X-շղթայակցված իխտիոզ (Armenian Wikipedia)

Analysis of information sources in references of the Wikipedia article "X-շղթայակցված իխտիոզ" in Armenian language version.

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24nih.gov

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13doi.org

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2harvard.edu

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2plos.org

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1omim.org

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archive.org

«Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis». Am. J. Hum. Genet. 50 (3): 483–91. 1992 թ․ մարտ. PMC 1684279. PMID 1539590.
«Steroid sulphatase in man: a non inactivated X-locus with partial gene dosage compensation». Hum. Genet. 65 (4): 355–7. 1984. doi:10.1007/BF00291559. PMID 6582028.
«X-linked ichthyosis and X-linked placental sulfatase deficiency: a disease entity. Histochemical observations». Am. J. Pathol. 99 (2): 279–89. 1980. PMC 1903491. PMID 6929654.
«Basis for abnormal desquamation and permeability barrier dysfunction in RXLI». J. Invest. Dermatol. 122 (2): 314–9. 2004. doi:10.1046/j.1523-1747.2003.22258.x. PMID 15009711.

bmj.com

jmg.bmj.com

Brcic, Lucija; Underwood, Jack FG; Kendall, Kimberley M.; Caseras, Xavier; Kirov, George; Davies, William (2020). «Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank». Journal of Medical Genetics. 57 (10): 692–698. doi:10.1136/jmedgenet-2019-106676. PMC 7525778. PMID 32139392.

doi.org

«Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis». Proc. Natl. Acad. Sci. U.S.A. 84 (13): 4519–23. 1987. Bibcode:1987PNAS...84.4519B. doi:10.1073/pnas.84.13.4519. PMC 305121. PMID 3474618.
«Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis». Proc. Natl. Acad. Sci. U.S.A. 84 (24): 9248–51. 1987 թ․ դեկտեմբեր. Bibcode:1987PNAS...84.9248B. doi:10.1073/pnas.84.24.9248. PMC 299730. PMID 3480541.
«Ichthyosis: etiology, diagnosis, and management». Am J Clin Dermatol. 4 (2): 81–95. 2003. doi:10.2165/00128071-200304020-00002. PMID 12553849.
Brcic, Lucija; Underwood, Jack FG; Kendall, Kimberley M.; Caseras, Xavier; Kirov, George; Davies, William (2020). «Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank». Journal of Medical Genetics. 57 (10): 692–698. doi:10.1136/jmedgenet-2019-106676. PMC 7525778. PMID 32139392.
«Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis». Hum. Mol. Genet. 14 (13): 1795–803. 2005. doi:10.1093/hmg/ddi186. PMID 15888481.
«Steroid sulphatase in man: a non inactivated X-locus with partial gene dosage compensation». Hum. Genet. 65 (4): 355–7. 1984. doi:10.1007/BF00291559. PMID 6582028.
«Carrier identification by FISH analysis in isolated cases of X-linked ichthyosis». Am. J. Med. Genet. 102 (2): 146–8. 2001 թ․ օգոստոս. doi:10.1002/ajmg.1450. PMID 11477606.
Valdes-Flores M, Kofman-Alfaro SH, Jimenez-Vaca AL, Cuevas-Covarrubias SA (2001 թ․ օգոստոս). «Carrier identification by FISH analysis in isolated cases of X-linked ichthyosis». Am. J. Med. Genet. 102 (2): 146–8. doi:10.1002/ajmg.1450. PMID 11477606.
«Immunohistochemical analysis of steroid sulfatase in human tissues». J. Steroid Biochem. Mol. Biol. 105 (1–5): 115–23. 2007. doi:10.1016/j.jsbmb.2006.12.105. PMID 17604157.
«Steroid sulfatase: molecular biology, regulation, and inhibition». Endocr. Rev. 26 (2): 171–202. 2005 թ․ ապրիլ. doi:10.1210/er.2004-0003. PMID 15561802.
«Basis for abnormal desquamation and permeability barrier dysfunction in RXLI». J. Invest. Dermatol. 122 (2): 314–9. 2004. doi:10.1046/j.1523-1747.2003.22258.x. PMID 15009711.
Cotellessa C, Cuevas-Covarrubias SA, Valeri P, Fargnoli MC, Peris K (2005). «Topical tazarotene 0.05% versus glycolic acid 70% treatment in X-linked ichthyosis due to extensive deletion of the STS gene». Acta Derm. Venereol. 85 (4): 346–8. doi:10.1080/00015550510026613. PMID 16191859.
Freiberg RA, Choate KA, Deng H, Alperin ES, Shapiro LJ, Khavari PA (1997). «A model of corrective gene transfer in X-linked ichthyosis». Hum. Mol. Genet. 6 (6): 927–33. doi:10.1093/hmg/6.6.927. PMID 9175741.

harvard.edu

ui.adsabs.harvard.edu

«Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis». Proc. Natl. Acad. Sci. U.S.A. 84 (13): 4519–23. 1987. Bibcode:1987PNAS...84.4519B. doi:10.1073/pnas.84.13.4519. PMC 305121. PMID 3474618.
«Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis». Proc. Natl. Acad. Sci. U.S.A. 84 (24): 9248–51. 1987 թ․ դեկտեմբեր. Bibcode:1987PNAS...84.9248B. doi:10.1073/pnas.84.24.9248. PMC 299730. PMID 3480541.

nih.gov

pubmed.ncbi.nlm.nih.gov

«Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis». Proc. Natl. Acad. Sci. U.S.A. 84 (13): 4519–23. 1987. Bibcode:1987PNAS...84.4519B. doi:10.1073/pnas.84.13.4519. PMC 305121. PMID 3474618.
«Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis». Proc. Natl. Acad. Sci. U.S.A. 84 (24): 9248–51. 1987 թ․ դեկտեմբեր. Bibcode:1987PNAS...84.9248B. doi:10.1073/pnas.84.24.9248. PMC 299730. PMID 3480541.
«Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis». Am. J. Hum. Genet. 50 (3): 483–91. 1992 թ․ մարտ. PMC 1684279. PMID 1539590.
«Ichthyosis: etiology, diagnosis, and management». Am J Clin Dermatol. 4 (2): 81–95. 2003. doi:10.2165/00128071-200304020-00002. PMID 12553849.
Brcic, Lucija; Underwood, Jack FG; Kendall, Kimberley M.; Caseras, Xavier; Kirov, George; Davies, William (2020). «Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank». Journal of Medical Genetics. 57 (10): 692–698. doi:10.1136/jmedgenet-2019-106676. PMC 7525778. PMID 32139392.
«Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis». Hum. Mol. Genet. 14 (13): 1795–803. 2005. doi:10.1093/hmg/ddi186. PMID 15888481.
«Placental sulfatase deficiency: maternal and fetal expression of steroid sulfatase deficiency and X-linked ichthyosis». Obstet Gynecol Surv. 41 (7): 401–13. 1986. PMID 3531932.
«Steroid sulphatase in man: a non inactivated X-locus with partial gene dosage compensation». Hum. Genet. 65 (4): 355–7. 1984. doi:10.1007/BF00291559. PMID 6582028.
«Carrier identification by FISH analysis in isolated cases of X-linked ichthyosis». Am. J. Med. Genet. 102 (2): 146–8. 2001 թ․ օգոստոս. doi:10.1002/ajmg.1450. PMID 11477606.
«The biochemical identification of carrier state in mothers of sporadic cases of X-linked recessive ichthyosis». Genet. Couns. 6 (2): 103–7. 1995. PMID 7546451.
Valdes-Flores M, Kofman-Alfaro SH, Jimenez-Vaca AL, Cuevas-Covarrubias SA (2001 թ․ օգոստոս). «Carrier identification by FISH analysis in isolated cases of X-linked ichthyosis». Am. J. Med. Genet. 102 (2): 146–8. doi:10.1002/ajmg.1450. PMID 11477606.
«Immunohistochemical analysis of steroid sulfatase in human tissues». J. Steroid Biochem. Mol. Biol. 105 (1–5): 115–23. 2007. doi:10.1016/j.jsbmb.2006.12.105. PMID 17604157.
«Steroid sulfatase: molecular biology, regulation, and inhibition». Endocr. Rev. 26 (2): 171–202. 2005 թ․ ապրիլ. doi:10.1210/er.2004-0003. PMID 15561802.
«X-linked ichthyosis and X-linked placental sulfatase deficiency: a disease entity. Histochemical observations». Am. J. Pathol. 99 (2): 279–89. 1980. PMC 1903491. PMID 6929654.
«Basis for abnormal desquamation and permeability barrier dysfunction in RXLI». J. Invest. Dermatol. 122 (2): 314–9. 2004. doi:10.1046/j.1523-1747.2003.22258.x. PMID 15009711.
Cotellessa C, Cuevas-Covarrubias SA, Valeri P, Fargnoli MC, Peris K (2005). «Topical tazarotene 0.05% versus glycolic acid 70% treatment in X-linked ichthyosis due to extensive deletion of the STS gene». Acta Derm. Venereol. 85 (4): 346–8. doi:10.1080/00015550510026613. PMID 16191859.
Freiberg RA, Choate KA, Deng H, Alperin ES, Shapiro LJ, Khavari PA (1997). «A model of corrective gene transfer in X-linked ichthyosis». Hum. Mol. Genet. 6 (6): 927–33. doi:10.1093/hmg/6.6.927. PMID 9175741.

ncbi.nlm.nih.gov

«Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis». Proc. Natl. Acad. Sci. U.S.A. 84 (13): 4519–23. 1987. Bibcode:1987PNAS...84.4519B. doi:10.1073/pnas.84.13.4519. PMC 305121. PMID 3474618.
«Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis». Proc. Natl. Acad. Sci. U.S.A. 84 (24): 9248–51. 1987 թ․ դեկտեմբեր. Bibcode:1987PNAS...84.9248B. doi:10.1073/pnas.84.24.9248. PMC 299730. PMID 3480541.
«Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis». Am. J. Hum. Genet. 50 (3): 483–91. 1992 թ․ մարտ. PMC 1684279. PMID 1539590.
Brcic, Lucija; Underwood, Jack FG; Kendall, Kimberley M.; Caseras, Xavier; Kirov, George; Davies, William (2020). «Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank». Journal of Medical Genetics. 57 (10): 692–698. doi:10.1136/jmedgenet-2019-106676. PMC 7525778. PMID 32139392.
Chatterjee S, Humby T, Davies W (2016) Behavioural and psychiatric phenotypes in men and boys with X-linked ichthyosis: evidence from a worldwide online survey. PLoS One 11(10):e0164417 PMID 27711218 doi:10.1371/journal.pone.0164417 URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0164417
Cavenagh A, Chatterjee S, Davies W (2019) Behavioural and psychiatric phenotypes in female carriers of genetic mutations associated with X-linked ichthyosis. PLoS One 14(2):e0212330 PMID 30768640 doi:10.1371/journal.pone.0212330 URL:https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0212330
«X-linked ichthyosis and X-linked placental sulfatase deficiency: a disease entity. Histochemical observations». Am. J. Pathol. 99 (2): 279–89. 1980. PMC 1903491. PMID 6929654.

omim.org

Մենդելյան ժառանգում (OMIM) ICHTHYOSIS, X-LINKED -308100

oxfordjournals.org

hmg.oxfordjournals.org

Freiberg RA, Choate KA, Deng H, Alperin ES, Shapiro LJ, Khavari PA (1997). «A model of corrective gene transfer in X-linked ichthyosis». Hum. Mol. Genet. 6 (6): 927–33. doi:10.1093/hmg/6.6.927. PMID 9175741.

plos.org

journals.plos.org

Chatterjee S, Humby T, Davies W (2016) Behavioural and psychiatric phenotypes in men and boys with X-linked ichthyosis: evidence from a worldwide online survey. PLoS One 11(10):e0164417 PMID 27711218 doi:10.1371/journal.pone.0164417 URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0164417
Cavenagh A, Chatterjee S, Davies W (2019) Behavioural and psychiatric phenotypes in female carriers of genetic mutations associated with X-linked ichthyosis. PLoS One 14(2):e0212330 PMID 30768640 doi:10.1371/journal.pone.0212330 URL:https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0212330