BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 3868422)

  • 1. Detection of heterozygotes of X-linked ichthyosis by measuring steroid sulphatase activity of lymphocytes. Mode of inheritance in three families.
    Okano M; Kitano Y; Nakamura T; Matsuzawa Y
    Br J Dermatol; 1985 Dec; 113(6):645-9. PubMed ID: 3868422
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Steroid sulphatase deficiency in patients initially diagnosed as ichthyosis vulgaris or recessive X-linked ichthyosis.
    Yoshiike T; Matsui T; Ogawa H
    Br J Dermatol; 1985 Apr; 112(4):431-3. PubMed ID: 3857937
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Placental sulfatase deficiency: maternal and fetal expression of steroid sulfatase deficiency and X-linked ichthyosis.
    Bradshaw KD; Carr BR
    Obstet Gynecol Surv; 1986 Jul; 41(7):401-13. PubMed ID: 3531932
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency.
    Ballabio A; Parenti G; Napolitano E; Di Natale P; Andria G
    Hum Genet; 1985; 70(4):315-7. PubMed ID: 3860470
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lipoprotein electrophoresis in recessive X-linked ichthyosis.
    Ibsen HH; Brandrup F; Blaabjerg O; Lykkesfeldt G
    Acta Derm Venereol; 1986; 66(1):59-62. PubMed ID: 2424217
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome.
    Ballabio A; Parenti G; Tippett P; Mondello C; Di Maio S; Tenore A; Andria G
    Hum Genet; 1986 Mar; 72(3):237-40. PubMed ID: 3007328
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hair root analysis in X-linked ichthyosis.
    Dancis J; Jansen V; Hutzler J
    J Inherit Metab Dis; 1983; 6(4):173-7. PubMed ID: 6422158
    [TBL] [Abstract][Full Text] [Related]  

  • 8. X-linked recessive ichthyosis. Reinvestigation of a family first described in 1928.
    Schlammadinger J; Meyer JC; Vajda I; Szabó G
    Dermatologica; 1987; 175(5):217-23. PubMed ID: 3479355
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The effect of steroid sulphatase on stratum corneum shedding in patients with X-linked ichthyosis.
    Yoshiike T; Matsui T; Kimura T; Yamada H; Ogawa H
    Br J Dermatol; 1985 Dec; 113(6):641-3. PubMed ID: 3868421
    [TBL] [Abstract][Full Text] [Related]  

  • 10. X chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis).
    Cooke A; Gillard EF; Yates JR; Mitchell MJ; Aitken DA; Weir DM; Affara NA; Ferguson-Smith MA
    Hum Genet; 1988 May; 79(1):49-52. PubMed ID: 3163320
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Heterozygote detection in steroid sulphatase deficiency.
    Müller CR; Migl B; Ropers HH; Happle R
    Lancet; 1980 Mar; 1(8167):546-7. PubMed ID: 6102271
    [No Abstract]   [Full Text] [Related]  

  • 12. Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome.
    Ballabio A; Sebastio G; Carrozzo R; Parenti G; Piccirillo A; Persico MG; Andria G
    Hum Genet; 1987 Dec; 77(4):338-41. PubMed ID: 3480263
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Absence of testicular steroid sulphatase activity in a boy with recessive X-linked ichthyosis and testicular maldescent.
    Lykkesfeldt G; Müller J; Skakkebaek NE; Bruun E; Lykkesfeldt AE
    Eur J Pediatr; 1985 Sep; 144(3):273-4. PubMed ID: 2865141
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Steroid sulphatase deficiency disease.
    Lykkesfeldt G; Høyer H; Ibsen HH; Brandrup F
    Clin Genet; 1985 Sep; 28(3):231-7. PubMed ID: 2866054
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X-linked recessive ichthyosis in three sisters: evidence for homozygosity.
    Mevorah B; Frenk E; Müller CR; Ropers HH
    Br J Dermatol; 1981 Dec; 105(6):711-7. PubMed ID: 6947821
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency).
    Gillard EF; Affara NA; Yates JR; Goudie DR; Lambert J; Aitken DA; Ferguson-Smith MA
    Nucleic Acids Res; 1987 May; 15(10):3977-85. PubMed ID: 2884621
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial lyonisation of steroid sulphatase gene in single hair roots.
    Willems PJ; de Bruijn HW; Groenhuis A; Mooyaart BR; Berger R
    J Inherit Metab Dis; 1986; 9(2):156-62. PubMed ID: 3091922
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A fluorimetric assay of steroid sulphatase in leukocytes: evidence for two genetically different enzymes with arylsulphatase C activity.
    van Diggelen OP; Konstantinidou AE; Bousema MT; Boer M; Bakx T; Jöbsis AC
    J Inherit Metab Dis; 1989; 12(3):273-80. PubMed ID: 2533306
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Carrier identification in steroid sulphatase deficiency and recessive X-linked ichthyosis.
    Lykkesfeldt G; Lykkesfeldt AE
    Acta Derm Venereol; 1986; 66(2):134-8. PubMed ID: 2424236
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Steroid sulfatase of human leukocytes and epidermis and the diagnosis of recessive X-linked ichthyosis.
    Epstein EH; Leventhal ME
    J Clin Invest; 1981 May; 67(5):1257-62. PubMed ID: 6939689
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.