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Items: 1 to 20 of 68

1.

TACI mutation p.Lys154Ter identified in Good Syndrome.

Margraf RL, Coonrod EM, Durtschi JD, Augustine NH, Voelkerding KV, Hill HR, Kumánovics A.

Clin Immunol. 2013 Jan;146(1):10-2. doi: 10.1016/j.clim.2012.10.006. Epub 2012 Oct 31. No abstract available.

PMID:
23165285
2.

TACI mutation in Good's Syndrome: in search of a genetic basis.

Sáenz-Cuesta M, Martínez-Pomar N, de Gracia J, Echaniz P, Villegas E, Prada A, Otaegui D, Matamoros N, Cuadrado E.

Clin Immunol. 2012 Oct;145(1):27-30. doi: 10.1016/j.clim.2012.07.014. Epub 2012 Aug 4. No abstract available.

PMID:
22922270
3.

Incidence of the C104R TACI Mutation in Patients With Primary Antibody Deficiency.

Lucena JM, Burillo Sanz S, Núñez-Roldan A, Sánchez B.

J Investig Allergol Clin Immunol. 2015;25(5):378-9. No abstract available.

4.

BAFF-R mutations in Good's syndrome.

Lougaris V, Vitali M, Baronio M, Tampella G, Plebani A.

Clin Immunol. 2014 Jul;153(1):91-3. doi: 10.1016/j.clim.2014.04.002. Epub 2014 Apr 13. No abstract available.

PMID:
24727458
5.

TACI mutation in common variable immunodeficiency and IgA deficiency.

Rachid R, Castigli E, Geha RS, Bonilla FA.

Curr Allergy Asthma Rep. 2006 Sep;6(5):357-62. Review.

PMID:
16899196
6.

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. doi: 10.1007/s10875-009-9317-5. Epub 2009 Jul 23.

PMID:
19629655
7.

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. doi: 10.1097/ACI.0b013e3283141200. Review.

PMID:
18978466
8.

Identification of a novel immunosubversion mechanism mediated by a virologue of the B-lymphocyte receptor TACI.

Grant JR, Moise AR, Jefferies WA.

Clin Vaccine Immunol. 2007 Jul;14(7):907-17. Epub 2007 May 30.

9.

Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency.

Castigli E, Wilson S, Garibyan L, Rachid R, Bonilla F, Schneider L, Morra M, Curran J, Geha R.

Nat Genet. 2007 Apr;39(4):430-1. No abstract available.

PMID:
17392798
10.

Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes.

Pulvirenti F, Zuntini R, Milito C, Specchia F, Spadaro G, Danieli MG, Pession A, Quinti I, Ferrari S.

J Immunol Res. 2016;2016:8390356. doi: 10.1155/2016/8390356. Epub 2016 Mar 30.

11.

TACI, isotype switching, CVID and IgAD.

Castigli E, Geha RS.

Immunol Res. 2007;38(1-3):102-11.

PMID:
17917015
12.

Primary antibody deficiency syndromes.

Wood PM.

Curr Opin Hematol. 2010 Jul;17(4):356-61. doi: 10.1097/MOH.0b013e328338f69e. Review.

PMID:
20442656
13.

Immunological characteristics and two novel mutations in TACI in a cohort of 28 pediatric patients with common variable immunodeficiency.

Almejún MB, Sajaroff E, Galicchio M, Oleastro M, Bernasconi A, Zelazko M, Danielian S.

J Clin Immunol. 2012 Feb;32(1):89-97. doi: 10.1007/s10875-011-9613-8. Epub 2011 Nov 11.

PMID:
22076597
14.

Phenotypic and clinical heterogeneity associated with monoallelic TNFRSF13B-A181E mutations in common variable immunodeficiency.

Dong X, Hoeltzle MV, Hagan JB, Park MA, Li JT, Abraham RS.

Hum Immunol. 2010 May;71(5):505-11. doi: 10.1016/j.humimm.2010.02.002. Epub 2010 Mar 12.

PMID:
20156508
15.

Functional analysis of transmembrane activator and calcium-modulating cyclophilin ligand interactor (TACI) mutations associated with common variable immunodeficiency.

Fried AJ, Rauter I, Dillon SR, Jabara HH, Geha RS.

J Allergy Clin Immunol. 2011 Jul;128(1):226-228.e1. doi: 10.1016/j.jaci.2011.01.048. Epub 2011 Mar 21. No abstract available.

16.

Rare mutations in TNFRSF13B increase the risk of asthma symptoms in Swedish children.

Janzi M, Melén E, Kull I, Wickman M, Hammarström L.

Genes Immun. 2012 Jan;13(1):59-65. doi: 10.1038/gene.2011.55. Epub 2011 Aug 18.

PMID:
21850030
17.

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. doi: 10.1016/j.humimm.2012.05.001. Epub 2012 May 22.

PMID:
22627058
18.

Molecular cloning and functional characterization of murine transmembrane activator and CAML interactor (TACI) with chromosomal localization in human and mouse.

von Bülow GU, Russell H, Copeland NG, Gilbert DJ, Jenkins NA, Bram RJ.

Mamm Genome. 2000 Aug;11(8):628-32.

PMID:
10920230
19.

TNFRSF13B/TACI alterations in Greek patients with antibody deficiencies.

Speletas M, Mamara A, Papadopoulou-Alataki E, Iordanakis G, Liadaki K, Bardaka F, Kanariou M, Germenis AE.

J Clin Immunol. 2011 Aug;31(4):550-9. doi: 10.1007/s10875-011-9536-4. Epub 2011 May 6.

PMID:
21547394
20.

Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency.

Pan-Hammarström Q, Salzer U, Du L, Björkander J, Cunningham-Rundles C, Nelson DL, Bacchelli C, Gaspar HB, Offer S, Behrens TW, Grimbacher B, Hammarström L.

Nat Genet. 2007 Apr;39(4):429-30. No abstract available.

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