Molecular Forms of beta-N-Acetylhexosaminidase in Epstein-Barr Virus-Transformed Lymphoid Cell Lines from Normal Subjects and Patients with Tay-Sachs Disease
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1432-1033.1983.tb07509.x/fullpdf
Reference57 articles.
1. N-Acetyl-β-glucosaminidases in human spleen
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3. Studies on Human β-d-N-Acetylhexosaminidases
4. Hexosaminidase C in Tay-Sachs and sandhoff disease
5. Studies on Hexosaminidase C in Cultured Skin Fibroblasts from Patients with Sandhoff's Disease
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1. Surface expression of low density lipoprotein receptor in EBV-transformed lymphocytes: characterization and use for studying familial hypercholesterolemia;Atherosclerosis;1997-06
2. Significance of two point mutations present in each HEXB allele of patients with adult GM2 gangliosidosis (Sandhoff disease) Homozygosity for the Ile207 → Val substitution is not associated with a clinical or biochemical phenotype;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;1996-11
3. Arylsulfatases A and B in EBV-transformed lymphoid cell lines: Studies on their molecular forms in cells from patients with inborn sulfatase deficiencies. Comparative diagnostic value of enzymatic assays;Clinica Chimica Acta;1991-10
4. Influence of chain length of pyrene fatty acids on their uptake and metabolism by Epstein–Barr-virus-transformed lymphoid cell lines from a patient with multisystemic lipid storage myopathy and from control subjects;Biochemical Journal;1990-07-01
5. Metabolism of pyrenedecanoic acid in Epstein-Barr virus-transformed lymphoid cell lines from normal subjects and from a patient with multisystemic lipid storage myopathy;Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism;1989-09
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