BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 24817258)

  • 1. RAG1 reversion mosaicism in a patient with Omenn syndrome.
    Crestani E; Choo S; Frugoni F; Lee YN; Richards S; Smart J; Notarangelo LD
    J Clin Immunol; 2014 Jul; 34(5):551-4. PubMed ID: 24817258
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Three faces of recombination activating gene 1 (RAG1) mutations.
    Patiroglu T; Akar HH; Van Der Burg M
    Acta Microbiol Immunol Hung; 2015 Dec; 62(4):393-401. PubMed ID: 26689875
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency.
    Wada T; Toma T; Okamoto H; Kasahara Y; Koizumi S; Agematsu K; Kimura H; Shimada A; Hayashi Y; Kato M; Yachie A
    Blood; 2005 Sep; 106(6):2099-101. PubMed ID: 15845893
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Modeling altered T-cell development with induced pluripotent stem cells from patients with RAG1-dependent immune deficiencies.
    Brauer PM; Pessach IM; Clarke E; Rowe JH; Ott de Bruin L; Lee YN; Dominguez-Brauer C; Comeau AM; Awong G; Felgentreff K; Zhang YH; Bredemeyer A; Al-Herz W; Du L; Ververs F; Kennedy M; Giliani S; Keller G; Sleckman BP; Schatz DG; Bushman FD; Notarangelo LD; Zúñiga-Pflücker JC
    Blood; 2016 Aug; 128(6):783-93. PubMed ID: 27301863
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia.
    Alsmadi O; Al-Ghonaium A; Al-Muhsen S; Arnaout R; Al-Dhekri H; Al-Saud B; Al-Kayal F; Al-Saud H; Al-Mousa H
    BMC Med Genet; 2009 Nov; 10():116. PubMed ID: 19912631
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.
    Lee YN; Frugoni F; Dobbs K; Walter JE; Giliani S; Gennery AR; Al-Herz W; Haddad E; LeDeist F; Bleesing JH; Henderson LA; Pai SY; Nelson RP; El-Ghoneimy DH; El-Feky RA; Reda SM; Hossny E; Soler-Palacin P; Fuleihan RL; Patel NC; Massaad MJ; Geha RS; Puck JM; Palma P; Cancrini C; Chen K; Vihinen M; Alt FW; Notarangelo LD
    J Allergy Clin Immunol; 2014 Apr; 133(4):1099-108. PubMed ID: 24290284
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of anti-herpes simplex virus antibody-producing B cells in a patient with an atypical RAG1 immunodeficiency.
    Kumaki S; Villa A; Asada H; Kawai S; Ohashi Y; Takahashi M; Hakozaki I; Nitanai E; Minegishi M; Tsuchiya S
    Blood; 2001 Sep; 98(5):1464-8. PubMed ID: 11520796
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Recombination-activating gene 1 (Rag1)-deficient mice with severe combined immunodeficiency treated with lentiviral gene therapy demonstrate autoimmune Omenn-like syndrome.
    van Til NP; Sarwari R; Visser TP; Hauer J; Lagresle-Peyrou C; van der Velden G; Malshetty V; Cortes P; Jollet A; Danos O; Cassani B; Zhang F; Thrasher AJ; Fontana E; Poliani PL; Cavazzana M; Verstegen MM; Villa A; Wagemaker G
    J Allergy Clin Immunol; 2014 Apr; 133(4):1116-23. PubMed ID: 24332219
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical, immunologic, and genetic characteristics of RAG mutations in 15 Chinese patients with SCID and Omenn syndrome.
    Bai X; Liu J; Zhang Z; Liu C; Zhang Y; Tang W; Dai R; Wu J; Tang X; Zhang Y; Ding Y; Jiang L; Zhao X
    Immunol Res; 2016 Apr; 64(2):497-507. PubMed ID: 26476733
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Similar recombination-activating gene (RAG) mutations result in similar immunobiological effects but in different clinical phenotypes.
    IJspeert H; Driessen GJ; Moorhouse MJ; Hartwig NG; Wolska-Kusnierz B; Kalwak K; Pituch-Noworolska A; Kondratenko I; van Montfrans JM; Mejstrikova E; Lankester AC; Langerak AW; van Gent DC; Stubbs AP; van Dongen JJ; van der Burg M
    J Allergy Clin Immunol; 2014 Apr; 133(4):1124-33. PubMed ID: 24418478
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Compound heterozygous mutation of Rag1 leading to Omenn syndrome.
    Matthews AG; Briggs CE; Yamanaka K; Small TN; Mooster JL; Bonilla FA; Oettinger MA; Butte MJ
    PLoS One; 2015; 10(4):e0121489. PubMed ID: 25849362
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lack of nonfunctional B-cell receptor rearrangements in a patient with normal B cell numbers despite partial RAG1 deficiency and atypical SCID/Omenn syndrome.
    Ohm-Laursen L; Nielsen C; Fisker N; Lillevang ST; Barington T
    J Clin Immunol; 2008 Sep; 28(5):588-92. PubMed ID: 18592361
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenotypical heterogeneity in RAG-deficient patients from a highly consanguineous population.
    Meshaal SS; El Hawary RE; Abd Elaziz DS; Eldash A; Alkady R; Lotfy S; Mauracher AA; Opitz L; Pachlopnik Schmid J; van der Burg M; Chou J; Galal NM; Boutros JA; Geha R; Elmarsafy AM
    Clin Exp Immunol; 2019 Feb; 195(2):202-212. PubMed ID: 30307608
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Clinical phenotype and gene diagnostic analysis of Omenn syndrome].
    Wang YQ; Cui YX; Feng J
    Zhonghua Er Ke Za Zhi; 2013 Jan; 51(1):64-8. PubMed ID: 23527934
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation c.256_257delAA in RAG1 Gene in Polish Children with Severe Combined Immunodeficiency: Diversity of Clinical Manifestations.
    Szaflarska A; Rutkowska-Zapała M; Kotula M; Gruca A; Grabowska A; Lenart M; Surman M; Trzyna E; Mordel A; Pituch-Noworolska A; Siedlar M
    Arch Immunol Ther Exp (Warsz); 2016 Dec; 64(Suppl 1):177-183. PubMed ID: 28083621
    [TBL] [Abstract][Full Text] [Related]  

  • 16. From Severe Combined Immunodeficiency to Omenn syndrome after hematopoietic stem cell transplantation in a RAG1 deficient family.
    Martinez-Martinez L; Vazquez-Ortiz M; Gonzalez-Santesteban C; Martin-Nalda A; Vicente A; Plaza AM; Badell I; Alsina L; de la Calle-Martin O
    Pediatr Allergy Immunol; 2012 Nov; 23(7):660-6. PubMed ID: 22882342
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome.
    Zhang ZY; Zhao XD; Jiang LP; Liu EM; Cui YX; Wang M; Wei H; Yu J; An YF; Yang XQ
    Pediatr Allergy Immunol; 2011 Aug; 22(5):482-7. PubMed ID: 21771083
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Omenn syndrome--review of several phenotypes of Omenn syndrome and RAG1/RAG2 mutations in Japan.
    Kato M; Kimura H; Seki M; Shimada A; Hayashi Y; Morio T; Kumaki S; Ishida Y; Kamachi Y; Yachie A
    Allergol Int; 2006 Jun; 55(2):115-9. PubMed ID: 17075247
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Leaky severe combined immunodeficiency and aberrant DNA rearrangements due to a hypomorphic RAG1 mutation.
    Giblin W; Chatterji M; Westfield G; Masud T; Theisen B; Cheng HL; DeVido J; Alt FW; Ferguson DO; Schatz DG; Sekiguchi J
    Blood; 2009 Mar; 113(13):2965-75. PubMed ID: 19126872
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    Chen R; Lukianova E; van der Loeff IS; Spegarova JS; Willet JDP; James KD; Ryder EJ; Griffin H; IJspeert H; Gajbhiye A; Lamoliatte F; Marin-Rubio JL; Woodbine L; Lemos H; Swan DJ; Pintar V; Sayes K; Ruiz-Morales ER; Eastham S; Dixon D; Prete M; Prigmore E; Jeggo P; Boyes J; Mellor A; Huang L; van der Burg M; Engelhardt KR; Stray-Pedersen A; Erichsen HC; Gennery AR; Trost M; Adams DJ; Anderson G; Lorenc A; Trynka G; Hambleton S
    Sci Immunol; 2024 May; 9(95):eade5705. PubMed ID: 38787962
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.