106 related articles for article (PubMed ID: 23124046)
1. Identification of a novel mutation in ZAP70 and prenatal diagnosis in a Turkish family with severe combined immunodeficiency disorder.
Karaca E; Karakoc-Aydiner E; Bayrak OF; Keles S; Sevli S; Barlan IB; Yuksel A; Chatila TA; Ozen M
Gene; 2013 Jan; 512(2):189-93. PubMed ID: 23124046
[TBL] [Abstract][Full Text] [Related]
2. SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling.
Hauck F; Blumenthal B; Fuchs S; Lenoir C; Martin E; Speckmann C; Vraetz T; Mannhardt-Laakmann W; Lambert N; Gil M; Borte S; Audrain M; Schwarz K; Lim A; Schamel WW; Fischer A; Ehl S; Rensing-Ehl A; Picard C; Latour S
Clin Immunol; 2015 Dec; 161(2):103-9. PubMed ID: 26187144
[TBL] [Abstract][Full Text] [Related]
3. Novel compound heterozygous mutations in ZAP70 in a Chinese patient with leaky severe combined immunodeficiency disorder.
Liu Q; Wang YP; Liu Q; Zhao Q; Chen XM; Xue XH; Zhou LN; Ding Y; Tang XM; Zhao XD; Zhang ZY
Immunogenetics; 2017 Apr; 69(4):199-209. PubMed ID: 28124082
[TBL] [Abstract][Full Text] [Related]
4. A novel zeta-associated protein 70 homozygous mutation causing combined immunodeficiency presenting as neonatal autoimmune hemolytic anemia.
Ling E; Broides A; Ling G; Shubinsky G; Hadad N; Nahum A; Simon AJ; Lev A; Somech R
Immunol Res; 2021 Feb; 69(1):100-106. PubMed ID: 33484432
[TBL] [Abstract][Full Text] [Related]
5. Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency.
Turul T; Tezcan I; Artac H; de Bruin-Versteeg S; Barendregt BH; Reisli I; Sanal O; van Dongen JJ; van der Burg M
Eur J Pediatr; 2009 Jan; 168(1):87-93. PubMed ID: 18509675
[TBL] [Abstract][Full Text] [Related]
6. Characterization of ζ-associated protein, 70 kd (ZAP70)-deficient human lymphocytes.
Roifman CM; Dadi H; Somech R; Nahum A; Sharfe N
J Allergy Clin Immunol; 2010 Dec; 126(6):1226-33.e1. PubMed ID: 20864151
[TBL] [Abstract][Full Text] [Related]
7. Hypomorphic mutation of ZAP70 in human results in a late onset immunodeficiency and no autoimmunity.
Picard C; Dogniaux S; Chemin K; Maciorowski Z; Lim A; Mazerolles F; Rieux-Laucat F; Stolzenberg MC; Debre M; Magny JP; Le Deist F; Fischer A; Hivroz C
Eur J Immunol; 2009 Jul; 39(7):1966-76. PubMed ID: 19548248
[TBL] [Abstract][Full Text] [Related]
8. Clinical, Immunological, and Genetic Features in 49 Patients With ZAP-70 Deficiency: A Systematic Review.
Sharifinejad N; Jamee M; Zaki-Dizaji M; Lo B; Shaghaghi M; Mohammadi H; Jadidi-Niaragh F; Shaghaghi S; Yazdani R; Abolhassani H; Aghamohammadi A; Azizi G
Front Immunol; 2020; 11():831. PubMed ID: 32431715
[No Abstract] [Full Text] [Related]
9. A novel Zap70 mutation with reduced protein stability demonstrates the rate-limiting threshold for Zap70 in T-cell receptor signalling.
Cauwe B; Tian L; Franckaert D; Pierson W; Staats KA; Schlenner SM; Liston A
Immunology; 2014 Mar; 141(3):377-87. PubMed ID: 24164480
[TBL] [Abstract][Full Text] [Related]
10. Novel Compound Heterozygous ZAP70 R37G A507T Mutations in Infant with Severe Immunodeficiency.
Benavides N; White JC; Sanmillan ML; Thomas M; Le T; Caywood E; Giraudo CG
J Clin Immunol; 2023 Dec; 44(1):27. PubMed ID: 38129328
[TBL] [Abstract][Full Text] [Related]
11. Severe combined immunodeficiency with absence of peripheral blood CD8+ T cells due to ZAP-70 deficiency.
Elder ME; Hope TJ; Parslow TG; Umetsu DT; Wara DW; Cowan MJ
Cell Immunol; 1995 Oct; 165(1):110-7. PubMed ID: 7671314
[TBL] [Abstract][Full Text] [Related]
12. ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency.
Chan AC; Kadlecek TA; Elder ME; Filipovich AH; Kuo WL; Iwashima M; Parslow TG; Weiss A
Science; 1994 Jun; 264(5165):1599-601. PubMed ID: 8202713
[TBL] [Abstract][Full Text] [Related]
13. Limitation of TREC-based newborn screening for ZAP70 Severe Combined Immunodeficiency.
Grazioli S; Bennett M; Hildebrand KJ; Vallance H; Turvey SE; Junker AK
Clin Immunol; 2014 Jul; 153(1):209-10. PubMed ID: 24797280
[No Abstract] [Full Text] [Related]
14. Combined immunodeficiency caused by pathogenic variants in the
Mongellaz C; Vicente R; Noroski LM; Noraz N; Courgnaud V; Chinen J; Faria E; Zimmermann VS; Taylor N
Front Immunol; 2023; 14():1155883. PubMed ID: 37313400
[TBL] [Abstract][Full Text] [Related]
15. MHC class I ligation of human T cells activates the ZAP70 and p56lck tyrosine kinases, leads to an alternative phenotype of the TCR/CD3 zeta-chain, and induces apoptosis.
Skov S; Bregenholt S; Claesson MH
J Immunol; 1997 Apr; 158(7):3189-96. PubMed ID: 9120273
[TBL] [Abstract][Full Text] [Related]
16. Selection transduction defect (STD) due to Zap-70 kinase deficiency.
Roifman CM
Immunodeficiency; 1995; 5(3):193-211. PubMed ID: 7749439
[TBL] [Abstract][Full Text] [Related]
17. Silent brain infarcts in two patients with zeta chain-associated protein 70 kDa (ZAP70) deficiency.
Akar HH; Patiroglu T; Akyildiz BN; Tekerek NU; Doğan MS; Doğanay S; van der Burg M; Dusunsel R
Clin Immunol; 2015 May; 158(1):88-91. PubMed ID: 25805655
[TBL] [Abstract][Full Text] [Related]
18. Defining combined immunodeficiency.
Roifman CM; Somech R; Kavadas F; Pires L; Nahum A; Dalal I; Grunebaum E
J Allergy Clin Immunol; 2012 Jul; 130(1):177-83. PubMed ID: 22664165
[TBL] [Abstract][Full Text] [Related]
19. Temperature-sensitive ZAP70 mutants degrading through a proteasome-independent pathway. Restoration of a kinase domain mutant by Cdc37.
Matsuda S; Suzuki-Fujimoto T; Minowa A; Ueno H; Katamura K; Koyasu S
J Biol Chem; 1999 Dec; 274(49):34515-8. PubMed ID: 10574909
[TBL] [Abstract][Full Text] [Related]
20. A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70.
Chan AY; Punwani D; Kadlecek TA; Cowan MJ; Olson JL; Mathes EF; Sunderam U; Fu SM; Srinivasan R; Kuriyan J; Brenner SE; Weiss A; Puck JM
J Exp Med; 2016 Feb; 213(2):155-65. PubMed ID: 26783323
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]