Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 100

Similar articles for PubMed (Select 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. doi: 10.1038/npp.2011.314. Epub 2011 Dec 21.

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. doi: 10.1016/j.psyneuen.2011.06.006. Epub 2011 Jul 1.

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. doi: 10.1016/j.psyneuen.2012.12.002. Epub 2012 Dec 29.

4.

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 15;66(4):360-7. doi: 10.1016/j.biopsych.2009.01.001. Epub 2009 Feb 28.

5.

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. doi: 10.1136/jmg.2008.057729. Epub 2008 Apr 15.

PMID:
18413370
6.

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 5;147B(8):1531-5. doi: 10.1002/ajmg.b.30873.

PMID:
18937300
7.

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. doi: 10.1111/j.1601-183X.2010.00672.x. Epub 2011 Jan 24.

8.

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 25;527(2):578-83. doi: 10.1016/j.gene.2013.06.018. Epub 2013 Jun 18.

PMID:
23791652
9.

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.

PMID:
20941942
10.

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. doi: 10.1016/j.jdermsci.2011.07.006. Epub 2011 Aug 27.

PMID:
21945601
11.

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 5;153B(8):1417-24. doi: 10.1002/ajmg.b.31120. Epub 2010 Sep 22.

12.
13.

Postnatal changes in serotonergic innervation to the hippocampus of methyl-CpG-binding protein 2-null mice.

Isoda K, Morimoto M, Matsui F, Hasegawa T, Tozawa T, Morioka S, Chiyonobu T, Nishimura A, Yoshimoto K, Hosoi H.

Neuroscience. 2010 Feb 17;165(4):1254-60. doi: 10.1016/j.neuroscience.2009.11.036. Epub 2009 Nov 22.

PMID:
19932741
14.

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. doi: 10.1038/npp.2014.115. Epub 2014 May 20.

15.

Loss of brain-derived neurotrophic factor gene allele exacerbates brain monoamine deficiencies and increases stress abnormalities of serotonin transporter knockout mice.

Ren-Patterson RF, Cochran LW, Holmes A, Sherrill S, Huang SJ, Tolliver T, Lesch KP, Lu B, Murphy DL.

J Neurosci Res. 2005 Mar 15;79(6):756-71.

PMID:
15672416
16.

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.

17.

[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. Chinese.

18.

Behavioral and neurochemical characterization of mice deficient in the N-type Ca2+ channel alpha1B subunit.

Nakagawasai O, Onogi H, Mitazaki S, Sato A, Watanabe K, Saito H, Murai S, Nakaya K, Murakami M, Takahashi E, Tan-No K, Tadano T.

Behav Brain Res. 2010 Mar 17;208(1):224-30. doi: 10.1016/j.bbr.2009.11.042. Epub 2009 Dec 4.

PMID:
19963013
19.

Mice with reduced brain-derived neurotrophic factor expression show decreased choline acetyltransferase activity, but regular brain monoamine levels and unaltered emotional behavior.

Chourbaji S, Hellweg R, Brandis D, Zörner B, Zacher C, Lang UE, Henn FA, Hörtnagl H, Gass P.

Brain Res Mol Brain Res. 2004 Feb 5;121(1-2):28-36.

PMID:
14969734
20.

X-linked ichthyosis without STS deficiency: clinical, genetical, and molecular studies.

Robledo R, Melis P, Schillinger E, Casciano I, Balazs I, Rinaldi A, Siniscalco M, Filippi G.

Am J Med Genet. 1995 Nov 6;59(2):143-8.

PMID:
8588575
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk