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U Ramenghi

Showing results (31-40 of 51) with videos related to

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Blood|November 1, 1991
In vitro growth and regulation of bone marrow enriched CD34+ hematopoietic progenitors in Diamond-Blackfan anemiaG P Bagnara, G Zauli, L Vitale, et al.
Nature Genetics|April 1, 1995
X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP geneA Villa, L Notarangelo, P Macchi, et al.
Stem Cells (Dayton, Ohio)|July 1, 1993
Production of interleukin 6, leukemia inhibitory factor and granulocyte-macrophage colony stimulating factor by peripheral blood mononuclear cells in Fanconi's anemiaG P Bagnara, L Bonsi, P Strippoli, et al.
Blood|July 15, 1992
Effect of stem cell factor on colony growth from acquired and constitutional (Fanconi) aplastic anemiaG P Bagnara, P Strippoli, L Bonsi, et al.
Human Genetics|January 1, 1997
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A geneA Savoia, M R Piemontese, M Savino, et al.
Experimental Hematology|November 14, 1997
Diamond-Blackfan anemia: expansion of erythroid progenitors in vitro by IL-9, but exclusion of a significant pathogenetic role for the IL-9 gene and the hematopoietic gene cluster on chromosome 5qI Dianzani, E Garelli, N Crescenzio, et al.
Blood|March 15, 1996
Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemiaI Dianzani, E Garelli, C Dompè, et al.
Blood Cells, Molecules & Diseases|December 9, 2000
Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian populationU Ramenghi, M F Campagnoli, E Garelli, et al.
Blood|May 16, 2000
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancerU Ramenghi, S Bonissoni, G Migliaretti, et al.
Diabetes|March 15, 2001
Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseasesS DeFranco, S Bonissoni, F Cerutti, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Blood|November 1, 1991
In vitro growth and regulation of bone marrow enriched CD34+ hematopoietic progenitors in Diamond-Blackfan anemiaG P Bagnara, G Zauli, L Vitale, et al.
Nature Genetics|April 1, 1995
X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP geneA Villa, L Notarangelo, P Macchi, et al.
Stem Cells (Dayton, Ohio)|July 1, 1993
Production of interleukin 6, leukemia inhibitory factor and granulocyte-macrophage colony stimulating factor by peripheral blood mononuclear cells in Fanconi's anemiaG P Bagnara, L Bonsi, P Strippoli, et al.
Blood|July 15, 1992
Effect of stem cell factor on colony growth from acquired and constitutional (Fanconi) aplastic anemiaG P Bagnara, P Strippoli, L Bonsi, et al.
Human Genetics|January 1, 1997
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A geneA Savoia, M R Piemontese, M Savino, et al.
Experimental Hematology|November 14, 1997
Diamond-Blackfan anemia: expansion of erythroid progenitors in vitro by IL-9, but exclusion of a significant pathogenetic role for the IL-9 gene and the hematopoietic gene cluster on chromosome 5qI Dianzani, E Garelli, N Crescenzio, et al.
Blood|March 15, 1996
Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemiaI Dianzani, E Garelli, C Dompè, et al.
Blood Cells, Molecules & Diseases|December 9, 2000
Diamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian populationU Ramenghi, M F Campagnoli, E Garelli, et al.
Blood|May 16, 2000
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancerU Ramenghi, S Bonissoni, G Migliaretti, et al.
Diabetes|March 15, 2001
Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseasesS DeFranco, S Bonissoni, F Cerutti, et al.
Pageof 6