Similar articles for PMID: 3480541

Year	Number of Results
1954	1
1956	1
1957	2
1959	1
1963	1
1979	4
1980	9
1981	11
1982	7
1983	18
1984	12
1985	17
1986	16
1987	18
1988	9
1989	7
1990	8
1991	2
1992	3
1993	1
1995	2
1996	1
1997	3
1998	1
2000	1
2002	1
2011	1
2012	1
2014	2
2015	1
2016	1
2018	1
2019	1
2020	1
2023	2
2024	0

1

Cloning of a cDNA for steroid sulfatase: frequent occurrence of gene deletions in patients with recessive X chromosome-linked ichthyosis.

Bonifas JM, Morley BJ, Oakey RE, Kan YW, Epstein EH Jr. Bonifas JM, et al. Proc Natl Acad Sci U S A. 1987 Dec;84(24):9248-51. doi: 10.1073/pnas.84.24.9248. Proc Natl Acad Sci U S A. 1987. PMID: 3480541 Free PMC article.

2

Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report.

Vasilyeva TA, Marakhonov AV, Tebieva IS, Kadyshev VV, Borovikov AO, Markova ZG, Chukhrova AL, Ginter EK, Kutsev SI, Zinchenko RA. Vasilyeva TA, et al. Int J Mol Sci. 2023 Feb 24;24(5):4515. doi: 10.3390/ijms24054515. Int J Mol Sci. 2023. PMID: 36901946 Free PMC article.

3

SulfAtlas, the sulfatase database: state of the art and new developments.

Stam M, Lelièvre P, Hoebeke M, Corre E, Barbeyron T, Michel G. Stam M, et al. Nucleic Acids Res. 2023 Jan 6;51(D1):D647-D653. doi: 10.1093/nar/gkac977. Nucleic Acids Res. 2023. PMID: 36318251 Free PMC article.

4

Is X-linked Recessive Ichthyosis a High Risk for Basal Cell Carcinoma?

Wakumoto K, Yoshida Y, Yamamoto O. Wakumoto K, et al. Yonago Acta Med. 2020 Feb 20;63(1):92-94. doi: 10.33160/yam.2020.02.012. eCollection 2020 Feb. Yonago Acta Med. 2020. PMID: 32158339 Free PMC article.

5

Editorial: Relevance of Steroid Biosynthesis, Metabolism and Transport in Pathophysiology and Drug Discovery.

Rižner TL. Rižner TL. Front Pharmacol. 2019 Mar 26;10:245. doi: 10.3389/fphar.2019.00245. eCollection 2019. Front Pharmacol. 2019. PMID: 30971920 Free PMC article. No abstract available.

6

Multiple Sulfatase Deficiency: A Case Series With a Novel Mutation.

Hijazi L, Kashgari A, Alfadhel M. Hijazi L, et al. J Child Neurol. 2018 Nov;33(13):820-824. doi: 10.1177/0883073818790851. Epub 2018 Aug 20. J Child Neurol. 2018. PMID: 30124108

7

Sulfatase activities are regulated by the interaction of the sulfatase-modifying factor 1 with SUMF2.

Zito E, Fraldi A, Pepe S, Annunziata I, Kobinger G, Di Natale P, Ballabio A, Cosma MP. Zito E, et al. EMBO Rep. 2016 Dec;17(12):1901. doi: 10.15252/embr.201570010. EMBO Rep. 2016. PMID: 27909074 Free PMC article.

8

Neonatal multiple sulfatase deficiency with a novel mutation and review of the literature.

Nur BG, Mıhçı E, Pepe S, Biberoğlu G, Ezgü FS, Ballabio A, Öztekin O, Dursun O. Nur BG, et al. Turk J Pediatr. 2014 Jul-Aug;56(4):418-22. Turk J Pediatr. 2014. PMID: 25818962 Review.

9

High levels of oxysterol sulfates in serum of patients with steroid sulfatase deficiency.

Sánchez-Guijo A, Oji V, Hartmann MF, Schuppe HC, Traupe H, Wudy SA. Sánchez-Guijo A, et al. J Lipid Res. 2015 Feb;56(2):403-12. doi: 10.1194/jlr.M055608. Epub 2014 Dec 11. J Lipid Res. 2015. PMID: 25502769 Free PMC article.

10

Evaluation of sulfatase-directed quinone methide traps for proteomics.

Lenger J, Schröder M, Ennemann EC, Müller B, Wong CH, Noll T, Dierks T, Hanson SR, Sewald N. Lenger J, et al. Bioorg Med Chem. 2012 Jan 15;20(2):622-7. doi: 10.1016/j.bmc.2011.04.044. Epub 2011 Apr 24. Bioorg Med Chem. 2012. PMID: 21570853 Free PMC article.

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