114 related articles for article (PubMed ID: 37211057)
1. Combined immunodeficiency and impaired PI3K signaling in a patient with biallelic LCP2 variants.
Edwards ESJ; Ojaimi S; Ngui J; Seo GH; Kim J; Chunilal S; Yablonski D; O'Hehir RE; van Zelm MC
J Allergy Clin Immunol; 2023 Sep; 152(3):807-813.e7. PubMed ID: 37211057
[TBL] [Abstract][Full Text] [Related]
2. Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects.
Lev A; Lee YN; Sun G; Hallumi E; Simon AJ; Zrihen KS; Levy S; Beit Halevi T; Papazian M; Shwartz N; Somekh I; Levy-Mendelovich S; Wolach B; Gavrieli R; Vernitsky H; Barel O; Javasky E; Stauber T; Ma CA; Zhang Y; Amariglio N; Rechavi G; Hendel A; Yablonski D; Milner JD; Somech R
J Exp Med; 2021 Mar; 218(3):. PubMed ID: 33231617
[TBL] [Abstract][Full Text] [Related]
3. Combined immunodeficiency due to MALT1 mutations, treated by hematopoietic cell transplantation.
Punwani D; Wang H; Chan AY; Cowan MJ; Mallott J; Sunderam U; Mollenauer M; Srinivasan R; Brenner SE; Mulder A; Claas FH; Weiss A; Puck JM
J Clin Immunol; 2015 Feb; 35(2):135-46. PubMed ID: 25627829
[TBL] [Abstract][Full Text] [Related]
4. The opposing effects of two gene defects in STX11 and SLP76 on the disease in a patient with an inborn error of immunity.
Mansour R; El-Hassan R; El-Orfali Y; Saidu A; Al-Kalamouni H; Chen Q; Benamar M; Dbaibo G; Hanna-Wakim R; Chatila TA; Massaad MJ
J Allergy Clin Immunol; 2023 Dec; 152(6):1597-1606. PubMed ID: 37595757
[TBL] [Abstract][Full Text] [Related]
5. SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related Lymphoma.
Lev A; Asleh M; Levy S; Lee YN; Simon AJ; Stepensky P; Nalbandyan K; Nahum A; Ben-Harosh M; Yablonski D; Broides A; Somech R
J Clin Immunol; 2023 Apr; 43(3):625-635. PubMed ID: 36474126
[TBL] [Abstract][Full Text] [Related]
6. A case of aberrant CD8 T cell-restricted IL-7 signaling with a Janus kinase 3 defect-associated atypical severe combined immunodeficiency.
Khanolkar A; Wilks JD; Liu G; Simpson BM; Caparelli EA; Kirschmann DA; Bergerson J; Fuleihan RL
Immunol Res; 2020 Feb; 68(1):13-27. PubMed ID: 32215810
[TBL] [Abstract][Full Text] [Related]
7. T
Stepensky P; Keller B; Shamriz O; von Spee-Mayer C; Friedmann D; Shadur B; Unger S; Fuchs S; NaserEddin A; Rumman N; Amro S; Molho Pessach V; Abuzaitoun O; Somech R; Elpeleg O; Ehl S; Warnatz K
J Clin Immunol; 2018 May; 38(4):527-536. PubMed ID: 29948574
[TBL] [Abstract][Full Text] [Related]
8. Kinetics of T-cell development of umbilical cord blood transplantation in severe T-cell immunodeficiency disorders.
Knutsen AP; Wall DA
J Allergy Clin Immunol; 1999 May; 103(5 Pt 1):823-32. PubMed ID: 10329816
[TBL] [Abstract][Full Text] [Related]
9. Combined immunodeficiency caused by a novel homozygous NFKB1 mutation.
Mandola AB; Sharfe N; Nagdi Z; Dadi H; Vong L; Merico D; Ngan B; Reid B; Roifman CM
J Allergy Clin Immunol; 2021 Feb; 147(2):727-733.e2. PubMed ID: 32980423
[TBL] [Abstract][Full Text] [Related]
10. Dominant Splice Site Mutations in PIK3R1 Cause Hyper IgM Syndrome, Lymphadenopathy and Short Stature.
Petrovski S; Parrott RE; Roberts JL; Huang H; Yang J; Gorentla B; Mousallem T; Wang E; Armstrong M; McHale D; MacIver NJ; Goldstein DB; Zhong XP; Buckley RH
J Clin Immunol; 2016 Jul; 36(5):462-71. PubMed ID: 27076228
[TBL] [Abstract][Full Text] [Related]
11. Combined immunodeficiency caused by a loss-of-function mutation in DNA polymerase delta 1.
Cui Y; Keles S; Charbonnier LM; Julé AM; Henderson L; Celik SC; Reisli I; Shen C; Xie WJ; Schmitz-Abe K; Wu H; Chatila TA
J Allergy Clin Immunol; 2020 Jan; 145(1):391-401.e8. PubMed ID: 31629014
[TBL] [Abstract][Full Text] [Related]
12. Diagnosis and Treatment of a Patient With Severe Combined Immunodeficiency Due to a Novel Homozygous Mutation in the IL-7Rα Chain.
Mansour R; Bsat YE; Fadel A; El-Orfali Y; Noun D; Tarek N; Kabbara N; Abboud M; Massaad MJ
Front Immunol; 2022; 13():867837. PubMed ID: 35418989
[TBL] [Abstract][Full Text] [Related]
13. Combined immunodeficiency evolving into predominant CD4+ lymphopenia caused by somatic chimerism in JAK3.
Ban SA; Salzer E; Eibl MM; Linder A; Geier CB; Santos-Valente E; Garncarz W; Lion T; Ott R; Seelbach C; Boztug K; Wolf HM
J Clin Immunol; 2014 Nov; 34(8):941-53. PubMed ID: 25205547
[TBL] [Abstract][Full Text] [Related]
14. Evaluation of B-cell intracellular signaling by monitoring the PI3K-Akt axis in patients with common variable immunodeficiency and activated phosphoinositide 3-kinase delta syndrome.
Del Pino-Molina L; Torres Canizales JM; Rodríguez-Pena R; López-Granados E
Cytometry B Clin Cytom; 2021 Jul; 100(4):460-466. PubMed ID: 32961022
[TBL] [Abstract][Full Text] [Related]
15. DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency.
Volk T; Pannicke U; Reisli I; Bulashevska A; Ritter J; Björkman A; Schäffer AA; Fliegauf M; Sayar EH; Salzer U; Fisch P; Pfeifer D; Di Virgilio M; Cao H; Yang F; Zimmermann K; Keles S; Caliskaner Z; Güner SÜ; Schindler D; Hammarström L; Rizzi M; Hummel M; Pan-Hammarström Q; Schwarz K; Grimbacher B
Hum Mol Genet; 2015 Dec; 24(25):7361-72. PubMed ID: 26476407
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Dysregulated PI3K Signaling in B Cells of CVID Patients.
Harder I; Münchhalfen M; Andrieux G; Boerries M; Grimbacher B; Eibel H; Maccari ME; Ehl S; Wienands J; Jellusova J; Warnatz K; Keller B
Cells; 2022 Jan; 11(3):. PubMed ID: 35159274
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. A partial deficiency of interleukin-7R alpha is sufficient to abrogate T-cell development and cause severe combined immunodeficiency.
Roifman CM; Zhang J; Chitayat D; Sharfe N
Blood; 2000 Oct; 96(8):2803-7. PubMed ID: 11023514
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]