These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 36529093)

  • 61. Radiosensitive SCID patients with Artemis gene mutations show a complete B-cell differentiation arrest at the pre-B-cell receptor checkpoint in bone marrow.
    Noordzij JG; Verkaik NS; van der Burg M; van Veelen LR; de Bruin-Versteeg S; Wiegant W; Vossen JM; Weemaes CM; de Groot R; Zdzienicka MZ; van Gent DC; van Dongen JJ
    Blood; 2003 Feb; 101(4):1446-52. PubMed ID: 12406895
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Hypomorphic Rag mutations can cause destructive midline granulomatous disease.
    De Ravin SS; Cowen EW; Zarember KA; Whiting-Theobald NL; Kuhns DB; Sandler NG; Douek DC; Pittaluga S; Poliani PL; Lee YN; Notarangelo LD; Wang L; Alt FW; Kang EM; Milner JD; Niemela JE; Fontana-Penn M; Sinal SH; Malech HL
    Blood; 2010 Aug; 116(8):1263-71. PubMed ID: 20489056
    [TBL] [Abstract][Full Text] [Related]  

  • 63. A human severe combined immunodeficiency (SCID) condition with increased sensitivity to ionizing radiations and impaired V(D)J rearrangements defines a new DNA recombination/repair deficiency.
    Nicolas N; Moshous D; Cavazzana-Calvo M; Papadopoulo D; de Chasseval R; Le Deist F; Fischer A; de Villartay JP
    J Exp Med; 1998 Aug; 188(4):627-34. PubMed ID: 9705945
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Unrelated Hematopoietic Cell Transplantation in a Patient with Combined Immunodeficiency with Granulomatous Disease and Autoimmunity Secondary to RAG Deficiency.
    John T; Walter JE; Schuetz C; Chen K; Abraham RS; Bonfim C; Boyce TG; Joshi AY; Kang E; Carvalho BT; Mahajerin A; Nugent D; Puthenveetil G; Soni A; Su H; Cowan MJ; Notarangelo L; Buchbinder D
    J Clin Immunol; 2016 Oct; 36(7):725-32. PubMed ID: 27539235
    [TBL] [Abstract][Full Text] [Related]  

  • 65. A new gene involved in DNA double-strand break repair and V(D)J recombination is located on human chromosome 10p.
    Moshous D; Li L; Chasseval R; Philippe N; Jabado N; Cowan MJ; Fischer A; de Villartay JP
    Hum Mol Genet; 2000 Mar; 9(4):583-8. PubMed ID: 10699181
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Rag-1 mutations associated with B-cell-negative scid dissociate the nicking and transesterification steps of V(D)J recombination.
    Li W; Chang FC; Desiderio S
    Mol Cell Biol; 2001 Jun; 21(12):3935-46. PubMed ID: 11359901
    [TBL] [Abstract][Full Text] [Related]  

  • 67. 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]  

  • 68. 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]  

  • 69. Generation of recombination activating gene-1-deficient neonatal piglets: a model of T and B cell deficient severe combined immune deficiency.
    Ito T; Sendai Y; Yamazaki S; Seki-Soma M; Hirose K; Watanabe M; Fukawa K; Nakauchi H
    PLoS One; 2014; 9(12):e113833. PubMed ID: 25437445
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Immunological assessment of a patient with Omenn syndrome resulting from compound heterozygous mutations in the RAG1 gene.
    Mou W; Yang Z; Wang X; Hei M; Wang Y; Gui J
    Immunogenetics; 2023 Aug; 75(4):385-393. PubMed ID: 37269334
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Intrathymic restriction and peripheral expansion of the T-cell repertoire in Omenn syndrome.
    Signorini S; Imberti L; Pirovano S; Villa A; Facchetti F; Ungari M; Bozzi F; Albertini A; Ugazio AG; Vezzoni P; Notarangelo LD
    Blood; 1999 Nov; 94(10):3468-78. PubMed ID: 10552957
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Novel RAG1 mutation in a case of severe combined immunodeficiency.
    Zhang J; Quintal L; Atkinson A; Williams B; Grunebaum E; Roifman CM
    Pediatrics; 2005 Sep; 116(3):e445-9. PubMed ID: 16061569
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Unusual phenotype in patients with a hypomorphic mutation in the DCLRE1C gene: IgG hypergammaglobulinemia with IgA and IgE deficiency.
    Nahum A; Somech R; Shubinsky G; Levy J; Broides A
    Clin Immunol; 2020 Apr; 213():108366. PubMed ID: 32092471
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Clinical and immunological manifestations of patients with atypical severe combined immunodeficiency.
    Felgentreff K; Perez-Becker R; Speckmann C; Schwarz K; Kalwak K; Markelj G; Avcin T; Qasim W; Davies EG; Niehues T; Ehl S
    Clin Immunol; 2011 Oct; 141(1):73-82. PubMed ID: 21664875
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Mutations in Recombination Activating Gene 1 and 2 in patients with severe combined immunodeficiency disorders in Egypt.
    Meshaal S; El Hawary R; Elsharkawy M; Mousa RK; Farid RJ; Abd Elaziz D; Alkady R; Galal N; Massaad MJ; Boutros J; Elmarsafy A
    Clin Immunol; 2015 Jun; 158(2):167-73. PubMed ID: 25869295
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV.
    Buck D; Moshous D; de Chasseval R; Ma Y; le Deist F; Cavazzana-Calvo M; Fischer A; Casanova JL; Lieber MR; de Villartay JP
    Eur J Immunol; 2006 Jan; 36(1):224-35. PubMed ID: 16358361
    [TBL] [Abstract][Full Text] [Related]  

  • 77. 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]  

  • 78. Complete arrest from pro- to pre-B cells in a case of B cell-negative severe combined immunodeficiency (SCID) without recombinase activating gene (RAG) mutations.
    Agematsu K; Nagumo H; Hokibara S; Mori T; Wada T; Yachie A; Kanegane H; Miyawaki T; Sugita K; Karasuyama H; Komiyama A
    Clin Exp Immunol; 2001 Jun; 124(3):461-4. PubMed ID: 11472408
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Signal joint formation is inhibited in murine scid preB cells and fibroblasts in substrates with homopolymeric coding ends.
    Sun T; Ezekiel UR; Erskine L; Agulo R; Bozek G; Roth D; Storb U
    Mol Immunol; 1999 Jun; 36(8):551-8. PubMed ID: 10475610
    [TBL] [Abstract][Full Text] [Related]  

  • 80. A hypomorphic Artemis human disease allele causes aberrant chromosomal rearrangements and tumorigenesis.
    Jacobs C; Huang Y; Masud T; Lu W; Westfield G; Giblin W; Sekiguchi JM
    Hum Mol Genet; 2011 Feb; 20(4):806-19. PubMed ID: 21147755
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.