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GFPT1
High-Throughput Discovery of Novel Developmental Phenotypes
Pdf 2019; 572: 402-6
Glutamine Deprivation Triggers NAGK-Dependent Hexosamine Salvage
Functional Dependency Analysis Identifies Potential Druggable
Transcriptome Analysis of Differentially Expressed Mrna Related to Pigeon Muscle Development
Downloaded Per Proteome Cohort Via the Web- Site Links of Table 1, Also Providing Information on the Deposited Spectral Datasets
GFPT1 Mutations in Congenital Myasthenic Syndrome Cause
Mutations in Gfpt1 and Skiv2l2 Cause Distinct
Enrichment of in Vivo Transcription Data from Dietary Intervention
Congenital Myasthenic Syndrome Caused by a Frameshift Insertion Mutation In
High GFPT1 Expression Predicts Unfavorable Outcomes in Patients
GFPT2-Expressing Cancer-Associated Fibroblasts Mediate Metabolic Reprogramming in Human Lung Adenocarcinoma
Manuscript Final Dec23 2020 SI
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Glutamine: Fructose-6-Phosphate Aminotransferase 2 (GFPT2)
MPI Depletion Enhances O-Glcnacylation of P53 And
Glycolysis and Glutaminolysis Cooperatively Control T Cell Function
Schwann Cell Reprogramming and Lung Cancer Progression: a Meta-Analysis of Transcriptome Data
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High-Throughput Discovery of Novel Developmental Phenotypes Mary E
GFPT1 / GFAT1 (332-699, His-Tag) Human Protein Product Data
Anti-GFPT1 (Aa 525-681) Polyclonal Antibody (DPABH-12096) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Functional Roles of Fructose PNAS PLUS
High-Throughput Discovery of Novel Developmental Phenotypes
Using CRISPR/Cas9 to Identify Gene Interactions with Hexosamine Biosynthesis and N-Glycan Remodeling Pathway Enzymes
A GFPT1 Deficient Mouse Model of Congenital Myasthenic Syndrome
Table 10: H. Sapiens Recon 1 Network Confidence Scores and Citations
Exploring the Function of Glutamine Fructose-6-Phosphate Transaminase (Gfpt2) in Embryonic Development
Iron Deficiency Reprograms Phosphorylation Signaling and Reduces O-Glcnac Pathways in Neuronal Cells
Ncomms11612.Pdf
Amyloid-‐‑Β Precursor Protein APP Down
Proteomics of Primary Uveal Melanoma: Insights Into Metastasis and Protein Biomarkers
Epigenomic Signature of the Progeroid Cockayne Syndrome Exposes Distinct and Common Features with Physiological Ageing
Congenital Myasthenic Syndrome Due to Compound Heterozygous Mutations in the GFPT1 Gene
RNA-Seq Based Genetic Variant Discovery Provides New Insights
Reports Report
Mouse Gfpt1 Conditional Knockout Project (CRISPR/Cas9)
Mediates Genetic Susceptibility to Chronic Kidney Disease