168 related articles for article (PubMed ID: 30622570)
21. Generation of novel Il2rg-knockout mice with clustered regularly interspaced short palindromic repeats (CRISPR) and Cas9.
Byambaa S; Uosaki H; Hara H; Nagao Y; Abe T; Shibata H; Nureki O; Ohmori T; Hanazono Y
Exp Anim; 2020 Apr; 69(2):189-198. PubMed ID: 31801915
[TBL] [Abstract][Full Text] [Related]
22. Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency.
Puck JM; Pepper AE; Henthorn PS; Candotti F; Isakov J; Whitwam T; Conley ME; Fischer RE; Rosenblatt HM; Small TN; Buckley RH
Blood; 1997 Mar; 89(6):1968-77. PubMed ID: 9058718
[TBL] [Abstract][Full Text] [Related]
23. Intact B-Cell Signaling and Function With Host B-Cells 47 Years After Transplantation for X-SCID.
Deal C; Thauland TJ; Stiehm ER; Garcia-Lloret MI; Butte MJ
Front Immunol; 2020; 11():415. PubMed ID: 32265911
[No Abstract] [Full Text] [Related]
24. A novel X-linked mutation in IL2RG associated with early-onset inflammatory bowel disease: a case report of twin brothers.
Rayzan E; Sadeghalvad M; Shahkarami S; Zoghi S; Aryan Z; Mahdaviani SA; Boztug K; Rezaei N
J Med Case Rep; 2023 Jul; 17(1):307. PubMed ID: 37461086
[TBL] [Abstract][Full Text] [Related]
25. Two mutational hotspots in the interleukin-2 receptor gamma chain gene causing human X-linked severe combined immunodeficiency.
Pepper AE; Buckley RH; Small TN; Puck JM
Am J Hum Genet; 1995 Sep; 57(3):564-71. PubMed ID: 7668284
[TBL] [Abstract][Full Text] [Related]
26. Targeted genome editing restores T cell differentiation in a humanized X-SCID pluripotent stem cell disease model.
Alzubi J; Pallant C; Mussolino C; Howe SJ; Thrasher AJ; Cathomen T
Sci Rep; 2017 Sep; 7(1):12475. PubMed ID: 28963568
[TBL] [Abstract][Full Text] [Related]
27. A reversion of an IL2RG mutation in combined immunodeficiency providing competitive advantage to the majority of CD8+ T cells.
Kuijpers TW; van Leeuwen EM; Barendregt BH; Klarenbeek P; aan de Kerk DJ; Baars PA; Jansen MH; de Vries N; van Lier RA; van der Burg M
Haematologica; 2013 Jul; 98(7):1030-8. PubMed ID: 23403317
[TBL] [Abstract][Full Text] [Related]
28. X-linked severe combined immunodeficiency due to a novel mutation complicated with hemophagocytic lymphohistiocytosis and presented with invagination: A case report.
Patiroglu T; Haluk Akar H; van den Burg M; Unal E; Akyildiz BN; Tekerek NU; Yilmaz E
Eur J Microbiol Immunol (Bp); 2014 Sep; 4(3):174-6. PubMed ID: 25215194
[TBL] [Abstract][Full Text] [Related]
29. Transplantation of human cells into Interleukin-2 receptor gamma gene knockout pigs under several conditions.
Hasegawa K; Nakano K; Nagaya M; Watanabe M; Uchikura A; Matsunari H; Umeyama K; Kobayashi E; Nagashima H
Regen Ther; 2022 Dec; 21():62-72. PubMed ID: 35765545
[TBL] [Abstract][Full Text] [Related]
30. The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1.
Puck JM; Deschênes SM; Porter JC; Dutra AS; Brown CJ; Willard HF; Henthorn PS
Hum Mol Genet; 1993 Aug; 2(8):1099-104. PubMed ID: 8401490
[TBL] [Abstract][Full Text] [Related]
31. Efficient detection of thirty-seven new IL2RG mutations in human X-linked severe combined immunodeficiency.
Niemela JE; Puck JM; Fischer RE; Fleisher TA; Hsu AP
Clin Immunol; 2000 Apr; 95(1 Pt 1):33-8. PubMed ID: 10794430
[TBL] [Abstract][Full Text] [Related]
32. Severe combined immunodeficiency in Serbia and Montenegro between years 1986 and 2010: a single-center experience.
Pasic S; Vujic D; Veljković D; Slavkovic B; Mostarica-Stojkovic M; Minic P; Minic A; Ristic G; Giliani S; Villa A; Sobacchi C; Lilić D; Abinun M
J Clin Immunol; 2014 Apr; 34(3):304-8. PubMed ID: 24481607
[TBL] [Abstract][Full Text] [Related]
33. Mutational landscape of severe combined immunodeficiency patients from Turkey.
Firtina S; Yin Ng Y; Hatirnaz Ng O; Kiykim A; Aydiner E; Nepesov S; Camcioglu Y; Sayar EH; Reisli I; Torun SH; Cogurlu T; Uygun D; Simsek IE; Kaya A; Cipe F; Cagdas D; Yucel E; Cekic S; Uygun V; Baris S; Ozen A; Ozbek U; Sayitoglu M
Int J Immunogenet; 2020 Dec; 47(6):529-538. PubMed ID: 32445296
[TBL] [Abstract][Full Text] [Related]
34. Clinical characteristics and mutation analysis of X-linked severe combined immunodeficiency in China.
Zhang C; Zhang ZY; Wu JF; Tang XM; Yang XQ; Jiang LP; Zhao XD
World J Pediatr; 2013 Feb; 9(1):42-7. PubMed ID: 22105576
[TBL] [Abstract][Full Text] [Related]
35. Novel
Rutkowska-Zapała M; Szaflarska A; Kluczewska A; Ciȩciwa J; Plewka J; Michalska A; Siedlar M
Front Pediatr; 2022; 10():858166. PubMed ID: 35498802
[TBL] [Abstract][Full Text] [Related]
36. Il2rg gene-targeted severe combined immunodeficiency pigs.
Suzuki S; Iwamoto M; Saito Y; Fuchimoto D; Sembon S; Suzuki M; Mikawa S; Hashimoto M; Aoki Y; Najima Y; Takagi S; Suzuki N; Suzuki E; Kubo M; Mimuro J; Kashiwakura Y; Madoiwa S; Sakata Y; Perry ACF; Ishikawa F; Onishi A
Cell Stem Cell; 2012 Jun; 10(6):753-758. PubMed ID: 22704516
[TBL] [Abstract][Full Text] [Related]
37. A novel splice donor mutation in
Zhang X; Jiang W; Jin Z; Wang X; Song X; Huang S; Zhang M; Lu H
Front Oncol; 2023; 13():1282678. PubMed ID: 37901335
[TBL] [Abstract][Full Text] [Related]
38. Female germ line mosaicism as the origin of a unique IL-2 receptor gamma-chain mutation causing X-linked severe combined immunodeficiency.
Puck JM; Pepper AE; Bédard PM; Laframboise R
J Clin Invest; 1995 Feb; 95(2):895-9. PubMed ID: 7860773
[TBL] [Abstract][Full Text] [Related]
39. Maternal mosaicism for a novel interleukin-2 receptor gamma-chain mutation causing X-linked severe combined immunodeficiency in a Navajo kindred.
O'Marcaigh AS; Puck JM; Pepper AE; De Santes K; Cowan MJ
J Clin Immunol; 1997 Jan; 17(1):29-33. PubMed ID: 9049783
[TBL] [Abstract][Full Text] [Related]
40. Identification of checkpoints in human T-cell development using severe combined immunodeficiency stem cells.
Wiekmeijer AS; Pike-Overzet K; IJspeert H; Brugman MH; Wolvers-Tettero IL; Lankester AC; Bredius RG; van Dongen JJ; Fibbe WE; Langerak AW; van der Burg M; Staal FJ
J Allergy Clin Immunol; 2016 Feb; 137(2):517-526.e3. PubMed ID: 26441229
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]