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Publications by Mengfatt Ho
Hereditary Sensory Neuropathy Type 1 Mutations Confer Dominant Negative Effects on Serine Palmitoyltransferase, Critical for Sphingolipid Synthesis
Journal of Clinical Investigation
Medicine
Related publications
Hereditary Sensory Neuropathy Type I
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Hereditary Sensory Neuropathy Type 1 Is Caused by the Accumulation of Two Neurotoxic Sphingolipids
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Dermal Melanocyte Hamartoma and Hereditary Motor and Sensory Neuropathy Type 2A
Acta Dermato-Venereologica
Dermatology
Medicine
A Mammalian Homolog of the YeastLCB1Encodes a Component of Serine Palmitoyltransferase, the Enzyme Catalyzing the First Step in Sphingolipid Synthesis
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
A Model of Hereditary Sensory and Autonomic Neuropathy Type 1 Reveals a Role of Glycosphingolipids in Neuronal Polarity
Journal of Neuroscience
Neuroscience
Diaphragmatic Weakness in Hereditary Motor and Sensory Neuropathy.
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
The LCB2 Gene of Saccharomyces and the Related LCB1 Gene Encode Subunits of Serine Palmitoyltransferase, the Initial Enzyme in Sphingolipid Synthesis.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Autosomal Recessive Forms of Hereditary Motor and Sensory Neuropathy.
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Proximal Dominant Hereditary Motor and Sensory Neuropathy With Proximal Dominance Association With Mutation in the TRK-Fused Gene
JAMA Neurology
Neurology
