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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.
Genomics|February 1, 1993
Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22O Parolini, J F Hejtmancik, R C Allen, et al.
Human Genetics|December 1, 1991
Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WASL D Notarangelo, O Parolini, F Porta, et al.
Scandinavian Journal of Immunology|July 8, 2016
Mesenchymal Stromal Cells Protect Endothelial Cells from Cytotoxic T Lymphocyte-Induced LysisE F Cahill, T Sax, I Hartmann, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 12, 2000
Anti-inflammatory effects of sodium butyrate on human monocytes: potent inhibition of IL-12 and up-regulation of IL-10 productionM D Säemann, G A Böhmig, C H Osterreicher, et al.
Cell|January 29, 1993
Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemiaS Tsukada, D C Saffran, D J Rawlings, et al.
Oncogene|August 19, 2007
Diacylglycerol kinase-alpha phosphorylation by Src on Y335 is required for activation, membrane recruitment and Hgf-induced cell motilityG Baldanzi, S Cutrupi, F Chianale, et al.
Annals of Hematology|September 12, 2002
Analysis of SH2D1A mutations in patients with severe Epstein-Barr virus infections, Burkitt's lymphoma, and Hodgkin's lymphomaO Parolini, B Kagerbauer, I Simonitsch-Klupp, et al.
Toxicology and Applied Pharmacology|November 16, 2004
Target-specific action of organochlorine compounds in reproductive and nonreproductive tissues of estrogen-reporter male miceR Villa, E Bonetti, M L Penza, et al.
British Journal of Haematology|June 20, 1998
Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1)G S Wengler, S Giliani, M Fiorini, et al.
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