Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

L D Notarangelo

Showing results (141-150 of 165) with videos related to

Pageof 17
Sort By:
European Journal of Immunology|April 1, 1997
A novel 4-kb interleukin-13 receptor alpha mRNA expressed in human B, T, and endothelial cells encoding an alternate type-II interleukin-4/interleukin-13 receptorJ F Gauchat, E Schlagenhauf, N P Feng, et al.
Blood|February 3, 1998
Development of autologous, oligoclonal, poorly functioning T lymphocytes in a patient with autosomal recessive severe combined immunodeficiency caused by defects of the Jak3 tyrosine kinaseD Brugnoni, L D Notarangelo, A Sottini, et al.
Nature Genetics|July 11, 2000
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosisA Frattini, P J Orchard, C Sobacchi, et al.
Clinical and Experimental Immunology|June 8, 2012
Comparison of American and European practices in the management of patients with primary immunodeficienciesH S Hernandez-Trujillo, H Chapel, V Lo Re, et al.
Blood|May 11, 2018
Hypomorphic <i>Rag1</i> mutations alter the preimmune repertoire at early stages of lymphoid developmentL M Ott de Bruin, M Bosticardo, A Barbieri, et al.
Immunological Reviews|February 24, 2001
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a modelL D Notarangelo, S Giliani, C Mazza, et al.
Immunity|December 1, 1996
Signaling via IL-2 and IL-4 in JAK3-deficient severe combined immunodeficiency lymphocytes: JAK3-dependent and independent pathwaysS A Oakes, F Candotti, J A Johnston, et al.
Lancet (London, England)|November 30, 1996
In-utero transplantation of parental CD34 haematopoietic progenitor cells in a patient with X-linked severe combined immunodeficiency (SCIDXI)G S Wengler, A Lanfranchi, T Frusca, et al.
Transplantation Proceedings|September 29, 1999
Immune reconstitution after in utero bone marrow transplantation in a fetus with severe combined immunodeficiency with natural killer cellsJ Gil, F Porta, J Bartolomé, et al.
Genes and Immunity|January 9, 2015
A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferationN Clemente, E Boggio, C L Gigliotti, et al.
Pageof 17

Showing results (141-150 of 165) with videos related to

Sort By:
Pageof 17
European Journal of Immunology|April 1, 1997
A novel 4-kb interleukin-13 receptor alpha mRNA expressed in human B, T, and endothelial cells encoding an alternate type-II interleukin-4/interleukin-13 receptorJ F Gauchat, E Schlagenhauf, N P Feng, et al.
Blood|February 3, 1998
Development of autologous, oligoclonal, poorly functioning T lymphocytes in a patient with autosomal recessive severe combined immunodeficiency caused by defects of the Jak3 tyrosine kinaseD Brugnoni, L D Notarangelo, A Sottini, et al.
Nature Genetics|July 11, 2000
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosisA Frattini, P J Orchard, C Sobacchi, et al.
Clinical and Experimental Immunology|June 8, 2012
Comparison of American and European practices in the management of patients with primary immunodeficienciesH S Hernandez-Trujillo, H Chapel, V Lo Re, et al.
Blood|May 11, 2018
Hypomorphic <i>Rag1</i> mutations alter the preimmune repertoire at early stages of lymphoid developmentL M Ott de Bruin, M Bosticardo, A Barbieri, et al.
Immunological Reviews|February 24, 2001
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a modelL D Notarangelo, S Giliani, C Mazza, et al.
Immunity|December 1, 1996
Signaling via IL-2 and IL-4 in JAK3-deficient severe combined immunodeficiency lymphocytes: JAK3-dependent and independent pathwaysS A Oakes, F Candotti, J A Johnston, et al.
Lancet (London, England)|November 30, 1996
In-utero transplantation of parental CD34 haematopoietic progenitor cells in a patient with X-linked severe combined immunodeficiency (SCIDXI)G S Wengler, A Lanfranchi, T Frusca, et al.
Transplantation Proceedings|September 29, 1999
Immune reconstitution after in utero bone marrow transplantation in a fetus with severe combined immunodeficiency with natural killer cellsJ Gil, F Porta, J Bartolomé, et al.
Genes and Immunity|January 9, 2015
A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferationN Clemente, E Boggio, C L Gigliotti, et al.
Pageof 17