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L D Notarangelo

Showing results (91-100 of 165) with videos related to

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American Journal of Human Genetics|January 1, 1992
Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivationE Maestrini, S Rivella, C Tribioli, et al.
Human Mutation|October 23, 2001
Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiencyL D Notarangelo, P Mella, A Jones, et al.
European Journal of Pediatrics|October 1, 1992
Carrier detection in X-linked adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysisL D Notarangelo, O Parolini, G Baiguini, et al.
Bone Marrow Transplantation|January 1, 1991
Use of the highly polymorphic DNA marker CRI-S232 for monitoring of engraftment and chimerism following bone marrow transplantationL D Notarangelo, O Parolini, F Porta, et al.
The Journal of Pathology|August 26, 1998
Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndromeF Facchetti, L Blanzuoli, W Vermi, et al.
Annals of the Rheumatic Diseases|May 1, 1986
IgG subclass serum levels in juvenile chronic arthritisA Martini, A Plebani, A Ravelli, et al.
Lancet (London, England)|August 28, 1993
Absence of xid mutation in X-linked agammaglobulinaemiaI Vorechovsky, J N Zhou, L Hammarström, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 22, 1998
Monocytes from Wiskott-Aldrich patients display reduced chemotaxis and lack of cell polarization in response to monocyte chemoattractant protein-1 and formyl-methionyl-leucyl-phenylalanineR Badolato, S Sozzani, F Malacarne, et al.
Human Mutation|April 13, 1999
Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. OnlineF X Arrendondo-Vega, I Santisteban, L D Notarangelo, et al.
Haematologica|November 1, 1995
Expansion of large granular lymphocyte subsets in Wiskott-Aldrich syndromeA Plebani, P Airò, D Brugnoni, et al.
Pageof 17

Showing results (91-100 of 165) with videos related to

Sort By:
Pageof 17
American Journal of Human Genetics|January 1, 1992
Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivationE Maestrini, S Rivella, C Tribioli, et al.
Human Mutation|October 23, 2001
Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiencyL D Notarangelo, P Mella, A Jones, et al.
European Journal of Pediatrics|October 1, 1992
Carrier detection in X-linked adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysisL D Notarangelo, O Parolini, G Baiguini, et al.
Bone Marrow Transplantation|January 1, 1991
Use of the highly polymorphic DNA marker CRI-S232 for monitoring of engraftment and chimerism following bone marrow transplantationL D Notarangelo, O Parolini, F Porta, et al.
The Journal of Pathology|August 26, 1998
Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndromeF Facchetti, L Blanzuoli, W Vermi, et al.
Annals of the Rheumatic Diseases|May 1, 1986
IgG subclass serum levels in juvenile chronic arthritisA Martini, A Plebani, A Ravelli, et al.
Lancet (London, England)|August 28, 1993
Absence of xid mutation in X-linked agammaglobulinaemiaI Vorechovsky, J N Zhou, L Hammarström, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 22, 1998
Monocytes from Wiskott-Aldrich patients display reduced chemotaxis and lack of cell polarization in response to monocyte chemoattractant protein-1 and formyl-methionyl-leucyl-phenylalanineR Badolato, S Sozzani, F Malacarne, et al.
Human Mutation|April 13, 1999
Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. OnlineF X Arrendondo-Vega, I Santisteban, L D Notarangelo, et al.
Haematologica|November 1, 1995
Expansion of large granular lymphocyte subsets in Wiskott-Aldrich syndromeA Plebani, P Airò, D Brugnoni, et al.
Pageof 17