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PYGL
PYGL Rabbit Polyclonal Antibody
Molecular Diagnosis of Glycogen Storage Disease and Disorders with Overlapping Clinical Symptoms by Massive Parallel Sequencing
Six Glycolysis-Related Genes As Prognostic Risk Markers Can Predict the Prognosis of Patients with Head and Neck Squamous Cell Carcinoma
Muscle Glycogen Phosphorylase and Its Functional Partners in Health and Disease
Linking Glycogen and Senescence in Cancer Cells
Extracellular Vesicles Released By
Carbohydrate and Amino Acid Metabolism As Hallmarks for Innate Immune Cell Activation and Function
Targeting Glycogen Metabolism: a Novel Strategy to Inhibit Cancer Cell Growth?
Supplementary Table 2: Energy Metabolism Related Genes
Absence of HIF1A Leads to Glycogen Accumulation and an Inflammatory Response That Enables Pancreatic Tumor Growth
PYGL (C3): Sc-517597
The Mcardle Disease Handbook a Guide to the Scientific and Medical Research Into Mcardle Disease Explained in Plain English
Glycogen Shortage During Fasting Triggers Liver–Brain–Adipose Neurocircuitry to Facilitate Fat Utilization
Glycogen Storage Disease Type VI
PYGL Gene Glycogen Phosphorylase L
Human Glycogen Phosphorylase, Liver (PYGL) ELISA
Metabolic and Microenvironmental Determinants of Breast Cancer
Diagnosis and Management of Glycogen Storage Diseases Type VI and IX: a Clinical Practice Resource of the American College of Medical Genetics and Genomics (ACMG)
Top View
Elucidating the Role of Hepatic Ppp1r3b in Glucose and Lipid Metabolism
1 Title: Phenotype Consequences of Myophosphorylase Dysfunction
PYGL Rabbit Pab
Leptin Signaling Regulates Glucose Homeostasis, but Not Adipostasis, in the Zebrafish
Anti-PYGL Antibody
PYGL Polyclonal Antibody Catalog Number:55429-1-AP
Extracellular Vesicles Released by Cardiomyocytes in a Doxorubicin
Systematic Surveys of Iron Homeostasis Mechanisms Reveal Ferritin Superfamily and Nucleotide Surveillance Regulation to Be Modif
Human Glycogen Phosphorylase, Liver (PYGL) ELISA
Clinical and Genetic Spectrum of Glycogen Storage Disease in Iranian
Molecular Diagnosis of Mcardle Disease Using Whole-Exome Sequencing
PYGB/L/M (N-20): Sc-46347
Polarity Protein AF6 Controls Hepatic Glucose Homeostasis and Insulin Sensitivity by Modulating IRS1/AKT Insulin Pathway in an SHP2-Dependent Manner
ELISA Kit for Glycogen Phosphorylase, Liver (PYGL)
Novel PYGL Mutations in Chinese Children Leading to Glycogen
Identification and Characterization of a Novel Splice Site Mutation Associated with Glycogen Storage Disease Type VI in Two Unre
Zhu-Gan Decoction Alleviated Non-Alcoholic Fatty Liver Disease Via
Mutations in the Liver Glycogen Phosphorylase Gene (PYGL) Underlying Glycogenosis Type VI (Hers Disease) Barbara Burwinkel,1 Henk D