المؤلفون: Park, JS, Cederroth, CR, Basinou, V, Meltser, I, Lundkvist, G, Canlon, B

المساهمون: 105212, 박, 정섭

مصطلحات موضوعية: ARNTL Transcription Factors, Animals, Brain-Derived Neurotrophic Factor, Cells, Cultured, Circadian Clocks, Cryptochromes, DNA-Binding Proteins, Inferior Colliculi, Male, Mice, Inbred CBA, Noise, Nuclear Receptor Subfamily 1, Group D, Member 1, Period Circadian Proteins, Photoperiod, Transcription Factors

العلاقة: J002706474; http://repository.ajou.ac.kr/handle/201003/14962Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871986Test/; The Journal of neuroscience, 36(20). : 5509-5519, 2016

الإتاحة: https://doi.org/10.1523/JNEUROSCI.3616-15.2016Test
http://repository.ajou.ac.kr/handle/201003/14962Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871986Test/

المؤلفون: Idrizbegovic, E, Bogdanovic, N, Willott, J F, Canlon, B

المصدر: Faculty Research 2000 - 2009

مصطلحات موضوعية: Age-Factors, Aging, Animals, Calcium-Binding-Protein-Vitamin-D-Dependent, Calcium-Binding-Proteins, Cell-Count, Cell-Survival, Cochlear-Nucleus, Female, Hearing-Loss-Central, Heredodegenerative-Disorders-Nervous, Immunohistochemistry, Male, Mice, Mice-Inbred-C57BL, Neuronal-Plasticity, Neurons, Parvalbumins, Research-Support-Non-U, Gov't, Research-Support-U, Gov't-P, Species-Specificity, Up-Regulation

العلاقة: https://mouseion.jax.org/stfb2000_2009/810Test; http://dx.doi.org/doi:10.1016/j.neurobiolaging.2003.11.004Test

الإتاحة: https://doi.org/10.1016/j.neurobiolaging.2003.11.004Test
https://mouseion.jax.org/stfb2000_2009/810Test

المؤلفون: Patricia Perez-Carpena, Patrick May, Joseph Sollini, Juan Manuel Espinosa-Sanchez, Alvaro Gallego-Martinez, Barbara Canlon, Sana Amanat, Jose A. Lopez-Escamez, Angel Batuecas-Caletrio, Andrés Soto-Varela, Christopher R. Cederroth, Ismael Aran

المساهمون: Fonds National de la Recherche - FnR [sponsor], Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group) [research center], [Amanat,S, Gallego-Martinez,A, Perez-Carpena,P, Espinosa-Sanchez,JM, Lopez-Escamez,JA] a Otology & Neurotology Group CTS495, Department of Genomic Medicine, GENYO-Centre for Genomics and Oncological Research-Pfizer/University of Granada/ Junta de Andalucía, PTS, Granada, Spain. [Sollini,J, Cederroth,CR] Hearing Sciences, Division of Clinical Neuroscience, School of Medicine, University of Nottingham, Nottingham, UK. [Perez-Carpena,P, Lopez-Escamez,JA] c Department of Otolaryngology, Instituto de Investigacion Biosanitaria, ibs.Granada, Hospital Universitario Virgen de las Nieves, Granada, Spain. [Aran,I] Department of Otolaryngology, Complexo Hospitalario de Pontevedra, Pontevedra, Spain. [Soto-Varela,A] e Division of Otoneurology, Department of Otorhinolaryngology, Complexo Hospitalario Universitario, Santiago de Compostela, Spain. [Batuecas-Caletrio,A] Department of Otolaryngology, Hospital Universitario de Salamanca, IBSAL Salamanca, Spain. [Canlon,B, Cederroth,CR] Laboratory of Experimental Audiology, Department of Physiology and Pharmacology, Karolinska Institute, Stockholm, Sweden. [May,P] Bioinformatics Core, Luxembourg Centre for System Biomedicine, University of Luxemburg, Esch-sur-Alzette, Luxembourg. [Cederroth,CR] National Institute for Health Research (NIHR) Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust, Ropewalk House, Nottingham, UK. [Lopez-Escamez,JA] Department of Surgery, Division of Otolaryngology, University of Granada, Granada, Spain, This study has been funded by H2020 MSCA-ITN-2016–722046, the H2020-SC1-2019-848261, and the GNP-182 GENDER-Net Co-Plus Fund (JALE and CRC). The project leading to these results has received funding from 'la Caixa' Foundation (ID 100010434), under agreement LCF/PR/DE18/52010002 (JALE). This project is a part of European School of Interdisciplinary Tinnitus (ESIT) research and Sana Amanat is a PhD student in Biomedicine Program at the University of Granada. CRC received additional funding from Svenska Läkaresällskapet (SLS- 779681 ), Hörselforskningsfonden (503). The data handling for STOP and SweGen cohorts were enabled by resources provided by the Swedish National Infrastructure for Computing (SNIC) at UPPMAX partially funded by the Swedish Research Council through Grant agreement No. 2018-05973 . The time provided by JS was funded by the University of Nottingham, Nottingham Research Fellowship. PM was supported by the BMBF Treat-ION Grant ( 01GM1907 ) and the DFG Research Unit FOR2715 (FNR INTER/DFG/17/ 11583046 )., Sollini, Joseph

المصدر: EBioMedicine
Digibug: Repositorio Institucional de la Universidad de Granada
Universidad de Granada (UGR)
EBioMedicine, Vol 66, Iss, Pp 103309-(2021)
Digibug. Repositorio Institucional de la Universidad de Granada
instname

مصطلحات موضوعية: 0301 basic medicine, Male, Exome sequencing, Medicine (General), Phenomena and Processes::Genetic Phenomena::Phenotype [Medical Subject Headings], Disciplines and Occupations::Natural Science Disciplines::Biological Science Disciplines::Biology::Genetics::Genetic Research::Gene Ontology [Medical Subject Headings], Psychiatry and Psychology::Mental Disorders [Medical Subject Headings], Anatomy::Nervous System::Synapses [Medical Subject Headings], Bioinformatics, Severity of Illness Index, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Genetic Association Studies [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Cytoskeletal Proteins [Medical Subject Headings], Mice, Tinnitus, 0302 clinical medicine, Organisms::Eukaryota::Animals [Medical Subject Headings], Missense mutation, 050207 economics, Anatomy::Nervous System::Neurons [Medical Subject Headings], Exome, Diseases::Otorhinolaryngologic Diseases::Ear Diseases::Labyrinth Diseases::Endolymphatic Hydrops::Meniere Disease [Medical Subject Headings], education.field_of_study, 050208 finance, Geographical Locations::Geographic Locations::Europe::Scandinavia::Sweden [Medical Subject Headings], 05 social sciences, Extreme phenotype, Family aggregation, Brain, General Medicine, Axon initial segment, 3. Good health, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Data Collection::Health Surveys::Health Status Indicators::Patient Acuity::Severity of Illness Index [Medical Subject Headings], Phenotype, Disciplines and Occupations::Natural Science Disciplines::Biological Science Disciplines::Biology::Computational Biology [Medical Subject Headings], 030220 oncology & carcinogenesis, Medicine, Disciplines and Occupations::Natural Science Disciplines::Biological Science Disciplines::Biology::Genetics::Genomics [Medical Subject Headings], Female, Genetics & genetic processes [F10] [Life sciences], medicine.symptom, Phenomena and Processes::Genetic Phenomena::Genetic Variation [Medical Subject Headings], Génétique & processus génétiques [F10] [Sciences du vivant], Fenotipo, Research Paper, Population, Check Tags::Male [Medical Subject Headings], General Biochemistry, Genetics and Molecular Biology, Epilepsia, Diseases::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Disease Susceptibility::Genetic Predisposition to Disease [Medical Subject Headings], 03 medical and health sciences, R5-920, 0502 economics and business, medicine, otorhinolaryngologic diseases, Segmento inicial del axón, Animals, Humans, Genetic Predisposition to Disease, Diseases::Otorhinolaryngologic Diseases::Ear Diseases::Hearing Disorders::Tinnitus [Medical Subject Headings], Generalized epilepsy, education, Genetic studies, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Alleles, Genetic Association Studies, Phenomena and Processes::Biological Phenomena [Medical Subject Headings], Sweden, Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Rodentia::Muridae::Murinae::Mice [Medical Subject Headings], Epilepsy, Secuenciación del exoma completo, Estudios de asociación genética, business.industry, Enfermedad de Meniere, Acúfeno, Computational Biology, Genetic Variation, Anatomy::Nervous System::Central Nervous System::Brain [Medical Subject Headings], Diseases::Nervous System Diseases::Central Nervous System Diseases::Brain Diseases::Epilepsy::Epilepsy, Generalized [Medical Subject Headings], medicine.disease, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Data Collection::Questionnaires::Self Report [Medical Subject Headings], 030104 developmental biology, Gene Ontology, Check Tags::Female [Medical Subject Headings], Meniere disease, Synapses, business, exome sequencing

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document; PDF

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69b8b540fb9be7a6d76365326bd18b58Test
https://pubmed.ncbi.nlm.nih.gov/33813136Test