(Q45104348)

9 December 2017

title

Prospect for enzyme therapy in glycogenosis II variants: a study on cultured muscle cells (English)

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9 December 2017

A T van der Ploeg

1

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9 December 2017

P A Bolhuis

2

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9 December 2017

R A Wolterman

3

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9 December 2017

J W Visser

4

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9 December 2017

M C Loonen

5

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9 December 2017

H F Busch

6

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9 December 2017

A J Reuser

7

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9 December 2017

publication date

1 September 1988

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9 December 2017

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9 December 2017

volume

235

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9 December 2017

issue

7

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9 December 2017

page(s)

392-396

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https://scigraph.springernature.com/pub.10.1007/bf00314479

9 December 2017

exact match

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cites work

Adult-onset acid maltase deficiency. Morphologic and biochemical abnormalities reproduced in in cultured muscle

1 reference

12 December 2020

Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood, and adult types

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12 December 2020

A quantitative technique for growing human adult skeletal muscle in culture starting from mononucleated cells

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12 December 2020

Uptake and stability of human and bovine acid α-glucosidase in cultured fibroblasts and skeletal muscle cells from glycogenosis type II patients

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12 December 2020

Retention of differentiation potentialities during prolonged cultivation of myogenic cells

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12 December 2020

Bovine generalised glycogenosis type II. Uptake of lysosomal alpha-glucosidase by cultured skeletal muscle and reversal of glycogen accumulation

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12 December 2020

Breakdown of lysosomal glycogen in cultured fibroblasts from glycogenosis type II patients after uptake of acid alpha-glucosidase

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12 December 2020

Residual acid maltase activity in late-onset acid maltase deficiency

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12 December 2020

Bone marrow transplantation for glycogen storage disease type II (Pompé's disease)

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12 December 2020

Free-energy carriers in human cultured muscle cells

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12 December 2020

Immunocytochemical analysis of normal and acid maltase-deficient muscle cultures

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12 December 2020

Immunocytochemistry of lysosomal hydrolases and their precursor forms in normal and mutant human cells

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12 December 2020

Marrow transplantation in genetic disease

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12 December 2020

Transport and processing of endocytosed lysosomal alpha-glucosidase in cultured human skin fibroblasts

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12 December 2020

Demonstration of acid alpha-glucosidase in different types of Pompe disease by use of an immunochemical method

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12 December 2020

Phosphohexosyl components of a lysosomal enzyme are recognized by pinocytosis receptors on human fibroblasts

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12 December 2020

Lysosomes in type II glycogenosis. Changes during administration of extract from Aspergillus niger

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12 December 2020

The application of bone marrow transplantation to the treatment of genetic diseases

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12 December 2020

Infantile acid maltase deficiency. I. Muscle fiber destruction after lysosomal rupture

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12 December 2020

Clinical diversity in glycogenosis type II. Biosynthesis and in situ localization of acid alpha-glucosidase in mutant fibroblasts

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12 December 2020

Defects in synthesis, phosphorylation, and maturation of acid alpha-glucosidase in glycogenosis type II

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12 December 2020

Isolation and characterization of a precursor form of lysosomal alpha-glucosidase from human urine

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12 December 2020

Protein measurement with the Folin phenol reagent

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12 December 2020

The use of leucocytes as an aid in the diagnosis of a variant of glycogen storage disease type II (Pompe's disease).

1 reference

12 December 2020

Fluorescamine: A Reagent for Assay of Amino Acids, Peptides, Proteins, and Primary Amines in the Picomole Range

1 reference

12 December 2020

Use of a monoclonal antibody to distinguish between precursor and mature forms of human lysosomal alpha-glucosidase

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12 December 2020

Glycogen, its chemistry and morphologic appearance in the electron microscope. I. A modified OsO 4 fixative which selectively contrasts glycogen

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00314479

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Dimensions Publication ID

9 December 2017

1036566528

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