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المؤلفون: Heiko, Witt, Miklos Sahin Toth, Olfert, Landt, Jian Min Chen, Thilo, Kahne, Drenth, Joost P. H., Zoltan, Kukor, Edit, Szepessy, Walter, Halangk, Stefan, Dahm, Klaus, Rohde, Hans Ulrich Schulz, Cedric Le Marechal, Nejat, Akar, Ammann, Rudolf W., Kaspar, Truninger, Mario, Bargetzi, Eesh, Bhatia, Carlo, Castellani, Giulia Martina Cavestro, Milos, Cerny, DESTRO-BISOL, Giovanni, Spedini, Gabriella, Hans, Eiberg, Jansen, Jan B. M. J., Monika, Koudova, Eva, Rausova, Milan, Macek, Macek Jr, M., Nuria, Malats, Real, Francisco X., Hans Jurgen Menzel, Pedro, Moral, Roberta, Galavotti, Pier Franco Pignatti, Olga, Rickards, Julius, Spicak, Narcis Octavian Zarnescu, Wolfgang, Bock, Gress, Thomas M., Helmut, Friess, Johann, Ockenga, Hartmut, Schmidt, Roland, Pfutzer, Matthias, Lohr, Peter, Simon, Frank Ulrich Weiss, Lerch, Markus M., Niels, Teich, Volker, Keim, Thomas, Berg, Bertram, Wiedenmann, Werner, Luck, David Alexander Groneberg, Michael, Becker, Thomas, Keil, Andreas, Kage, Jana, Bernardova, Markus, Braun, Claudia, Guldner, Juliane, Halangk, Jonas, Rosendahl, Ulrike, Witt, Matthias, Treiber, Renate, Nickel, Claude, Ferec
المساهمون: Witt, H, SAHIN TOTH, M, Landt, O, Chen, Jm, Kahne, T, Drenth, Jp, Kukor, Z, Szepessy, E, Halangk, W, Dahm, S, Rohde, K, Schulz, Hu, LE MARECHAL, C, Akar, N, Ammann, Rw, Truninger, K, Bargetzi, M, Bhatia, E, Castellani, C, Cavestro, GIULIA MARTINA, Cerny, M, DESTRO BISOL, G, Spedini, G, Eiberg, H, Jansen, Jb, Koudova, M, Rausova, E, MACEK M., Jr, Malats, N, Real, Fx, Menzel, Hj, Moral, P, Galavotti, R, Pignatti, Pf, Rickards, O, Spicak, J, Zarnescu, No, Bock, W, Gress, Tm, Friess, H, Ockenga, J, Schmidt, H, Pfutzer, R, Lohr, M, Simon, P, Weiss, Fu, Lerch, Mm, Teich, N, Keim, V, Berg, T, Wiedenmann, B, Luck, W, Groneberg, Da, Becker, M, Keil, T, Kage, A, Bernardova, J, Braun, M, Guldner, C, Halangk, J, Rosendahl, J, Witt, U, Treiber, M, Nickel, R, Ferec, C.
المصدر: Nature Genetics, 38, 6, pp. 668-73
Recercat. Dipósit de la Recerca de Catalunya
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Nature Genetics, 38, 668-73
Karolinska Institutetمصطلحات موضوعية: trypsin inhibitor, Models, Molecular, Enteropeptidase, Pancreatic disease, Membrane transport and intracellular motility [NCMLS 5], arginine, genetic risk, chemistry.chemical_compound, Models, proteinosis, Trypsin, Pancreatic Secretory Trypsin Inhibitor, PRSS1 gene, enteropeptidase, medicine.diagnostic_test, adult, Hydrolysis, cationic trypsinogen, protection, unclassified drug, enzyme activity, female, priority journal, risk factor, CHRONIC PANCREATITIS, protein degradation, Trypsinogen, medicine.drug, medicine.medical_specialty, anionic trypsinogen, Proteolysis, Biology, Article, male, Internal medicine, Genetics, medicine, Matrix-Assisted Laser Desorption-Ionization, Humans, PRSS2, controlled study, human, Molecular gastro-enterology and hepatology [IGMD 2], gene, DNA Primers, Genetic polymorphism, catalysis, Base Sequence, Spectrometry, disease predisposition, Molecular, cationic trypsinogen prss1, glycine, pancreatic secretory trypsin inhibitor spink1, trypsin, trypsinogen, article, chronic pancreatitis, codon, genetic susceptibility, major clinical study, nucleotide sequence, Chronic Disease, Haplotypes, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Mass, medicine.disease, Tripsinogen, Tripsina, Settore BIO/18 - Genetica, Endocrinology, Genetic defects of metabolism [UMCN 5.1], Pancreatitis, chemistry, Genètica
وصف الملف: application/pdf
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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
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المؤلفون: Michael Becker, Heiko Witt
المصدر: Journal of Pediatric Gastroenterology and Nutrition. 34:125-136
مصطلحات موضوعية: Pancreatic disease, Trypsinogen, Cystic Fibrosis Transmembrane Conductance Regulator, chemistry.chemical_compound, Prevalence, Humans, Medicine, Trypsin, Child, Chromosomes, Human, Pair 14, Genetics, Chromosomes, Human, Pair 12, business.industry, Gastroenterology, medicine.disease, α1 antitrypsin, Pancreatitis, chemistry, Trypsin Inhibitor, Kazal Pancreatic, alpha 1-Antitrypsin, Chronic Disease, Mutation, Pediatrics, Perinatology and Child Health, Chromosomes, Human, Pair 5, business, Chromosomes, Human, Pair 7
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المؤلفون: Heiko Witt
المصدر: Pancreatology. 1:432-438
مصطلحات موضوعية: Serine Proteinase Inhibitors, Endocrinology, Diabetes and Metabolism, Cystic Fibrosis Transmembrane Conductance Regulator, Gene mutation, medicine.disease_cause, Humans, Medicine, Trypsin, Family history, Child, Gene, Genetic testing, Genetics, Mutation, Hepatology, medicine.diagnostic_test, business.industry, Gastroenterology, Single-strand conformation polymorphism, medicine.disease, Pancreatitis, alpha 1-Antitrypsin, Chronic Disease, Trypsinogen, Restriction fragment length polymorphism, business
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المؤلفون: A. Kage, U Lass, Olfert Landt, W Luck, M Classen, Hans Christian Hennies, Heiko Witt, Michael Becker
المصدر: Nature Genetics. 25:213-216
مصطلحات موضوعية: Male, Adolescent, Genotype, Trypsinogen, Trypsin inhibitor, DNA Mutational Analysis, Mutation, Missense, Biology, medicine.disease_cause, Models, Biological, Linkage Disequilibrium, chemistry.chemical_compound, Genetics, medicine, Humans, PRSS2, Missense mutation, Child, Pancreatic Secretory Trypsin Inhibitor, Hereditary pancreatitis, Mutation, Polymorphism, Genetic, Exons, medicine.disease, Molecular biology, Introns, Haplotypes, Pancreatitis, chemistry, Trypsin Inhibitor, Kazal Pancreatic, Chronic Disease, Chromosomes, Human, Pair 5, Female, Lod Score
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المؤلفون: Michael Becker, Heiko Witt, W Luck
المصدر: Gastroenterology. 117:7-10
مصطلحات موضوعية: Male, Pancreatic disease, Adolescent, Trypsinogen, Molecular Sequence Data, Protein Sorting Signals, Biology, Polymerase Chain Reaction, Loss of heterozygosity, chemistry.chemical_compound, Cations, medicine, Humans, PRSS2, Amino Acid Sequence, Child, Polymorphism, Single-Stranded Conformational, Genetics, Hereditary pancreatitis, Hepatology, Gastroenterology, Infant, Single-strand conformation polymorphism, medicine.disease, Trypsin, Molecular biology, Pancreatitis, chemistry, Child, Preschool, Chronic Disease, Mutation, Female, medicine.drug
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المؤلفون: Thomas von Hahn, Ulrich Beuers, Bertram Wiedenmann, Renate Nickel, Peter Neuhaus, Thomas Berg, Tobias Müller, J. Halangk, Gero Puhl, Konrad Neumann, Heiko Witt
المساهمون: Amsterdam Gastroenterology Endocrinology Metabolism, Gastroenterology and Hepatology
المصدر: Scandinavian journal of gastroenterology, 43(5), 584-592. Informa Healthcare
مصطلحات موضوعية: Adult, Male, Alcoholic liver disease, Receptor complex, Lipopolysaccharide, Adolescent, Genotype, CD14, Lipopolysaccharide Receptors, Chronic liver disease, Proinflammatory cytokine, chemistry.chemical_compound, medicine, Humans, Genetic Predisposition to Disease, Receptors, Immunologic, Receptor, Child, Liver Diseases, Alcoholic, Aged, business.industry, Liver Diseases, Gastroenterology, Genetic Variation, Hepatitis C, Chronic, Middle Aged, medicine.disease, Molecular biology, Toll-Like Receptor 4, chemistry, Immunology, Chronic Disease, TLR4, Female, business
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المؤلفون: Narcis O. Zarnescu, Renate Nickel, Joost P.H. Drenth, Milos Cerny, Carlo Castellani, J. Halangk, Francisco X. Real, Gourdas Choudhuri, Andreas Kage, Hartmut Schmidt, Thomas M. Gress, Kaspar Truninger, Maria Grazia Romanelli, Hans-Ulrich Schulz, Andrew N. Kingsnorth, Monika Koudova, Matthias Treiber, Matthias Pietschmann, Olga Rickards, Niels Teich, Hans-Jürgen Menzel, Julius Spicak, Jonas Rosendahl, Derek A. O'Reilly, Nejat Akar, Gian Franco De Stefano, Rudolf W. Ammann, Johann Ockenga, Heiko Witt, David A. Groneberg, Pier Franco Pignatti, Andrew G. Demaine, Olfert Landt, Sadiq S. Sikora, Cinzia Battagia, Eesh Bhatia, Mario Bargetzi, Pedro Moral, Frank Ulrich Weiss, Jan B.M.J. Jansen
المصدر: Treiber, Matthias; Schulz, Hans-Ulrich; Landt, Olfert; Drenth, Joost P H; Castellani, Carlo; Real, Francisco X; Akar, Nejat; Ammann, Rudolf W; Bargetzi, Mario; Bhatia, Eesh; Demaine, Andrew Glenn; Battagia, Cinzia; Kingsnorth, Andrew; O'Reilly, Derek; Truninger, Kaspar; Koudova, Monika; Spicak, Julius; Cerny, Milos; Menzel, Hans-Jürgen; Moral, Pedro; ... (2006). Keratin 8 sequence variants in patients with pancreatitis and pancreatic cancer. Journal of molecular medicine JMM, 84(12), pp. 1015-22. Berlin: Springer 10.1007/s00109-006-0096-7 <http://dx.doi.org/10.1007/s00109-006-0096-7>
Journal of Molecular Medicine-Jmm, 84, 12, pp. 1015-22
Journal of Molecular Medicine-Jmm, 84, 1015-22مصطلحات موضوعية: Male, Pathology, Pancreatic disease, Pancreatitis, Alcoholic, Membrane transport and intracellular motility [NCMLS 5], Gastroenterology, Cohort Studies, Gene Frequency, Drug Discovery, keratin 8, acute pancreatitis, chronic pancreatitis, pancreatic carcinoma, Genetics (clinical), Geography, Middle Aged, Acute Disease, Molecular Medicine, Adenocarcinoma, Acute pancreatitis, Female, Carcinoma, Pancreatic Ductal, Adult, medicine.medical_specialty, Heterozygote, acute pancreatitis, Black People, White People, chronic pancreatitis, Asian People, Internal medicine, Pancreatic cancer, medicine, Carcinoma, Humans, keratin 8, Molecular gastro-enterology and hepatology [IGMD 2], Exocrine pancreatic insufficiency, Alleles, Aged, Retrospective Studies, Polymorphism, Genetic, pancreatic carcinoma, business.industry, Keratin-8, Case-control study, Genetic Variation, medicine.disease, Pancreatic Neoplasms, Pancreatitis, Genetic defects of metabolism [UMCN 5.1], Case-Control Studies, Chronic Disease, business
وصف الملف: application/pdf
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المؤلفون: Renate Nickel, T Berg, Olfert Landt, Peter Neuhaus, Bertram Wiedenmann, Gero Puhl, Heiko Witt, J. Halangk, Tobias Mueller, Andreas Kage, W Luck
المصدر: Scopus-Elsevier
مصطلحات موضوعية: Genetically modified mouse, Adult, Liver Cirrhosis, Guanine, Adolescent, Hepatitis, Viral, Human, Mutation, Missense, Biology, Electronic Letter, Keratin 18, Liver disease, Cytosine, Keratin, Genetics, medicine, Humans, Histidine, Intermediate filament, Child, Genetics (clinical), Aged, chemistry.chemical_classification, Liver injury, Aged, 80 and over, Keratin-8, Liver Diseases, Wild type, Middle Aged, medicine.disease, Molecular biology, Hepatitis, Autoimmune, chemistry, Immunology, Chronic Disease, Keratin 8, Keratins, Tyrosine
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المؤلفون: Helen Beranek, Hans-Ulrich Schulz, Volker Keim, Niels Teich, Joachim Mössner, Heiko Witt
المصدر: European journal of gastroenterologyhepatology. 15(11)
مصطلحات موضوعية: Genetic Markers, Pathology, medicine.medical_specialty, Pancreatic disease, Pancreatitis, Alcoholic, Trypsinogen, Gene mutation, digestive system, Gastroenterology, chemistry.chemical_compound, Gene Frequency, Internal medicine, medicine, Humans, Promoter Regions, Genetic, Hereditary pancreatitis, Polymorphism, Genetic, Hepatology, business.industry, Tumor Necrosis Factor-alpha, Case-control study, medicine.disease, Penetrance, digestive system diseases, Interleukin-10, Interleukin 10, chemistry, Pancreatitis, Case-Control Studies, Chronic Disease, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16e35848a5545c2c27ebbec88f389b24
https://pubmed.ncbi.nlm.nih.gov/14560157