Prosaposin: threshold rescue and analysis of the "neuritogenic" region in transgenic mice (Q44123136)

30 November 2017

Prosaposin: threshold rescue and analysis of the "neuritogenic" region in transgenic mice (English)

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30 November 2017

Ying Sun

1

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30 November 2017

Xiaoyang Qi

2

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30 November 2017

David P Witte

3

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30 November 2017

Elvira Ponce

4

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30 November 2017

Keiji Kondoh

5

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30 November 2017

Brian Quinn

6

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30 November 2017

Gregory A Grabowski

7

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30 November 2017

language of work or name

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1 August 2002

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Molecular Genetics and Metabolism

30 November 2017

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30 November 2017

76

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30 November 2017

4

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30 November 2017

271-286

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

30 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated by lactosylceramide accumulation

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Insertion in the mRNA of a metachromatic leukodystrophy patient with sphingolipid activator protein-1 deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

A mutation in the saposin A domain of the sphingolipid activator protein (prosaposin) gene results in a late-onset, chronic form of globoid cell leukodystrophy in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipids.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Identification of the neurotrophic factor sequence of prosaposin

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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Identification of prosaposin as a neurotrophic factor

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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Functional organization of saposin C. Definition of the neurotrophic and acid beta-glucosidase activation regions

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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Prosaposin facilitates sciatic nerve regeneration in vivo

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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

A hydrophilic peptide comprising 18 amino acid residues of the prosaposin sequence has neurotrophic activity in vitro and in vivo.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Conformational and amino acid residue requirements for the saposin C neuritogenic effect

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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Role of prosaposin in the male reproductive system: effect of prosaposin inactivation on the testis, epididymis, prostate, and seminal vesicles

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Pathological study of mice with total deficiency of sphingolipid activator proteins (SAP knockout mice).

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Prosaposin: promoter analysis and central-nervous-system-preferential elements for expression in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Proteolytic processing patterns of prosaposin in insect and mammalian cells

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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Successive isolation and separation of the major lipid fractions including gangliosides from single biological samples.

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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Murine PGK-1 promoter drives widespread but not uniform expression in transgenic mice.

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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Ex vivo localization of the mouse saposin C activation region for acid beta-glucosidase

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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Variegated gene expression in mice.

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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

The distribution of lipids in the human nervous system. II. Lipid composition of human fetal and infant brain.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

A Comprehensive Study of the Postnatal Changes in the Concentration of the Lipids of Developing Rat Brain*

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Acid sphingomyelinase deficient mice: a model of types A and B Niemann-Pick disease

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Light and electron microscopic analysis of the central and peripheral nervous systems of acid sphingomyelinase-deficient mice resulting from gene targeting

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Mouse model for the lysosomal disorder galactosialidosis and correction of the phenotype with overexpressing erythroid precursor cells

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Neurotrophin regulation of the developing nervous system: analyses of knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

Severe peripheral sensory neuron loss and modest motor neuron reduction in mice with combined deficiency of brain-derived neurotrophic factor, neurotrophin 3 and neurotrophin 4/5.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900114-2

7 January 2021

10.1016/S1096-7192(02)00114-2

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DOI

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30 November 2017

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