The sulfatase gene family (Q34433161)

2 August 2017

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title

The sulfatase gene family (English)

1 reference

2 August 2017

G Parenti

1

1 reference

PubMed ID

9229115

2 August 2017

G Meroni

series ordinal

2

1 reference

PubMed ID

9229115

2 August 2017

A Ballabio

series ordinal

3

1 reference

2 August 2017

1 June 1997

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Current Opinion in Genetics & Development

2 August 2017

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2 August 2017

7

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2 August 2017

386-391

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2 August 2017

3

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A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy

2 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

The evolutionary conservation of a novel protein modification, the conversion of cysteine to serinesemialdehyde in arylsulfatase from Volvox carteri

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase protein

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Structure of a human lysosomal sulfatase

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

cDNA cloning, nucleotide sequence and expression of the gene for arylsulfatase in the sea urchin (Hemicentrotus pulcherrimus) embryo.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

An inducible arylsulfatase of Volvox carteri with properties suitable for a reporter-gene system. Purification, characterization and molecular cloning.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

The pseudoautosomal regions of the human sex chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Cloning and expression of the mouse pseudoautosomal steroid sulphatase gene (Sts).

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Sequence of the human iduronate 2-sulfatase (IDS) gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human iduronate-2-sulfate sulfatase locus

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Presence of an IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Maternal and fetal sequelae of anticoagulation during pregnancy

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Targeted disruption of the arylsulfatase B gene results in mice resembling the phenotype of mucopolysaccharidosis VI

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Treatment of Late Infantile Metachromatic Leukodystrophy by Bone Marrow Transplantation

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Correction of steroid sulfatase deficiency by gene transfer into basal cells of tissue-cultured epidermis from patients with recessive X-linked ichthyosis

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Arylsulfatase B activities and glycosaminoglycan levels in retrovirally transduced mucopolysaccharidosis type VI cells. Prospects for gene therapy

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Retroviral-mediated transfer of the iduronate-2-sulfatase gene into lymphocytes for treatment of mild Hunter syndrome (mucopolysaccharidosis type II)

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

Gene therapy for metachromatic leukodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2897%2980153-0

7 January 2021

10.1016/S0959-437X(97)80153-0

Identifiers

DOI

1 reference

2 August 2017

1 reference

PubMed ID

9229115