Biochemistry, Genetics and Molecular Biology
Alkaline Phosphatase
100%
Isoenzyme
100%
Disease Classification
100%
Pyridoxal Phosphate
80%
ALPL
40%
Pyridoxine
40%
Vitamin B6
40%
Mineralization
20%
Enzymatic Hydrolysis
20%
Autosomal Dominant Inheritance
20%
Pyrophosphate
20%
Rickets
20%
Loss of Function Mutation
20%
Osteomalacia
20%
Posttranslational Modification
20%
Missense
20%
Autosomal Recessive Inheritance
20%
Inborn Error of Metabolism
20%
Adolescence
20%
Blood Plasma
20%
Phosphatase
20%
Keyphrases
Hypophosphatasia
100%
Nosology
100%
Pediatric Research
100%
Isoenzymes
33%
Pyridoxal 5′-phosphate
26%
Alkaline Phosphatase
20%
Puberty
13%
Liver
6%
Hydrolysis
6%
Autosomal Dominant
6%
Kidney
6%
Pediatric
6%
Pediatric Patients
6%
Skeletal Disorders
6%
Rickets
6%
Osteomalacia
6%
Inorganic Pyrophosphate
6%
Natural Substrate
6%
Phosphohydrolase
6%
Gain-of-function mutation
6%
Post-translational Modification
6%
Cell Surface
6%
Potent Inhibitor
6%
Alkaline Phosphatase Level
6%
Physiological Changes
6%
Perinatal Hypophosphatasia
6%
Inborn Errors of Metabolism
6%
Autosomal Recessive Inheritance
6%
Vitamin B6
6%
Wide-ranging
6%
Alkaline Phosphatase Gene
6%
Missense
6%
Phosphate Levels
6%
Superabundance
6%
Tooth Loss
6%
ALPL Gene
6%
Developing Teeth
6%
Vitamin B6-dependent Epilepsy
6%
Medicine and Dentistry
Pediatrics
100%
Nosology
100%
Hypophosphatasia
100%
Alkaline Phosphatase
31%
Isoenzyme
31%
Pyridoxal 5 Phosphate
25%
Pyridoxine
12%
Biological Marker
6%
Epileptic Seizure
6%
Pediatrics Patient
6%
Cell Surface
6%
Loss of Function Mutation
6%
Disease
6%
Urinary System
6%
Dual-Energy X-Ray Absorptiometry
6%
Autosomal Recessive Inheritance
6%
Autosomal Dominant Inheritance
6%
Rickets
6%
Skeleton
6%
Mineralization
6%
Osteomalacia
6%
Inborn Error of Metabolism
6%
Pyrophosphate
6%
Phosphatase
6%
Adolescence
6%
Enzymatic Hydrolysis
6%
Periodontal Disease
6%
Bone Disease
6%
Post-Translational Modification
6%