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Arylsulfatase:CCnc:Pt:Ser/Plas:Qn

Known as: S--arilsulfatasi, arilsulfatasa:concentración catalítica:punto en el tiempo:suero:cuantitativo, Arylsulfatases [Catalytique/Volume] Sérum/Plasma ; Numérique 
 
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
Introduction Dopamine (DA) binds to five receptors (DAR), classified by their ability to increase (D1R-like) or decrease (D2R… Expand
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2007
2007
Successful gene therapy approaches for metachromatic leukodystrophy (MLD), based either on hematopoietic stem/progenitor cells… Expand
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2001
2001
Arylsulfatase A (ASA)-deficient mice represent an animal model for the fatal lysosomal storage disease metachromatic… Expand
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1999
1999
Arylsulfatase A (ASA)-deficient (-/-) mice and ASA(+/+) controls were constructed as a transgenic model for the lysosomal storage… Expand
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1999
1999
Insulator DNAs functionally isolate neighboring genes by blocking interactions between distal cis-regulatory elements and… Expand
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Highly Cited
1996
Highly Cited
1996
Metachromatic leukodystrophy is a lysosomal sphingolipid storage disorder caused by the deficiency of arylsulfatase A. The… Expand
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Review
1991
Review
1991
  • P. Laidler
  • Folia medica Cracoviensia
  • 1991
  • Corpus ID: 45839286
Arylsulfatase A was isolated from urine and human liver. The enzyme was homogeneous with respect to charge and had high specific… Expand
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1991
1991
Fragments of the arylsulfatase A (ARSA) gene from a patient with juvenile-onset metachromatic leukodystrophy (MLD) were amplified… Expand
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Highly Cited
1990
Highly Cited
1990
A 14-kb genomic clone containing the entire gene of human lysosomal arylsulfatase A was isolated. The arylsulfatase A gene is… Expand
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1987
1987
Pseudo arylsulfatase A deficiency, an asymptomatic condition, and metachromatic leukodystrophy, a severe neurodegenerative… Expand
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