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المؤلفون: Bernhard, Steiner, Jonas, Rosendahl, Heiko, Witt, Niels, Teich, Volker, Keim, Hans-Ulrich, Schulz, Roland, Pfützer, Matthias, Löhr, Matthias, Lühr, Thomas M, Gress, Renate, Nickel, Olfert, Landt, Monika, Koudova, Milan, Macek, Antoni, Farre, Teresa, Casals, Marie-Claire, Desax, Sabina, Gallati, Macarena, Gomez-Lira, Marie Pierre, Audrezet, Claude, Férec, Marie, des Georges, Mireille, Claustres, Kaspar, Truninger
المساهمون: Institute of Medical Microbiology [Zurich], Universität Zürich [Zürich] = University of Zurich (UZH), Etablissement Français du Sang Bretagne, EFS, Department of Gastroenterology, University of Marburg, Department of Biology and Medical Genetics, Charles University Prague, Medical School and University, The Weatherall Institute of Molecular Medicine, University of Oxford [Oxford], Génétique, génomique fonctionnelle et biotechnologies (UMR 1078) (GGB), Institut Brestois Santé Agro Matière (IBSAM), Université de Brest (UBO)-Université de Brest (UBO)-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire de génétique des maladies rares. Pathologie moleculaire, etudes fonctionnelles et banque de données génétiques (LGMR), IFR3, Université Montpellier 1 (UM1)-Université Montpellier 1 (UM1)-Université de Montpellier (UM)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), University of Zurich, Truninger, K
المصدر: Human Mutation
Human Mutation, Wiley, 2011, 32 (8), pp.912-920. ⟨10.1002/humu.21511⟩
HUMAN MUTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instnameمصطلحات موضوعية: Male, 10039 Institute of Medical Genetics, [SDV]Life Sciences [q-bio], Cystic Fibrosis Transmembrane Conductance Regulator, medicine.disease_cause, Gastroenterology, Vas Deferens, Male Urogenital Diseases, Genotype, Genetics(clinical), CFTR, Child, Genetics (clinical), Genetics, 0303 health sciences, Mutation, education.field_of_study, integumentary system, musculoskeletal, neural, and ocular physiology, 030305 genetics & heredity, Vas deferens, Middle Aged, 3. Good health, idiopathic chronic pancreatitis, medicine.anatomical_structure, Trypsin Inhibitor, Kazal Pancreatic, CBAVD, Adult, 2716 Genetics (clinical), medicine.medical_specialty, Adolescent, Genetic counseling, Population, 610 Medicine & health, Biology, Young Adult, 03 medical and health sciences, 1311 Genetics, Pancreatitis, Chronic, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, education, Infertility, Male, 030304 developmental biology, Haplotype, Epistasis, Genetic, Heterozygote advantage, medicine.disease, nervous system diseases, Haplotypes, 570 Life sciences, biology, Pancreatitis, Carrier Proteins
وصف الملف: Steiner_et_al,_Common_CFTR_haplotypes.pdf - application/pdf
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المؤلفون: Stefan Taube, Justus Welke, V. Weich, Manfred Wiese, Christoph Sarrazin, Hermann E. Wasmuth, Eckart Schreier, Eckart Schott, Frank Lammert, J. Halangk, Golo Ahlenstiel, Ulrich Spengler, Heiko Witt, Uwe Goebel, Thomas Berg, Andreas Mas Marques, B. Schlosser, Tobias Mueller
المصدر: Infection, Genetics and Evolution. 9:847-852
مصطلحات موضوعية: Adult, Male, Microbiology (medical), Genotype, Combination therapy, Hepatitis C virus, Remission, Spontaneous, Biology, medicine.disease_cause, Antiviral Agents, Polymorphism, Single Nucleotide, Microbiology, Young Adult, chemistry.chemical_compound, Interferon, Genetics, medicine, Humans, 3' Untranslated Regions, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Aged, Ribavirin, Remission Induction, Exons, Hepatitis C, Hepatitis C, Chronic, Middle Aged, medicine.disease, Virology, Cross-Sectional Studies, Logistic Models, Infectious Diseases, Receptors, LDL, chemistry, Case-Control Studies, Multivariate Analysis, LDL receptor, Immunology, Female, Interferons, Viral hepatitis, medicine.drug
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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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المؤلفون: Holger Hinrichsen, Carolin Fitz, Bertram Wiedenmann, Christoph Sarrazin, Peter Neuhaus, Konrad Neumann, Heiko Witt, Thomas Berg, Gero Puhl, J. Halangk, Tobias Mueller
المصدر: Genetic Testing and Molecular Biomarkers. 13:407-414
مصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, Genotype, Hepatitis C virus, Angiotensinogen, Biology, medicine.disease_cause, Chronic liver disease, Linkage Disequilibrium, Young Adult, Gene Frequency, Risk Factors, Hepatic Stellate Cells, medicine, Humans, Liver Diseases, Alcoholic, Allele frequency, Alleles, Genetics (clinical), Aged, Aged, 80 and over, Liver Diseases, Genetic Variation, General Medicine, Hepatitis C, Hepatitis C, Chronic, Middle Aged, medicine.disease, Fibrosis, Angiotensin II, Genotype frequency, Case-Control Studies, Immunology, Disease Progression, Female, Viral hepatitis
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::086d107a6aa5d47a9ac7a6647ba30eb6
https://doi.org/10.1089/gtmb.2008.0135 -
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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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المؤلفون: Christoph Sarrazin, Hartwig Klinker, Gerlinde Teuber, Tobias Mueller, Thomas Berg, Holger Hinrichsen, Gero Puhl, J. Halangk, Peter Buggisch, V. Weich, Konrad Neumann, Bertram Wiedenmann, A. Bergk, Peter Neuhaus, Olfert Landt, Heiko Witt
المصدر: Journal of Hepatology. 49:339-345
مصطلحات موضوعية: Adult, Liver Cirrhosis, Male, Cirrhosis, Adolescent, Genotype, medicine.medical_treatment, Single-nucleotide polymorphism, Liver transplantation, Polymorphism, Single Nucleotide, Cohort Studies, Gene Frequency, Risk Factors, Fibrosis, Germany, medicine, Humans, Genetic Predisposition to Disease, Risk factor, Aged, Aged, 80 and over, Hepatology, medicine.diagnostic_test, business.industry, Complement C5, Hepatitis C, Hepatitis C, Chronic, Middle Aged, medicine.disease, Europe, Haplotypes, Liver biopsy, Immunology, Female, business, Viral hepatitis
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المؤلفون: Michael J. McMahon, Derek A. O'Reilly, Michael Larvin, Mark T Cartmell, Andrew N. Kingsnorth, Andrew G. Demaine, Sakhawat H. Rahman, Andreas Kage, Michael Becker, Olfert Landt, Kevin Sargen, Heiko Witt, Hans-Ulrich Schulz
المصدر: European Journal of Gastroenterology & Hepatology. 20:726-731
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Pancreatic disease, Adolescent, medicine.medical_treatment, Trypsin inhibitor, Polymerase Chain Reaction, Gastroenterology, Pathogenesis, Gene Frequency, Polymorphism (computer science), Internal medicine, Humans, Medicine, Genetic Predisposition to Disease, Age of Onset, Polymorphism, Single-Stranded Conformational, Aged, Aged, 80 and over, Protease, Hepatology, business.industry, Odds ratio, Middle Aged, medicine.disease, Phenotype, Endocrinology, Pancreatitis, Trypsin Inhibitor, Kazal Pancreatic, Acute Disease, Acute pancreatitis, Female, Carrier Proteins, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0ec0ba9e578834685b459dca383cdd5
https://doi.org/10.1097/meg.0b013e3282f5728c -
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المؤلفون: Tamás Molnár, Rene H. M. te Morsche, Heiko Witt, Zsofia Nemoda, Joost P.H. Drenth, Ákos Pap, Jan B.M.J. Jansen, Sundaresan Santhosh
المصدر: Pancreas, 36, 317-20
Pancreas, 36, 3, pp. 317-20مصطلحات موضوعية: Adult, Male, Heterozygote, medicine.medical_specialty, Adolescent, Endocrinology, Diabetes and Metabolism, Membrane transport and intracellular motility [NCMLS 5], Polymorphism, Single Nucleotide, Endocrinology, Gene Frequency, Pancreatitis, Chronic, Internal medicine, Internal Medicine, medicine, Humans, PRSS2, Trypsin, Molecular gastro-enterology and hepatology [IGMD 2], Child, Alleles, Loss function, Aged, DNA Primers, Aged, 80 and over, Hungary, Base Sequence, Hepatology, Anionic Trypsinogen, business.industry, Middle Aged, medicine.disease, Genetic defects of metabolism [UMCN 5.1], Amino Acid Substitution, Case-Control Studies, Trypsinogen, Pancreatitis, Female, business
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79ec296835d000090eed5a243099f071
https://doi.org/10.1097/mpa.0b013e31815db4b3 -
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المؤلفون: Dirk J. de Jong, Carsten Büning, Sabine Buhner, Herbert Büning, Ferenc Nagy, Olfert Landt, János Lonovics, Andreas Kage, Hartmut Schmidt, Verena Haas, Daniel C. Baumgart, Heiko Witt, Andreas Sturm, Herbert Lochs, Tahir Durmus, Tamás Molnár, Enno Gentz, Theodor Todorov, Renate Nickel, Janine Büttner, Thomas Fiedler, Joost P.H. Drenth
المصدر: Journal of Crohn's and Colitis, 1, 70-6
Journal of Crohn's and Colitis, 1, 2, pp. 70-6مصطلحات موضوعية: medicine.medical_specialty, Crohn's disease, business.industry, Gastroenterology, Membrane transport and intracellular motility [NCMLS 5], General Medicine, Disease, medicine.disease, Inflammatory bowel disease, Ulcerative colitis, Genotype frequency, Pathogenesis and modulation of inflammation [N4i 1], Genetic defects of metabolism [UMCN 5.1], Internal medicine, Genotype, Cohort, Immunology, medicine, Molecular gastro-enterology and hepatology [IGMD 2], business, ATG16L1
وصف الملف: application/pdf
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المؤلفون: Tobias Müller, Eckart Schott, J. Halangk, A. Bergk, Heiko Witt, M. Pascu, Thomas Berg, Gero Puhl, Florian van Boemmel, V. Weich, Bertram Wiedenmann
المصدر: European Journal of Gastroenterology & Hepatology. 19:947-951
مصطلحات موضوعية: Adult, Male, Hepatitis B virus, Adolescent, Genotype, Cholangitis, Sclerosing, Hepacivirus, Autoimmune hepatitis, Chronic liver disease, medicine.disease_cause, Polymorphism, Single Nucleotide, Hepatitis B, Chronic, Primary biliary cirrhosis, Gene Frequency, Orthohepadnavirus, Antigens, CD, Liver Cirrhosis, Alcoholic, medicine, Humans, CTLA-4 Antigen, Aged, Hepatitis, Chronic, Aged, 80 and over, Autoimmune disease, Chi-Square Distribution, Hepatology, biology, Liver Cirrhosis, Biliary, business.industry, Gastroenterology, Hepatitis C, Chronic, Middle Aged, Hepatitis B, biology.organism_classification, medicine.disease, Fatty Liver, Hepatitis, Autoimmune, Hepadnaviridae, Case-Control Studies, Immunology, Female, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ab3c868936d87ee81dac68fbd2433d1
https://doi.org/10.1097/meg.0b013e3282efa240
Full Text via ClinicalKey