-
1
المؤلفون: Gunnar Kleinau, Harald Jüppner, Sarah Paisdzior, Heiko Krude, John Gregory, Dirk Schnabel, Mehul T. Dattani, Thomas J. Gardella, Louise C. Wilson, Michael Mannstadt, Detlef Bockenhauer, Ian Tully, Jeremy Allgrove, Sarah Kiff, Heike Biebermann, Patrick Scheerer, Monica Reyes, Annette Grüters
مصطلحات موضوعية: 0301 basic medicine, Male, medicine.medical_specialty, Heterozygote, Gs alpha subunit, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, DNA Mutational Analysis, Puberty, Precocious, 030209 endocrinology & metabolism, Context (language use), Biology, medicine.disease_cause, Biochemistry, Bone and Bones, Adenylyl cyclase, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Endocrinology, Loss of Function Mutation, Internal medicine, medicine, GNAS complex locus, Chromogranins, GTP-Binding Protein alpha Subunits, Gs, Humans, Receptor, Pseudohypoparathyroidism, Clinical Research Articles, Alleles, G protein-coupled receptor, Mutation, Biochemistry (medical), medicine.disease, 030104 developmental biology, Phenotype, chemistry, Amino Acid Substitution, Gain of Function Mutation, biology.protein, Female, Maternal Inheritance, Hyponatremia
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6549249d249e21c347aa4043aa794a5dTest
https://europepmc.org/articles/PMC6380466Test/ -
2
المؤلفون: Oliver Blankenstein, Maria E. Craig, Michaela Brückner-Spieler, Anne-Marie Stoehr, Heiko Krude, Peter Kühnen, Paulina E Aleksander, Erwin Lankes, Dirk Schnabel, Andrea Ernert, Walter Stäblein, Annette Grüters
المصدر: Yearbook of Paediatric Endocrinology.
مصطلحات موضوعية: Male, endocrine system, Pediatrics, medicine.medical_specialty, Adolescent, Endocrinology, Diabetes and Metabolism, Intelligence, Clinical Biochemistry, Levothyroxine, 030209 endocrinology & metabolism, Context (language use), Carotid Intima-Media Thickness, Biochemistry, Body Mass Index, Young Adult, 03 medical and health sciences, Neonatal Screening, 0302 clinical medicine, Endocrinology, Quality of life, 030225 pediatrics, Internal medicine, Congenital Hypothyroidism, medicine, Humans, Newborn screening, business.industry, Biochemistry (medical), Infant, Newborn, Wechsler Scales, Wechsler Adult Intelligence Scale, medicine.disease, Congenital hypothyroidism, Thyroxine, Cross-Sectional Studies, Quality of Life, Triiodothyronine, Female, business, Body mass index, Cohort study, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12c7e261488b40464a19ca66e39c5aceTest
https://doi.org/10.1530/ey.15.3.7Test -
3
المؤلفون: Terry J. DeClue, Annette Grüters-Kieslich, Erwin Lankes, Amita Sharma, Cem Demirci, Dirk Schnabel, Monica Reyes, Harald Jüppner, Dov Tiosano
المصدر: Yearbook of Paediatric Endocrinology.
مصطلحات موضوعية: Male, 0301 basic medicine, Pediatric Obesity, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, medicine.disease_cause, Bioinformatics, Biochemistry, Epigenesis, Genetic, Cohort Studies, Exon, Endocrinology, GTP-Binding Protein alpha Subunits, Gs, Medicine, Child, Mutation, biology, food and beverages, Methylation, Phenotype, Child, Preschool, Pseudohypoparathyroidism, DNA methylation, Female, STX16, musculoskeletal diseases, medicine.medical_specialty, Adolescent, Context (language use), Syntaxin 16, 03 medical and health sciences, Internal medicine, Chromogranins, GNAS complex locus, Humans, Epigenetics, Clinical Research Articles, business.industry, fungi, Biochemistry (medical), Infant, DNA Methylation, medicine.disease, Obesity, 030104 developmental biology, biology.protein, business, Multiplex Polymerase Chain Reaction
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c51d6290f0d12e13e36b51e8d9f931ceTest
https://doi.org/10.1530/ey.15.11.8Test -
4
المؤلفون: Maren Rehders, Lars C. Moeller, Annette Grüters, Klaudia Brix, Heike Biebermann, Peter Kühnen, Anita Kinne, Jana Fischer, Dagmar Führer, Anne Müller, Gunnar Kleinau, Denise Zwanziger, Heiko Krude
المصدر: Journal of Molecular Endocrinology. 54:39-50
مصطلحات موضوعية: Models, Molecular, Monocarboxylic Acid Transporters, Mutant, Medizin, Mutation, Missense, Context (language use), Chromosomal translocation, Biology, Protein Structure, Secondary, Endocrinology, INDEL Mutation, Chlorocebus aethiops, Animals, Humans, Protein Structure, Quaternary, Molecular Biology, Monocarboxylate transporter, Symporters, Translocon, Major facilitator superfamily, Transmembrane protein, Protein Structure, Tertiary, Muscular Atrophy, Protein Transport, Transmembrane domain, Biochemistry, COS Cells, Mental Retardation, X-Linked, biology.protein, Muscle Hypotonia, Protein Multimerization, Protein Binding
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c005c2f78ccb3286db7aa629d6ffb11Test
https://doi.org/10.1530/jme-14-0272Test -
5
المؤلفون: Heiko Krude, Tulay Guran, Peter Kühnen, Annette Grüters, Heike Biebermann, Saygin Abali, Wei Chen, Abdullah Bereket, Serap Turan, Sebastian Fröhler
المساهمون: Kuehnen, Peter, Turan, Serap, Froehler, Sebastian, Gueran, Tuelay, Abali, Saygin, Biebermann, Heike, Bereket, Abdullah, Grueters, Annette, Chen, Wei, Krude, Heiko
المصدر: The Journal of Clinical Endocrinology & Metabolism. 99:E169-E176
مصطلحات موضوعية: Male, Turkey, endocrine system diseases, Endocrinology, Diabetes and Metabolism, DNA Mutational Analysis, GENOTYPE-PHENOTYPE CORRELATION, Clinical Biochemistry, Biochemistry, NONSYNDROMIC HEARING-LOSS, Cohort Studies, Endocrinology, Missense mutation, SYNDROME GENE PDS, Exome sequencing, Sanger sequencing, EVA, Thyroid, Pedigree, Congenital hypothyroidism, medicine.anatomical_structure, Sulfate Transporters, Thyroid Dysgenesis, symbols, Female, IODIDE TRANSPORTER, endocrine system, medicine.medical_specialty, Adolescent, ENLARGEMENT, Context (language use), Biology, Thyroid dysgenesis, symbols.namesake, Internal medicine, Congenital Hypothyroidism, VESTIBULAR AQUEDUCT, medicine, Humans, Genetic Association Studies, POLYMORPHISMS, ENDEMIC CRETINISM, Biochemistry (medical), Membrane Transport Proteins, Pendrin, medicine.disease, Case-Control Studies, Mutation, CELLS, biology.protein
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dc7148e569514673c72285e61bccef0Test
https://doi.org/10.1210/jc.2013-2619Test -
6
المؤلفون: Heike Biebermann, Daniela Handke, Heiko Krude, Peter Kühnen, Annette Grüters, Burkhard Wiesner, Gunnar Kleinau, Franziska Winkler, Jenny Eichhorst, Fergus J. Cameron, Burkhard Gerling, Anke Teichmann
المصدر: The Journal of Clinical Endocrinology & Metabolism. 97:E228-E232
مصطلحات موضوعية: medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, Amino Acid Motifs, Clinical Biochemistry, Biology, Transfection, Biochemistry, Protein Structure, Secondary, Receptors, G-Protein-Coupled, Substrate Specificity, Thyrotropin receptor, Endocrinology, Catalytic Domain, Internal medicine, Helix (Snails), Chlorocebus aethiops, medicine, Animals, Humans, Child, Receptor, Conserved Sequence, G protein-coupled receptor, Genetics, Biochemistry (medical), Infant, Newborn, Receptors, Thyrotropin, Transmembrane domain, HEK293 Cells, Structural Homology, Protein, COS Cells, Mutation, Motif (music), Signal Transduction
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ca878b66eaaf946d0d01a888dadc5d2Test
https://doi.org/10.1210/jc.2011-2106Test -
7
المؤلفون: Theda Wessel, Eva Klopocki, Klemens Raile, Monika Maringa, Jürgen Weber, Dorothee Deiss, Thomas Riebel, Annette Grüters, Denise Horn, Dominik N. Müller, Martin Holder, A. Galler, Reinhard Ullmann
المصدر: The Journal of Clinical Endocrinology & Metabolism. 94:2658-2664
مصطلحات موضوعية: Male, medicine.medical_specialty, Adolescent, Endocrinology, Diabetes and Metabolism, DNA Mutational Analysis, Clinical Biochemistry, Disease, Biochemistry, Maturity onset diabetes of the young, Cohort Studies, Endocrinology, Internal medicine, Diabetes mellitus, Humans, Medicine, Hepatocyte Nuclear Factor 1-beta, Comparative Genomic Hybridization, Type 1 diabetes, business.industry, Biochemistry (medical), medicine.disease, HNF1B, HNF1A, Hepatocyte nuclear factors, Diabetes Mellitus, Type 2, Female, Chromosome Deletion, business, Chromosomes, Human, Pair 17, Comparative genomic hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a923df7e45789b30995670755b59cc6Test
https://doi.org/10.1210/jc.2008-2189Test -
8
المؤلفون: Heike Biebermann, Andrea M. Müller, Gunnar Kleinau, Heiko Krude, Juliane Dinter, Carolin Leonie Wienchol, S Jacobi, Jessica Mühlhaus, C Höfig, J Meister, M Cöster, Annette Grüters, Torsten Schöneberg, Josef Köhrle, Jens Mittag
المصدر: Experimental and Clinical Endocrinology & Diabetes. 122
مصطلحات موضوعية: Endocrinology, Biochemistry, Endocrinology, Diabetes and Metabolism, Internal Medicine, General Medicine, Biology, G protein-coupled receptor
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::e25df59800f7bb6a087aeff6dd7dbd5dTest
https://doi.org/10.1055/s-0035-1547778Test -
9
المؤلفون: Annette Grüters, Anne Müller, Jana Fischer, Timo D. Müller, Heike Biebermann, Vera Knäuper, Gunnar Kleinau, Matthias H. Tschöp, Brinja Leinweber
المصدر: BMC Res. Notes 7:913 (2014)
BMC Research Notesمصطلحات موضوعية: Models, Molecular, Molecular Sequence Data, Short Report, Biology, Q1, General Biochemistry, Genetics and Molecular Biology, Receptors, G-Protein-Coupled, Mice, GTP-Binding Proteins, Constitutive activation, Extracellular, Enzyme-linked receptor, Animals, Humans, Inverse agonist, Amino Acid Sequence, GABBR2, GABBR1, Receptor, Signaling mechanism, G protein-coupled receptor, Medicine(all), G-protein coupled receptor 83, Binding Sites, Sequence Homology, Amino Acid, Biochemistry, Genetics and Molecular Biology(all), Cell Membrane, Antagonist, General Medicine, Protein Structure, Tertiary, Cell biology, HEK293 Cells, Biochemistry, COS Cells, Mutation, Mitogen-Activated Protein Kinases, Signal transduction, Signal Transduction
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfe2753fb0136feea7d2d766e964f645Test
https://doi.org/10.1186/1756-0500-7-913Test -
10
المؤلفون: Mojca Zerjav Tansek, Heiko Krude, Heike Biebermann, Primus E. Mullis, Dirk Schnabel, Annette Grüters, Pierre Theunissen
المصدر: The Journal of Clinical Endocrinology & Metabolism. 88:4633-4640
مصطلحات موضوعية: Thyroid Hormones, endocrine system, medicine.medical_specialty, Pro-Opiomelanocortin, Genotype, Endocrinology, Diabetes and Metabolism, DNA Mutational Analysis, Clinical Biochemistry, Thyroid Gland, Compound heterozygosity, Biochemistry, Endocrinology, Adrenocorticotropic Hormone, Proopiomelanocortin, Internal medicine, Adrenal insufficiency, Humans, POMC Gene Product, Medicine, Obesity, Hair Color, biology, business.industry, Body Weight, digestive, oral, and skin physiology, Biochemistry (medical), Thyroid, Infant, Newborn, Infant, medicine.disease, Peptide Fragments, Pro-Opiomelanocortin Deficiency, Phenotype, medicine.anatomical_structure, Child, Preschool, biology.protein, Basal Metabolism, Melanocortin, business, hormones, hormone substitutes, and hormone antagonists, Hormone
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::147bb5793ed2e373ea4d20944695c478Test
https://doi.org/10.1210/jc.2003-030502Test