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Michael W King, PhD | © 1996–2016 themedicalbiochemistrypage.org, LLC |
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Last modified: January 3, 2017
Abbreviations: definitions of abbreviations used in this site
Addison Disease
Adipose Tissue: not just a fat storage organ
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Acute intermittent porphyria
ALA dehydratase deficient porphyria
Alkaptonuria
All diseases: alphabetic listing of all disease discussion pages in this site
Amino acid metabolism
AMPK: Master metabolic regulator
Arginase deficiency: urea cycle defect
Argininosuccinate lyase deficiency: urea cycle defect
Argininosuccinate synthetase deficiency: urea cycle defect
Aspartylglucosaminuria: lysosomal storage disease
Aspirin function via lipid modulators of inflammation
Ataxia telangiectasia: defective DNA repair
Awards
Basic biochemistry of amino acids
Basic biochemistry of carbohydrates
Basic biochemistry of lipid classes
Basic biochemistry of nucleic acids
Bernard-Soulier syndrome giant platelet syndrome, blood coagulation defect
Bile acid synthesis and functions
Bioactive Lipids & Lipid-Sensing Receptors
Biochemistry of nerve transmission
Blood coagulation: hemostasis
Blood tests: collection of common blood test values
Carbamoylphosphate synthetase deficiency: urea cycle defect
Cell Cycle
Cholesterol synthesis and metabolism
Congenital disorders of glycosylation (CDG): defects in glycosylation
Congenital adrenal hyperplasias (CAH): defects in adrenal steroidogenesis
Congenital erythropoietic porphyria
Crigler-Najjar syndromes: bilirubin metabolism disorders
Cushing Syndrome
Cytochrome P450 Family Enzymes
Derivatives of amino acids
Dentatorubro-Pallidoluysian atrophy: trinucleotide repeat disorder
Diabetes: type 1 and type 2
Diabetic ketoacidosis
Dipeptidyl Peptidase 4, DPP4
Diseases and Disorders: listing of pages detailing various diseases and disorders
Diseases associated with defects in bilirubin metabolism
Diseases associated with defects in blood coagulation
Diseases associated with defects in connective tissue metabolism
Diseases associated with abnormal amino acid metabolism
Diseases associated with abnormal amino acid transport
Diseases associated with defects in DNA repair
Diseases associated with defects in fatty acid oxidation
Diseases associated with defects in metal transport and homeostasis
Diseases associated with abnormal fructose and galactose metabolism
Diseases associated with defects in proteins of oxygen transport
Diseases associated with defects in peroxisome function
Diseases associated with defects in purine nucleotide metabolism
Diseases associated with defects in pyrimidine nucleotide metabolism
Diseases associated with defects in the urea cycle
DNA metabolism
Dubin-Johnson syndrome: bilirubin metabolism disorder
Ehlers-Danlos syndrome: disorder in connective tissue metabolism
Eicosanoid Metabolism: prostaglandins, thromboxanes, leukotrienes, and lipoxins
Endocannabinoids
Enzyme kinetics
Erythropoietic porphyria
Ethanol (alcohol) Metabolism
Extracellular matrix
Fabry disease: lysosomal storage disease
Factor X deficiency: blood coagulation defect
Factor XI deficiency: blood coagulation defect
Factor XII deficiency: blood coagulation defect
Factor XIII deficiency: blood coagulation defect
Familial hypercholesterolemia
Farber lipogranulomatosis: lysosomal storage disease
Farnesoid X Receptors, FXRs
Fatty acid oxidation
Fragile X syndrome: trinucleotide repeat disorder
Fragile XE mental retardation: trinucleotide repeat disorder
Friedreich ataxia: trinucleotide repeat disorder
Fructose Metabolism
Fucosidosis: lysosomal storage disease
Fucosidosis: lysosomal storage disease
Galactose Metabolism
Gaucher disease: lysosomal storage disease
Genomic imprinting and disease
Gilbert syndrome: bilirubin metabolism disorder
Glanzmann thrombasthenia: blood coagulation disorder
Glossary: medical and clinical terms from site
Gluconeogenesis
Glucose-6-phosphate dehydrogenase deficiency
GLUT1 Deficiency Syndrome
Glycosaminoglycans and proteoglycans
Glycogen metabolism
Glycogen storage diseases listing
Glycogen storage disease 1: von Gierke disease
Glycogen storage disease 2: Pompe disease
Glycogen storage disease 3: Cori disease
Glycogen storage disease 4: Andersen disease
Glycogen storage disease 5: McArdle disease
Glycolysis
Glycoproteins: synthesis and clinical consequences
GM1 gangliosidosis: lysosomal storage disease
GM2 activator deficiency: lysosomal storage disease
Gout
Graves Disease
Growth factors
Gut-Brain: Interactions and Feeding Behaviors
Hereditary coproporphyria
Heme and porphyrin metabolism
Hemochromatosis
Hemoglobin and myoglobin
Hemophilia A
Hemophilia B
Hunter syndrome: mucopolysaccharidosis, lysosomal storage disease
Huntington disease: trinucleotide repeat disorder
Hurler-Scheie syndromes: mucopolysaccharidoses, lysosomal storage disease
Hyperlipoproteinemias
Hypolipoproteinemias
I-cell disease: mucolipidosis, lysosomal storage disease
Infantile Refsum disease (IRD): peroxisome biogenesis disorder
Insulin function
Ionic equilibria
Iron and Copper Homeostasis
Krabbe disease: lysosomal storage disease
Krill oil: composition and nutitional benefits
Large picture of adrenal steroid synthesis
Large picture of glycosaminoglycan degradation
Large picture of glycoprotein degradation
Large picture of heme biosynthesis
Large picture of hexosamine biosynthesis pathway, HBP
Large picture of sphingolipid degradation
Large picture of telomerase activities
Lesch-Nyhan disease: purine nucleotide metabolism disorder
Lipid Metabolism: fatty acid, triglyceride, and phospholipid synthesis
Lipoproteins and lipoprotein associated diseases
Lysosomal storage diseases listing
Liver X Receptors (LXRs)
α-Mannosidosis: lysosomal storage disease
β-Mannosidosis: lysosomal storage disease
Maple syrup urine disease
Marfan syndrome: disorder in connective tissue metabolism
Maroteaux-Lamy syndrome: mucopolysaccharidosis, lysosomal storage disease
Medium chain acyl-CoA dehydrogenase (MCAD) deficiency: fatty acid oxidation disorder
Membranes and Membrane Transport
Menkes disease: defect in copper homeostasis
Metabolic Syndrome: MetS
Metachromatic leukodystrophy: lysosomal storage disease
Minerals: Critical Micronutrients
Molecular biology tools in medicine
Morquio syndrome: mucopolysaccharidosis, lysosomal storage disease
Mucopolysaccharidoses listings
Muscle biochemistry
Myotonic dystrophy: trinucleotide repeat disorder
Niemann-Pick diseases: lysosomal storage diseases
Neonatal adrenoleukodystrophy: peroxisome biogenesis disorder
Nitrogen metabolism and the urea cycle
Nuclear receptors in metabolism
Nucleotide metabolism
Obesity: Metabolic Consequences
Omega-3 and -6 polyunsaturated fatty acids
Oncogenes
Opioids and Opioid Receptors
Ornithine transcarbamoylase deficiency: urea cycle disorder
Osteogenesis imperfecta: disorders in connective tissue metabolism
Oxidative phosphorylation
Pentose phosphate pathway
Peptide hormones and receptors
Peroxisome Prolifertor-Activated Receptors, PPARs
Phenylketonuria
Porphyria cutanea tarda
Porphyrias listing
Posttranslational Protein Modifications (PTM) and Protein Targeting
PPARγ Coactivator-1 (PGC-1) Family
Protein, Organelle, and Cell Turnover: ubiquitylation, apoptosis, autophagy
Protein C deficiency: blood coagulation disorder
Protein structure
Protein synthesis
Pseudo-Hurler polydystrophy: mucolipidosis, lysosomal storage disease
Pyruvate kinase deficiency: erythrocyte enzymopathy
Recent Updates: latest news about site updates
References: subject oriented listing of peer-reviewed references
Refsum disease: defect in α-oxidation of fatty acids
Regulation of gene expression
Resources Page: Page containing links to useful resources
Rhizomelic chondrodysplasia punctata, type 1 (RCDP1): peroxisome biogenesis disorder
Rotor syndrome: bilirubin metabolism disorder
Sandhoff disease: lysosomal storage disease
Sanfilippo syndromes: mucopolysaccharidoses, lysosomal storage disease
Severe combined immunodeficiency, SCID: defect in purine nucleotide metabolism
Sphingolipid Metabolism: sphingomyelins and gangliosides
Sialidosis: lysosomal storage disease
Sickle cell anemia
Signal transduction
Sly syndrome: mucopolysaccharidosis, lysosomal storage disease
Smith-Lemli-Opitz Syndrome: cholesterol biosynthesis defect
Spinobulbar muscular atrophy: trinucleotide repeat disorder
Spinocerebellar ataxias: trinucleotide repeat disorders
Steroid hormones
Table of peptide hormones
Tangier Disease: defective cholesterol homeostasis
Tay-Sachs disease: lysosomal storage disease
TCA cycle
α-Thalassemias
β-Thalassemias
The Medical Biochemistry Page awards
Thermodynamics review
Transcription
Trinucleotide repeat disorders listing
Tumor suppressors
Vitamins and Minerals
Variegate porphyria
von Willebrand disease: blood coagulation disorder
Wilson disease: defect in copper homeostasis
Wnts, BMPs and TGF-β signaling
Xeroderma pigmentosum: defective DNA repair
X-linked adrenoleukodystrophy: peroxisome biogenesis disorder
X-linked sideroblastic anemia: porphyrin biosynthesis disorder
Zellweger syndrome: peroxisome biogenesis disorder