(Q28204289)

1

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D J Hulme

2

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S B Brahmbhatt

3

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M Auer-Grumbach

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G A Nicholson

Hereditary sensory neuropathies

5

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language of work or name

English

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publication date

March 2001

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published in

Nature Genetics

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volume

27

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page(s)

309-12

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issue

3

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cites work

1 reference

7 January 2021

The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3.

1 reference

7 January 2021

Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22.

1 reference

7 January 2021

Serine palmitoyltransferase regulates de novo ceramide generation during etoposide-induced apoptosis

1 reference

7 January 2021

Lipoapoptosis in beta-cells of obese prediabetic fa/fa rats. Role of serine palmitoyltransferase overexpression

1 reference

7 January 2021

Production of ceramides causes apoptosis during early neural differentiation in vitro

1 reference

7 January 2021

A YAC-based transcript map of human chromosome 9q22.1-q22.3 encompassing the loci for hereditary sensory neuropathy type I and multiple self-healing squamous epithelioma

1 reference

7 January 2021

Human and murine serine-palmitoyl-CoA transferase--cloning, expression and characterization of the key enzyme in sphingolipid synthesis

1 reference

7 January 2021

Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci

1 reference

7 January 2021

Sphingolipid synthesis: identification and characterization of mammalian cDNAs encoding the Lcb2 subunit of serine palmitoyltransferase

1 reference

7 January 2021

Biosynthesis of sphingosine and dihydrosphingosine by cell-free systems from Hansenula ciferri

1 reference

7 January 2021

Inhibition of serine palmitoyltransferase in vitro and long-chain base biosynthesis in intact Chinese hamster ovary cells by beta-chloroalanine

1 reference

7 January 2021

A mammalian homolog of the yeast LCB1 encodes a component of serine palmitoyltransferase, the enzyme catalyzing the first step in sphingolipid synthesis

1 reference

7 January 2021

Sphingolipids--the enigmatic lipid class: biochemistry, physiology, and pathophysiology

1 reference

7 January 2021

Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene

1 reference

7 January 2021

Dideoxy fingerprinting (ddF): A rapid and efficient screen for the presence of mutations

1 reference

7 January 2021