Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C (sub)alpha -formylglycine generating enzyme
Article Abstract:
Research has been conducted on C (sub)alpha -formylglycine. Results demonstrate that genetic deficiency of C (sub)alpha -formylglycine leads to multiple sulfatase deficiency, and that C (sub)alpha -formylglycine-generating enzyme has been purified and its gene and mutations have been identified and discussed.
Publication Name: Cell
Subject: Biological sciences
ISSN: 0092-8674
Year: 2003
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tRNA structure goes from L to lambda
Article Abstract:
The authors discuss the publication on L-like structure of tRNA. The topics of interest include the designation of this structure as lambda-form where the tertiary interaction disruption is compensated by interactions with enzyme.
Publication Name: Cell
Subject: Biological sciences
ISSN: 0092-8674
Year: 2003
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The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases
Article Abstract:
Research has been conducted on multiple sulfatase deficiency. The authors have investigated the gene which is mutated in multiple sulfatase deficiency and can rescue enzymatic deficiency in patients' cell lines.
Publication Name: Cell
Subject: Biological sciences
ISSN: 0092-8674
Year: 2003
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