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 *

195 related articles for article (PubMed ID: 22189290)

  • 1. Altered serotonergic function may partially account for behavioral endophenotypes in steroid sulfatase-deficient mice.
    Trent S; Cassano T; Bedse G; Ojarikre OA; Humby T; Davies W
    Neuropsychopharmacology; 2012 Apr; 37(5):1267-74. PubMed ID: 22189290
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Steroid sulfatase-deficient mice exhibit endophenotypes relevant to attention deficit hyperactivity disorder.
    Trent S; Dennehy A; Richardson H; Ojarikre OA; Burgoyne PS; Humby T; Davies W
    Psychoneuroendocrinology; 2012 Feb; 37(2):221-9. PubMed ID: 21723668
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Biological mechanisms associated with increased perseveration and hyperactivity in a genetic mouse model of neurodevelopmental disorder.
    Trent S; Dean R; Veit B; Cassano T; Bedse G; Ojarikre OA; Humby T; Davies W
    Psychoneuroendocrinology; 2013 Aug; 38(8):1370-80. PubMed ID: 23276394
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits.
    Kent L; Emerton J; Bhadravathi V; Weisblatt E; Pasco G; Willatt LR; McMahon R; Yates JR
    J Med Genet; 2008 Aug; 45(8):519-24. PubMed ID: 18413370
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Converging pharmacological and genetic evidence indicates a role for steroid sulfatase in attention.
    Davies W; Humby T; Kong W; Otter T; Burgoyne PS; Wilkinson LS
    Biol Psychiatry; 2009 Aug; 66(4):360-7. PubMed ID: 19251250
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X-linked ichthyosis associated with psychosis and behavioral abnormalities: a case report.
    Malik A; Amer AB; Salama M; Haddad B; Alrifai MT; Balwi MA; Davies W; Eyaid W
    J Med Case Rep; 2017 Sep; 11(1):267. PubMed ID: 28934990
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder.
    Brookes KJ; Hawi Z; Kirley A; Barry E; Gill M; Kent L
    Am J Med Genet B Neuropsychiatr Genet; 2008 Dec; 147B(8):1531-5. PubMed ID: 18937300
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic and pharmacological modulation of the steroid sulfatase axis improves response control; comparison with drugs used in ADHD.
    Davies W; Humby T; Trent S; Eddy JB; Ojarikre OA; Wilkinson LS
    Neuropsychopharmacology; 2014 Oct; 39(11):2622-32. PubMed ID: 24842408
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Xp22.3 interstitial deletion: a recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation.
    Ben Khelifa H; Soyah N; Ben-Abdallah-Bouhjar I; Gritly R; Sanlaville D; Elghezal H; Saad A; Mougou-Zerelli S
    Gene; 2013 Sep; 527(2):578-83. PubMed ID: 23791652
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder.
    Stergiakouli E; Langley K; Williams H; Walters J; Williams NM; Suren S; Giegling I; Wilkinson LS; Owen MJ; O'Donovan MC; Rujescu D; Thapar A; Davies W
    Genes Brain Behav; 2011 Apr; 10(3):334-44. PubMed ID: 21255266
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients.
    Afzal S; Ramzan K; Ullah S; Wakil SM; Jamal A; Basit S; Waqar AB
    BMC Med Genet; 2020 Jan; 21(1):20. PubMed ID: 32005174
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Behavioural and psychiatric phenotypes in female carriers of genetic mutations associated with X-linked ichthyosis.
    Cavenagh A; Chatterjee S; Davies W
    PLoS One; 2019; 14(2):e0212330. PubMed ID: 30768640
    [TBL] [Abstract][Full Text] [Related]  

  • 13. X-linked ichthyosis: Clinical and molecular findings in 35 Italian patients.
    Diociaiuti A; Angioni A; Pisaneschi E; Alesi V; Zambruno G; Novelli A; El Hachem M
    Exp Dermatol; 2019 Oct; 28(10):1156-1163. PubMed ID: 29672931
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The detection of steroid sulfatase gene deletion (STS) in Egyptian males with X-linked ichthyosis.
    Abdel-Hamed MF; Hussein HA; Helmy NA; Elsaie ML
    J Drugs Dermatol; 2010 Oct; 9(10):1192-6. PubMed ID: 20941942
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations.
    Ramesh R; Chen H; Kukula A; Wakeling EL; Rustin MH; McLean WH
    J Dermatol Sci; 2011 Dec; 64(3):159-62. PubMed ID: 21945601
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Role of steroid sulfatase in steroid homeostasis and characterization of the sulfated steroid pathway: Evidence from steroid sulfatase deficiency.
    Sánchez-Guijo A; Neunzig J; Gerber A; Oji V; Hartmann MF; Schuppe HC; Traupe H; Bernhardt R; Wudy SA
    Mol Cell Endocrinol; 2016 Dec; 437():142-153. PubMed ID: 27531568
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in X-linked ichthyosis disrupt the active site structure of estrone/DHEA sulfatase.
    Ghosh D
    Biochim Biophys Acta; 2004 Dec; 1739(1):1-4. PubMed ID: 15607112
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Investigation of steroid sulfatase gene in two pedigrees with X-linked ichthyosis].
    Liu A; Xiao SX; Tan SS; Jiao T; Liu Y; Li XL; Zhou SN
    Di Yi Jun Yi Da Xue Xue Bao; 2005 Aug; 25(8):1023-5. PubMed ID: 16109567
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Polymorphisms of the steroid sulfatase (STS) gene are associated with attention deficit hyperactivity disorder and influence brain tissue mRNA expression.
    Brookes KJ; Hawi Z; Park J; Scott S; Gill M; Kent L
    Am J Med Genet B Neuropsychiatr Genet; 2010 Dec; 153B(8):1417-24. PubMed ID: 20862695
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deletion of exons 1-5 of the STS gene causing X-linked ichthyosis.
    Valdes-Flores M; Kofman-Alfaro SH; Vaca AL; Cuevas-Covarrubias SA
    J Invest Dermatol; 2001 Mar; 116(3):456-8. PubMed ID: 11231321
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.