-
1دورية أكاديمية
المؤلفون: Jan-Philipp Bodenbender, Valerio Marino, Julia Philipp, Anke Tropitzsch, Christoph Kernstock, Katarina Stingl, Melanie Kempf, Tobias B. Haack, Theresia Zuleger, Pascale Mazzola, Susanne Kohl, Nicole Weisschuh, Daniele Dell’Orco, Laura Kühlewein
المصدر: Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
مصطلحات موضوعية: TUBB4B, Hereditary retinal dystrophy, Leber congenital amaurosis, Retinitis pigmentosa, Hearing loss, Structural analysis, Medicine, Science
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2045-2322Test
-
2دورية أكاديمية
المؤلفون: Orlando Guntinas-Lichius, Dirk Arnold, Gerd Fabian Volk, Daniela Korth, Rene Aschenbach, Johann-Martin Hempel, Fritz Schneider, Thore Schade-Mann, Philipp Gamerdinger, Anke Tropitzsch, Hubert Löwenheim
المصدر: PLoS ONE, Vol 17, Iss 8, p e0272943 (2022)
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/1932-6203Test
-
3دورية أكاديمية
المؤلفون: Eusebia Schäfer, Ana-Elena Vedoveli, Giulia Righetti, Philipp Gamerdinger, Marlies Knipper, Anke Tropitzsch, Hans-Otto Karnath, Christoph Braun, Yiwen Li Hegner
المصدر: Frontiers in Neuroscience, Vol 15 (2021)
مصطلحات موضوعية: EEG, CI, TPO junction, repetition suppression, auditory, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fnins.2021.613101/fullTest; https://doaj.org/toc/1662-453XTest
-
4دورية أكاديمية
المؤلفون: Anke Tropitzsch, Marcus Müller, François Paquet-Durand, Frank Mayer, Hans-Georg Kopp, Andre Schrattenholz, Andrea Müller, Hubert Löwenheim
المصدر: Frontiers in Cellular Neuroscience, Vol 13 (2019)
مصطلحات موضوعية: cisplatin, ototoxicity, otoprotection, organ culture, PARP, hair cell loss, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/article/10.3389/fncel.2019.00406/fullTest; https://doaj.org/toc/1662-5102Test
-
5دورية أكاديمية
المؤلفون: Claudia Frick, Stefan Fink, Dominik Schmidbauer, Francis Rousset, Holger Eickhoff, Anke Tropitzsch, Benedikt Kramer, Pascal Senn, Rudolf Glueckert, Helge Rask-Andersen, Karl-Heinz Wiesmüller, Hubert Löwenheim, Marcus Müller
المصدر: Brain Sciences, Vol 10, Iss 9, p 580 (2020)
مصطلحات موضوعية: small-molecule BDNF mimetics, THF, NT-3, Trk receptors, SGN, murine postnatal model, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
-
6
المؤلفون: Thore Schade-Mann, Damaris Platzer, Anke Tropitzsch, Julia Philipp, Dominik Riss, Rudolfs Liepins, Alice Auinger, Clemens Honeder
المصدر: Abstract- und Posterband - 93. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn Interface - Fokus Mensch im Zeitalter der technisierten Medizin.
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::693e3994f0bb2e174d8f53dc02133e4dTest
https://doi.org/10.1055/s-0042-1747404Test -
7
المؤلفون: Thore Schade-Mann, Damaris Platzer, Anke Tropitzsch, Julia Philipp, Dominik Riss, Rudolfs Liepins, Alice Auinger, Clemens Honeder
المصدر: Abstract- und Posterband - 93. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn Interface - Fokus Mensch im Zeitalter der technisierten Medizin.
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::d62e1fe5b0640f185519b9713e613113Test
https://doi.org/10.1055/s-0042-1746801Test -
8
المؤلفون: Barbara Vona, Philipp Gamerdinger, Evgeny N. Imyanitov, Thore Schade-Mann, Saskia Biskup, Marcus Müller, Aboulfazl Rad, Grigoriy A. Yanus, Hubert Löwenheim, Björn Schulte, Anke Tropitzsch
المصدر: Human Mutation. 42:25-30
مصطلحات موضوعية: Heterozygote, Hearing loss, Hearing Loss, Sensorineural, RNA Splicing, Locus (genetics), Deafness, Biology, Collagen Type XI, 03 medical and health sciences, Genetics, medicine, Humans, Nonsyndromic deafness, Hearing Loss, Gene, Genetics (clinical), Organ system, 030304 developmental biology, Genetic testing, 0303 health sciences, medicine.diagnostic_test, 030305 genetics & heredity, Intron, medicine.disease, Pedigree, RNA splicing, medicine.symptom
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2373af06cff850d19856b4a11eb6b810Test
https://doi.org/10.1002/humu.24136Test -
9
المؤلفون: Natalia Trpchevska, Maxim B. Freidin, Linda Broer, Berthe C. Oosterloo, Shuyang Yao, Yitian Zhou, Barbara Vona, Charles Bishop, Argyro Bizaki-Vallaskangas, Barbara Canlon, Fabio Castellana, Daniel I. Chasman, Stacey Cherny, Kaare Christensen, Maria Pina Concas, Adolfo Correa, Ran Elkon, Jonas Mengel-From, Yan Gao, Anne B.S. Giersch, Giorgia Girotto, Alexander Gudjonsson, Vilmundur Gudnason, Nancy L. Heard-Costa, Ronna Hertzano, Jacob v.B. Hjelmborg, Jens Hjerling-Leffler, Howard J. Hoffman, Jaakko Kaprio, Johannes Kettunen, Kristi Krebs, Anna K. Kähler, Francois Lallemend, Lenore J. Launer, I-Min Lee, Hampton Leonard, Chuan-Ming Li, Hubert Lowenheim, Patrik K.E. Magnusson, Joyce van Meurs, Lili Milani, Cynthia C. Morton, Antti Mäkitie, Mike A. Nalls, Giuseppe Giovanni Nardone, Marianne Nygaard, Teemu Palviainen, Sheila Pratt, Nicola Quaranta, Joel Rämö, Elmo Saarentaus, Rodolfo Sardone, Claudia L. Satizabal, John M. Schweinfurth, Sudha Seshadri, Eric Shiroma, Eldad Shulman, Eleanor Simonsick, Christopher Spankovich, Anke Tropitzsch, Volker M. Lauschke, Patrick F. Sullivan, Andre Goedegebure, Christopher R. Cederroth, Frances M.K. Williams, Andries Paul Nagtegaal, Andres Metspalu, Mari Nelis, Reedik Mägi, Tõnu Esko
المساهمون: Tampere University, Clinical Medicine, Department of Otology and Oral Diseases, Institute for Molecular Medicine Finland, HUS Head and Neck Center, Clinicum, Korva-, nenä- ja kurkkutautien klinikka, Genetic Epidemiology, Genomics of Neurological and Neuropsychiatric Disorders, Complex Disease Genetics, Trpchevska, Natalia, Freidin, Maxim B, Broer, Linda, Oosterloo, Berthe C, Yao, Shuyang, Zhou, Yitian, Vona, Barbara, Bishop, Charle, Bizaki-Vallaskangas, Argyro, Canlon, Barbara, Castellana, Fabio, Chasman, Daniel I, Cherny, Stacey, Christensen, Kaare, Concas, Maria Pina, Correa, Adolfo, Elkon, Ran, Mengel-From, Jona, Gao, Yan, Giersch, Anne B S, Girotto, Giorgia, Gudjonsson, Alexander, Gudnason, Vilmundur, Heard-Costa, Nancy L, Hertzano, Ronna, Hjelmborg, Jacob V B, Hjerling-Leffler, Jen, Hoffman, Howard J, Kaprio, Jaakko, Kettunen, Johanne, Krebs, Kristi, Kähler, Anna K, Lallemend, Francoi, Launer, Lenore J, Lee, I-Min, Leonard, Hampton, Li, Chuan-Ming, Lowenheim, Hubert, Magnusson, Patrik K E, van Meurs, Joyce, Milani, Lili, Morton, Cynthia C, Mäkitie, Antti, Nalls, Mike A, Nardone, Giuseppe Giovanni, Nygaard, Marianne, Palviainen, Teemu, Pratt, Sheila, Quaranta, Nicola, Rämö, Joel, Saarentaus, Elmo, Sardone, Rodolfo, Satizabal, Claudia L, Schweinfurth, John M, Seshadri, Sudha, Shiroma, Eric, Shulman, Eldad, Simonsick, Eleanor, Spankovich, Christopher, Tropitzsch, Anke, Lauschke, Volker M, Sullivan, Patrick F, Goedegebure, Andre, Cederroth, Christopher R, Williams, Frances M K, Nagtegaal, Andries Paul, Internal Medicine, Otorhinolaryngology and Head and Neck Surgery
المصدر: Trpchevska, N, Freidin, M B, Broer, L, Oosterloo, B C, Yao, S, Zhou, Y, Vona, B, Bishop, C, Bizaki-vallaskangas, A, Canlon, B, Castellana, F, Chasman, D I, Cherny, S, Christensen, K, Concas, M P, Correa, A, Elkon, R, Mengel-from, J, Gao, Y, Giersch, A B S, Girotto, G, Gudjonsson, A, Gudnason, V, Heard-costa, N L, Hertzano, R, Hjelmborg, J V B, Hjerling-leffler, J, Hoffman, H J, Kaprio, J, Kettunen, J, Krebs, K, Kähler, A K, Lallemend, F, Launer, L J, Lee, I, Leonard, H, Li, C, Lowenheim, H, Magnusson, P K E, Van Meurs, J, Milani, L, Morton, C C, Mäkitie, A, Nalls, M A, Nardone, G G, Nygaard, M, Palviainen, T, Pratt, S, Quaranta, N, Rämö, J, Saarentaus, E, Sardone, R, Satizabal, C L, Schweinfurth, J M, Seshadri, S, Shiroma, E, Shulman, E, Simonsick, E, Spankovich, C, Tropitzsch, A, Lauschke, V M, Sullivan, P F, Goedegebure, A, Cederroth, C R, Williams, F M K, Nagtegaal, A P, Metspalu, A, Nelis, M, Mägi, R & Esko, T 2022, ' Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss ', American Journal of Human Genetics . https://doi.org/10.1016/j.ajhg.2022.04.010Test
American Journal of Human Genetics, 109(6), 1077-1091. Cell Press
The American Journal of Human Geneticsمصطلحات موضوعية: basal cells, hair cells, cochlea, spindle cell, ARHL, GWAS, genetics, hearing loss, root cells, spindle cells, stria vascularis, Animals, Cochlea, Genome-Wide Association Study, Humans, Mice, Stria Vascularis, Deafness, Hearing Loss, basal cell, hair cell, Hair-cells, Heritability, otorhinolaryngologic diseases, Genetics, Pathogenicity, Gwas data, Deafne, Ld score regression, Ganglion neurons, Genetics (clinical), Animal, 1184 Genetics, developmental biology, physiology, hearing lo, Stria Vasculari, Inner, 3142 Public health care science, environmental and occupational health, root cell, Differentiation, Degeneration, 3111 Biomedicine, genetic, Noise, Human
وصف الملف: fulltext; application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adc091fdf2ade424805f1d22909bade0Test
https://pubmed.ncbi.nlm.nih.gov/35580588Test -
10
المؤلفون: Anke Tropitzsch, Florian Battke, Andreas Heyd, Marcus Müller, Barbara Vona, Martin Schulze, Philipp Gamerdinger, Saskia Biskup, Hubert Löwenheim, Martin Holderried, S. Fehr, Björn Schulte, S Dofek, Thore Schade-Mann
المصدر: Ear and hearing. 43(3)
مصطلحات موضوعية: Proband, medicine.medical_specialty, Hearing loss, Population, Genes, Recessive, Biology, Speech and Hearing, Age Distribution, Internal medicine, otorhinolaryngologic diseases, medicine, Humans, Genetic Testing, TECTA, education, Genetic testing, Retrospective Studies, education.field_of_study, medicine.diagnostic_test, Serine Endopeptidases, Membrane Proteins, Neoplasm Proteins, Pedigree, Otorhinolaryngology, Genetic epidemiology, Cohort, Mutation, Medical genetics, medicine.symptom, Usher Syndromes
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f3318e77cef70b2560038a4dfb9857dTest
https://pubmed.ncbi.nlm.nih.gov/34753855Test