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SPTLC1
The Modulation of Sphingolipids by Human Cytomegalovirus and Its Influence on Viral Protein Accumulation and Growth
NICU Gene List Generator.Xlsx
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Myopathy Genes (HGNC) Neuropathy (HGNC) Neuromuscular Disease
Cldn19 Clic2 Clmp Cln3
Requisition for DNA Testing
Genetic Neuromuscular Disease *
The Debut of a Rational Treatment for an Inherited Neuropathy?
Investigating SPTLC1 Mutations on Protein and Lipid Profiles in HSN-I
Mutations in the SPTLC1 Gene Are a Cause of Juvenile Amyotrophic Lateral Sclerosis That May
Downregulation of Carnitine Acyl-Carnitine Translocase by Mirnas
Table S4. RAE Analysis of Dedifferentiated Liposarcoma
Oxidized Phospholipids Regulate Amino Acid Metabolism Through MTHFD2 to Facilitate Nucleotide Release in Endothelial Cells
Supplemental Figures 04 12 2017
Lupus Nephritis Supp Table 5
A Model of Hereditary Sensory and Autonomic Neuropathy Type 1 Reveals a Role of Glycosphingolipids in Neuronal Polarity
A Novel Mutation in the Stalk Domain of KIF5A Causes a Slowly Progressive Atypical Motor Syndrome
STAT3 Targets Suggest Mechanisms of Aggressive Tumorigenesis in Diffuse Large B Cell Lymphoma
Top View
Regulation of the Activity of Mammalian Serine Palmitoyltransferase
After a Review of the Current Available Literature, CGS Administrators Has Determined That Testing for the Following Genes/Gene
Subunit Composition of the Mammalian Serine-Palmitoyltransferase Defines the Spectrum of Straight and Methyl-Branched Long-Chain Bases
Characterization of Two Mutations in the SPTLC1 Subunit of Serine Palmitoyltransferase Associated with Hereditary Sensory and Autonomic Neuropathy Type I
SPTLC1 Gene Serine Palmitoyltransferase Long Chain Base Subunit 1
Comparative Transcriptome Profile Between Iberian Pig Varieties
Blueprint Genetics Charcot-Marie-Tooth Neuropathy
Targeted Genes and Methodology Details for Peripheral Neuropathy Gene Panels
Hereditary Sensory and Autonomic Neuropathy Type 1 (HSANI) Caused by a Novel Mutation in SPTLC2
Mutations in the SPTLC1 Gene Are a Cause of Amyotrophic Lateral Sclerosis That May Be Amenable to Serine Supplementation
'An Improved Method to Determine Serine Palmitoyltransferase Activity'
Download Requisition for DNA Testing
The Role of Sphingolipid Metabolism in Cutaneous Permeabilitybarrier Formation
Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-To-CMMRD Phenotypic Continuum
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Quantitative Analysis and Genome-Scale Modeling of Human CD4+ T-Cell Differentiation Reveals Subset-Specific Regulation of Glycosphingolipid Pathways
Early Limited Nitrosamine Exposures Exacerbate High Fat Diet-Mediated
Requisition for DNA Testing Reason for Referral: Sample Collection