These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 1680331)

  • 1. Synthesis and characterization of NBD-PS: a fluorescent analog of cerebroside arylsulfatase A deficiency disorders.
    Louis AI; Widen KE; Tsay KK; Fluharty AL
    Mol Chem Neuropathol; 1991 Apr; 14(2):113-30. PubMed ID: 1680331
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis of pyrene derivatives of cerebroside sulfate and their use for determining arylsulfatase A activity.
    Marchesini S; Viani P; Cestaro B; Gatt S
    Biochim Biophys Acta; 1989 Mar; 1002(1):14-9. PubMed ID: 2564282
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Impaired cerebroside sulfate hydrolysis in fibroblasts of sibs with "pseudo" arylsulfatase A deficiency without metachromatic leukodystrophy.
    Hreidarsson SJ; Thomas GH; Kihara H; Fluharty AL; Kolodny EH; Moser HW; Reynolds LW
    Pediatr Res; 1983 Sep; 17(9):701-4. PubMed ID: 6137805
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Metachromatic leukodystrophy caused by a partial cerebroside sulfatase.
    Kihara H; Fluharty AL; O'Brien JS; Fish CH
    Clin Genet; 1982 Apr; 21(4):253-61. PubMed ID: 6125284
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of metachromatic leukodystrophy in a family with pseudo arylsulfatase A deficiency by the cerebroside sulfate loading test.
    Kihara H; Ho CK; Fluharty AL; Tsay KK; Hartlage PL
    Pediatr Res; 1980 Mar; 14(3):224-7. PubMed ID: 6104322
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fluorescence assay of glucosylceramide glucosidase using NBD-cerebroside.
    Abe A; Shayman JA; Radin NS
    Lipids; 1992 Dec; 27(12):1052-4. PubMed ID: 1487952
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prevalence of partial cerebroside sulfate sulfatase (arylsulfatase A) defect in adult psychiatric patients.
    Shah SN; Johnson RC; Stone RK; Mahon-Haft H
    Biol Psychiatry; 1985 Jan; 20(1):50-7. PubMed ID: 2856894
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Croatian population data for arylsulfatase a pseudodeficiency-associated mutations in healthy subjects, and in patients with Alzheimer-type dementia and Down syndrome.
    Bognar SK; Furac I; Kubat M; Cosović C; Demarin V
    Arch Med Res; 2002; 33(5):473-7. PubMed ID: 12459318
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interfacial activation of porcine pancreatic phospholipase A(2) studied with 7-nitrobenz-2-oxa-1,3-diazol-4-yl-labeled lipids.
    Morales R; Fernández MS
    Arch Biochem Biophys; 2002 Feb; 398(2):221-8. PubMed ID: 11831853
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Diagnosis of arylsulfatase A deficiency in intact cultured cells using a fluorescent derivative of cerebroside sulfate.
    Bach G; Dagan A; Herz B; Gatt S
    Clin Genet; 1987 Apr; 31(4):211-7. PubMed ID: 2885115
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Arylsulfatase A pseudodeficiency: loss of a polyadenylylation signal and N-glycosylation site.
    Gieselmann V; Polten A; Kreysing J; von Figura K
    Proc Natl Acad Sci U S A; 1989 Dec; 86(23):9436-40. PubMed ID: 2574462
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An assay for the rapid detection of the arylsulfatase A pseudodeficiency allele facilitates diagnosis and genetic counseling for metachromatic leukodystrophy.
    Gieselmann V
    Hum Genet; 1991 Jan; 86(3):251-5. PubMed ID: 1671769
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency.
    Kappler J; Leinekugel P; Conzelmann E; Kleijer WJ; Kohlschütter A; Tønnesen T; Rochel M; Freycon F; Propping P
    Hum Genet; 1991 Mar; 86(5):463-70. PubMed ID: 1673113
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Arylsulfatase a gene polymorphisms in relapsing remitting multiple sclerosis: genotype-phenotype correlation and estimation of disease progression.
    Baronica KB; Mlinac K; Ozretić D; Vladić A; Bognar SK
    Coll Antropol; 2011 Jan; 35 Suppl 1():11-6. PubMed ID: 21648305
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthesis of a fluorescent derivative of glucosyl ceramide for the sensitive determination of glucocerebrosidase activity.
    Dinur T; Grabowski GA; Desnick RJ; Gatt S
    Anal Biochem; 1984 Jan; 136(1):223-34. PubMed ID: 6424502
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Use of mixed dispersion of fluorescent galactosylceramide and sodium dodecylsulfate for assaying galactosylceramide-beta-galactosidase and diagnosing Krabbe disease.
    Salvayre R; Gatt S
    Enzyme; 1985; 33(3):175-80. PubMed ID: 4054076
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pseudoarylsulfatase-A deficiency in the neurologically impaired patient.
    Farrell K; Applegarth DA; Toone JR; McLeod PM; Savage AV
    Can J Neurol Sci; 1985 Aug; 12(3):274-7. PubMed ID: 2864994
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic complementation in somatic cell hybrids of cerebroside sulfatase activator deficiency and metachromatic leukodystrophy fibroblasts.
    Kihara H; Tsay KK; Fluharty AL
    Hum Genet; 1984; 66(4):300-1. PubMed ID: 6144627
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Atypical metachromatic leukodystrophy? Problems with the biochemical diagnosis.
    Tønnesen T; Vrang C; Wiesmann UN; Christomanou H; Lou HO
    Hum Genet; 1984; 67(2):170-3. PubMed ID: 6146562
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dynamics of lipid chain attached fluorophore 7-nitrobenz-2-oxa-1,3-diazol-4-yl (NBD) in negatively charged membranes determined by NMR spectroscopy.
    Huster D; Müller P; Arnold K; Herrmann A
    Eur Biophys J; 2003 Mar; 32(1):47-54. PubMed ID: 12632206
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.