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1رسالة جامعية
المؤلفون: Elgadi, Abdelaziz
مصطلحات موضوعية: Thyroid hormones -- genetics, Thyroid hormones -- physiology, Hyperthyroidism -- genetics, Thyrotropin -- genetics, Neuromuscular diseases -- genetics, Mutation, Adipocytes -- metabolism
Degree: Diss. (sammanfattning) Stockholm : Karolinska institutet, 2008
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المؤلفون: Yolande F. M. Ramos, Tom Fiers, Jari Lahti, Tarunveer S. Ahluwalia, Elisa Kasbohm, Silvia Naitza, Hou-Feng Zheng, Charlotte Cerqueira, Ingrid Meulenbelt, Betina H. Thuesen, Ernst Rietzschel, Anne R. Cappola, John P. Walsh, Alessandro De Grandi, Johan G. Eriksson, Suzanne J. Brown, Jiaojiao Jing, Deborah Mascalzoni, Nicole Soranzo, Daniel Taliun, Margreet Kloppenburg, Purdey J Campbell, Kai-Uwe Eckardt, Yong Li, Mauro Pala, Marco Medici, Florian Kronenberg, Caterina Barbieri, Francesco Cucca, Allan Linneberg, Anna Köttgen, Bruce M. Psaty, Eric Boerwinkle, Ian J. Deary, Jennie Hui, Joris Deelen, Matthijs Moed, Astrid Petersmann, Graziano Ceresini, Michela Marina, Iris Postmus, Alice M. Arnold, Michiaki Kubo, J. Brent Richards, Marc De Buyzere, Henriette E. Meyer zu Schwabedissen, Eleonora Porcu, Christian Fuchsberger, Celia Di Munno, Dan E. Arking, David J. Stott, Toshiko Tanaka, Sofie Bekaert, Andrew A. Hicks, W. Edward Visser, Wouter den Hollander, Martin Gögele, Cinzia Sala, Peter P. Pramstaller, Georg Homuth, Yukinori Okada, Arne Astrup, Arif B. Ekici, Ulla T. Schultheiss, Richard A. Jensen, Christa Meisinger, Romana T. Netea-Maier, Rafael T. Mikolajczyk, Theo J. Visser, Marian Beekman, Michela Traglia, David C. Liewald, Koichi Matsuda, Thorkild I. A. Sørensen, Ilja M. Nolte, André G. Uitterlinden, David Schlessinger, Luigi Ferrrucci, Shuo Li, Alexander Teumer, Daniel Tiller, Sarah E. Harris, J. Wouter Jukema, Rajesh Rawal, Tim De Meyer, Kadri Haljas, Greet Roef, Yoichiro Kamatani, Karin Halina Greiser, Jean-Marc Kaufman, Serena Sanna, Bruce H. R. Wolffenbuttel, Scott Wilson, Daniela Toniolo, Ee Mun Lim, Stefan Groeneweg, Caroline S. Fox, Torben Hansen, Masato Akiyama, Christian Gieger, Layal Chaker, Tim D. Spector, Ian Ford, Martin den Heijer, P. Eline Slagboom, Elizabeth Selvin, Lambertus A. Kiemeney, Emil V. R. Appel, Niels Grarup, Diana van Heemst, Youri Taes, Robin P. Peeters, Henry Völzke, Cristian Pattaro, Daniel Medenwald, John M. Starr, Qiong Yang, Jerome I. Rotter, M. Arfan Ikram, Edoardo Fiorillo, Till Ittermann, Oluf Pedersen, Eero Kajantie, John Beilby, Tessel E. Galesloot, Fernando Rivadeneira, Paul Redmond, Bruno Lapauw
المساهمون: Lifelines Cohort Study, Alizadeh, B.Z., Boezen, H.M., Franke, L., van der Harst, P., Navis, G., Rots, M., Snieder, H., Swertz, M.A., Wijmenga, C., Life Course Epidemiology (LCE), Lifestyle Medicine (LM), Center for Liver, Digestive and Metabolic Diseases (CLDM), Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, Clinicum, University of Helsinki, Department of Psychology and Logopedics, Doctoral Programme in Cognition, Learning, Instruction and Communication, Medicum, Lastentautien yksikkö, Children's Hospital, HUS Children and Adolescents, Developmental Psychology Research Group, Internal medicine, AGEM - Endocrinology, metabolism and nutrition, Amsterdam Movement Sciences - Rehabilitation & Development, Amsterdam Movement Sciences - Restoration and Development, APH - Aging & Later Life, Epidemiology, Internal Medicine, Teumer, Alexander [0000-0002-8309-094X], Ahluwalia, Tarunveer S [0000-0002-7464-3354], Appel, Emil Vincent R [0000-0001-7704-6611], Astrup, Arne [0000-0001-8968-8996], Beekman, Marian [0000-0003-0585-6206], Beilby, John P [0000-0002-4915-2254], Ekici, Arif B [0000-0001-6099-7066], Grarup, Niels [0000-0001-5526-1070], Hansen, Torben [0000-0001-8748-3831], Hicks, Andrew A [0000-0001-6320-0411], Ikram, M Arfan [0000-0003-0372-8585], Jukema, J Wouter [0000-0002-3246-8359], Kamatani, Yoichiro [0000-0001-8748-5597], Kronenberg, Florian [0000-0003-2229-1120], Lahti, Jari [0000-0002-4310-5297], Li, Shuo [0000-0003-2331-2448], Liewald, David CM [0000-0002-0544-7368], Linneberg, Allan [0000-0002-0994-0184], Mascalzoni, Deborah [0000-0003-4156-1464], Meulenbelt, Ingrid [0000-0001-7786-7081], Netea-Maier, Romana T [0000-0002-9603-0460], Nolte, Ilja M [0000-0001-5047-4077], Okada, Yukinori [0000-0002-0311-8472], Ramos, Yolande FM [0000-0003-1459-413X], Richards, J Brent [0000-0002-3746-9086], Soranzo, Nicole [0000-0003-1095-3852], Yang, Qiong [0000-0002-3658-1375], Köttgen, Anna [0000-0002-4671-3714], Apollo - University of Cambridge Repository
المصدر: Nature communications, vol. 9, no. 1, pp. 4455
Nature Communications, 9(1):4455. Nature Publishing Group
Nature Communications, 9
Nature Communications, Vol 9, Iss 1, Pp 1-14 (2018)
Nature Communications
Teumer, A, Chaker, L, Groeneweg, S, Li, Y, Di Munno, C, Barbieri, C, Ahluwalia, T S, Astrup, A, Linneberg, A, Pedersen, O B, Sørensen, T I A & ThyroidOmics Consortium 2018, ' Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation ', Nature Communications, vol. 9, 4455 . https://doi.org/10.1038/s41467-018-06356-1
Nat. Commun. 9:4455 (2018)
Lifelines Cohort Study 2018, ' Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation ', Nature Communications, vol. 9, no. 1, 4455 . https://doi.org/10.1038/s41467-018-06356-1
Nat Commun
Nature Communications, 9:4455. Nature Publishing Group
Teumer, A, Chaker, L, Groeneweg, S, Li, Y, Di Munno, C, Barbieri, C, Schultheiss, U T, Traglia, M, Ahluwalia, T S, Akiyama, M, Appel, E V R, Arking, D E, Arnold, A, Astrup, A, Beekman, M, Beilby, J P, Bekaert, S, Boerwinkle, E, Brown, S J, De Buyzere, M, Campbell, P J, Ceresini, G, Cerqueira, C, Cucca, F, Deary, I J, Deelen, J, Eckardt, K-U, Ekici, A B, Eriksson, J G, Ferrrucci, L, Fiers, T, Fiorillo, E, Ford, I, Fox, C S, Fuchsberger, C, Galesloot, T E, Gieger, C, Gögele, M, De Grandi, A, Grarup, N, Greiser, K H, Haljas, K, Hansen, T, Harris, S E, van Heemst, D, den Heijer, M, Hicks, A A, Liewald, D C M, Redmond, P, Starr, J M, Stott, D J, Taes, Y E, Taliun, D, Toshiko, T, Thuesen, B, Tiller, D, Toniolo, D, Uitterlinden, A G, Visser, W E, Walsh, J P, Wilson, S G, Wolffenbuttel, B H R, Yang, Q, Zheng, H-F, Cappola, A R, Peeters, R P, Naitza, S, Völzke, H, Sanna, S, Köttgen, A, Visser, T J & Medici, M 2018, ' Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation ', Nature Communications, vol. 9, no. 1, pp. 1-14 . https://doi.org/10.1038/s41467-018-06356-1
NATURE COMMUNICATIONSمصطلحات موضوعية: 0301 basic medicine, Genetic variants, endocrine system diseases, Vascular damage Radboud Institute for Health Sciences [Radboudumc 16], Thyroid Gland, Thyrotropin, Metabolyzing hormone (AADAT), General Physics and Astronomy, EFFICIENT, Genome-wide association study, Thyroid hormone transporter (SLC17A4), Disease, VARIANTS, Bioinformatics, Hyperthyroidism, DISEASE, 0302 clinical medicine, SUBCLINICAL HYPOTHYROIDISM, Risk Factors, Genome-wide analysis, Chlorocebus aethiops, Faculty of Science, Medicine, lcsh:Science, POPULATION, RISK, education.field_of_study, Multidisciplinary, HERITABILITY, Thyroid disease, Thyroid, Thyroid dysfunction, ASSOCIATION, 3. Good health, medicine.anatomical_structure, Urological cancers Radboud Institute for Health Sciences [Radboudumc 15], COS Cells, Thyroid function, Sodium-Phosphate Cotransporter Proteins, Type I, Thyroid Hormones, endocrine system, PARTICIPANT DATA-ANALYSIS, Science, Population, 030209 endocrinology & metabolism, Rare cancers Radboud Institute for Molecular Life Sciences [Radboudumc 9], Polymorphism, Single Nucleotide, White People, Article, General Biochemistry, Genetics and Molecular Biology, MONOCARBOXYLATE TRANSPORTER-8, 03 medical and health sciences, All institutes and research themes of the Radboud University Medical Center, Hypothyroidism, Animals, Humans, ddc:610, education, METAANALYSIS, Genetic association, 2-Aminoadipate Transaminase, IDENTIFICATION, business.industry, Biology and Life Sciences, Biological Transport, General Chemistry, REFERENCE RANGE, medicine.disease, R1, 2-Aminoadipate Transaminase/genetics, 2-Aminoadipate Transaminase/metabolism, Cercopithecus aethiops, European Continental Ancestry Group, Gene Expression Regulation/genetics, Genome-Wide Association Study, Hyperthyroidism/genetics, Hyperthyroidism/physiopathology, Hypothyroidism/genetics, Hypothyroidism/physiopathology, Sodium-Phosphate Cotransporter Proteins, Type I/genetics, Sodium-Phosphate Cotransporter Proteins, Type I/metabolism, Thyroid Gland/metabolism, Thyroid Gland/physiopathology, Thyroid Hormones/genetics, Thyroid Hormones/metabolism, Thyrotropin/metabolism, 030104 developmental biology, Gene Expression Regulation, ATRIAL-FIBRILLATION, lcsh:Q, 3111 Biomedicine, business, Thyroid hormone regulation, Hormone
وصف الملف: application/pdf
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المؤلفون: Kaare Christensen, Mads Lillevang-Johansen, Laszlo Hegedüs, Thomas Heiberg Brix, Inge Petersen
المصدر: Lillevang-Johansen, M, Petersen, I, Christensen, K, Hegedüs, L & Brix, T H 2014, ' Is previous hyperthyroidism associated with long-term cognitive dysfunction? A twin study ', Clinical Endocrinology, vol. 80, no. 2, pp. 290-295 . https://doi.org/10.1111/cen.12255
مصطلحات موضوعية: Male, Pediatrics, medicine.medical_specialty, Time Factors, endocrine system diseases, Endocrinology, Diabetes and Metabolism, Denmark, Hyperthyroidism/genetics, Twins, Monozygotic/genetics, Neuropsychological Tests, Affect (psychology), Hyperthyroidism, Twins, Dizygotic/genetics, Cognition, Endocrinology, Internal medicine, Twins, Dizygotic, medicine, Humans, Cognitive skill, Registries, Cognition/physiology, Aged, Aged, 80 and over, Discordant Twin, business.industry, Confounding, Case-control study, Registries/statistics & numerical data, Twins, Monozygotic, Middle Aged, Health Surveys, Twin study, Cognitive test, Health Surveys/statistics & numerical data, Case-Control Studies, Female, Cognition Disorders, business, Cognition Disorders/genetics, Record linkage
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::958a3d01baf573838c88051a4242721a
https://portal.findresearcher.sdu.dk/da/publications/b7356142-11a8-4491-98cd-67fe87d4d972 -
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المؤلفون: Marc Klein, Carine Maenhaut, Martine Patey, Aline Hebrant, J Leclère, Jacques Emile Dumont, Wilma C G van Staveren, Jacqueline Van Sande, Frédérique Savagner, Pierre P. Roger, Claire Bournaud
المساهمون: I.R.I.B.H.M., Université libre de Bruxelles (ULB), Laboratoire d’anatomie et cytologie pathologique, Hôpital Robert Debré, CHU de Reims, Centre Hospitalier Universitaire de Nancy (CHU Nancy), Equipe 4, Centre de Recherche en Cancérologie de Lyon (UNICANCER/CRCL), Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM), Stress Oxydant et Pathologies Métaboliques (SOPAM), Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM), Archéologie Industrielle, Histoire, Patrimoine - Géographie, Développement, Environnement de la Caraïbe (AIHP-GEODE), Université des Antilles (UA), Adaptation, Climat Tropical, Exercice et Santé (ACTES), Walloon Excellence in Life sciences and BIOtechnology [Liège] (WELBIO)
المصدر: Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2009, 94 (7), pp.2602-2609. ⟨10.1210/jc.2008-2191⟩
The Journal of clinical endocrinology and metabolism, 94 (7مصطلحات موضوعية: Male, Endocrinology, Diabetes and Metabolism, [SDV]Life Sciences [q-bio], Clinical Biochemistry, Thyroid Gland, Gene Expression, medicine.disease_cause, Hyperthyroidism, Biochemistry, Adenoma -- metabolism, 0302 clinical medicine, Endocrinology, Cell-matrix adhesion, Child, Oligonucleotide Array Sequence Analysis, 0303 health sciences, Mutation, Thyroid, Sciences bio-médicales et agricoles, Middle Aged, Phenotype, Hyperthyroidism -- genetics, Gene Expression Regulation, Neoplastic, medicine.anatomical_structure, Female, Thyroid Neoplasms -- metabolism, Endocrine gland, Adenoma, Adult, medicine.medical_specialty, Adolescent, Thyroid Neoplasms -- complications, Molecular Sequence Data, 030209 endocrinology & metabolism, Context (language use), Biology, Models, Biological, Thyrotropin receptor, 03 medical and health sciences, Internal medicine, medicine, Adenoma -- complications, Adenoma -- genetics, Humans, Thyroid Neoplasms, Amino Acid Sequence, Thyroid Neoplasms -- genetics, 030304 developmental biology, Gene Expression Profiling, Biochemistry (medical), medicine.disease, Hyperthyroidism -- metabolism, Hyperthyroidism -- etiology, Thyroid Gland -- metabolism
وصف الملف: 2 full-text file(s): application/pdf; application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86da8263be1f903da2dde799b025a2fd
https://hal.univ-angers.fr/hal-03275655 -
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المؤلفون: Fulya Akin, Buenyamin Kaptanoglu, Sebahat Turgut, Mehmet Bastemir, Guenfer Turgut, Raziye Kursunluoglu
مصطلحات موضوعية: endocrine system diseases, genotype, polymerase chain reaction, thyroid peroxidase, Hyperthyroidism, glycoprotein P, Thyroiditis, ethnic group, thyrotropin, Exon, P-glycoprotein polymorphism, polycyclic compounds, MDR1, C3435T, multidrug resistance protein 1, restriction fragment length polymorphism, P-glycoprotein, Hashimoto disease, biology, integumentary system, Thyroid, article, Exons, General Medicine, Graves Disease, drug distribution, medicine.anatomical_structure, ATP Binding Cassette Transporter, Subfamily B, Member 1/*genetics/metabolism, Alleles, Genetic Predisposition to Disease, Genotype, Graves Disease/genetics/metabolism, Hashimoto Disease/genetics/metabolism, Humans, Hyperthyroidism/*genetics/metabolism, Hypothyroidism/*genetics/metabolism, Polymorphism, Genetic, Graves disease, blood sampling, medicine.medical_specialty, endocrine system, protein polymorphism, hormone blood level, Hashimoto Disease, gene frequency, Hypothyroidism, Internal medicine, Genetics, medicine, Distribution (pharmacology), controlled study, ATP Binding Cassette Transporter, Subfamily B, Member 1, human, free thyroxine index, Allele, protein expression, Molecular Biology, business.industry, medicine.disease, thyroid hormone, DNA isolation, major clinical study, free liothyronine index, Genotype frequency, Endocrinology, thyroglobulin antibody, biology.protein, liothyronine, business, Hormone
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::919b0e5e8d5f9e506b9d53270d3b57d1
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6دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
7مورد إلكتروني
المصدر: The Journal of clinical endocrinology and metabolism, 94 (7
مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adenoma -- complications, Adenoma -- genetics, Adenoma -- metabolism, Adolescent, Adult, Amino Acid Sequence, Child, Female, Gene Expression, Gene Expression Profiling, Gene Expression Regulation, Neoplastic, Humans, Hyperthyroidism -- etiology, Hyperthyroidism -- genetics, Hyperthyroidism -- metabolism, Male, Middle Aged, Models, Biological, Molecular Sequence Data, Oligonucleotide Array Sequence Analysis, Thyroid Gland -- metabolism, Thyroid Neoplasms -- complications, Thyroid Neoplasms -- genetics, Thyroid Neoplasms -- metabolism, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article
URL:
https://dipot.ulb.ac.be/dspace/bitstream/2013/51257/4/doi_26322.pdf https://dipot.ulb.ac.be/dspace/bitstream/2013/51257/1/HebrantJCEM2009.pdf http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51257 http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL -
8مورد إلكتروني
المصدر: The Journal of clinical endocrinology and metabolism, 94 (7
مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adenoma -- complications, Adenoma -- genetics, Adenoma -- metabolism, Adolescent, Adult, Amino Acid Sequence, Child, Female, Gene Expression, Gene Expression Profiling, Gene Expression Regulation, Neoplastic, Humans, Hyperthyroidism -- etiology, Hyperthyroidism -- genetics, Hyperthyroidism -- metabolism, Male, Middle Aged, Models, Biological, Molecular Sequence Data, Oligonucleotide Array Sequence Analysis, Thyroid Gland -- metabolism, Thyroid Neoplasms -- complications, Thyroid Neoplasms -- genetics, Thyroid Neoplasms -- metabolism, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article
URL:
https://dipot.ulb.ac.be/dspace/bitstream/2013/51257/4/doi_26322.pdf https://dipot.ulb.ac.be/dspace/bitstream/2013/51257/1/HebrantJCEM2009.pdf http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51257 http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL -
9مورد إلكتروني
المصدر: European journal of pediatrics, 167 (11
مصطلحات الفهرس: Sciences bio-médicales et agricoles, Child, Preschool, Cyclic AMP -- metabolism, Gene Expression -- genetics, Germ-Line Mutation -- genetics, Humans, Hyperthyroidism -- enzymology, Hyperthyroidism -- genetics, Immunoglobulins, Thyroid-Stimulating -- immunology, Infant, Newborn, Iodide Peroxidase -- metabolism, Male, Point Mutation -- genetics, Polymerase Chain Reaction, Polymorphism, Single Nucleotide -- genetics, Receptors, Thyrotropin -- genetics, Receptors, Thyrotropin -- immunology, Thyroxine -- blood, Transfection -- methods, Triiodothyronine -- blood, Valine -- metabolism, Activating mutation, Familial, TSH receptor, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article
URL:
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/52418 http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL -
10مورد إلكتروني
المصدر: Acta paediatrica, 94 (8
مصطلحات الفهرس: Sciences bio-médicales et agricoles, Child, Diagnosis, Differential, Genes, Dominant, Germ-Line Mutation, Humans, Hyperthyroidism -- diagnosis, Hyperthyroidism -- drug therapy, Hyperthyroidism -- genetics, Male, Methimazole -- therapeutic use, Neuromuscular Diseases -- diagnosis, Receptors, Thyrotropin -- genetics, Risk Assessment, Severity of Illness Index, Thyroid Function Tests, Endocrinology, Neuromuscular symptoms, Non-autoimmune hyperthyroidism, TSHR mutation, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article
URL:
https://dipot.ulb.ac.be/dspace/bitstream/2013/53300/3/53300.pdf http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/53300 http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL