Oral l-serine supplementation reduces production of neurotoxic deoxysphingolipids in mice and humans with hereditary sensory autonomic neuropathy type 1-Reference-Cited by-同舟云学术

Oral l-serine supplementation reduces production of neurotoxic deoxysphingolipids in mice and humans with hereditary sensory autonomic neuropathy type 1

Published:2011-12-01 Issue:12 Volume:121 Page:4735-4745
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Garofalo Kevin,Penno Anke,Schmidt Brian P.,Lee Ho-Joon,Frosch Matthew P.,von Eckardstein Arnold,Brown Robert H.,Hornemann Thorsten,Eichler Florian S.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference30 articles.

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

2. SPTLC1 is mutated in hereditary sensory neuropathy, type 1

3. Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I

4. Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I

5. Serine palmitoyltransferase, a key enzyme of sphingolipid metabolism

Cited by 178 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Enzymes of sphingolipid metabolism as transducers of metabolic inputs;Biochemical Society Transactions;2024-08-05

2. L-serine restored lysosomal failure in cells derived from patients with BPAN reducing iron accumulation with eliminating lipofuscin;Free Radical Biology and Medicine;2024-08

3. Serine and glycine physiology reversibly modulate retinal and peripheral nerve function;Cell Metabolism;2024-08

4. Serine Palmitoyltransferase (SPT)-related Neurodegenerative and Neurodevelopmental Disorders;Journal of Neuromuscular Diseases;2024-07-02

5. Ceramides are fuel gauges on the drive to cardiometabolic disease;Physiological Reviews;2024-07-01