(Q39626957)

13 September 2017

Characterization of lysosomal hydrolases that are elevated in Gaucher's disease (English)

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

23 April 2022

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

23 April 2022

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

23 April 2022

1 reference

K. D. Moffitt

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A101149

23 April 2022

J. P. Chambers

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A101149

23 April 2022

W. F. Diven

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A101149

23 April 2022

R. H. Glew

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A101149

23 April 2022

D. A. Wenger

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A101149

23 April 2022

D. F. Farrell

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A101149

23 April 2022

language of work or name

English

0 references

publication date

1 September 1978

1 reference

full work available at URL

13 September 2017

https://api.elsevier.com/content/article/PII:0003986178902746?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

https://api.elsevier.com/content/article/PII:0003986178902746?httpAccept=text/plain

23 April 2022

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Archives of Biochemistry and Biophysics

23 April 2022

published in

1 reference

13 September 2017

190

1 reference

13 September 2017

1

1 reference

13 September 2017

247-260

1 reference

METABOLISM OF GLUCOCEREBROSIDES. II. EVIDENCE OF AN ENZYMATIC DEFICIENCY IN GAUCHER'S DISEASE.

13 September 2017

2

18

221

Brady

1965

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

A microassay for Gaucher's disease

23 April 2022

4

60

391

Peters

1975

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Isolation of heat-stable glucocerebrosidase activators from the spleens of three variants of Gaucher's disease

23 April 2022

6

183

290

Peters

1977

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Tissue Acid Hydrolase Activities in Gaucher's Disease

23 April 2022

8

22

62

Ockerman

1968

0 references

Infantile Gaucher's Disease: Neuropathology, Acid Hydrolase Activities and Negative Staining Observations1

9

8

89

Verity

1977

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Glycolipids Isolated from the Spleen of Gaucher's Disease

23 April 2022

10

88

277

Makita

1966

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

LIPID CLASS COMPOSITION OF NORMAL HUMAN BRAIN AND VARIATIONS IN METACHROMATIC LEUCODYSTROPHY, TAY-SACHS, NIEMANN-PICK, CHRONIC GAUCHER'S AND ALZHEIMER'S DISEASES.

23 April 2022

12

42

404

Rouser

1965

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Lipid composition of the brain in infantile Gaucher's disease.

23 April 2022

13

19

81

French

1969

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Brain glycolipids in infantile Gaucher's disease

23 April 2022

14

29

379

Sudo

1977

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

THE CHEMICAL COMPOSITION OF BOVINE CNS MYELIN

23 April 2022

16

122

77

Norton

1965

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Lactosylceramide galactosidase: Comparison with other sphingolipid hydrolases in developing rat brain

23 April 2022

17

14

497

Radin

1969

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Lactosyl Ceramidosis: Normal Activity for Two Lactosyl Ceramide β-Galactosidases

23 April 2022

23

188

1310

Wenger

1975

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

The assay of arylsulphatases A and B in human urine

23 April 2022

24

4

453

Baum

1959

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Arylsulfatase B deficiency in Maroteaux-Lamy syndrome: Cellular studies and carrier identification

23 April 2022

25

9

475

Beratis

1975

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Tay-sachs disease. Detection of heterozygotes and homozygotes by serum hexosaminidase assay

23 April 2022

26

283

15

O'Brien

1970

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Composition of the membranous deposits occurring in Gaucher's disease

23 April 2022

27

156

626

Glew

1973

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Protein measurement with the Folin phenol reagent

23 April 2022

28

193

265

Lowry

0 references

Determination of serum acid phosphatase in gaucher's disease using 4-methylumbelliferyl phosphate

31

80

67

Chambers

1977

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

An improved method for the identification of patients and carriers of Krabbe's disease

23 April 2022

32

56

199

Wenger

1974

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

Mucopolysaccharidosis: secondarily induced abnormal distribution of lysosomal isoenzymes

23 April 2022

34

181

352

Kint

1973

1 reference

https://api.crossref.org/works/10.1016/0003-9861(78)90274-6

23 April 2022

Identifiers

1 reference

13 September 2017

1 reference