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NMNAT1
Nicotinamide Adenine Dinucleotide Is Transported Into Mammalian
Identification of Evolutionary and Kinetic Drivers of NAD-Dependent Signaling
An Alu-Mediated Duplication in NMNAT1, Involved in NAD Biosynthesis, Causes a Novel Syndrome, SHILCA, Affecting Multiple Tissues and Organs
ADHD) Gene Networks in Children of Both African American and European American Ancestry
Nicotinamide Mononucleotide Adenylyl Transferase- Mediated Axonal Protection Requires Enzymatic Activity but Not Increased Level
Measuring NAD+ and Related Metabolites Using Liquid Chromatography Mass Spectrometry
NMNAT1 Mutations Cause Leber Congenital Amaurosis
Nicotinamide Mononucleotide Adenylyltransferase Expression in Mitochondrial Matrix Delays Wallerian Degeneration
Potential Therapeutic Benefit of NAD+ Supplementation for Glaucoma And
(NF1) As a Breast Cancer Driver
Mutations in NMNAT1 Cause Leber Congenital Amaurosis and Identify a New Disease Pathway for Retinal Degeneration
[Frontiers in Bioscience 14, 410-431, January 1, 2009] 410 the NMN/Namn Adenylyltransferase (NMNAT) Protein Family Corinna Lau
NMNAT1 Mutations Cause Leber Congenital Amaurosis
Wasin Vol. 9 N. 4 2558.Pmd
Anterograde Regulation of Mitochondrial Genes and FGF21 Signaling by Hepatic LSD1
Nmnat1 Cannot Substitute for Wld to Delay Wallerian Degeneration
Spaceflight Influences Gene Expression, Photoreceptor
SARM1 Depletion Rescues NMNAT1 Dependent Photoreceptor Cell Death and Retinal Degeneration
Top View
Current Concepts of Genotype-Phenotype Correlations
98354 NMNAT1 (D7O4N) Rabbit Mab
NMNAT1 Is a Survival Factor in Actinomycin D-Induced Osteosarcoma Cell Death
Cyclex NMNAT1 Colorimetric Assay Kit Ver.2 for 100 Assays Cat# CY-1252V2
Programmed Axon Degeneration: from Mouse to Mechanism to Medicine
Pharmacological Bypass of NAD+ Salvage Pathway Protects Neurons
NMNAT1 Inhibits Axon Degeneration Via Blockade of SARM1-Mediated NAD Depletion
Targeted Deletion of Nmnat1 in Mouse Retina Leads to Early Severe Retinal Dystrophy Xiaolin Wang , Yu Fang , Rongsheng Liao , Ta
Research Article a Network Pharmacology-Based Study on the Anti-Lung Cancer Effect of Dipsaci Radix
NMNAT1 Mutations Cause Leber Congenital Amaurosis the Harvard
NMNAT1 (NM 022787) Human Recombinant Protein – TP304825 | Origene
NMNAT1 Mutations Cause Leber Congenital Amaurosis
Multiple Domain Interfaces Mediate SARM1 Autoinhibition
Stimulation of Nicotinamide Adenine Dinucleotide Biosynthetic Pathways Delays Axonal Degeneration After Axotomy
A Rise in NAD Precursor Nicotinamide Mononucleotide (NMN) After Injury Promotes Axon Degeneration
Nmnat1 Protects Neuronal Function Without Altering Phospho-Tau Pathology in a Mouse Model of Tauopathy Erik S
Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5'UTR Mutations and Copy-Number Variations Of
HHS Public Access Author Manuscript