128 related articles for article (PubMed ID: 8541866)
21. Sharing of a common gamma chain, gamma c, by the IL-2, IL-4, and IL-7 receptors: implications for X-linked severe combined immunodeficiency (XSCID).
Leonard WJ; Noguchi M; Russell SM
Adv Exp Med Biol; 1994; 365():225-32. PubMed ID: 7887307
[No Abstract] [Full Text] [Related]
22. The defective gene in X-linked severe combined immunodeficiency encodes a shared interleukin receptor subunit: implications for cytokine pleiotropy and redundancy.
Leonard WJ
Curr Opin Immunol; 1994 Aug; 6(4):631-5. PubMed ID: 7946053
[TBL] [Abstract][Full Text] [Related]
23. The molecular basis of X-linked severe combined immunodeficiency: the role of the interleukin-2 receptor gamma chain as a common gamma chain, gamma c.
Leonard WJ; Noguchi M; Russell SM; McBride OW
Immunol Rev; 1994 Apr; 138():61-86. PubMed ID: 8070818
[TBL] [Abstract][Full Text] [Related]
24. 'Bubble boy' paradox resolved.
Nowak R
Science; 1993 Dec; 262(5141):1818. PubMed ID: 8266068
[No Abstract] [Full Text] [Related]
25. Detection of a novel nonsense mutation in the interleukin 2 receptor gamma gene causing X-linked severe combined immunodeficiency.
Cohen L; Hirschfeld AF; Junker AK; Davis J; Turvey SE
Ann Allergy Asthma Immunol; 2006 Apr; 96(4):632. PubMed ID: 16680939
[No Abstract] [Full Text] [Related]
26. IL2RGbase: a database of gamma c-chain defects causing human X-SCID.
Puck JM
Immunol Today; 1996 Nov; 17(11):507-11. PubMed ID: 8961626
[No Abstract] [Full Text] [Related]
27. Interleukin-2 (IL-2) receptor gamma chain mutations in X-linked severe combined immunodeficiency disease result in the loss of high-affinity IL-2 receptor binding.
DiSanto JP; Dautry-Varsat A; Certain S; Fischer A; de Saint Basile G
Eur J Immunol; 1994 Feb; 24(2):475-9. PubMed ID: 8299698
[TBL] [Abstract][Full Text] [Related]
28. A novel splice-site mutation in the common gamma chain (gammac) gene IL2RG results in X-linked severe combined immunodeficiency with an atypical NK+ phenotype.
Ginn SL; Smyth C; Wong M; Bennetts B; Rowe PB; Alexander IE
Hum Mutat; 2004 May; 23(5):522-3. PubMed ID: 15108287
[TBL] [Abstract][Full Text] [Related]
29. Mosaicism in X-linked severe combined immunodeficiency.
Ting SS; Ziegler J; Leigh D; Kemp A; Lindeman R
J Pediatr; 1998 Oct; 133(4):575-6. PubMed ID: 9787703
[TBL] [Abstract][Full Text] [Related]
30. Two point mutations (313 + 1G --> A and 313 + 1G --> T) in the splice donor site of intron 3 of the low-density lipoprotein receptor gene are associated with familial hypercholesterolemia.
Jensen HK; Jensen LG; Hansen PS; Faergeman O; Gregersen N
Hum Mutat; 1996; 7(3):269-71. PubMed ID: 8829662
[No Abstract] [Full Text] [Related]
31. Comparison of five retrovirus vectors containing the human IL-2 receptor gamma chain gene for their ability to restore T and B lymphocytes in the X-linked severe combined immunodeficiency mouse model.
Avilés Mendoza GJ; Seidel NE; Otsu M; Anderson SM; Simon-Stoos K; Herrera A; Hoogstraten-Miller S; Malech HL; Candotti F; Puck JM; Bodine DM
Mol Ther; 2001 Apr; 3(4):565-73. PubMed ID: 11319919
[TBL] [Abstract][Full Text] [Related]
32. Arrested rearrangement of TCR V beta genes in thymocytes from children with X-linked severe combined immunodeficiency disease.
Sleasman JW; Harville TO; White GB; George JF; Barrett DJ; Goodenow MM
J Immunol; 1994 Jul; 153(1):442-8. PubMed ID: 8207253
[TBL] [Abstract][Full Text] [Related]
33. Interleukin-2 receptor gamma-chain mutations in severe combined immunodeficiency with B-lymphocytes.
Tsuge I; Matsuoka H; Abe T; Kamachi Y; Torii S
Eur J Pediatr; 1996 Dec; 155(12):1018-24. PubMed ID: 8956936
[TBL] [Abstract][Full Text] [Related]
34. A missense mutation in exon 4 of the human adenosine deaminase gene causes severe combined immunodeficiency.
Atasoy U; Norby-Slycord CJ; Markert ML
Hum Mol Genet; 1993 Aug; 2(8):1307-8. PubMed ID: 7691348
[No Abstract] [Full Text] [Related]
35. Substitution of A1498D in noncollagen domain of a5(IV) collagen chain associated with adult-onset X-linked Alport syndrome.
Tverskaya S; Bobrynina V; Tsalykova F; Ignatova M; Krasnopolskaya X; Evgrafov O
Hum Mutat; 1996; 7(2):149-50. PubMed ID: 8829632
[No Abstract] [Full Text] [Related]
36. WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
Derry JM; Kerns JA; Weinberg KI; Ochs HD; Volpini V; Estivill X; Walker AP; Francke U
Hum Mol Genet; 1995 Jul; 4(7):1127-35. PubMed ID: 8528199
[TBL] [Abstract][Full Text] [Related]
37. IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human disease.
Henthorn PS; Somberg RL; Fimiani VM; Puck JM; Patterson DF; Felsburg PJ
Genomics; 1994 Sep; 23(1):69-74. PubMed ID: 7829104
[TBL] [Abstract][Full Text] [Related]
38. X-linked severe combined immunodeficiency syndrome: the first Korean case with gamma c chain gene mutation and subsequent genetic counseling.
Jo EK; Kumaki S; Wei D; Tsuchiya S; Kanegane H; Song CH; Noh HY; Kim YO; Kim SY; Chung HY; Kim YH; Kook H
J Korean Med Sci; 2004 Feb; 19(1):123-6. PubMed ID: 14966353
[TBL] [Abstract][Full Text] [Related]
39. Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterization.
Mella P; Imberti L; Brugnoni D; Pirovano S; Candotti F; Mazzolari E; Bettinardi A; Fiorini M; De Mattia D; Martire B; Plebani A; Notarangelo LD; Giliani S
Clin Immunol; 2000 Apr; 95(1 Pt 1):39-50. PubMed ID: 10794431
[TBL] [Abstract][Full Text] [Related]
40. Restoration of lymphoid populations in a murine model of X-linked severe combined immunodeficiency by a gene-therapy approach.
Lo M; Bloom ML; Imada K; Berg M; Bollenbacher JM; Bloom ET; Kelsall BL; Leonard WJ
Blood; 1999 Nov; 94(9):3027-36. PubMed ID: 10556186
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]