-
1
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 -
2
المؤلفون: Clemens Ruppert, Malgorzata Wygrecka, Andreas Guenther, Phillipp Markart, Martina Korfei, I. Theruvath, Werner Seeger, Ulrich Pison, Heiko Witt, Reinhold E. Schmidt, Heinz Harbach
المصدر: European Respiratory Journal. 29:134-137
مصطلحات موضوعية: Adult, Male, Pulmonary and Respiratory Medicine, Pathology, medicine.medical_specialty, Genotype, DNA Mutational Analysis, medicine.disease_cause, Idiopathic pulmonary fibrosis, Gene Frequency, Pulmonary fibrosis, medicine, Humans, Idiopathic interstitial pneumonia, Aged, Mutation, Polymorphism, Genetic, Lung, business.industry, Respiratory disease, Interstitial lung disease, Surfactant protein C, Middle Aged, medicine.disease, Pulmonary Surfactant-Associated Protein C, respiratory tract diseases, medicine.anatomical_structure, Case-Control Studies, Immunology, Female, Lung Diseases, Interstitial, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58a05f2210edb607c364a15c6f681c50
https://doi.org/10.1183/09031936.00034406 -
3
المؤلفون: Rainer Dietz, Bakytbek Imanov, Mirsaid M. Mirrakhimov, Karl Josef Osterziel, Nana Bit-Avragim, Bernard Hoffmann, Reinhard Geßner, Dinara A. Usupbaeva, Raisa I. Rudenko, Andreas Perrot, Zhyldyz Kabaeva, Hajo Schmidt-Traub, Michal Tendera, Matthias Prager, Anna Wycisk, Heiko Witt
المصدر: Journal of Molecular Medicine. 83:468-477
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Pathology, Adolescent, Genotype, DNA Mutational Analysis, Molecular Sequence Data, Mutation, Missense, Biology, medicine.disease_cause, Left ventricular hypertrophy, Risk Factors, Germany, Internal medicine, Drug Discovery, Prevalence, medicine, Humans, Missense mutation, Amino Acid Sequence, Prospective Studies, Child, Kyrgyzstan, Genetics (clinical), Aged, Mutation, Myosin Heavy Chains, Hypertrophic cardiomyopathy, Cardiomyopathy, Hypertrophic, Middle Aged, medicine.disease, Penetrance, Pedigree, Molecular Medicine, Population study, Female, MYH7, Poland, Cardiac Myosins, Sequence Alignment
-
4
المؤلفون: Heiko Witt
المصدر: Gut. 52:31ii-41
مصطلحات موضوعية: Male, Paper, Pathology, medicine.medical_specialty, Pancreatic disease, Cystic Fibrosis, Pancreatitis, Alcoholic, Trypsinogen, medicine.disease_cause, Cystic fibrosis, Pathogenesis, chemistry.chemical_compound, Vas Deferens, medicine, Humans, Genetic Predisposition to Disease, Genetic testing, Mutation, Models, Genetic, biology, medicine.diagnostic_test, Gastroenterology, medicine.disease, Cystic fibrosis transmembrane conductance regulator, Pancreatitis, chemistry, Chronic Disease, Immunology, biology.protein
-
5
المؤلفون: Ellen van Binsbergen, Andreas R. Janecke, Thomas Müller, Helmut Denk, Helmut Ellemunter, Heiko Witt, Johann Deutsch, Bart van de Sluis, Ashish Bavdekar, Irmin Sternlieb, M. Stuart Tanner, Cisca Wijmenga, Alexandra Zhernakova, Helga Weirich-Schwaiger, Anand Pandit, W Müller
المساهمون: Faculteit Medische Wetenschappen/UMCG, Restoring Organ Function by Means of Regenerative Medicine (REGENERATE)
المصدر: Journal of Hepatology, 38(2), 164-168. ELSEVIER SCIENCE BV
مصطلحات موضوعية: Liver Cirrhosis, Candidate gene, Pathology, medicine.medical_specialty, Cirrhosis, Molecular Sequence Data, chemistry.chemical_element, Indian childhood cirrhosis, Hepatic copper, Exon, Liver Cirrhosis/genetics, Dogs, Hepatolenticular Degeneration, Medicine, Animals, Humans, Gene, Adaptor Proteins, Signal Transducing, Hepatology, Base Sequence, business.industry, Signal Transducing, Proteins, Chromosome, Adaptor Proteins, Infant, Metabolism, Inborn Errors/genetics, medicine.disease, Copper, Copper/adverse effects, Metabolism, chemistry, Proteins/genetics, business, Carrier Proteins, Metabolism, Inborn Errors, Inborn Errors/genetics
-
6
المؤلفون: M. G. Slieker, Carla Colombo, Roderick H. J. Houwen, D. Staab, Behrooz Z. Alizadeh, C. K. van der Ent, H. P. J. van der Doef, Manuela Seia, Renate Nickel, Heiko Witt
المصدر: Journal of Pediatric Gastroenterology & Nutrition. 50:347-349
مصطلحات موضوعية: Adult, Male, Meconium, congenital, hereditary, and neonatal diseases and abnormalities, Pathology, medicine.medical_specialty, Pancreatic disease, Adolescent, Cystic Fibrosis, Genotype, Ileus, Cystic Fibrosis Transmembrane Conductance Regulator, Meconium Ileus, Cystic fibrosis, Young Adult, Chloride Channels, medicine, Humans, Intestine obstruction, Child, biology, business.industry, Respiratory disease, Infant, Newborn, Gastroenterology, Genetic Variation, respiratory system, medicine.disease, digestive system diseases, Cystic fibrosis transmembrane conductance regulator, Europe, Pediatrics, Perinatology and Child Health, biology.protein, Female, business
-
7
المؤلفون: Hans-Dieter Walmrath, Heiko Witt, Paul Stevens, Claudia Sengler, Olfert Landt, Ulrich Pison, Renate Nickel, Andreas Günther, Ilka Frerking
المصدر: Critical Care Medicine. 33:2404-2406
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Pathology, ARDS, Adolescent, Genotype, Critical Care and Intensive Care Medicine, Gastroenterology, Internal medicine, Intensive care, Humans, Uteroglobin, Medicine, Allele frequency, Aged, Aged, 80 and over, Respiratory Distress Syndrome, Polymorphism, Genetic, medicine.diagnostic_test, Respiratory distress, business.industry, Respiratory disease, Infant, Newborn, Case-control study, Middle Aged, Prognosis, medicine.disease, Bronchoalveolar lavage, Case-Control Studies, Female, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2320ec9097c05e6f7cbd67941d3b42f
https://doi.org/10.1097/01.ccm.0000181526.24809.3e -
8
المؤلفون: Jonas Rosendahl, Matthias Blüher, Peter Kovacs, Robert Grützmann, Joost P.H. Drenth, Michael Stumvoll, Max Herms, Sebastian Weis, Peter Bugert, Moritz Jesinghaus, Volker Keim, Robert Schober, Henning Wittenburg, Claudia Ruffert, Joachim Mössner, Heiko Witt, Knut Krohn, Hans-Ulrich Schulz, Dorit Schleinitz
المصدر: PLoS One, 7, 5
PLoS ONE, Vol 7, Iss 5, p e37981 (2012)
PLoS One, 7
PLoS ONEمصطلحات موضوعية: Male, Pathology, Cirrhosis, HMOX1, lcsh:Medicine, Membrane transport and intracellular motility [NCMLS 5], Biochemistry, Gastroenterology, Pathogenesis, chemistry.chemical_compound, Liver Cirrhosis, Alcoholic, Molecular gastro-enterology and hepatology Membrane transport and intracellular motility [IGMD 2], Child, Promoter Regions, Genetic, lcsh:Science, Heme, Aged, 80 and over, Multidisciplinary, Middle Aged, Enzymes, Medicine, Acute pancreatitis, Female, Research Article, Adult, medicine.medical_specialty, Adolescent, Gastroenterology and Hepatology, Biology, Polymorphism, Single Nucleotide, Enzyme Regulation, Young Adult, Internal medicine, Genetics, medicine, Humans, Molecular gastro-enterology and hepatology [IGMD 2], Pancreas, Genetic Association Studies, Aged, Repetitive Sequences, Nucleic Acid, Inflammation, lcsh:R, Immunity, Human Genetics, Sequence Analysis, DNA, medicine.disease, Heme oxygenase, Pancreatitis, chemistry, Case-Control Studies, Genetics of Disease, Genetic Polymorphism, Hepatic stellate cell, Clinical Immunology, lcsh:Q, Heme Oxygenase-1, Population Genetics
وصف الملف: application/pdf
-
9
المؤلفون: Roland H. Pfützer, Hans Ulrich Schulz, Michael Stumvoll, Renate Nickel, Henning Wittenburg, Matthias Löhr, Niels Teich, Miklós Sahin-Tóth, Jonas Rosendahl, Richárd Szmola, Peter Kovacs, Volker Keim, Matthias Blüher, Joachim Mössner, Albrecht Hoffmeister, Heiko Witt, Thomas M. Gress, Johann Ockenga
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Proteases, Pathology, Endocrinology, Diabetes and Metabolism, Gastroenterology, Gene Frequency, Internal medicine, Pancreatitis, Chronic, medicine, MESOTRYPSINOGEN, Humans, In patient, Trypsin, PRSS3, Pancreatitis, chronic, Child, Gene, Aged, Aged, 80 and over, Original Paper, Hepatology, Base Sequence, business.industry, fungi, Infant, Newborn, food and beverages, Infant, Middle Aged, medicine.disease, Haplotypes, Child, Preschool, Mutation, Pancreatitis, MESOTRYPSIN, Female, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eb644c12e5731882e12676514b981ff
https://europepmc.org/articles/PMC2899151/ -
10
المؤلفون: Jan B.M.J. Jansen, Amit Kumar Dutta, Ashok Chacko, Santhosh Sundaresan, Heiko Witt, Rene H. M. te Morsche, Joost P.H. Drenth, Eesh Bhatia
المصدر: Pancreatology, 9, 145-9
Pancreatology, 9, 1-2, pp. 145-9مصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, Heterozygote, Endocrinology, Diabetes and Metabolism, Trypsin inhibitor, TROPICAL CALCIFIC PANCREATITIS, India, Membrane transport and intracellular motility [NCMLS 5], Pancreatitis, Chronic, Medicine, PRSS2, Humans, Genetic Predisposition to Disease, Trypsin, Molecular gastro-enterology and hepatology [IGMD 2], Hepatology, business.industry, Homozygote, Gastroenterology, Idiopathic pancreatitis, Calcinosis, Genetic Variation, Amino Acid Substitution, Genetic defects of metabolism [UMCN 5.1], Trypsin Inhibitor, Kazal Pancreatic, Trypsinogen, Female, business, Carrier Proteins