430 related articles for article (PubMed ID: 29867916)
1. Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.
de Valles-Ibáñez G; Esteve-Solé A; Piquer M; González-Navarro EA; Hernandez-Rodriguez J; Laayouni H; González-Roca E; Plaza-Martin AM; Deyà-Martínez Á; Martín-Nalda A; Martínez-Gallo M; García-Prat M; Del Pino-Molina L; Cuscó I; Codina-Solà M; Batlle-Masó L; Solís-Moruno M; Marquès-Bonet T; Bosch E; López-Granados E; Aróstegui JI; Soler-Palacín P; Colobran R; Yagüe J; Alsina L; Juan M; Casals F
Front Immunol; 2018; 9():636. PubMed ID: 29867916
[TBL] [Abstract][Full Text] [Related]
2. Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency.
Kutukculer N; Gulez N; Karaca NE; Aksu G; Berdeli A
J Clin Immunol; 2012 Dec; 32(6):1165-79. PubMed ID: 22699762
[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. 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]
5. Clinical variability of family members with the C104R mutation in transmembrane activator and calcium modulator and cyclophilin ligand interactor (TACI).
Koopmans W; Woon ST; Brooks AE; Dunbar PR; Browett P; Ameratunga R
J Clin Immunol; 2013 Jan; 33(1):68-73. PubMed ID: 22983507
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. The profile of IL-4, IL-5, IL-10 and GATA3 in patients with LRBA deficiency and CVID with no known monogenic disease: Association with disease severity.
Azizi G; Bagheri Y; Yazdani R; Zaki-Dizaji M; Jamee M; Jadidi-Niaragh F; Kamali AN; Abolhassani H; Aghamohammadi A
Allergol Immunopathol (Madr); 2019; 47(2):172-178. PubMed ID: 30193889
[TBL] [Abstract][Full Text] [Related]
8. Histocompatibility Complex Status and Mendelian Randomization Analysis in Unsolved Antibody Deficiency.
Abolhassani H; Lim CK; Aghamohammadi A; Hammarström L
Front Immunol; 2020; 11():14. PubMed ID: 32038658
[TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 16899196
[TBL] [Abstract][Full Text] [Related]
10. Sequence variants of the TNFRSF13B gene in Czech CVID and IgAD patients in the context of other populations.
Freiberger T; Ravčuková B; Grodecká L; Pikulová Z; Stikarovská D; Pešák S; Kuklínek P; Jarkovský J; Salzer U; Litzman J
Hum Immunol; 2012 Nov; 73(11):1147-54. PubMed ID: 22884984
[TBL] [Abstract][Full Text] [Related]
11. 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]
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. PubMed ID: 26100089
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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. PubMed ID: 22076597
[TBL] [Abstract][Full Text] [Related]
15. Identification of novel NFKB1 and ICOS frameshift variants in patients with CVID.
Liu A; Liu Q; Leng S; Zhang X; Feng Q; Peng J; Feng G
Clin Exp Immunol; 2023 Mar; 211(1):68-77. PubMed ID: 36571238
[TBL] [Abstract][Full Text] [Related]
16. An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene.
Sazzini M; Zuntini R; Farjadian S; Quinti I; Ricci G; Romeo G; Ferrari S; Calafell F; Luiselli D
Genes Immun; 2009 Sep; 10(6):566-78. PubMed ID: 19494827
[TBL] [Abstract][Full Text] [Related]
17. Common Variable Immunodeficiency with Genetic Defects Identified by Whole Exome Sequencing.
Li R; Zheng Y; Li Y; Zhang R; Wang F; Yang D; Ma Y; Mu X; Cao Z; Gao Z
Biomed Res Int; 2018; 2018():3724630. PubMed ID: 30363934
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 21547394
[TBL] [Abstract][Full Text] [Related]
19. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.
Tuijnenburg P; Lango Allen H; Burns SO; Greene D; Jansen MH; Staples E; Stephens J; Carss KJ; Biasci D; Baxendale H; Thomas M; Chandra A; Kiani-Alikhan S; Longhurst HJ; Seneviratne SL; Oksenhendler E; Simeoni I; de Bree GJ; Tool ATJ; van Leeuwen EMM; Ebberink EHTM; Meijer AB; Tuna S; Whitehorn D; Brown M; Turro E; Thrasher AJ; Smith KGC; Thaventhiran JE; Kuijpers TW;
J Allergy Clin Immunol; 2018 Oct; 142(4):1285-1296. PubMed ID: 29477724
[TBL] [Abstract][Full Text] [Related]
20. Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders.
van Schouwenburg PA; Davenport EE; Kienzler AK; Marwah I; Wright B; Lucas M; Malinauskas T; Martin HC; ; Lockstone HE; Cazier JB; Chapel HM; Knight JC; Patel SY
Clin Immunol; 2015 Oct; 160(2):301-14. PubMed ID: 26122175
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]