Mella P - Search Results

1

Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiency.

Notarangelo LD, Mella P, Jones A, de Saint Basile G, Savoldi G, Cranston T, Vihinen M, Schumacher RF. Notarangelo LD, et al. Among authors: mella p. Hum Mutat. 2001 Oct;18(4):255-63. doi: 10.1002/humu.1188. Hum Mutat. 2001. PMID: 11668610 Review.

2

Prenatal diagnosis of JAK3 deficient SCID.

Schumacher RF, Mella P, Lalatta F, Fiorini M, Giliani S, Villa A, Candotti F, Notarangelo LD. Schumacher RF, et al. Among authors: mella p. Prenat Diagn. 1999 Jul;19(7):653-6. Prenat Diagn. 1999. PMID: 10419614

3

Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterization.

Mella P, Imberti L, Brugnoni D, Pirovano S, Candotti F, Mazzolari E, Bettinardi A, Fiorini M, De Mattia D, Martire B, Plebani A, Notarangelo LD, Giliani S. Mella P, et al. Clin Immunol. 2000 Apr;95(1 Pt 1):39-50. doi: 10.1006/clim.2000.4842. Clin Immunol. 2000. PMID: 10794431

4

Molecular modeling of the Jak3 kinase domains and structural basis for severe combined immunodeficiency.

Vihinen M, Villa A, Mella P, Schumacher RF, Savoldi G, O'Shea JJ, Candotti F, Notarangelo LD. Vihinen M, et al. Among authors: mella p. Clin Immunol. 2000 Aug;96(2):108-18. doi: 10.1006/clim.2000.4880. Clin Immunol. 2000. PMID: 10900158

5

Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism.

Schumacher RF, Mella P, Badolato R, Fiorini M, Savoldi G, Giliani S, Villa A, Candotti F, Tampalini A, O'Shea JJ, Notarangelo LD. Schumacher RF, et al. Among authors: mella p. Hum Genet. 2000 Jan;106(1):73-9. doi: 10.1007/s004390051012. Hum Genet. 2000. PMID: 10982185

6

Combined immunodeficiencies due to defects in signal transduction: defects of the gammac-JAK3 signaling pathway as a model.

Notarangelo LD, Giliani S, Mella P, Schumacher RF, Mazza C, Savoldi G, Rodriguez-Pérez C, Badolato R, Mazzolari E, Porta F, Candotti F, Ugazio AG. Notarangelo LD, et al. Among authors: mella p. Immunobiology. 2000 Aug;202(2):106-19. doi: 10.1016/s0171-2985(00)80058-3. Immunobiology. 2000. PMID: 10993286 Review.

7

Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model.

Notarangelo LD, Giliani S, Mazza C, Mella P, Savoldi G, Rodriguez-Pérez C, Mazzolari E, Fiorini M, Duse M, Plebani A, Ugazio AG, Vihinen M, Candotti F, Schumacher RF. Notarangelo LD, et al. Among authors: mella p. Immunol Rev. 2000 Dec;178:39-48. doi: 10.1034/j.1600-065x.2000.17812.x. Immunol Rev. 2000. PMID: 11213805 Review.

8

Eleven novel JAK3 mutations in patients with severe combined immunodeficiency-including the first patients with mutations in the kinase domain.

Mella P, Schumacher RF, Cranston T, de Saint Basile G, Savoldi G, Notarangelo LD. Mella P, et al. Hum Mutat. 2001 Oct;18(4):355-6. doi: 10.1002/humu.1199. Hum Mutat. 2001. PMID: 11668621

9

Cytokine-mediated signalling and early defects in lymphoid development.

Giliani S, Mella P, Savoldi G, Mazzolari E. Giliani S, et al. Among authors: mella p. Curr Opin Allergy Clin Immunol. 2005 Dec;5(6):519-24. doi: 10.1097/01.all.0000191889.35516.b6. Curr Opin Allergy Clin Immunol. 2005. PMID: 16264332 Review.

10

In-utero transplantation of parental CD34 haematopoietic progenitor cells in a patient with X-linked severe combined immunodeficiency (SCIDXI).

Wengler GS, Lanfranchi A, Frusca T, Verardi R, Neva A, Brugnoni D, Giliani S, Fiorini M, Mella P, Guandalini F, Mazzolari E, Pecorelli S, Notarangelo LD, Porta F, Ugazio AG. Wengler GS, et al. Among authors: mella p. Lancet. 1996 Nov 30;348(9040):1484-7. doi: 10.1016/s0140-6736(96)09392-0. Lancet. 1996. PMID: 8942778

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