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Items: 1 to 20 of 356

1.
2.

Reduced BAFF-R and increased TACI expression in common variable immunodeficiency.

Barbosa RR, Silva SL, Silva SP, Melo AC, Pereira-Santos MC, Barata JT, Hammarström L, Cascalho M, Sousa AE.

J Clin Immunol. 2014 Jul;34(5):573-83. doi: 10.1007/s10875-014-0047-y.

PMID:
24809296
3.

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.

PMID:
22627058
4.

Impaired selective cytokine production by CD4(+) T cells in Common Variable Immunodeficiency associated with the absence of memory B cells.

Berrón-Ruiz L, López-Herrera G, Vargas-Hernández A, Santos-Argumedo L, López-Macías C, Isibasi A, Segura-Méndez NH, Bonifaz L.

Clin Immunol. 2016 May;166-167:19-26. doi: 10.1016/j.clim.2016.03.013. Epub 2016 Apr 4.

PMID:
27057998
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. doi: 10.1007/s10875-009-9317-5.

PMID:
19629655
6.

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
7.

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. doi: 10.1111/iji.12217. Review.

PMID:
26096648
8.

TACI mutations and impaired B-cell function in subjects with CVID and healthy heterozygotes.

Martinez-Gallo M, Radigan L, Almejún MB, Martínez-Pomar N, Matamoros N, Cunningham-Rundles C.

J Allergy Clin Immunol. 2013 Feb;131(2):468-76. doi: 10.1016/j.jaci.2012.10.029.

9.

TACI, isotype switching, CVID and IgAD.

Castigli E, Geha RS.

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

PMID:
17917015
10.

Age-matched reference values for B-lymphocyte subpopulations and CVID classifications in children.

Schatorjé EJ, Gemen EF, Driessen GJ, Leuvenink J, van Hout RW, van der Burg M, de Vries E.

Scand J Immunol. 2011 Nov;74(5):502-10. doi: 10.1111/j.1365-3083.2011.02609.x.

11.

Molecular basis of common variable immunodeficiency.

Castigli E, Geha RS.

J Allergy Clin Immunol. 2006 Apr;117(4):740-6; quiz 747. Review.

PMID:
16630927
12.

TNF receptor superfamily member 13b (TNFRSF13B) hemizygosity reveals transmembrane activator and CAML interactor haploinsufficiency at later stages of B-cell development.

Romberg N, Virdee M, Chamberlain N, Oe T, Schickel JN, Perkins T, Cantaert T, Rachid R, Rosengren S, Palazzo R, Geha R, Cunningham-Rundles C, Meffre E.

J Allergy Clin Immunol. 2015 Nov;136(5):1315-25. doi: 10.1016/j.jaci.2015.05.012.

13.

Lymphocytes and B-cell abnormalities in patients with common variable immunodeficiency (CVID).

Berrón-Ruiz L, López-Herrera G, Vargas-Hernández A, Mogica-Martínez D, García-Latorre E, Blancas-Galicia L, Espinosa-Rosales FJ, Santos-Argumedo L.

Allergol Immunopathol (Madr). 2014 Jan-Feb;42(1):35-43. doi: 10.1016/j.aller.2012.07.016.

PMID:
23305827
14.

Expressions of BAFF/BAFF receptors and their correlation with disease activity in Chinese SLE patients.

Zhao LD, Li Y, Smith MF Jr, Wang JS, Zhang W, Tang FL, Tian XP, Wang HY, Zhang FC, Ba DN, He W, Zhang X.

Lupus. 2010 Nov;19(13):1534-49. doi: 10.1177/0961203310375268.

PMID:
20974656
15.

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.

PMID:
18204790
16.

Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease.

Warnatz K, Denz A, Dräger R, Braun M, Groth C, Wolff-Vorbeck G, Eibel H, Schlesier M, Peter HH.

Blood. 2002 Mar 1;99(5):1544-51.

17.

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.

PMID:
20156508
18.

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.

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. doi: 10.1111/j.1365-2249.2008.03863.x.

20.

Common variable immunodeficiency. Old questions are getting clearer.

Blanco-Quirós A, Solís-Sánchez P, Garrote-Adrados JA, Arranz-Sanz E.

Allergol Immunopathol (Madr). 2006 Nov-Dec;34(6):263-75. Review.

PMID:
17173844

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