166 related articles for article (PubMed ID: 18254984)
1. Screening of functional and positional candidate genes in families with common variable immunodeficiency.
Salzer U; Neumann C; Thiel J; Woellner C; Pan-Hammarström Q; Lougaris V; Hagena T; Jung J; Birmelin J; Du L; Metin A; Webster DA; Plebani A; Moschese V; Hammarström L; Schäffer AA; Grimbacher B
BMC Immunol; 2008 Feb; 9():3. PubMed ID: 18254984
[TBL] [Abstract][Full Text] [Related]
2. Genes associated with common variable immunodeficiency: one diagnosis to rule them all?
Bogaert DJ; Dullaers M; Lambrecht BN; Vermaelen KY; De Baere E; Haerynck F
J Med Genet; 2016 Sep; 53(9):575-90. PubMed ID: 27250108
[TBL] [Abstract][Full Text] [Related]
3. Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder.
Keller MD; Pandey R; Li D; Glessner J; Tian L; Henrickson SE; Chinn IK; Monaco-Shawver L; Heimall J; Hou C; Otieno FG; Jyonouchi S; Calabrese L; van Montfrans J; Orange JS; Hakonarson H
J Allergy Clin Immunol; 2016 Aug; 138(2):544-550.e4. PubMed ID: 27016798
[TBL] [Abstract][Full Text] [Related]
4. A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family.
Lougaris V; Gallizzi R; Vitali M; Baronio M; Salpietro A; Bergbreiter A; Salzer U; Badolato R; Plebani A
Hum Immunol; 2012 Aug; 73(8):836-9. PubMed ID: 22627058
[TBL] [Abstract][Full Text] [Related]
5. Novel mutations in TACI (TNFRSF13B) causing common variable immunodeficiency.
Mohammadi J; Liu C; Aghamohammadi A; Bergbreiter A; Du L; Lu J; Rezaei N; Amirzargar AA; Moin M; Salzer U; Pan-Hammarström Q; Hammarström L
J Clin Immunol; 2009 Nov; 29(6):777-85. PubMed ID: 19629655
[TBL] [Abstract][Full Text] [Related]
6. Age-related changes in BAFF and APRIL profiles and upregulation of BAFF and APRIL expression in patients with primary antibody deficiency.
Jin R; Kaneko H; Suzuki H; Arai T; Teramoto T; Fukao T; Kondo N
Int J Mol Med; 2008 Feb; 21(2):233-8. PubMed ID: 18204790
[TBL] [Abstract][Full Text] [Related]
7. Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: clinical and immunologic outcomes in heterozygotes.
Zhang L; Radigan L; Salzer U; Behrens TW; Grimbacher B; Diaz G; Bussel J; Cunningham-Rundles C
J Allergy Clin Immunol; 2007 Nov; 120(5):1178-85. PubMed ID: 17983875
[TBL] [Abstract][Full Text] [Related]
8. Evaluation of cytokine genetic polymorphisms in adult patients with common variable immunodeficiency: A single-center study.
Perovic D; Perovic V; Pravica V; Bonaci-Nikolic B; Mijanovic R; Bunjevacki V
Immunol Lett; 2016 Aug; 176():97-104. PubMed ID: 27288995
[TBL] [Abstract][Full Text] [Related]
9. Translational mini-review series on immunodeficiency: molecular defects in common variable immunodeficiency.
Bacchelli C; Buckridge S; Thrasher AJ; Gaspar HB
Clin Exp Immunol; 2007 Sep; 149(3):401-9. PubMed ID: 17697196
[TBL] [Abstract][Full Text] [Related]
10. TACI, isotype switching, CVID and IgAD.
Castigli E; Geha RS
Immunol Res; 2007; 38(1-3):102-11. PubMed ID: 17917015
[TBL] [Abstract][Full Text] [Related]
11. Analysis of genetic defects in patients with the common variable immunodeficiency phenotype in a single Taiwanese tertiary care hospital.
Lee WI; Huang JL; Kuo ML; Lin SJ; Chen LC; Chen MT; Jaing TH
Ann Allergy Asthma Immunol; 2007 Nov; 99(5):433-42. PubMed ID: 18051214
[TBL] [Abstract][Full Text] [Related]
12. TACItly changing tunes: farewell to a yin and yang of BAFF receptor and TACI in humoral immunity? New genetic defects in common variable immunodeficiency.
Salzer U; Grimbacher B
Curr Opin Allergy Clin Immunol; 2005 Dec; 5(6):496-503. PubMed ID: 16264328
[TBL] [Abstract][Full Text] [Related]
13. ICOS deficiency in patients with common variable immunodeficiency.
Salzer U; Maul-Pavicic A; Cunningham-Rundles C; Urschel S; Belohradsky BH; Litzman J; Holm A; Franco JL; Plebani A; Hammarstrom L; Skrabl A; Schwinger W; Grimbacher B
Clin Immunol; 2004 Dec; 113(3):234-40. PubMed ID: 15507387
[TBL] [Abstract][Full Text] [Related]
14. Transmembrane activator and calcium-modulator and cyclophilin ligand interactor mutations in common variable immunodeficiency.
Lee JJ; Ozcan E; Rauter I; Geha RS
Curr Opin Allergy Clin Immunol; 2008 Dec; 8(6):520-6. PubMed ID: 18978466
[TBL] [Abstract][Full Text] [Related]
15. Deconstructing common variable immunodeficiency by genetic analysis.
Schäffer AA; Salzer U; Hammarström L; Grimbacher B
Curr Opin Genet Dev; 2007 Jun; 17(3):201-12. PubMed ID: 17467261
[TBL] [Abstract][Full Text] [Related]
16. Molecular basis of common variable immunodeficiency.
Castigli E; Geha RS
J Allergy Clin Immunol; 2006 Apr; 117(4):740-6; quiz 747. PubMed ID: 16630927
[TBL] [Abstract][Full Text] [Related]
17. Genetics of common variable immunodeficiency: role of transmembrane activator and calcium modulator and cyclophilin ligand interactor.
Sathkumara HD; De Silva NR; Handunnetti S; De Silva AD
Int J Immunogenet; 2015 Aug; 42(4):239-53. PubMed ID: 26096648
[TBL] [Abstract][Full Text] [Related]
18. Mutational analysis of human BLyS in patients with common variable immunodeficiency.
Losi CG; Salzer U; Gatta R; Lougaris V; Cattaneo G; Meini A; Soresina A; Grimbacher B; Plebani A
J Clin Immunol; 2006 Jul; 26(4):396-9. PubMed ID: 16838132
[TBL] [Abstract][Full Text] [Related]
19. TACI mutations and disease susceptibility in patients with common variable immunodeficiency.
Poodt AE; Driessen GJ; de Klein A; van Dongen JJ; van der Burg M; de Vries E
Clin Exp Immunol; 2009 Apr; 156(1):35-9. PubMed ID: 19210517
[TBL] [Abstract][Full Text] [Related]
20. Rare variants at 16p11.2 are associated with common variable immunodeficiency.
Maggadottir SM; Li J; Glessner JT; Li YR; Wei Z; Chang X; Mentch FD; Thomas KA; Kim CE; Zhao Y; Hou C; Wang F; Jørgensen SF; Perez EE; Sullivan KE; Orange JS; Karlsen TH; Chapel H; Cunningham-Rundles C; Hakonarson H
J Allergy Clin Immunol; 2015 Jun; 135(6):1569-77. PubMed ID: 25678086
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]