BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 15702055)

  • 1. A novel mutation in the interleukin-2 receptor gamma gene as the cause of lymphopenia in a neonate vertically exposed to human immunodeficiency virus.
    Neubert J; Meindl A; Theisen A; Adams O; Schulz A; Feyen O; Niehues T
    Pediatr Infect Dis J; 2005 Feb; 24(2):187-9. PubMed ID: 15702055
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [A first pilot study on the neonatal screening of primary immunodeficiencies in Spain: TRECS and KRECS identify severe T- and B-cell lymphopenia].
    Olbrich P; de Felipe B; Delgado-Pecellin C; Rodero R; Rojas P; Aguayo J; Marquez J; Casanovas J; Sánchez B; Lucena JM; Ybot-Gonzalez P; Borte S; Neth O
    An Pediatr (Barc); 2014 Nov; 81(5):310-7. PubMed ID: 25278007
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. LMO2 and gene therapy for severe combined immunodeficiency.
    Fischer A; Abina SH; Thrasher A; von Kalle C; Cavazzana-Calvo M
    N Engl J Med; 2004 Jun; 350(24):2526-7; author reply 2526-7. PubMed ID: 15190153
    [No Abstract]   [Full Text] [Related]  

  • 6. Haemophagocytic lymphohistiocytosis in X-linked severe combined immunodeficiency.
    Grunebaum E; Zhang J; Dadi H; Roifman CM
    Br J Haematol; 2000 Mar; 108(4):834-7. PubMed ID: 10792291
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Carrier and prenatal diagnosis of X-linked severe combined immunodeficiency: mutation detection methods and utilization.
    Puck JM; Middelton L; Pepper AE
    Hum Genet; 1997 May; 99(5):628-33. PubMed ID: 9150730
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of the gammac chain among 27 unrelated Japanese patients with X-linked severe combined immunodeficiency (X-SCID).
    Kumaki S; Ishii N; Minegishi M; Ohashi Y; Hakozaki I; Nonoyama S; Imai K; Morio T; Tsuge I; Sakiyama Y; Miyanoshita A; Miura J; Mayumi M; Heike T; Katamura K; Takada H; Izumi I; Kamizono J; Hibi S; Sasaki H; Kimura M; Kikuta A; Date Y; Sako M; Tanaka H; Sano K; Sugamura K; Tsuchiya S
    Hum Genet; 2000 Oct; 107(4):406-8. PubMed ID: 11129345
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans.
    Noguchi M; Yi H; Rosenblatt HM; Filipovich AH; Adelstein S; Modi WS; McBride OW; Leonard WJ
    Cell; 1993 Apr; 73(1):147-57. PubMed ID: 8462096
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linking newborn severe combined immunodeficiency screening with targeted exome sequencing: A case report.
    Patel DR; Yu H; Wong LC; Lupski JR; Seeborg FO; Rider NL; Martinez CA; Orange JS; Hanson C
    J Allergy Clin Immunol Pract; 2017; 5(5):1442-1444. PubMed ID: 28438538
    [No Abstract]   [Full Text] [Related]  

  • 13. Activation of the T-cell oncogene LMO2 after gene therapy for X-linked severe combined immunodeficiency.
    McCormack MP; Rabbitts TH
    N Engl J Med; 2004 Feb; 350(9):913-22. PubMed ID: 14985489
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Mutations causing severe combined immunodeficiency: detection with a custom resequencing microarray.
    Lebet T; Chiles R; Hsu AP; Mansfield ES; Warrington JA; Puck JM
    Genet Med; 2008 Aug; 10(8):575-85. PubMed ID: 18641513
    [TBL] [Abstract][Full Text] [Related]  

  • 16. T-Cell Receptor Excision Circles in HIV-Exposed, Uninfected Newborns Measured During a National Newborn Screening Program for Severe Combined Immunodeficiency.
    Warszawski J; Thomas C; Dialla O; Garrait V; Dollfus C; Reliquet V; Clech L; Dert C; Mandelbrot L; Audrain M; Blanche S;
    J Pediatr; 2018 Nov; 202():311-314.e2. PubMed ID: 29980289
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Three novel mutations in the interleukin-2 receptor gamma chain gene in four Japanese patients with X-linked severe combined immunodeficiency.
    Minegishi Y; Ishii N; Maeda H; Takagi S; Tsuchida M; Okawa H; Sugamura K; Yata J
    Hum Genet; 1995 Dec; 96(6):681-3. PubMed ID: 8522327
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-linked severe combined immunodeficiency with gamma delta T cells.
    Jung EY; Heike T; Katamura K; Kimata H; Ohmori K; Morikawa Y; Ishii N; Mayumi M
    Acta Paediatr Jpn; 1997 Aug; 39(4):442-7. PubMed ID: 9316288
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector.
    Gaspar HB; Parsley KL; Howe S; King D; Gilmour KC; Sinclair J; Brouns G; Schmidt M; Von Kalle C; Barington T; Jakobsen MA; Christensen HO; Al Ghonaium A; White HN; Smith JL; Levinsky RJ; Ali RR; Kinnon C; Thrasher AJ
    Lancet; 2004 Dec 18-31; 364(9452):2181-7. PubMed ID: 15610804
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2R gamma chain gene by single-strand conformation polymorphism analysis.
    Clark PA; Lester T; Genet S; Jones AM; Hendriks R; Levinsky RJ; Kinnon C
    Hum Genet; 1995 Oct; 96(4):427-32. PubMed ID: 7557965
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.