Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions
Year:
2016
Type of item:
Articolo in Rivista
Tipologia ANVUR:
Articolo su rivista
Language:
Inglese
Referee:
No
Name of journal:
Journal of Allergy and Clinical Immunonology
ISSN of journal:
0091-6749
N° Volume:
138
Number or Folder:
1
:
Elsevier Science
Page numbers:
229-240
Keyword:
CRKL; DiGeorge syndrome; IL-2; T-cell receptor activation; c-Fos; proliferation; signal transducer and activator of transcription 5
Short description of contents:
Partial DiGeorge syndrome (pDGS) is caused by deletion of the 22q11.2 region. Within this region lies CrK-like (CRKL), a gene encoding an adapter protein belonging to the Crk family that is involved in the signaling cascade of IL-2, stromal cell-derived factor 1α, and type I interferon. Although recurrent infections can be observed in patients with deletion of chromosome 22 syndrome, the immune pathogenesis of this condition is yet not fully understood.
Product ID:
94158
Handle IRIS:
11562/952205
Last Modified:
November 15, 2022
Bibliographic citation:
Giacomelli, Mauro; Kumar, Rajesh; Soresina, Annarosa; Tamassia, Nicola; Lorenzini, Tiziana; Moratto, Daniele; Gasperini, Sara; Cassatella, Marco Antonio; Plebani, Alessandro; Lougaris, Vassilios; Badolato, Raffaele,
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions«Journal of Allergy and Clinical Immunonology»
, vol. 138
, n. 1
, 2016
, pp. 229-240