Zollo M - Search Results

1

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. Among authors: zollo m. Genomics. 1989 Jan;4(1):36-40. doi: 10.1016/0888-7543(89)90311-x. Genomics. 1989. PMID: 2644167 Clinical Trial.

2

Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiency.

Ballabio A, Zollo M, Carrozzo R, Caiulo A, Zuffardi O, Cascioli CF, Viggiano D, Strisciuglio P. Ballabio A, et al. Among authors: zollo m. Am J Med Genet. 1991 Nov 1;41(2):184-7. doi: 10.1002/ajmg.1320410210. Am J Med Genet. 1991. PMID: 1785631

3

Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification.

Ballabio A, Ranier JE, Chamberlain JS, Zollo M, Caskey CT. Ballabio A, et al. Among authors: zollo m. Hum Genet. 1990 May;84(6):571-3. doi: 10.1007/BF00210812. Hum Genet. 1990. PMID: 2338343 Free article.

4

Molecular characterization of a gene of the 'EGF family' expressed in undifferentiated human NTERA2 teratocarcinoma cells.

Ciccodicola A, Dono R, Obici S, Simeone A, Zollo M, Persico MG. Ciccodicola A, et al. Among authors: zollo m. EMBO J. 1989 Jul;8(7):1987-91. doi: 10.1002/j.1460-2075.1989.tb03605.x. EMBO J. 1989. PMID: 2792079 Free PMC article.

5

Molecular studies of marsupial X chromosomes reveal limited sequence homology of mammalian X-linked genes.

Kaslow DC, Migeon BR, Persico MG, Zollo M, VandeBerg JL, Samollow PB. Kaslow DC, et al. Among authors: zollo m. Genomics. 1987 Sep;1(1):19-28. doi: 10.1016/0888-7543(87)90100-5. Genomics. 1987. PMID: 2822568

6

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. Among authors: zollo m. Development. 1987;101 Suppl:127-32. doi: 10.1242/dev.101.Supplement.127. Development. 1987. PMID: 3503710

7

Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3).

Mastroianni N, De Fusco M, Zollo M, Arrigo G, Zuffardi O, Bettinelli A, Ballabio A, Casari G. Mastroianni N, et al. Among authors: zollo m. Genomics. 1996 Aug 1;35(3):486-93. doi: 10.1006/geno.1996.0388. Genomics. 1996. PMID: 8812482

8

Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor.

Meroni G, Reymond A, Alcalay M, Borsani G, Tanigami A, Tonlorenzi R, Lo Nigro C, Messali S, Zollo M, Ledbetter DH, Brent R, Ballabio A, Carrozzo R. Meroni G, et al. Among authors: zollo m. EMBO J. 1997 May 15;16(10):2892-906. doi: 10.1093/emboj/16.10.2892. EMBO J. 1997. PMID: 9184233 Free PMC article.

9

Identification by shotgun sequencing, genomic organization, and functional analysis of a fourth arylsulfatase gene (ARSF) from the Xp22.3 region.

Puca AA, Zollo M, Repetto M, Andolfi G, Guffanti A, Simon G, Ballabio A, Franco B. Puca AA, et al. Among authors: zollo m. Genomics. 1997 Jun 1;42(2):192-9. doi: 10.1006/geno.1997.4716. Genomics. 1997. PMID: 9192838

10

A method to direct sequence cosmid LAWRIST16 clones.

Repetto M, Ballabio A, Zollo M. Repetto M, et al. Among authors: zollo m. DNA Seq. 1997;7(3-4):229-33. doi: 10.3109/10425179709034041. DNA Seq. 1997. PMID: 9254019

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