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 *

116 related articles for article (PubMed ID: 8128316)

  • 1. The UDP-galactose translocator gene is mapped to band Xp11.23-p11.22 containing the Wiskott-Aldrich syndrome locus.
    Hara T; Yamauchi M; Takahashi E; Hoshino M; Aoki K; Ayusawa D; Kawakita M
    Somat Cell Mol Genet; 1993 Nov; 19(6):571-5. PubMed ID: 8128316
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Wiskott-Aldrich syndrome: new molecular and biochemical insights.
    Peacocke M; Siminovitch KA
    J Am Acad Dermatol; 1992 Oct; 27(4):507-19. PubMed ID: 1401301
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3.
    Kwan SP; Lehner T; Hagemann T; Lu B; Blaese M; Ochs H; Wedgwood R; Ott J; Craig IW; Rosen FS
    Genomics; 1991 May; 10(1):29-33. PubMed ID: 1675197
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Molecular genetic diagnosis of Wiskott-Aldrich syndrome].
    Orth U; Rosenkranz W; Schwinger E; Holzgreve W; Gal A
    Monatsschr Kinderheilkd; 1993 Sep; 141(9):728-31. PubMed ID: 8413349
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome.
    Arveiler B; de Saint-Basile G; Fischer A; Griscelli C; Mandel JL
    Am J Hum Genet; 1990 May; 46(5):906-11. PubMed ID: 1971143
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Assignment of the human moesin gene (MSN) to chromosome region Xq11.2-->q12.
    Kishino T; Ariga T; Soejima H; Tamura T; Ohta T; Jinno Y; Yonemura S; Sato N; Tsukita S; Tsukita S
    Cytogenet Cell Genet; 1994; 66(3):167-9. PubMed ID: 8125014
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Wiskott-Aldrich syndrome.
    Peacocke M; Siminovitch KA
    Semin Dermatol; 1993 Sep; 12(3):247-54. PubMed ID: 8105860
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers.
    Kwan SP; Sandkuyl LA; Blaese M; Kunkel LM; Bruns G; Parmley R; Skarshaug S; Page DC; Ott J; Rosen FS
    Genomics; 1988 Jul; 3(1):39-43. PubMed ID: 2906042
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome.
    Derry JM; Ochs HD; Francke U
    Cell; 1994 Aug; 78(4):635-44. PubMed ID: 8069912
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human UDP-galactose translocator: molecular cloning of a complementary DNA that complements the genetic defect of a mutant cell line deficient in UDP-galactose translocator.
    Miura N; Ishida N; Hoshino M; Yamauchi M; Hara T; Ayusawa D; Kawakita M
    J Biochem; 1996 Aug; 120(2):236-41. PubMed ID: 8889805
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expression of human Wiskott-Aldrich syndrome protein in patients' cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteins.
    Huang MM; Tsuboi S; Wong A; Yu XJ; Oh-Eda M; Derry JM; Francke U; Fukuda M; Weinberg KI; Kohn DB
    Gene Ther; 2000 Feb; 7(4):314-20. PubMed ID: 10694812
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Close linkage of hypervariable marker DXS255 to disease locus of Wiskott-Aldrich syndrome.
    de Saint Basile G; Arveiler B; Fraser NJ; Boyd Y; Graig IW; Griscelli G; Fischer A
    Lancet; 1989 Dec; 2(8675):1319-21. PubMed ID: 2574264
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An Alu-mediated deletion at Xp11.23 leading to Wiskott-Aldrich syndrome.
    Lutskiy MI; Jones LN; Rosen FS; Remold-O'Donnell E
    Hum Genet; 2002 May; 110(5):515-9. PubMed ID: 12073025
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome.
    Greer WL; Somani AK; Kwong PC; Peacocke M; Rubin LA; Siminovitch KA
    Genomics; 1990 Mar; 6(3):568-71. PubMed ID: 2328995
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosome.
    Derry JM; Wiedemann P; Blair P; Wang Y; Kerns JA; Lemahieu V; Godfrey VL; Wilkinson JE; Francke U
    Genomics; 1995 Sep; 29(2):471-7. PubMed ID: 8666397
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers.
    De Saint-Basile G; Schlegel N; Caniglia M; Le Deist F; Kaplan C; Lecompte T; Piller F; Fischer A; Griscelli C
    Ann Hematol; 1991 Aug; 63(2):107-10. PubMed ID: 1912030
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Manifestations and linkage analysis in X-linked autoimmunity-immunodeficiency syndrome.
    Ferguson PJ; Blanton SH; Saulsbury FT; McDuffie MJ; Lemahieu V; Gastier JM; Francke U; Borowitz SM; Sutphen JL; Kelly TE
    Am J Med Genet; 2000 Feb; 90(5):390-7. PubMed ID: 10706361
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Carrier detection in Wiskott-Aldrich syndrome: combined use of M27 beta for X-inactivation studies and as a linked probe.
    Goodship J; Carter J; Espanol T; Boyd Y; Malcolm S; Levinsky RJ
    Blood; 1991 Jun; 77(12):2677-81. PubMed ID: 2043768
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome.
    Peacocke M; Siminovitch KA
    Proc Natl Acad Sci U S A; 1987 May; 84(10):3430-3. PubMed ID: 3472214
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The scurfy mouse mutant has previously unrecognized hematological abnormalities and resembles Wiskott-Aldrich syndrome.
    Lyon MF; Peters J; Glenister PH; Ball S; Wright E
    Proc Natl Acad Sci U S A; 1990 Apr; 87(7):2433-7. PubMed ID: 2320565
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.