Cause inherited diseases like cystic fibrosis. Medical search. Frequent questions

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Anatomy23

Cells, Cultured Sweat Sputum Lung Cell Line Respiratory Mucosa Nasal Mucosa Fibroblasts Respiratory System Epithelial Cells Liver Bronchi Mucus Meconium Trachea Sweat Glands Epithelium Exocrine Glands Hepatic Stellate Cells Myofibroblasts Pancreas Vas Deferens Kidney

Organisms10

Pseudomonas aeruginosa Mice, Inbred C57BL Mice, Inbred CFTR Burkholderia cepacia Burkholderia cepacia complex Achromobacter denitrificans Burkholderia cenocepacia Stenotrophomonas maltophilia Burkholderia Mice, Knockout

Diseases33

Cystic Fibrosis Fibrosis Genetic Diseases, Inborn Disease Models, Animal Pseudomonas Infections Inflammation Autoimmune Diseases Neoplasms Arthritis, Rheumatoid Burkholderia Infections Endomyocardial Fibrosis Idiopathic Pulmonary Fibrosis Exocrine Pancreatic Insufficiency Genetic Predisposition to Disease Liver Cirrhosis Retroperitoneal Fibrosis Syndrome Bronchiectasis Lung Diseases Aspergillosis, Allergic Bronchopulmonary Oral Submucous Fibrosis Respiratory Tract Infections Liver Cirrhosis, Experimental Chronic Disease Ureteral Obstruction Bronchopneumonia Disease Progression Pneumonia, Bacterial Gram-Negative Bacterial Infections Peritoneal Fibrosis Ileus Intestinal Obstruction Opportunistic Infections

Chemicals and Drugs45

Cystic Fibrosis Transmembrane Conductance Regulator Ferrochelatase Codon, Nonsense Chlorides Chloride Channels Membrane Proteins Tobramycin DNA Pancreatin Pancreatic Extracts RNA, Messenger Anti-Bacterial Agents DNA Primers Genetic Markers Expectorants Alginates Proteins Bleomycin Pancrelipase Aminophenols Leukocyte Elastase Amiloride Hexuronic Acids Colistin Glucuronic Acid Hydroxyproline Mucins Colforsin Cyclic AMP Trypsinogen Transforming Growth Factor beta Bicarbonates Collagen Carbon Tetrachloride Biological Markers Interleukin-8 Anions Adenosine Triphosphate Epithelial Sodium Channels Iodides Aerosols ortho-Aminobenzoates Collagen Type III Collagen Type I Recombinant Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment32

Disease Models, Animal Pedigree Models, Biological Genetic Testing Genetic Therapy DNA Mutational Analysis Chromosome Mapping Polymerase Chain Reaction Neonatal Screening Forced Expiratory Volume Respiratory Function Tests Amino Acid Substitution Lung Transplantation Heterozygote Detection Models, Genetic Reverse Transcriptase Polymerase Chain Reaction Transfection Sequence Analysis, DNA Mucociliary Clearance Models, Molecular Vital Capacity Liver Cirrhosis, Experimental Administration, Inhalation Drainage, Postural Bronchoalveolar Lavage Fluid Respiratory Therapy Severity of Illness Index Biopsy Heart-Lung Transplantation Nebulizers and Vaporizers Breath Tests Prenatal Diagnosis

Phenomena and Processes34

Mutation Phenotype Mutation, Missense Heredity Signal Transduction Codon, Nonsense Genetic Linkage Base Sequence Heterozygote Genotype Point Mutation Exons Amino Acid Sequence Genetic Predisposition to Disease Alleles Genome, Human Forced Expiratory Volume Germ-Line Mutation Gene Expression Genetic Vectors Amino Acid Substitution Polymorphism, Genetic Genetic Markers Polymorphism, Single Nucleotide Transfection Sequence Homology, Amino Acid Mucociliary Clearance Ion Transport Vital Capacity Time Factors Homozygote Nutritional Status Biofilms Gene Expression Regulation

Disciplines and Occupations2

Computational Biology Genetic Counseling

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups1

Infant, Newborn

Health Care6

Genetic Testing Neonatal Screening Family Health Genetic Counseling Severity of Illness Index Nutritional Status

Geographicals1

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

Cystic Fibrosis Cystic Fibrosis Transmembrane Conductance Regulator Fibrosis Genetic Diseases, Inborn Mutation Phenotype Disease Models, Animal Pseudomonas Infections Inflammation Pseudomonas aeruginosa Autoimmune Diseases Cells, Cultured Pedigree Sweat Mice, Inbred C57BL India Mutation, Missense Sputum Neoplasms Heredity Models, Biological Molecular Sequence Data Mice, Inbred CFTR Arthritis, Rheumatoid Genetic Testing Ferrochelatase Signal Transduction Codon, Nonsense Burkholderia Infections Genetic Linkage Burkholderia cepacia Genetic Therapy Base Sequence Chlorides DNA Mutational Analysis Endomyocardial Fibrosis Heterozygote Idiopathic Pulmonary Fibrosis Genotype Lung Point Mutation Exons Amino Acid Sequence Exocrine Pancreatic Insufficiency Chromosome Mapping Genetic Predisposition to Disease Liver Cirrhosis Cell Line Polymerase Chain Reaction Alleles Chloride Channels Respiratory Mucosa Membrane Proteins Genome, Human Tobramycin Nasal Mucosa DNA Pancreatin Fibroblasts Neonatal Screening Forced Expiratory Volume Germ-Line Mutation Retroperitoneal Fibrosis Burkholderia cepacia complex Syndrome Respiratory Function Tests Pancreatic Extracts Respiratory System Bronchiectasis Gene Expression Family Health Lung Diseases Epithelial Cells Liver Genetic Vectors RNA, Messenger Anti-Bacterial Agents Amino Acid Substitution Polymorphism, Genetic Computational Biology Bronchi Lung Transplantation Mucus Heterozygote Detection DNA Primers Genetic Markers Polymorphism, Single Nucleotide Models, Genetic Reverse Transcriptase Polymerase Chain Reaction Meconium Expectorants Alginates Proteins Bleomycin Transfection Pancrelipase Sequence Analysis, DNA Trachea Achromobacter denitrificans Sequence Homology, Amino Acid

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