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1دورية أكاديمية
المؤلفون: Marques, Oriana, Rosa, Ana, Leite, Luciana, Faustino, Paula, Rêma, Alexandra, Martins da Silva, Berta, Porto, Graça, Lopes, Carlos
المصدر: Cancer Microenvironment: Official Journal of the International Cancer Microenvironment Society. December 2016 9(2-3):85-91
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المؤلفون: Pierre Brissot, Aline Morgan Alvarenga, Flávio Augusto Naoum, Rodolfo D. Cançado, Theo G M Oliveira, Paula Fernanda Silva Fonseca, Carla Luana Dinardo, Nathália Kozikas da Silva, Paulo Caleb Junior Lima Santos, Jacilene Barbosa da Silva Monteiro
المساهمون: Universidade Federal de São Paulo, Universidade de São Paulo (USP), Nutrition, Métabolismes et Cancer (NuMeCan), Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES), Fundação de Amparo à Pesquisa do Estado de São Paulo, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Universidade de São Paulo = University of São Paulo (USP), Université de Rennes (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)
المصدر: Blood Cells, Molecules and Diseases
Blood Cells, Molecules and Diseases, Elsevier, 2020, 84, pp.102444. ⟨10.1016/j.bcmd.2020.102444⟩
Blood Cells, Molecules and Diseases, 2020, 84, pp.102444. ⟨10.1016/j.bcmd.2020.102444⟩مصطلحات موضوعية: Adult, Male, Heterozygote, Bone Morphogenetic Protein 6, BMP6, medicine.disease_cause, 03 medical and health sciences, Exon, 0302 clinical medicine, Hepcidin, Genotype, medicine, Humans, Point Mutation, Iron overload, Sequencing, Molecular Biology, Gene, Hemochromatosis, 030304 developmental biology, Genetics, 0303 health sciences, Mutation, [SDV.GEN]Life Sciences [q-bio]/Genetics, biology, Homozygote, Cell Biology, Hematology, Middle Aged, Non-homozygous genotype for the HFE p.Cys282Tyr, medicine.disease, Phenotype, 3. Good health, Bone morphogenetic protein 6, 030220 oncology & carcinogenesis, biology.protein, Molecular Medicine, Female
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3Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype
المؤلفون: Sonia Distante, Ben Marris, Albert Altes, Alberto Piperno, Rodolfo D. Cançado, Paul C. Adams, Robert W. Evans, John Ryan, Graça Porto, Ioav Cabantchik, Emerência Teixeira, Annick Vanclooster, Dianne Prince, Desley White, Paulo Caleb Junior Lima Santos, Patricia J. Evans, Dorine W. Swinkels, Domenico Girelli, Mayka Sanchez, Gordon D. McLaren, Ketil Toska, Rolf Hultcrantz, Pierre Brissot, Brigitte Pineau, Elizabeta Nemeth, Peter Nielsen, Tomas Ganz, Nils Milman, Barbara Butzeck
المساهمون: Adams, P, Altes, A, Brissot, P, Butzeck, B, Cabantchik, I, Cançado, R, Distante, S, Evans, P, Evans, R, Ganz, T, Girelli, D, Hultcrantz, R, Mclaren, G, Marris, B, Milman, N, Nemeth, E, Nielsen, P, Pineau, B, Piperno, A, Porto, G, Prince, D, Ryan, J, Sanchez, M, Santos, P, Swinkels, D, Teixeira, E, Toska, K, Vanclooster, A, White, D
المصدر: Hepatology International
مصطلحات موضوعية: Male, Pediatrics, medicine.medical_specialty, Homozygous genotype, Guidelines, p.Cys282Tyr, Hereditary Hemochromatosis, guidelines, treatment, 03 medical and health sciences, 0302 clinical medicine, Phlebotomy, medicine, Humans, Hemochromatosis Protein, Hemochromatosis, Final version, Hepatology, business.industry, Homozygote, hereditary hemochromatosis, medicine.disease, Chelation Therapy, Diet, 030220 oncology & carcinogenesis, Hereditary hemochromatosis, Medical training, 030211 gastroenterology & hepatology, Female, hereditary hemochromatosis, HFE, p.Cys282Tyr, HFE, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a728a5d65c1e59cf0a3989bf3759033a
https://ora.ox.ac.uk/objects/uuid:dd16cf4c-126c-4bfb-9f6a-fb79ca535d8d -
4دورية أكاديمية
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المؤلفون: Pelucchi, S, Galimberti, S, Greni, F, Rametta, R, Mariani, R, Pelloni, I, Girelli, D, Busti, F, Ravasi, G, Valsecchi, M, Valenti, L, Piperno, A
المساهمون: Pelucchi, S, Galimberti, S, Greni, F, Rametta, R, Mariani, R, Pelloni, I, Girelli, D, Busti, F, Ravasi, G, Valsecchi, M, Valenti, L, Piperno, A
المصدر: Journal of gastroenterology and hepatology. 31(7)
مصطلحات موضوعية: Genetic Markers, Liver Cirrhosis, Male, Carcinoma, Hepatocellular, Genotype, Homozygote, Liver Neoplasms, PCSK7, single nucleotide polymorphism, iron, Ishak score, p.Cys282Tyr, Middle Aged, p.Cys282Tyr, Cohort Studies, iron, Ishak score, Italy, single nucleotide polymorphism, Risk Factors, PCSK7, Humans, Hemochromatosis, Subtilisins, Hemochromatosis Protein, Alleles
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المؤلفون: Graça Porto, Carlos Lopes, Berta Martins da Silva, Luciana Leite, Alexandra Rêma, Oriana Marques, Paula Faustino, Ana Margarida Rosa
مصطلحات موضوعية: 0301 basic medicine, Hepcidina, Cancer Research, Cell type, Iron, Short Communication, Transferrin receptor, Compound heterozygosity, p.Cys282Tyr, Cancro, Loss of heterozygosity, 03 medical and health sciences, Breast cancer, Hepcidin, Breast Cancer, Genotype, Medicine, Modificadores Genéticos, biology, business.industry, medicine.disease, Doenças Genéticas, Ferritin, High Iron FE, 030104 developmental biology, Oncology, Immunology, biology.protein, HFE, Metabolismo do Ferro, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd3765347a2ae11ee88400abf5860ca2
https://europepmc.org/articles/PMC5264664/ -
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المؤلفون: Sara Bernabini, Caterina Aurizi, Francesca Clementina Radio, Diana Giannarelli, Fiammetta Sorge, G. Biolcati, Carmelilia De Bernardo, Irene Giotti, Silvia Majore, Francesca Torricelli, Paola Grammatico
المصدر: Blood cells, moleculesdiseases. 55(1)
مصطلحات موضوعية: Male, TMPRSS6, Genotype, Iron, Bone Morphogenetic Protein 2, BMP2, FTL, HAMP, Hereditary hemochromatosis, Iron overload, P.Cys282Tyr, Penetrance defect, SLC40A1, TFR2, Molecular Biology, Molecular Medicine, Hematology, Cell Biology, Penetrance, Biology, Polymorphism, Single Nucleotide, Gene Frequency, Hepcidins, Receptors, Transferrin, Missense mutation, Humans, Allele, Hemochromatosis Protein, Allele frequency, Gene, Cation Transport Proteins, Alleles, Genetics, Histocompatibility Antigens Class I, Serine Endopeptidases, Transferrin, Membrane Proteins, Phenotype, Apoferritins, Ferritins, Female, Gene-Environment Interaction, Hemochromatosis
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المؤلفون: Bardou-Jacquet, Edouard, Philip, Julie, Lorho, Richard, Ropert, Martine, Latournerie, Marianne, Houssel-Debry, Pauline, Guyader, Dominique, Loreal, Olivier, Boudjema, Karim, Brissot, Pierre
المساهمون: Foie, métabolismes et cancer, Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Service des maladies du foie, Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Hôpital Pontchaillou-Centre Hospitalier Universitaire [Rennes], Service de Chirurgie Hépatobiliaire et Digestive [Rennes] = Hepatobiliary and Digestive Surgery [Rennes], CHU Pontchaillou [Rennes], Centre de référence des surcharges en fer rares d'origine génétique, Laboratoire de biochimie générale, Hôpital Pontchaillou-CHU Pontchaillou [Rennes], Microenvironnement et remodelage, Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )-Service des maladies du foie, Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Hôpital Pontchaillou-Centre Hospitalier Universitaire [Rennes]-Hôpital Pontchaillou-Centre Hospitalier Universitaire [Rennes], Supported by the Association Fer et Foie and The French National reference center for rare iron overload diseases of genetic origin., Université de Rennes (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Service des maladies du foie [CHU Rennes], Centre Hospitalier Universitaire [Rennes], Université de Rennes (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )-Université de Rennes (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )-Service des maladies du foie [CHU Rennes], Centre Hospitalier Universitaire [Rennes]-Centre Hospitalier Universitaire [Rennes], Le Corre, Morgane
المصدر: Hepatology
Hepatology, Wiley-Blackwell, 2014, 59 (3), pp.839-847. ⟨10.1002/hep.26570⟩
Hepatology, 2014, 59 (3), pp.839-847. ⟨10.1002/hep.26570⟩مصطلحات موضوعية: Hepicidin, [SDV.MHEP.HEG]Life Sciences [q-bio]/Human health and pathology/Hépatology and Gastroenterology, Hemochromatosis, HFE, iron overload, p.Cys282Tyr, [SDV.MHEP.HEG] Life Sciences [q-bio]/Human health and pathology/Hépatology and Gastroenterology, Liver Transplantation
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9دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.
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