(Q71905303)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7618436%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

Sphingolipid activator proteins in the neuronal ceroid-lipofuscinoses: an immunological study (English)

1 reference

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22 October 2019

1 reference

J Tyynelä

1

1 reference

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22 October 2019

M Baumann

2

1 reference

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22 October 2019

M Henseler

3

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22 October 2019

K Sandhoff

4

1 reference

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22 October 2019

M Haltia

5

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22 October 2019

publication date

1 January 1995

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22 October 2019

published in

Acta Neuropathologica

1 reference

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22 October 2019

volume

89

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22 October 2019

issue

5

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22 October 2019

page(s)

391-398

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A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples

22 October 2019

cites work

1 reference

12 December 2020

Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis)

1 reference

12 December 2020

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

12 December 2020

A variant of Jansky-Bielschowsky disease

1 reference

12 December 2020

A cerebrosidesulfatase from swine kidney

1 reference

12 December 2020

Glycosphingolipid specificity of the human sulfatide activator protein

1 reference

12 December 2020

Storage of saposins A and D in infantile neuronal ceroid-lipofuscinosis

1 reference

12 December 2020

Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common gene

1 reference

12 December 2020

Batten disease: past, present, and future.

1 reference

12 December 2020

Mutational analysis in a patient with a variant form of Gaucher disease caused by SAP-2 deficiency

1 reference

12 December 2020

Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: incorporation of linkage disequilibrium in multipoint analysis

1 reference

12 December 2020

Saposin A: second cerebrosidase activator protein

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12 December 2020

The adult and a new late adult forms of neuronal ceroid lipofuscinosis

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12 December 2020

Distribution of saposins (sphingolipid activator proteins) in tissues of lysosomal storage disease patients

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12 December 2020

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

1 reference

12 December 2020

Distribution of prosaposin-like immunoreactivity in rat brain

1 reference

12 December 2020

Activator proteins and topology of lysosomal sphingolipid catabolism.

1 reference

12 December 2020

Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16

1 reference

12 December 2020

Distribution of saposin proteins (sphingolipid activator proteins) in lysosomal storage and other diseases

1 reference

12 December 2020

The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase

1 reference

12 December 2020

Mapping the gene for juvenile onset neuronal ceroid lipofuscinosis to chromosome 16 by linkage analysis

1 reference

12 December 2020

Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)

1 reference

12 December 2020

Saposin proteins: structure, function, and role in human lysosomal storage disorders

1 reference

12 December 2020

Immunocytochemical localization of sphingolipid activator protein 2 (SAP-2) in normal and SAP-deficient fibroblasts.

1 reference

12 December 2020

Saposins: structure, function, distribution, and molecular genetics

1 reference

12 December 2020

Characterization of a mutation in a family with saposin B deficiency: a glycosylation site defect

1 reference

12 December 2020

Additional biochemical findings in a patient and fetal sibling with a genetic defect in the sphingolipid activator protein (SAP) precursor, prosaposin. Evidence for a deficiency in SAP-1 and for a normal lysosomal neuraminidase

1 reference

12 December 2020

Genetic heterogeneity in neuronal ceroid lipofuscinosis (NCL): evidence that the late-infantile subtype (Jansky-Bielschowsky disease; CLN2) is not an allelic form of the juvenile or infantile subtypes

1 reference

12 December 2020

Intracellular trafficking of glycosphingolipids: role of sphingolipid activator proteins in the topology of endocytosis and lysosomal digestion

1 reference

12 December 2020

Neuronal ceroid-lipofuscinosis (Batten's disease): relationship to amaurotic family idiocy?

1 reference

12 December 2020

Sphingolipid activator protein D (sap-D) stimulates the lysosomal degradation of ceramide in vivo

1 reference

12 December 2020

Sulfatide activator protein. Alternative splicing that generates three mRNAs and a newly found mutation responsible for a clinical disease

1 reference

12 December 2020

Detection of a point mutation in sphingolipid activator protein-1 mRNA in patients with a variant form of metachromatic leukodystrophy

1 reference

12 December 2020

Mutation in the sphingolipid activator protein 2 in a patient with a variant of Gaucher disease

1 reference

12 December 2020

Infantile type of so-called neuronal ceroid-lipofuscinosis. 2. Morphological and biochemical studies

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00307641

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7618436%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

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