Neonatal th deficiency. Medical search. Frequent questions

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Anatomy25

Th2 Cells Th1 Cells Th17 Cells Liver Cells, Cultured T-Lymphocytes, Helper-Inducer Fibroblasts Erythrocytes Spleen CD4-Positive T-Lymphocytes T-Lymphocytes Cell Line Brain Skin Lung T-Lymphocyte Subsets B-Lymphocytes Macrophages Dendritic Cells Mitochondria Kidney Lymphocytes T-Lymphocytes, Regulatory Bone and Bones Neutrophils

Organisms10

Mice, Knockout Mice, Inbred C57BL Mice, Transgenic Mice, Mutant Strains Mice, Inbred BALB C Animals, Newborn Mice, 129 Strain Rats, Sprague-Dawley Rats, Inbred Strains Mice, Inbred Strains

Diseases88

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 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 Disease Models, Animal Factor XIII Deficiency Leukocyte-Adhesion Deficiency Syndrome Factor X Deficiency Ornithine Carbamoyltransferase Deficiency Disease Adrenal Hyperplasia, Congenital Choline Deficiency Cytochrome-c Oxidase Deficiency Amino Acid Metabolism, Inborn Errors Lecithin Acyltransferase Deficiency Biotinidase Deficiency Yin Deficiency Lipid Metabolism, Inborn Errors Hypopituitarism Carbohydrate Metabolism, Inborn Errors Purine-Pyrimidine Metabolism, Inborn Errors Body Weight Dwarfism, Pituitary Anemia, Hemolytic Potassium Deficiency Platelet Storage Pool Deficiency Growth Disorders Inflammation Dihydropyrimidine Dehydrogenase Deficiency Brain Diseases, Metabolic, Inborn Pyruvate Dehydrogenase Complex Deficiency Disease Scurvy Mitochondrial Diseases Severe Combined Immunodeficiency Syndrome Anemia, Hemolytic, Congenital Nonspherocytic Vitamin K Deficiency Bleeding Anemia Anemia, Macrocytic Homocystinuria Brain Diseases, Metabolic Xerophthalmia Agammaglobulinemia Rickets Disease Susceptibility Yang Deficiency Glycogen Storage Disease Anemia, Megaloblastic Hyperlipoproteinemia Type I Multiple Carboxylase Deficiency Malabsorption Syndromes Mevalonate Kinase Deficiency Goiter Multiple Acyl Coenzyme A Dehydrogenase Deficiency Pregnancy Complications Autoimmune Diseases Hypogonadism Leigh Disease Adrenal Insufficiency Hyperammonemia Muscular Diseases Common Variable Immunodeficiency Pregnancy Complications, Hematologic Anemia, Pernicious Lesch-Nyhan Syndrome Hypothyroidism

Chemicals and Drugs63

Iron Iodine Zinc Cytokines RNA, Messenger Vitamin B 12 Ferritins Interleukin-17 Interferon-gamma Interleukin-4 Vitamin D alpha 1-Antitrypsin Fatty Acids, Essential Vitamin A Human Growth Hormone Steroid 21-Hydroxylase Hemoglobins Iron, Dietary Copper Folic Acid Selenium Methylmalonic Acid Carnitine Glucosephosphate Dehydrogenase Acyl-CoA Dehydrogenases Membrane Proteins Thiamine Interleukin-12 Acyl-CoA Dehydrogenase Biological Markers Carrier Proteins GATA3 Transcription Factor DNA-Binding Proteins DNA Primers Complement C6 Immunoglobulin G Homocysteine DNA Growth Hormone Ovalbumin Biotinidase Interleukin-10 Complement C2 Transcription Factors Transcobalamins Adenosine Deaminase Interleukins Transferrin Tyrosine 3-Monooxygenase Sulfatases Recombinant Proteins Receptors, Transferrin Pyridoxine Trace Elements Mannose-Binding Lectin Codon, Nonsense Thyroid Hormones Cholesterol Hydroxocobalamin Protoporphyrins Pyrithiamine Complement C4 Complement C7

Analytical, Diagnostic and Therapeutic Techniques and Equipment23

Disease Models, Animal Pedigree Body Weight Lymphocyte Activation Erythrocyte Indices Flow Cytometry Reverse Transcriptase Polymerase Chain Reaction Polymerase Chain Reaction DNA Mutational Analysis Reference Values Prevalence Blotting, Western Organ Size Hematocrit Immunohistochemistry Crosses, Genetic Risk Factors Case-Control Studies Heterozygote Detection Models, Biological Enzyme-Linked Immunosorbent Assay Gene Targeting Neonatal Screening

Phenomena and Processes41

Th1-Th2 Balance Mutation Phenotype Homozygote Heterozygote Base Sequence Diet Pregnancy Cell Differentiation Body Weight Signal Transduction Time Factors Lymphocyte Activation Gene Expression Regulation Consanguinity Genotype Amino Acid Sequence Erythrocyte Indices Point Mutation Nutritional Status Alleles Mutation, Missense Gene Deletion Homeostasis Exons Gene Expression Apoptosis Organ Size Disease Susceptibility Aging Cell Proliferation Genes, Recessive Hematocrit Up-Regulation Oxidative Stress Nutritional Requirements Lipid Metabolism Down-Regulation Immunity, Innate Frameshift Mutation Codon, Nonsense

Disciplines and Occupations1

Immunohistochemistry

Technology, Industry, Agriculture3

Dietary Supplements Food, Fortified Trace Elements

Humanities6

History, 19th Century History, 17th Century History, 20th Century History, 18th Century History, 16th Century History, 15th Century

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Prevalence

Named Groups1

Infant, Newborn

Health Care5

Nutritional Status Prevalence Risk Factors Case-Control Studies Neonatal Screening

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

Th2 Cells Th1 Cells Th17 Cells Vitamin A Deficiency Deficiency Diseases alpha 1-Antitrypsin Deficiency Vitamin B 12 Deficiency Vitamin D Deficiency Folic Acid Deficiency IgA Deficiency Thiamine Deficiency Mice, Knockout Glucosephosphate Dehydrogenase Deficiency Magnesium Deficiency Anemia, Iron-Deficiency Vitamin E Deficiency Ascorbic Acid Deficiency Immunologic Deficiency Syndromes Protein C Deficiency IgG Deficiency Mice, Inbred C57BL Vitamin B 6 Deficiency Th1-Th2 Balance Factor V Deficiency Iron Riboflavin Deficiency Mutation Antithrombin III Deficiency Metabolism, Inborn Errors Vitamin K Deficiency Factor VII Deficiency Factor XI Deficiency Protein Deficiency Phenotype Anemia, Hypochromic Vitamin B Deficiency Disease Models, Animal Iodine Factor XIII Deficiency Zinc Leukocyte-Adhesion Deficiency Syndrome Factor X Deficiency Liver Ornithine Carbamoyltransferase Deficiency Disease Homozygote Adrenal Hyperplasia, Congenital Cells, Cultured Choline Deficiency Heterozygote Pedigree Cytochrome-c Oxidase Deficiency Amino Acid Metabolism, Inborn Errors Mice, Transgenic Cytokines Molecular Sequence Data Lecithin Acyltransferase Deficiency Biotinidase Deficiency Base Sequence RNA, Messenger Mice, Mutant Strains Vitamin B 12 Ferritins Diet Interleukin-17 Yin Deficiency Interferon-gamma Interleukin-4 Vitamin D Mice, Inbred BALB C Pregnancy Infant, Newborn Lipid Metabolism, Inborn Errors alpha 1-Antitrypsin Hypopituitarism Carbohydrate Metabolism, Inborn Errors T-Lymphocytes, Helper-Inducer Fatty Acids, Essential Vitamin A Purine-Pyrimidine Metabolism, Inborn Errors Cell Differentiation Human Growth Hormone Steroid 21-Hydroxylase Fibroblasts Body Weight Signal Transduction History, 19th Century Hemoglobins Erythrocytes Time Factors Iron, Dietary Lymphocyte Activation Copper Dwarfism, Pituitary Gene Expression Regulation Anemia, Hemolytic Folic Acid Dietary Supplements Potassium Deficiency Platelet Storage Pool Deficiency Growth Disorders

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