These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
87 related articles for article (PubMed ID: 22926078)
1. Role of SNAP29, LZTR1 and P2RXL1 genes on immune regulation in a patient with atypical 0.5 Mb deletion in 22q11.2 region. de Queiroz Soares DC; Dutra RL; D'angioli Costa Quaio CR; Melaragno MI; Kulikowski LD; Torres LC; Kim CA Clin Immunol; 2012 Oct; 145(1):55-8. PubMed ID: 22926078 [No Abstract] [Full Text] [Related]
3. Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS. McDonald-McGinn DM; Fahiminiya S; Revil T; Nowakowska BA; Suhl J; Bailey A; Mlynarski E; Lynch DR; Yan AC; Bilaniuk LT; Sullivan KE; Warren ST; Emanuel BS; Vermeesch JR; Zackai EH; Jerome-Majewska LA J Med Genet; 2013 Feb; 50(2):80-90. PubMed ID: 23231787 [TBL] [Abstract][Full Text] [Related]
4. A 39-year-old father is diagnosed in adulthood as having partial DiGeorge anomaly with a combined T- and B-cell immunodeficiency after diagnosis of the condition in his daughter. Campbell JM; Knutsen AP; Becker BA Ann Allergy Asthma Immunol; 2008 Jun; 100(6):620-1. PubMed ID: 18592832 [No Abstract] [Full Text] [Related]
6. Association between polymorphism of the SNAP29 gene promoter region and schizophrenia. Wonodi I; Hong LE; Avila MT; Buchanan RW; Carpenter WT; Stine OC; Mitchell BD; Thaker GK Schizophr Res; 2005 Oct; 78(2-3):339-41. PubMed ID: 15908182 [No Abstract] [Full Text] [Related]
7. Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR). McQuade L; Christodoulou J; Budarf M; Sachdev R; Wilson M; Emanuel B; Colley A Am J Med Genet; 1999 Sep; 86(1):27-33. PubMed ID: 10440825 [TBL] [Abstract][Full Text] [Related]
8. The immune deficiency of chromosome 22q11.2 deletion syndrome. Morsheimer M; Brown Whitehorn TF; Heimall J; Sullivan KE Am J Med Genet A; 2017 Sep; 173(9):2366-2372. PubMed ID: 28627729 [TBL] [Abstract][Full Text] [Related]
9. Inherited t(9;22) as the cause of DiGeorge syndrome: a case report. Shuib S; Abdul Latif Z; Abidin NZ; Akmal SN; Zakaria Z Malays J Pathol; 2009 Dec; 31(2):133-6. PubMed ID: 20514857 [TBL] [Abstract][Full Text] [Related]
10. A prospective study of influenza vaccination and a comparison of immunologic parameters in children and adults with chromosome 22q11.2 deletion syndrome (digeorge syndrome/velocardiofacial syndrome). Jawad AF; Prak EL; Boyer J; McDonald-McGinn DM; Zackai E; McDonald K; Sullivan KE J Clin Immunol; 2011 Dec; 31(6):927-35. PubMed ID: 21863400 [TBL] [Abstract][Full Text] [Related]
11. Low thymic output in the 22q11.2 deletion syndrome measured by CCR9+CD45RA+ T cell counts and T cell receptor rearrangement excision circles. Lima K; Abrahamsen TG; Foelling I; Natvig S; Ryder LP; Olaussen RW Clin Exp Immunol; 2010 Jul; 161(1):98-107. PubMed ID: 20491792 [TBL] [Abstract][Full Text] [Related]
12. CEDNIK syndrome results from loss-of-function mutations in SNAP29. Fuchs-Telem D; Stewart H; Rapaport D; Nousbeck J; Gat A; Gini M; Lugassy Y; Emmert S; Eckl K; Hennies HC; Sarig O; Goldsher D; Meilik B; Ishida-Yamamoto A; Horowitz M; Sprecher E Br J Dermatol; 2011 Mar; 164(3):610-6. PubMed ID: 21073448 [TBL] [Abstract][Full Text] [Related]
18. A novel function for SNAP29 (synaptosomal-associated protein of 29 kDa) in mast cell phagocytosis. Wesolowski J; Caldwell V; Paumet F PLoS One; 2012; 7(11):e49886. PubMed ID: 23185475 [TBL] [Abstract][Full Text] [Related]
19. Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11.2 microdeletion and partial DiGeorge syndrome. Eberle P; Berger C; Junge S; Dougoud S; Büchel EV; Riegel M; Schinzel A; Seger R; Güngör T Clin Exp Immunol; 2009 Feb; 155(2):189-98. PubMed ID: 19040613 [TBL] [Abstract][Full Text] [Related]