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1
المؤلفون: Heiko Witt, Sebastian Müller, Rupino W. Griffioen, Franz Rüschendorf, Claudia Sengler, Young-Ae Lee, Renate Nickel, Ulrich Wahn, Simona Eva Zitnik, Paolo Meglio
المصدر: Pediatric Allergy and Immunology. 20:551-555
مصطلحات موضوعية: Allergy, Genotype, Eggs, Immunology, Immunoglobulin E, medicine.disease_cause, Dermatitis, Atopic, Atopy, Allergen, Immunopathology, Anti-Allergic Agents, Humans, Immunology and Allergy, Medicine, Egg Hypersensitivity, Sensitization, Asthma, Interleukin-13, biology, business.industry, Genetic Variation, Infant, Atopic dermatitis, Allergens, medicine.disease, Cetirizine, Treatment Outcome, medicine.anatomical_structure, Child, Preschool, Pediatrics, Perinatology and Child Health, biology.protein, business, Food Hypersensitivity
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2
المؤلفون: Ulrich Wahn, Sabina Illi, Young-Ae Lee, Steffi Humberdros, Katja C. Beier, Renate Nickel, Franz Rüschendorf, Susanne Lau, Eckard Hamelmann, Heiko Witt
المصدر: Pediatric Allergy and Immunology. 20:242-245
مصطلحات موضوعية: Antigens, Differentiation, T-Lymphocyte, Allergy, Genotype, Immunology, Population, Immunoglobulin E, Airborne allergen, Cohort Studies, Inducible T-Cell Co-Stimulator Protein, Allergic sensitization, Atopy, Gene Frequency, Hypersensitivity, medicine, Humans, Immunology and Allergy, Genetic Predisposition to Disease, Prospective Studies, Child, Promoter Regions, Genetic, education, Alleles, Asthma, education.field_of_study, biology, business.industry, Atopic dermatitis, Allergens, medicine.disease, Europe, Pediatrics, Perinatology and Child Health, biology.protein, business
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3
المؤلفون: Renate Nickel, Dirk J. de Jong, Daniel C. Baumgart, Joost P.H. Drenth, Heiko Witt, Ferenc Nagy, Herbert Lochs, Olfert Landt, H. Schmidt, János Lonovics, Sabine Buhner, Janine Büttner, Andreas Sturm, Thomas Fiedler, Carsten Büning, T Molnár
المصدر: Alimentary Pharmacology & Therapeutics. 26:1025-1033
مصطلحات موضوعية: Crohn's disease, medicine.medical_specialty, Hepatology, business.industry, Gastroenterology, Single-nucleotide polymorphism, Disease, medicine.disease, Ulcerative colitis, Inflammatory bowel disease, Genotype frequency, Internal medicine, Genotype, Immunology, medicine, Pharmacology (medical), Colitis, business
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4
المؤلفون: Jan Maarten Cobben, Nienke E. Verbeek, Markus M. Lerch, Fowzan S. Alkuraya, Manuel Oltra Benavent, Celina Guzman, Nima Rezaei, Abdullah Alrajoudi, Özgür Kirbiyik, Martin Zenker, Charu Deshpande, Carlos A. Venegas-Vega, Prajnya Ranganath, Fouad Ali, Marie-Claude Addor, Erick Richmond, Eva-Lena Stattin, Lynette A. Gillis, Débora Romeo Bertola, David B. Everman, Klaus-Michael Keller, Maja Sukalo, Gesche Düker, Clara D.M. van Karnebeek, Heiko Witt, Zhifeng Liu, Julia Mayerle, Jiad N. Mcheik, Crésio Alves, Bita Bozorgmehr, Stephanie Spranger, Amy Shealy, Ankur Singh, Koumudi Godbole, Ariane Fiedler, Jan Liebelt, Gonul Ogur, Carsten Bergmann
المساهمون: Ondokuz Mayıs Üniversitesi, ANS - Amsterdam Neuroscience, Other Research, Human Genetics, Paediatric Genetics
المصدر: HUMAN MUTATION
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Human mutation, 35(5), 521-531. Wiley-Liss Inc.مصطلحات موضوعية: medicine.medical_specialty, Hearing Loss, Sensorineural, Ubiquitin-Protein Ligases, Dwarfism, Nose, Biology, medicine.disease_cause, UBR1, Short stature, aplasia of alae nasi, Frameshift mutation, Anus, Imperforate, Hypothyroidism, Ectodermal Dysplasia, Intellectual Disability, Internal medicine, Databases, Genetic, Genetics, medicine, Humans, Missense mutation, Abnormalities, Multiple, Allele, Exocrine pancreatic insufficiency, Growth Disorders, Genetics (clinical), cognitive impairment, Mutation, Pancreatic Diseases, medicine.disease, exocrine pancreatic insufficiency, Phenotype, Endocrinology, Johanson–Blizzard syndrome, Sensorineural hearing loss, medicine.symptom, Johanson-Blizzard syndrome
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5
المؤلفون: V. Weich, Thomas Berg, Heiko Witt, Eckart Schott, Tobias Müller, A. Bergk, J. Halangk, Konrad Neumann, Gero Puhl, Bertram Wiedenmann
المصدر: Journal of Viral Hepatitis. :070806205932002
مصطلحات موضوعية: Male, Hepatitis C virus, Mutation, Missense, Single-nucleotide polymorphism, Hepacivirus, Biology, Chronic liver disease, medicine.disease_cause, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Cohort Studies, Immune system, Belgium, Interferon, Virology, Genetic variation, medicine, Humans, Innate immune system, Hepatology, Haplotype, Genetic Variation, Interferon-alpha, virus diseases, Hepatitis C, Chronic, medicine.disease, digestive system diseases, Blood, Logistic Models, Treatment Outcome, Infectious Diseases, Toll-Like Receptor 7, Case-Control Studies, Immunology, Female, medicine.drug
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