BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

274 related articles for article (PubMed ID: 34868061)

  • 1. Reversion Mosaicism in Primary Immunodeficiency Diseases.
    Miyazawa H; Wada T
    Front Immunol; 2021; 12():783022. PubMed ID: 34868061
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Revertant somatic mosaicism in primary immunodeficiency diseases].
    Wada T
    Nihon Rinsho Meneki Gakkai Kaishi; 2014; 37(6):447-53. PubMed ID: 25748128
    [TBL] [Abstract][Full Text] [Related]  

  • 3. In vivo reversion to normal of inherited mutations in humans.
    Hirschhorn R
    J Med Genet; 2003 Oct; 40(10):721-8. PubMed ID: 14569115
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Somatic mosaicism in primary immune deficiencies.
    Wada T; Candotti F
    Curr Opin Allergy Clin Immunol; 2008 Dec; 8(6):510-4. PubMed ID: 18978464
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Somatic mosaicism in Wiskott--Aldrich syndrome suggests in vivo reversion by a DNA slippage mechanism.
    Wada T; Schurman SH; Otsu M; Garabedian EK; Ochs HD; Nelson DL; Candotti F
    Proc Natl Acad Sci U S A; 2001 Jul; 98(15):8697-702. PubMed ID: 11447283
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Revertant somatic mosaicism in the Wiskott-Aldrich syndrome.
    Davis BR; Candotti F
    Immunol Res; 2009; 44(1-3):127-31. PubMed ID: 19129986
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mosaicism of NK cells in a patient with Wiskott-Aldrich syndrome.
    Lutskiy MI; Beardsley DS; Rosen FS; Remold-O'Donnell E
    Blood; 2005 Oct; 106(8):2815-7. PubMed ID: 15985539
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Second-site mutation in the Wiskott-Aldrich syndrome (WAS) protein gene causes somatic mosaicism in two WAS siblings.
    Wada T; Konno A; Schurman SH; Garabedian EK; Anderson SM; Kirby M; Nelson DL; Candotti F
    J Clin Invest; 2003 May; 111(9):1389-97. PubMed ID: 12727931
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency.
    Hirschhorn R; Yang DR; Puck JM; Huie ML; Jiang CK; Kurlandsky LE
    Nat Genet; 1996 Jul; 13(3):290-5. PubMed ID: 8673127
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Investigating the Variation of TREC/KREC in Combined Immunodeficiencies.
    Shakerian L; Nourizadeh M; Badalzadeh M; Fazlollahi MR; Shokouhi Shoormasti R; Saghafi S; Esmaeili B; Alizadeh Z; Borte S; Houshmand M; Hammarström L; Pourpak Z
    Iran J Allergy Asthma Immunol; 2021 Aug; 20(4):402-412. PubMed ID: 34418894
    [TBL] [Abstract][Full Text] [Related]  

  • 11. IKAROS-Associated Diseases in 2020: Genotypes, Phenotypes, and Outcomes in Primary Immune Deficiency/Inborn Errors of Immunity.
    Kuehn HS; Nunes-Santos CJ; Rosenzweig SD
    J Clin Immunol; 2021 Jan; 41(1):1-10. PubMed ID: 33392855
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myeloid malignancies with somatic
    Alfayez M; Wang SA; Bannon SA; Kontoyiannis DP; Kornblau SM; Orange JS; Mace EM; DiNardo CD
    Leuk Lymphoma; 2019 Aug; 60(8):2025-2033. PubMed ID: 30648453
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multiple independent second-site mutations in two siblings with somatic mosaicism for Wiskott-Aldrich syndrome.
    Boztug K; Germeshausen M; Avedillo Díez I; Gulacsy V; Diestelhorst J; Ballmaier M; Welte K; Maródi L; Chernyshova L; Klein C
    Clin Genet; 2008 Jul; 74(1):68-74. PubMed ID: 18479478
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Revertant T lymphocytes in a patient with Wiskott-Aldrich syndrome: analysis of function and distribution in lymphoid organs.
    Trifari S; Scaramuzza S; Catucci M; Ponzoni M; Mollica L; Chiesa R; Cattaneo F; Lafouresse F; Calvez R; Vermi W; Medicina D; Castiello MC; Marangoni F; Bosticardo M; Doglioni C; Caniglia M; Aiuti A; Villa A; Roncarolo MG; Dupré L
    J Allergy Clin Immunol; 2010 Feb; 125(2):439-448.e8. PubMed ID: 20159256
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and Immunological Characterization of Combined Immunodeficiency Due to TFRC Mutation in Eight Patients.
    Aljohani AH; Al-Mousa H; Arnaout R; Al-Dhekri H; Mohammed R; Alsum Z; Nicolas-Jilwan M; Alrogi F; Al-Muhsen S; Alazami AM; Al-Saud B
    J Clin Immunol; 2020 Nov; 40(8):1103-1110. PubMed ID: 32851577
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recombination-induced revertant mosaicism in ichthyosis with confetti and loricrin keratoderma.
    Nomura T
    J Dermatol Sci; 2020 Feb; 97(2):94-100. PubMed ID: 31928837
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiple patients with revertant mosaicism in a single Wiskott-Aldrich syndrome family.
    Wada T; Schurman SH; Jagadeesh GJ; Garabedian EK; Nelson DL; Candotti F
    Blood; 2004 Sep; 104(5):1270-2. PubMed ID: 15142877
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction.
    Gross M; Hanenberg H; Lobitz S; Friedl R; Herterich S; Dietrich R; Gruhn B; Schindler D; Hoehn H
    Cytogenet Genome Res; 2002; 98(2-3):126-35. PubMed ID: 12697994
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Primary Immune Regulatory Disorders and Targeted Therapies.
    Kolukısa B; Barış S
    Turk J Haematol; 2021 Feb; 38(1):1-14. PubMed ID: 33442967
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Somatic recombination underlies frequent revertant mosaicism in loricrin keratoderma.
    Suzuki S; Nomura T; Miyauchi T; Takeda M; Fujita Y; Nishie W; Akiyama M; Ishida-Yamamoto A; Shimizu H
    Life Sci Alliance; 2019 Feb; 2(1):. PubMed ID: 30718378
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.