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Fabio Candotti

Showing results (61-70 of 143) with videos related to

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Cell Transplantation|September 8, 2017
Expansion of Hepatic and Hematopoietic Stem Cells Utilizing Mouse Embryonic Liver ExplantsSatdarshan P S Monga, Yi Tang, Fabio Candotti, et al.
Blood|August 1, 2002
Reconstitution of lymphoid development and function in ZAP-70-deficient mice following gene transfer into bone marrow cellsMakoto Otsu, Marcos Steinberg, Christophe Ferrand, et al.
Orphanet Journal of Rare Diseases|December 20, 2015
Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiencyHirsh D Komarow, Robert Sokolic, Michael S Hershfield, et al.
Human Gene Therapy|February 28, 2002
Flow cytometry analysis of adenosine deaminase (ADA) expression: a simple and reliable tool for the assessment of ADA-deficient patients before and after gene therapyMakoto Otsu, Michael S Hershfield, Laura M Tuschong, et al.
Molecular Genetics and Metabolism|December 4, 2014
In vitro functional correction of Hermansky-Pudlak Syndrome type-1 by lentiviral-mediated gene transferYasuhiro Ikawa, Richard Hess, Heidi Dorward, et al.
Current Opinion in Allergy and Clinical Immunology|January 31, 2004
Cytokines and their role in lymphoid development, differentiation and homeostasisSigrun R Hofmann, Rachel Ettinger, Yong-Jie Zhou, et al.
Disease Models & Mechanisms|November 16, 2019
A model for reticular dysgenesis shows impaired sensory organ development and hair cell regeneration linked to cellular stressAlberto Rissone, Erin Jimenez, Kevin Bishop, et al.
Science Translational Medicine|June 25, 2010
Nuclear role of WASp in the pathogenesis of dysregulated TH1 immunity in human Wiskott-Aldrich syndromeMatthew D Taylor, Sanjoy Sadhukhan, Ponnappa Kottangada, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 4, 2006
Functional interaction of common gamma-chain and growth hormone receptor signaling apparatusMarsilio Adriani, Corrado Garbi, Giada Amodio, et al.
The Journal of Clinical Investigation|May 3, 2003
Second-site mutation in the Wiskott-Aldrich syndrome (WAS) protein gene causes somatic mosaicism in two WAS siblingsTaizo Wada, Akihiro Konno, Shepherd H Schurman, et al.
Pageof 15

Showing results (61-70 of 143) with videos related to

Sort By:
Pageof 15
Cell Transplantation|September 8, 2017
Expansion of Hepatic and Hematopoietic Stem Cells Utilizing Mouse Embryonic Liver ExplantsSatdarshan P S Monga, Yi Tang, Fabio Candotti, et al.
Blood|August 1, 2002
Reconstitution of lymphoid development and function in ZAP-70-deficient mice following gene transfer into bone marrow cellsMakoto Otsu, Marcos Steinberg, Christophe Ferrand, et al.
Orphanet Journal of Rare Diseases|December 20, 2015
Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiencyHirsh D Komarow, Robert Sokolic, Michael S Hershfield, et al.
Human Gene Therapy|February 28, 2002
Flow cytometry analysis of adenosine deaminase (ADA) expression: a simple and reliable tool for the assessment of ADA-deficient patients before and after gene therapyMakoto Otsu, Michael S Hershfield, Laura M Tuschong, et al.
Molecular Genetics and Metabolism|December 4, 2014
In vitro functional correction of Hermansky-Pudlak Syndrome type-1 by lentiviral-mediated gene transferYasuhiro Ikawa, Richard Hess, Heidi Dorward, et al.
Current Opinion in Allergy and Clinical Immunology|January 31, 2004
Cytokines and their role in lymphoid development, differentiation and homeostasisSigrun R Hofmann, Rachel Ettinger, Yong-Jie Zhou, et al.
Disease Models & Mechanisms|November 16, 2019
A model for reticular dysgenesis shows impaired sensory organ development and hair cell regeneration linked to cellular stressAlberto Rissone, Erin Jimenez, Kevin Bishop, et al.
Science Translational Medicine|June 25, 2010
Nuclear role of WASp in the pathogenesis of dysregulated TH1 immunity in human Wiskott-Aldrich syndromeMatthew D Taylor, Sanjoy Sadhukhan, Ponnappa Kottangada, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 4, 2006
Functional interaction of common gamma-chain and growth hormone receptor signaling apparatusMarsilio Adriani, Corrado Garbi, Giada Amodio, et al.
The Journal of Clinical Investigation|May 3, 2003
Second-site mutation in the Wiskott-Aldrich syndrome (WAS) protein gene causes somatic mosaicism in two WAS siblingsTaizo Wada, Akihiro Konno, Shepherd H Schurman, et al.
Pageof 15