Medicine and Dentistry
Congenital Diaphragm Hernia
100%
Glycogen Storage Disease Type II
100%
Patient
72%
Stromal Cell
50%
1,4 Alpha Glucan Branching Enzyme
50%
Glycogen
50%
Pathogenesis
33%
Development
33%
Glycogen Metabolism
33%
Glucose Uptake
33%
Glycogen Synthesis
33%
Skeletal Muscle
33%
Protein
33%
Diseases
33%
Enzyme Replacement Therapy
33%
Differentiation
27%
Analysis
22%
Therapeutic Procedure
16%
Diaphragm
16%
Congenital Disorder
16%
Congenital Malformation
16%
Etiology
16%
Pulmonary Hypoplasia
16%
Lung
16%
Cells
16%
Cell Surface Protein
16%
Muscle Biopsy
16%
UTP-glucose-1-phosphate Uridylyltransferase
16%
Glucan 1,4 Alpha Glucosidase
16%
Glycogen Synthase
16%
Glucose Transporter 4
16%
Glycogenin
16%
Disease Course
16%
Phenotype
16%
Biopsy
16%
Enzyme Activity
16%
Myopathy
16%
Enzyme
16%
Adult
16%
Muscle
16%
Muscle Atrophy
16%
Mass Spectrum
16%
Extracellular Matrix
11%
Combination Therapy
11%
Gene
11%
Donor
11%
Mineralization
11%
In Vitro
5%
Cell Population
5%
Adipocyte
5%
Biochemistry, Genetics and Molecular Biology
Intestine Innervation
100%
Glycogen Branching Enzyme
50%
Lysozyme
50%
Glycogen
50%
CD24
37%
Mouse
33%
Glycogen Metabolism
33%
Glycogenesis
33%
Skeletal Muscle
33%
Protein
33%
Glucose Transport
33%
Intestine
25%
CD90
25%
Fluorescence Activated Cell Sorting
25%
Staining
25%
Glycogenin
16%
Glycogen Synthase
16%
Reduction (Chemistry)
16%
Glucose Transporter
16%
Enzyme Activity
16%
Glucose
16%
Mass Spectrometry
16%
Acid Alpha-Glucosidase
16%
Phenotype
16%
Glial Cells
12%
Flow Cytometry
12%
Health
12%
Transcriptome
12%
RNA Sequence
12%
Immunology and Microbiology
Bone Marrow
100%
Cells
66%
Differentiation
27%
Cell Surface
22%
Mineralization
11%
Tissues
11%
Electric Potential
11%
Gene
11%
Extracellular Matrix
11%
Bone
5%
Cell Heterogeneity
5%
Cell Population
5%
Homeostasis
5%
Adipocyte
5%
Cell Activity
5%
Cell Adhesion
5%
Biological Product
5%
