megarbane, et al.
The Journal of Experimental Medicine|February 14, 2007
WASP regulates suppressor activity of human and murine CD4(+)CD25(+)FOXP3(+) natural regulatory T cellsFrancesco Marangoni, Sara Trifari, Samantha Scaramuzza, et al.
Oncotarget|October 21, 2015
Chromosome transplantation as a novel approach for correcting complex genomic disordersMarianna Paulis, Alessandra Castelli, Lucia Susani, et al.
Bone|June 22, 2018
Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1Eleonora Palagano, Giulia Zuccarini, Paolo Prontera, et al.
Pageof 17