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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

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]  

  • 2. Immunologic defects in 22q11.2 deletion syndrome.
    McLean-Tooke A; Barge D; Spickett GP; Gennery AR
    J Allergy Clin Immunol; 2008 Aug; 122(2):362-7, 367.e1-4. PubMed ID: 18485468
    [TBL] [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]  

  • 5.
    Keser V; Lachance JB; Alam SS; Lim Y; Scarlata E; Kaur A; Zhang TF; Lv S; Lachapelle P; O'Flaherty C; Golden JA; Jerome-Majewska LA
    Commun Biol; 2019; 2():375. PubMed ID: 31633066
    [TBL] [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]  

  • 13. Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
    Jawad AF; McDonald-Mcginn DM; Zackai E; Sullivan KE
    J Pediatr; 2001 Nov; 139(5):715-23. PubMed ID: 11713452
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.
    Staple L; Andrews T; McDonald-McGinn D; Zackai E; Sullivan KE
    Pediatr Allergy Immunol; 2005 May; 16(3):226-30. PubMed ID: 15853951
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architecture.
    Tuţulan-Cuniţă AC; Budişteanu M; Papuc SM; Dupont JM; Blancho D; Lebbar A; Viot G; Lungeanu A; Arghir A
    Psychiatry Res; 2012 May; 197(3):356-7. PubMed ID: 22365273
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
    Sullivan KE
    Immunol Allergy Clin North Am; 2008 May; 28(2):353-66. PubMed ID: 18424337
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ocular manifestations of 22q11.2 microduplication.
    Cordovez JA; Capasso J; Lingao MD; Sadagopan KA; Spaeth GL; Wasserman BN; Levin AV
    Ophthalmology; 2014 Jan; 121(1):392-398. PubMed ID: 23972321
    [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]  

  • 20. Deletion 22q11: spectrum of associated disorders.
    Hay BN
    Semin Pediatr Neurol; 2007 Sep; 14(3):136-9. PubMed ID: 17980310
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.