Patients with ptps deficiency. Medical search. Frequent questions

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Anatomy14

Cells, Cultured Fibroblasts Liver Cell Line COS Cells Erythrocytes Brain Cell Line, Tumor Skin Mitochondria T-Lymphocytes Spleen Bone and Bones Kidney

Organisms6

Mice, Knockout Mice, Inbred C57BL Mice, Mutant Strains Mice, Transgenic Mice, 129 Strain Animals, Newborn

Diseases86

Vitamin A Deficiency Deficiency Diseases alpha 1-Antitrypsin Deficiency Vitamin B 12 Deficiency Vitamin D Deficiency Folic Acid Deficiency IgA Deficiency Thiamine Deficiency Glucosephosphate Dehydrogenase Deficiency Magnesium Deficiency Anemia, Iron-Deficiency Vitamin E Deficiency Ascorbic Acid Deficiency Immunologic Deficiency Syndromes Protein C Deficiency IgG Deficiency Amino Acid Metabolism, Inborn Errors Vitamin B 6 Deficiency Factor V Deficiency Riboflavin Deficiency Antithrombin III Deficiency Metabolism, Inborn Errors Vitamin K Deficiency Factor VII Deficiency Factor XI Deficiency Protein Deficiency Anemia, Hypochromic Vitamin B Deficiency Factor XIII Deficiency Leukocyte-Adhesion Deficiency Syndrome Factor X Deficiency Ornithine Carbamoyltransferase Deficiency Disease Adrenal Hyperplasia, Congenital Choline Deficiency Cytochrome-c Oxidase Deficiency Disease Models, Animal Lecithin Acyltransferase Deficiency Biotinidase Deficiency Yin Deficiency Lipid Metabolism, Inborn Errors Hypopituitarism Carbohydrate Metabolism, Inborn Errors Purine-Pyrimidine Metabolism, Inborn Errors Dwarfism, Pituitary Anemia, Hemolytic Potassium Deficiency Platelet Storage Pool Deficiency Body Weight Growth Disorders Dihydropyrimidine Dehydrogenase Deficiency Brain Diseases, Metabolic, Inborn Pyruvate Dehydrogenase Complex Deficiency Disease Mitochondrial Diseases Anemia, Hemolytic, Congenital Nonspherocytic Vitamin K Deficiency Bleeding Scurvy Severe Combined Immunodeficiency Anemia Syndrome Anemia, Macrocytic Homocystinuria Brain Diseases, Metabolic Xerophthalmia Rickets Agammaglobulinemia Glycogen Storage Disease Anemia, Megaloblastic Hyperlipoproteinemia Type I Yang Deficiency Multiple Carboxylase Deficiency Malabsorption Syndromes Mevalonate Kinase Deficiency Multiple Acyl Coenzyme A Dehydrogenase Deficiency Goiter Hypogonadism Leigh Disease Adrenal Insufficiency Hyperammonemia Inflammation Pregnancy Complications Pregnancy Complications, Hematologic Anemia, Pernicious Muscular Diseases Disease Susceptibility Lesch-Nyhan Syndrome Common Variable Immunodeficiency

Chemicals and Drugs76

Protein Tyrosine Phosphatases Protein Tyrosine Phosphatase, Non-Receptor Type 1 Phosphorus-Oxygen Lyases Protein Tyrosine Phosphatase, Non-Receptor Type 2 Receptor-Like Protein Tyrosine Phosphatases, Class 7 Protein Tyrosine Phosphatase, Non-Receptor Type 3 Receptor-Like Protein Tyrosine Phosphatases, Class 4 Protein Tyrosine Phosphatase, Non-Receptor Type 11 Receptor-Like Protein Tyrosine Phosphatases, Class 2 Receptor-Like Protein Tyrosine Phosphatases, Class 3 Protein Tyrosine Phosphatases, Non-Receptor Vanadates Protein Tyrosine Phosphatase, Non-Receptor Type 6 Protein Tyrosine Phosphatase, Non-Receptor Type 12 Iron Biopterin Enzyme Inhibitors Iodine Zinc Tyrosine RNA, Messenger Neopterin Intracellular Signaling Peptides and Proteins GTP Cyclohydrolase Hydrogen Peroxide Vitamin B 12 Ferritins Phosphotyrosine SH2 Domain-Containing Protein Tyrosine Phosphatases Vitamin D alpha 1-Antitrypsin Fatty Acids, Essential Steroid 21-Hydroxylase Cysteine Molecular Probes Vitamin A Human Growth Hormone Protein-Tyrosine Kinases Recombinant Proteins Hemoglobins Iron, Dietary Copper Receptors, Platelet-Derived Growth Factor DNA, Complementary Folic Acid Selenium Receptor, Insulin Reactive Oxygen Species Methylmalonic Acid Alcohol Oxidoreductases Isoenzymes Carnitine Acyl-CoA Dehydrogenases Glucosephosphate Dehydrogenase Thiamine Acyl-CoA Dehydrogenase Membrane Proteins Complement C6 Homocysteine Carrier Proteins Biotinidase Growth Hormone Complement C2 Transcobalamins Adenosine Deaminase DNA Primers Transferrin DNA Biological Markers Sulfatases Receptors, Transferrin DNA-Binding Proteins Mannose-Binding Lectin Pyridoxine Codon, Nonsense Hydroxocobalamin

Analytical, Diagnostic and Therapeutic Techniques and Equipment22

Pedigree Disease Models, Animal Polymerase Chain Reaction Models, Molecular Sequence Alignment Cloning, Molecular Models, Biological Body Weight Erythrocyte Indices Crystallography, X-Ray Transfection Drug Design DNA Mutational Analysis Mutagenesis, Site-Directed Prevalence Organ Size Blotting, Western Reference Values Reverse Transcriptase Polymerase Chain Reaction Hematocrit Heterozygote Detection Crosses, Genetic

Phenomena and Processes52

Mutation Signal Transduction Phosphorylation Amino Acid Sequence Catalytic Domain Base Sequence Substrate Specificity Oxidation-Reduction Phenotype Homozygote Heterozygote Diet Enzyme Activation Kinetics Gene Expression Sequence Homology, Amino Acid Molecular Structure Binding Sites Gene Expression Regulation, Enzymologic src Homology Domains Body Weight Consanguinity Pregnancy Protein Binding Genotype Erythrocyte Indices Protein Structure, Tertiary Transfection Point Mutation Mutation, Missense Nutritional Status Alleles Gene Deletion Time Factors Catalysis Gene Expression Regulation Exons Structure-Activity Relationship Homeostasis Organ Size Genes, Recessive Apoptosis Protein Conformation Hematocrit Aging Oxidative Stress Nutritional Requirements Lipid Metabolism Disease Susceptibility Frameshift Mutation Cell Differentiation Codon, Nonsense

Disciplines and Occupations1

Technology, Industry, Agriculture2

Dietary Supplements Food, Fortified

Information Science4

Molecular Sequence Data Amino Acid Sequence Base Sequence Prevalence

Named Groups1

Infant, Newborn

Health Care2

Nutritional Status Prevalence

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Technology, Industry, Agriculture Information Science Named Groups Health Care

Protein Tyrosine Phosphatases Protein Tyrosine Phosphatase, Non-Receptor Type 1 Phosphorus-Oxygen Lyases Vitamin A Deficiency Deficiency Diseases Protein Tyrosine Phosphatase, Non-Receptor Type 2 alpha 1-Antitrypsin Deficiency Receptor-Like Protein Tyrosine Phosphatases, Class 7 Vitamin B 12 Deficiency Protein Tyrosine Phosphatase, Non-Receptor Type 3 Vitamin D Deficiency Receptor-Like Protein Tyrosine Phosphatases, Class 4 Folic Acid Deficiency IgA Deficiency Thiamine Deficiency Protein Tyrosine Phosphatase, Non-Receptor Type 11 Receptor-Like Protein Tyrosine Phosphatases, Class 2 Glucosephosphate Dehydrogenase Deficiency Receptor-Like Protein Tyrosine Phosphatases, Class 3 Magnesium Deficiency Anemia, Iron-Deficiency Vitamin E Deficiency Ascorbic Acid Deficiency Mice, Knockout Protein Tyrosine Phosphatases, Non-Receptor Vanadates Protein Tyrosine Phosphatase, Non-Receptor Type 6 Immunologic Deficiency Syndromes Protein C Deficiency IgG Deficiency Amino Acid Metabolism, Inborn Errors Mutation Molecular Sequence Data Vitamin B 6 Deficiency Signal Transduction Protein Tyrosine Phosphatase, Non-Receptor Type 12 Phosphorylation Factor V Deficiency Iron Biopterin Amino Acid Sequence Riboflavin Deficiency Antithrombin III Deficiency Mice, Inbred C57BL Metabolism, Inborn Errors Vitamin K Deficiency Catalytic Domain Factor VII Deficiency Base Sequence Factor XI Deficiency Protein Deficiency Substrate Specificity Anemia, Hypochromic Vitamin B Deficiency Enzyme Inhibitors Factor XIII Deficiency Cells, Cultured Leukocyte-Adhesion Deficiency Syndrome Iodine Oxidation-Reduction Zinc Phenotype Tyrosine Factor X Deficiency Ornithine Carbamoyltransferase Deficiency Disease Adrenal Hyperplasia, Congenital Fibroblasts Homozygote RNA, Messenger Neopterin Choline Deficiency Liver Intracellular Signaling Peptides and Proteins Cytochrome-c Oxidase Deficiency Heterozygote Pedigree GTP Cyclohydrolase Cell Line Disease Models, Animal Lecithin Acyltransferase Deficiency Biotinidase Deficiency Hydrogen Peroxide Vitamin B 12 Ferritins Phosphotyrosine Diet Yin Deficiency Polymerase Chain Reaction Models, Molecular SH2 Domain-Containing Protein Tyrosine Phosphatases Lipid Metabolism, Inborn Errors Vitamin D Enzyme Activation alpha 1-Antitrypsin Mice, Mutant Strains Hypopituitarism Carbohydrate Metabolism, Inborn Errors Kinetics Gene Expression Sequence Homology, Amino Acid

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