Similar articles for PMID: 3032454

Year	Number of Results
1979	1
1980	5
1981	4
1982	3
1983	6
1984	6
1985	6
1986	7
1987	16
1988	5
1989	6
1990	8
1991	2
1992	5
1994	2
1995	4
1996	4
1997	2
1999	1
2000	3
2001	2
2003	1
2008	1
2010	1
2013	1
2020	1
2024	0

1

Cloning and expression of steroid sulfatase cDNA and the frequent occurrence of deletions in STS deficiency: implications for X-Y interchange.

Yen PH, Allen E, Marsh B, Mohandas T, Wang N, Taggart RT, Shapiro LJ. Yen PH, et al. Cell. 1987 May 22;49(4):443-54. doi: 10.1016/0092-8674(87)90447-8. Cell. 1987. PMID: 3032454

2

Molecular studies of deletions at the human steroid sulfatase locus.

Shapiro LJ, Yen P, Pomerantz D, Martin E, Rolewic L, Mohandas T. Shapiro LJ, et al. Proc Natl Acad Sci U S A. 1989 Nov;86(21):8477-81. doi: 10.1073/pnas.86.21.8477. Proc Natl Acad Sci U S A. 1989. PMID: 2813406 Free PMC article.

3

Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase.

Conary JT, Lorkowski G, Schmidt B, Pohlmann R, Nagel G, Meyer HE, Krentler C, Cully J, Hasilik A, von Figura K. Conary JT, et al. Biochem Biophys Res Commun. 1987 Apr 29;144(2):1010-7. doi: 10.1016/s0006-291x(87)80064-5. Biochem Biophys Res Commun. 1987. PMID: 3034252

4

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.

5

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. Gillard EF, et al. Nucleic Acids Res. 1987 May 26;15(10):3977-85. doi: 10.1093/nar/15.10.3977. Nucleic Acids Res. 1987. PMID: 2884621 Free PMC article.

6

Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis.

Ballabio A, Parenti G, Carrozzo R, Sebastio G, Andria G, Buckle V, Fraser N, Craig I, Rocchi M, Romeo G, et al. Ballabio A, et al. Proc Natl Acad Sci U S A. 1987 Jul;84(13):4519-23. doi: 10.1073/pnas.84.13.4519. Proc Natl Acad Sci U S A. 1987. PMID: 3474618 Free PMC article.

7

The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: evidence for an inversion of the Y chromosome during primate evolution.

Yen PH, Marsh B, Allen E, Tsai SP, Ellison J, Connolly L, Neiswanger K, Shapiro LJ. Yen PH, et al. Cell. 1988 Dec 23;55(6):1123-35. doi: 10.1016/0092-8674(88)90257-7. Cell. 1988. PMID: 3203382

8

Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels.

Ballabio A, Carrozzo R, Parenti G, Gil A, Zollo M, Persico MG, Gillard E, Affara N, Yates J, Ferguson-Smith MA, et al. Ballabio A, et al. Genomics. 1989 Jan;4(1):36-40. doi: 10.1016/0888-7543(89)90311-x. Genomics. 1989. PMID: 2644167 Clinical Trial.

9

Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: evidence for an ancestral pseudoautosomal gene?

Fraser N, Ballabio A, Zollo M, Persico G, Craig I. Fraser N, et al. Development. 1987;101 Suppl:127-32. doi: 10.1242/dev.101.Supplement.127. Development. 1987. PMID: 3503710

10

Steroid sulfatase gene in XX males.

Mohandas TK, Stern HJ, Meeker CA, Passage MB, Müller U, Page DC, Yen PH, Shapiro LJ. Mohandas TK, et al. Am J Hum Genet. 1990 Feb;46(2):369-76. Am J Hum Genet. 1990. PMID: 2301402 Free PMC article.

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