TNFRSF13Bbase mutation publications
2010
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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(5): 505-11
[PubMed abstract].
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Lymphocyte characteristics in children with common variable immunodeficiency.
van de Ven AA, van de Corput L, van Tilburg CM, Tesselaar K, van Gent R, Sanders EA, Boes M, Bloem AC, van Montfrans JM
Clin Immunol 2010(1): 63-71
[PubMed abstract].
2009
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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(1): 35-9
[PubMed abstract].
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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(6): 777-85
[PubMed abstract].
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Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8.
Waldrep ML, Zhuang Y, Schroeder HW
BMC Med Genet 2009(): 100
[PubMed abstract].
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Role of TNFRSF13B variants in patients with common variable immunodeficiency.
Martínez-Pomar N, Detková D, Arostegui JI, Alvarez A, Soler-Palacín P, Vidaller A, Espanol T, Sampalo A, de Gracia J, Hernandez M, Yagüe J, Matamoros N
Blood 2009(13): 2846-8
[PubMed abstract].
2006
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TACI mutation with invasive polyclonal CD8+ T-cell lymphoproliferation in a patient with common variable immunodeficiency.
Berglund LJ, Jones GJ, Murali R, Fulcher DA
J Allergy Clin Immunol 2006(4): 870-7
[PubMed abstract].
2005
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TACI is mutant in common variable immunodeficiency and IgA deficiency.
Castigli E, Wilson SA, Garibyan L, Rachid R, Bonilla F, Schneider L, Geha RS
Nat Genet 2005(8): 829-34
[PubMed abstract].
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Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.
Salzer U, Chapel HM, Webster AD, Pan-Hammarström Q, Schmitt-Graeff A, Schlesier M, Peter HH, Rockstroh JK, Schneider P, Schäffer AA, Hammarström L, Grimbacher B
Nat Genet 2005(8): 820-8
[PubMed abstract].
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