Literatura académica sobre el tema "Phenotype"
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Artículos de revistas sobre el tema "Phenotype"
Moser, Lukas, Silvan Hess, Henrik Behrend y Michael Hirschmann. "Variability of functional knee phenotypes in osteoarthritic knees shows that a more personalized approach in TKA is needed". Orthopaedic Journal of Sports Medicine 8, n.º 5_suppl4 (1 de mayo de 2020): 2325967120S0030. http://dx.doi.org/10.1177/2325967120s00300.
Texto completoRoemer, F., J. Collins, T. Neogi, M. Crema y A. Guermazi. "FRI0421 RATES OF PROGRESSION DIFFER BETWEEN STRUCTURAL PHENOTYPES OF KNEE OSTEOARTHRITIS: A SECONDARY ANALYSIS FROM THE FNIH COHORT". Annals of the Rheumatic Diseases 79, Suppl 1 (junio de 2020): 808.1–809. http://dx.doi.org/10.1136/annrheumdis-2020-eular.1802.
Texto completoCarmina, Enrico y Rogerio A. Lobo. "Comparing Lean and Obese PCOS in Different PCOS Phenotypes: Evidence That the Body Weight Is More Important Than the Rotterdam Phenotype in Influencing the Metabolic Status". Diagnostics 12, n.º 10 (25 de septiembre de 2022): 2313. http://dx.doi.org/10.3390/diagnostics12102313.
Texto completoPostoeva, A. V., I. V. Dvoryashina, A. V. Kudryavtsev y V. A. Postoev. "Prevalence of metabolic phenotypes among citizens of Arctic area of the Russian Federation (in Arkhangelsk city setting)". Obesity and metabolism 20, n.º 1 (22 de mayo de 2023): 34–42. http://dx.doi.org/10.14341/omet12926.
Texto completoLusczek, Elizabeth R., Nicholas E. Ingraham, Basil S. Karam, Jennifer Proper, Lianne Siegel, Erika S. Helgeson, Sahar Lotfi-Emran et al. "Characterizing COVID-19 clinical phenotypes and associated comorbidities and complication profiles". PLOS ONE 16, n.º 3 (31 de marzo de 2021): e0248956. http://dx.doi.org/10.1371/journal.pone.0248956.
Texto completode Koning-Tijssen, M. "One gene many phenotypes, one phenotype many genes". Journal of the Neurological Sciences 405 (octubre de 2019): 11. http://dx.doi.org/10.1016/j.jns.2019.10.028.
Texto completoXiromerisiou, Georgia, Henry Houlden, Nikolaos Scarmeas, Maria Stamelou, Eleanna Kara, John Hardy, Andrew J. Lees et al. "THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations". Movement Disorders 27, n.º 10 (17 de agosto de 2012): 1290–94. http://dx.doi.org/10.1002/mds.25146.
Texto completoFerguson, Amy Christina, Sophie Thrippleton, David Henshall, Ed Whittaker, Bryan Conway, Malcolm MacLeod, Rainer Malik et al. "Frequency and Phenotype Associations of Rare Variants in 5 Monogenic Cerebral Small Vessel Disease Genes in 200,000 UK Biobank Participants". Neurology Genetics 8, n.º 5 (24 de agosto de 2022): e200015. http://dx.doi.org/10.1212/nxg.0000000000200015.
Texto completoZhou, Xue, Keijiro Nakamura, Naohiko Sahara, Masako Asami, Yasutake Toyoda, Yoshinari Enomoto, Hidehiko Hara et al. "Exploring and Identifying Prognostic Phenotypes of Patients with Heart Failure Guided by Explainable Machine Learning". Life 12, n.º 6 (24 de mayo de 2022): 776. http://dx.doi.org/10.3390/life12060776.
Texto completoSpring, Michele D., Jason C. Sousa, Qigui Li, Christian A. Darko, Meshell N. Morrison, Sean R. Marcsisin, Kristin T. Mills et al. "Determination of Cytochrome P450 Isoenzyme 2D6 (CYP2D6) Genotypes and Pharmacogenomic Impact on Primaquine Metabolism in an Active-Duty US Military Population". Journal of Infectious Diseases 220, n.º 11 (24 de septiembre de 2019): 1761–70. http://dx.doi.org/10.1093/infdis/jiz386.
Texto completoTesis sobre el tema "Phenotype"
Moses, Lorraine. "Phenotypic factors influencing Mycobacterium tuberculosis phenotype". Thesis, Stellenbosch : Stellenbosch University, 2002. http://hdl.handle.net/10019.1/52997.
Texto completoSailer, Zachary. "Predicting Phenotypes in Sparsely Sampled Genotype-Phenotype Maps". Thesis, University of Oregon, 2019. http://hdl.handle.net/1794/24231.
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Arbon, Jed. "Phenotype-genotype correlation between the Hippo pathway and 3D craniofacial phenotypes". Thesis, University of Iowa, 2016. https://ir.uiowa.edu/etd/3042.
Texto completoHabib, Farhat Abbas. "Genotype-phenotype correlation using phylogenetic trees". Columbus, Ohio : Ohio State University, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1187297400.
Texto completoBloomfield, Kelly Louise y n/a. "Investigation of the Role of Thioredoxin in the Invasive Phenotype and its Interaction with the Transcription Factor Sp1". Griffith University. School of Biomolecular and Biomedical Science, 2003. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20031021.120018.
Texto completoBloomfield, Kelly Louise. "Investigation of the Role of Thioredoxin in the Invasive Phenotype and its Interaction with the Transcription Factor Sp1". Thesis, Griffith University, 2003. http://hdl.handle.net/10072/366170.
Texto completoThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Biomolecular and Biomedical Sciences
Full Text
Ried, Janina S. "Phenotype set enrichment analysis". Diss., Ludwig-Maximilians-Universität München, 2013. http://nbn-resolving.de/urn:nbn:de:bvb:19-158079.
Texto completoAlsbou, Mohammed. "Dissecting phenotype-genoype relationships". Thesis, University of Liverpool, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.443925.
Texto completoARDISSONE, ANNA. "Mitochondrial diseases related to mtDNA in childhood: genotype-phenotype correlation and characterization of novel phenotypes". Doctoral thesis, Università degli Studi di Milano-Bicocca, 2020. http://hdl.handle.net/10281/262917.
Texto completoMitochondrial diseases (MD) are a clinically heterogeneous group of disorders that arise as a result of dysfunction of the mitochondrial respiratory chain (RC) and oxidative phosphorylation (OXPHOS). Mitochondrial functions are under the control of two different genomes: mitochondrial DNA (mtDNA) and nuclear genome (nDNA). Childhood phenotypes are often associated with nDNA mutations; in recent years, new-generation sequencing technologies (Next Generation Sequencing-NGS) have identified novel causative genes; in collaboration with other centers we contributed to the definition of phenotype associated with the new identified disease genes. The application of this technique has also been extended to the study of mtDNA: even if more than 100 mutations and deletions in mtDNA have been described in association with an extremely heterogeneous spectrum of clinical presentations, only a few of them are associated with well-defined clinical syndromes in childhood. We performed a systematic evaluation of clinical, instrumental, metabolic and biochemical data of a large cohort of patients affected by the most common MD in childhood: Leigh syndrome. We analyzed in this population, genotype-phenotype correlation in nDNA and mtDNA gene associated cases in order to identify diagnostic clues for mtDNA related Leigh syndrome. In genetically unresolved cases and various phenotypes (Leigh syndrome, leukodystropy..), we performed mtDNA screening using next-generation sequencing (NGS) technologies in order to assess, with high accuracy, point mutations and single or multiple large deletions, both in homoplasmic or heteroplasmic state. We identified both novel and known mutations associated to unexpected phenotype (i.e. CO3 gene). Our data better define and expand the phenotypic spectrum of mtDNA-MD in childhood.
Gale, Christopher Robert Keith. "Newborn feeding and infant phenotype". Thesis, Imperial College London, 2013. http://hdl.handle.net/10044/1/39361.
Texto completoLibros sobre el tema "Phenotype"
Zielonka, Stefan y Simon Krah, eds. Genotype Phenotype Coupling. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-4939-9853-1.
Texto completoZielonka, Stefan y Simon Krah, eds. Genotype Phenotype Coupling. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3279-6.
Texto completoSue, Malcolm y Goodship Timothy H. J, eds. Genotype to phenotype. 2a ed. Oxford: BIOS Scientific, 2001.
Buscar texto completovan, Gils Jan A., ed. The flexible phenotype: Towards a body-centred integration of ecology, physiology, and behaviour. Oxford: Oxford University Press, 2010.
Buscar texto completoFeldbauer, Roman. Machine Learning for Microbial Phenotype Prediction. Wiesbaden: Springer Fachmedien Wiesbaden, 2016. http://dx.doi.org/10.1007/978-3-658-14319-0.
Texto completoSavagner, Pierre. Rise and Fall of Epithelial Phenotype. Boston, MA: Springer US, 2005. http://dx.doi.org/10.1007/0-387-28671-3.
Texto completo1947-, Friedman J. M. y Riccardi Vincent M. 1940-, eds. Neurofibromatosis: Phenotype, natural history, and pathogenesis. 3a ed. Baltimore: Johns Hopkins University Press, 1999.
Buscar texto completoE, Eichner June, ed. Neurofibromatosis: Phenotype, natural history, and pathogenesis. Baltimore: Johns Hopkins University Press, 1986.
Buscar texto completoeditor, Fielding Roger A., Sieber Cornel editor, Vellas, B. J. (Bruno J.), editor y Nestlé Nutrition Institute, eds. Frailty: Pathophysiology, phenotype and patient care. Basel, Switzerland: Karger, 2015.
Buscar texto completoPontarotti, Pierre, ed. Evolutionary Biology: Biodiversification from Genotype to Phenotype. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-19932-0.
Texto completoCapítulos de libros sobre el tema "Phenotype"
Frank, J. Howard, J. Howard Frank, Michael C. Thomas, Allan A. Yousten, F. William Howard, Robin M. Giblin-davis, John B. Heppner et al. "Phenotype". En Encyclopedia of Entomology, 2841. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_2899.
Texto completoHahn, Martin y Rohan Palmer. "Phenotype". En Encyclopedia of Clinical Neuropsychology, 2673. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_1861.
Texto completoManrubia, Susanna C. "Phenotype". En Encyclopedia of Astrobiology, 1224–25. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1179.
Texto completoHahn, Martin y Rohan Palmer. "Phenotype". En Encyclopedia of Clinical Neuropsychology, 1934. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-79948-3_1861.
Texto completoMcCarthy, Jeanette. "Phenotype". En Encyclopedia of Behavioral Medicine, 1471–72. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-1005-9_713.
Texto completoNahler, Gerhard. "phenotype". En Dictionary of Pharmaceutical Medicine, 140. Vienna: Springer Vienna, 2009. http://dx.doi.org/10.1007/978-3-211-89836-9_1061.
Texto completoHahn, Martin y Rohan Palmer. "Phenotype". En Encyclopedia of Clinical Neuropsychology, 1. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56782-2_1861-2.
Texto completoManrubia, Susanna. "Phenotype". En Encyclopedia of Astrobiology, 1851–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1179.
Texto completoTsui, Nancy B. Y. y Johnson Y. N. Lau. "Phenotype". En Encyclopedia of Gerontology and Population Aging, 1–5. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-69892-2_939-1.
Texto completoSander, Jana. "Phenotype". En Encyclopedia of Child Behavior and Development, 1084. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-0-387-79061-9_2134.
Texto completoActas de conferencias sobre el tema "Phenotype"
Liu, Weizhen, Jiayu Tan, Guangyu Lan, Ao Li, Dongye Li, Le Zhao, Xiaohui Yuan y Nanqing Dong. "Benchmarking Fish Dataset and Evaluation Metric in Keypoint Detection - Towards Precise Fish Morphological Assessment in Aquaculture Breeding". En Thirty-Third International Joint Conference on Artificial Intelligence {IJCAI-24}. California: International Joint Conferences on Artificial Intelligence Organization, 2024. http://dx.doi.org/10.24963/ijcai.2024/816.
Texto completoHartmann, Morten y Tim Goedeweeck. "Adapting a Genotype-phenotype Mapping to Phenotypic Complexity". En 2009 NASA/ESA Conference on Adaptive Hardware and Systems (AHS). IEEE, 2009. http://dx.doi.org/10.1109/ahs.2009.47.
Texto completoPeng, Jiajie, Weiwei Hui y Xuequn Shang. "Measuring phenotype-phenotype similarity through the interactome". En 2017 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2017. http://dx.doi.org/10.1109/bibm.2017.8217911.
Texto completoTsvelaya, V. A., M. M. Slotvitsky, A. A. Aitova, S. A. Romanova y K. I. Agladze. "TISSUE ENGINEERING AS A TOOL FOR RESEARCH AND DEVELOPMENT OF POTENTIAL THERAPIES FOR THE PROCESSES OF ARRHYTHMIAS". En X Международная конференция молодых ученых: биоинформатиков, биотехнологов, биофизиков, вирусологов и молекулярных биологов — 2023. Novosibirsk State University, 2023. http://dx.doi.org/10.25205/978-5-4437-1526-1-219.
Texto completoPeng, Jiajie, Hansheng Xue, Yukai Shao, Xuequn Shang, Yadong Wang y Jin Chen. "Measuring phenotype semantic similarity using Human Phenotype Ontology". En 2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2016. http://dx.doi.org/10.1109/bibm.2016.7822617.
Texto completoMorales, F. L., C. Gao, T. Stoeger, A. Pawlowski, P. Nannapaneni, D. H. Schneider, M. Kang et al. "Capturing Phenotypic Manifestations of Severe Pneumonia Through the Human Phenotype Ontology". En American Thoracic Society 2022 International Conference, May 13-18, 2022 - San Francisco, CA. American Thoracic Society, 2022. http://dx.doi.org/10.1164/ajrccm-conference.2022.205.1_meetingabstracts.a5150.
Texto completoOtter, Tim. "Genotype, phenotype and ontogeny". En the 2005 workshops. New York, New York, USA: ACM Press, 2005. http://dx.doi.org/10.1145/1102256.1102323.
Texto completoGKOUTOS, G. V., E. C. J. GREEN, A. M. MALLON, J. M. HANCOCK y D. DAVIDSON. "BUILDING MOUSE PHENOTYPE ONTOLOGIES". En Proceedings of the Pacific Symposium. WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812704856_0018.
Texto completoWATERS, DENNIS P. "LANGUAGE AS EXTENDED PHENOTYPE?" En Proceedings of the 8th International Conference (EVOLANG8). WORLD SCIENTIFIC, 2010. http://dx.doi.org/10.1142/9789814295222_0122.
Texto completoFerri, Sebastian, Ramona Sorrentino, Carlo Chessari, Giovanni Terranova, Teresa Augelletti, Raffaele Campisi, Enrico Heffler, Nunzio Crimi y Sabrina Genco. "Bronchiectasis: understanding the phenotype". En ERS International Congress 2017 abstracts. European Respiratory Society, 2017. http://dx.doi.org/10.1183/1393003.congress-2017.pa3594.
Texto completoInformes sobre el tema "Phenotype"
Daniel W McDonald y Ronald B Michaels. Plant Phenotype Characterization System. Office of Scientific and Technical Information (OSTI), septiembre de 2005. http://dx.doi.org/10.2172/850165.
Texto completoDubbin, K. R., D. R. Gray, K. A. Anderson y M. L. Moya. Metamaterials for Mechanically Directing Cell Phenotype. Office of Scientific and Technical Information (OSTI), abril de 2020. http://dx.doi.org/10.2172/1614964.
Texto completoKoutcher, Jason. Imaging Prostate Cancer (Pca) Phenotype and Evolution. Fort Belvoir, VA: Defense Technical Information Center, octubre de 2014. http://dx.doi.org/10.21236/ada612861.
Texto completoWalker, Cheryl. TSC2 Happloinsufficiency Leads to a Mutator Phenotype. Fort Belvoir, VA: Defense Technical Information Center, noviembre de 2007. http://dx.doi.org/10.21236/ada481229.
Texto completoLelievre, Sophie A. How Does Nuclear Organization Maintain Normal Mammary Phenotype? Fort Belvoir, VA: Defense Technical Information Center, marzo de 2005. http://dx.doi.org/10.21236/ada436884.
Texto completoLeievre, Sophie A. How Does Nuclear Organization Maintain Normal Mammary Phenotype. Fort Belvoir, VA: Defense Technical Information Center, julio de 2001. http://dx.doi.org/10.21236/ada396710.
Texto completoMartin, Sandra L. y Hannah V. Carey. Translating the Hibernation Phenotype to Human Trauma Care. Fort Belvoir, VA: Defense Technical Information Center, septiembre de 2008. http://dx.doi.org/10.21236/ada500737.
Texto completoLelievre, Sophie A. How Does Nuclear Organization Maintain Normal Mammary Phenotype. Fort Belvoir, VA: Defense Technical Information Center, julio de 2002. http://dx.doi.org/10.21236/ada408754.
Texto completoWilson, Sarah, Ingrid Scheffer, Valerie Yap, Alan Connelly y Neil McLachlan. Identifying Neurobiological Markers of the Broader Autism Phenotype. Fort Belvoir, VA: Defense Technical Information Center, septiembre de 2013. http://dx.doi.org/10.21236/ada601230.
Texto completoWilson, Sarah, Ingrid Scheffer y Valerie Yap. Identifying Neurobiological Markers of the Broader Autism Phenotype. Fort Belvoir, VA: Defense Technical Information Center, enero de 2015. http://dx.doi.org/10.21236/ada621217.
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