(Q68352801)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4214804%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

title

The use of quantiatative cytochemical analyses in rapid prenatal detection and somatic cell genetic studies of metabolic diseases (English)

1 reference

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23 September 2019

author name string

H Galjaard

1

1 reference

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23 September 2019

A Hoogeveen

2

1 reference

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23 September 2019

W Keijzer

3

1 reference

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23 September 2019

E De Wit-Verbeek

4

1 reference

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23 September 2019

C Vlek-Noot

5

1 reference

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23 September 2019

publication date

1 September 1974

1 reference

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The Histochemical Journal

23 September 2019

published in

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23 September 2019

volume

6

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23 September 2019

issue

5

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23 September 2019

page(s)

491-509

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Interallelic Complementation in Hybrid Cells Derived from Human Diploid Strains Deficient in Galactose-1-Phosphate Uridyl Transferase Activity

23 September 2019

cites work

1 reference

12 December 2020

Transport and storage of amniotic fluid samples for prenatal diagnosis of metabolic diseases

1 reference

12 December 2020

Glycogen storage diseases

1 reference

12 December 2020

Prenatal detection of genetic disorders

1 reference

12 December 2020

The quantitative histochemistry of hypothalamus. I. Pentose shunt enzymes in the activated supraoptic nucleus of the rat.

1 reference

12 December 2020

The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase

1 reference

12 December 2020

Use of cell culture techniques in diagnosis and studies of inherited disease

1 reference

12 December 2020

1 reference

12 December 2020

Prenatal diagnosis of type II glycogenosis (Pompe's disease) using microchemical analyses

1 reference

12 December 2020

DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS

1 reference

12 December 2020

Treatment of Metachromatic Leukodystrophy in Fibroblasts by Enzyme Replacement

1 reference

12 December 2020

Methodology of the quantitative cytochemical analysis of single or small numbers of cultured cells

1 reference

12 December 2020

Correction of the Enzymic Defect in Cultured Fibroblasts from Patients with Fabry's Disease: Treatment with Purified α-Galactosidase from Ficin

1 reference

12 December 2020

The single-active-X: functional differentiation at the chromosome level

1 reference

12 December 2020

Prenatal genetic diagnosis. 3.

1 reference

12 December 2020

Linkage analysis using somatic cell hybrids

1 reference

12 December 2020

Hurler's syndrome: a genetic study of clones in cell culture with particular reference to the Lyon hypothesis

1 reference

12 December 2020

A modified uronic acid carbazole reaction

1 reference

12 December 2020

Tissue culture and antenatal detection of molecular diseases

1 reference

12 December 2020

X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations

1 reference

12 December 2020

Uptake of beta-glucuronidase by deficient human fibroblasts

1 reference

12 December 2020

QUANTITATIVE CYTOCHEMICAL STUDIES ON INTERPHASE GROWTH. I. DETERMINATION OF DNA, RNA AND MASS CONTENT OF AGE DETERMINED MOUSE FIBROBLASTS IN VITRO AND OF INTERCELLULAR VARIATION IN GENERATION TIME

1 reference

12 December 2020

Hypoxanthine-guanine phosphoribosyltransferase deficiency: chemical agents selective for mutant or normal cultured fibroblasts in mixed and heterozygote cultures

1 reference

12 December 2020

Genetic Heterogeneity of Xeroderma Pigmentosum demonstrated by Somatic Cell Hybridization

1 reference

12 December 2020

Mammalian oocytes: X chromosome activity

1 reference

12 December 2020

A method for rapid prenatal diagnosis of glycogenosis II (Pompe's disease).

1 reference

12 December 2020

The quantitative histochemistry of the brain; histological sampling.

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

Hybrid Cells Derived from Mouse and Man : Artificial Heterokaryons of Mammalian Cells from Different Species

1 reference

12 December 2020

Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 reference

12 December 2020

Sanfilippo disease type B: enzyme replacement and metabolic correction in cultured fibroblasts

1 reference

12 December 2020

An example of rapid prenatal diagnosis of Fabry's disease using microtechniques

1 reference

12 December 2020

Evidence for intergenic complementation in hybrid cells derived from two human diploid strains each carrying an X-linked mutation

1 reference

12 December 2020

Genetic Inactivation of the α-Galactosidase Locus in Carriers of Fabry's Disease

1 reference

12 December 2020

A hypothesis for I-cell disease: defective hydrolases that do not enter lysosomes

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01003266

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4214804%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

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