BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 26689875)

  • 21. Mutations in the RNA component of RNase mitochondrial RNA processing might cause Omenn syndrome.
    Roifman CM; Gu Y; Cohen A
    J Allergy Clin Immunol; 2006 Apr; 117(4):897-903. PubMed ID: 16630949
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Analysis of mutations and recombination activity in RAG-deficient patients.
    Asai E; Wada T; Sakakibara Y; Toga A; Toma T; Shimizu T; Nampoothiri S; Imai K; Nonoyama S; Morio T; Muramatsu H; Kamachi Y; Ohara O; Yachie A
    Clin Immunol; 2011 Feb; 138(2):172-7. PubMed ID: 21131235
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Highly variable clinical phenotypes of hypomorphic RAG1 mutations.
    Avila EM; Uzel G; Hsu A; Milner JD; Turner ML; Pittaluga S; Freeman AF; Holland SM
    Pediatrics; 2010 Nov; 126(5):e1248-52. PubMed ID: 20956421
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Leaky RAG Deficiency in Adult Patients with Impaired Antibody Production against Bacterial Polysaccharide Antigens.
    Geier CB; Piller A; Linder A; Sauerwein KM; Eibl MM; Wolf HM
    PLoS One; 2015; 10(7):e0133220. PubMed ID: 26186701
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Partial correction of immunodeficiency by lentiviral vector gene therapy in mouse models carrying
    Castiello MC; Di Verniere M; Draghici E; Fontana E; Penna S; Sereni L; Zecchillo A; Minuta D; Uva P; Zahn M; Gil-Farina I; Annoni A; Iaia S; Ott de Bruin LM; Notarangelo LD; Pike-Overzet K; Staal FJT; Villa A; Capo V
    Front Immunol; 2023; 14():1268620. PubMed ID: 38022635
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A variant of SCID with specific immune responses and predominance of gamma delta T cells.
    Ehl S; Schwarz K; Enders A; Duffner U; Pannicke U; Kühr J; Mascart F; Schmitt-Graeff A; Niemeyer C; Fisch P
    J Clin Invest; 2005 Nov; 115(11):3140-8. PubMed ID: 16211094
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Clinical characteristics of human recombination activating gene 1 mutations in 8 immunodeficiency patients with diverse phenotypes].
    Yu G; Wang WJ; Liu DR; Tao ZF; Hui XY; Hou J; Sun JQ; Wang XC
    Zhonghua Er Ke Za Zhi; 2018 Mar; 56(3):186-191. PubMed ID: 29518828
    [No Abstract]   [Full Text] [Related]  

  • 28. Detection of RAG mutations and prenatal diagnosis in families presenting with either T-B- severe combined immunodeficiency or Omenn's syndrome.
    Tabori U; Mark Z; Amariglio N; Etzioni A; Golan H; Biloray B; Toren A; Rechavi G; Dalal I
    Clin Genet; 2004 Apr; 65(4):322-6. PubMed ID: 15025726
    [TBL] [Abstract][Full Text] [Related]  

  • 29.
    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]  

  • 30. Recombinase-activating gene 1 immunodeficiency: different immunological phenotypes in three siblings.
    Pasic S; Djuricic S; Ristic G; Slavkovic B
    Acta Paediatr; 2009 Jun; 98(6):1062-4. PubMed ID: 19243569
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Atypical Omenn Syndrome Due to RAG2 Gene Mutation, a Case Report.
    Pourvali A; Arshi S; Nabavi M; Bemanian MH; Shokri S; Shahrooei M; Rezaei N; Fallahpour M
    Iran J Immunol; 2019 Dec; 16(4):334-338. PubMed ID: 31885011
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Recent advances in understanding RAG deficiencies.
    Gennery A
    F1000Res; 2019; 8():. PubMed ID: 30800289
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. [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]  

  • 36. A novel homozygous
    Melika S; Hossein E; Mona S; Elham R; Samaneh Z; Sepideh S; Raul Jimenez H; Ana K; Kaan B; Nima R
    Allergol Immunopathol (Madr); 2021; 49(4):91-97. PubMed ID: 34224223
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency.
    Kutukculer N; Gulez N; Karaca NE; Aksu G; Berdeli A
    Ital J Pediatr; 2012 Mar; 38():8. PubMed ID: 22424479
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Relative CD4 lymphopenia and a skewed memory phenotype are the main immunologic abnormalities in a child with Omenn syndrome due to homozygous RAG1-C2633T hypomorphic mutation.
    McCusker C; Hotte S; Le Deist F; Hirschfeld AF; Mitchell D; Nguyen VH; Gagnon R; Mazer B; Turvey SE; Jabado N
    Clin Immunol; 2009 Jun; 131(3):447-55. PubMed ID: 19246248
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 12.