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Artykuły w czasopismach na temat "Phenotype"
Moser, Lukas, Silvan Hess, Henrik Behrend i 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, nr 5_suppl4 (1.05.2020): 2325967120S0030. http://dx.doi.org/10.1177/2325967120s00300.
Pełny tekst źródłaRoemer, F., J. Collins, T. Neogi, M. Crema i 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 (czerwiec 2020): 808.1–809. http://dx.doi.org/10.1136/annrheumdis-2020-eular.1802.
Pełny tekst źródłaCarmina, Enrico, i 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, nr 10 (25.09.2022): 2313. http://dx.doi.org/10.3390/diagnostics12102313.
Pełny tekst źródłaPostoeva, A. V., I. V. Dvoryashina, A. V. Kudryavtsev i V. A. Postoev. "Prevalence of metabolic phenotypes among citizens of Arctic area of the Russian Federation (in Arkhangelsk city setting)". Obesity and metabolism 20, nr 1 (22.05.2023): 34–42. http://dx.doi.org/10.14341/omet12926.
Pełny tekst źródłaLusczek, Elizabeth R., Nicholas E. Ingraham, Basil S. Karam, Jennifer Proper, Lianne Siegel, Erika S. Helgeson, Sahar Lotfi-Emran i in. "Characterizing COVID-19 clinical phenotypes and associated comorbidities and complication profiles". PLOS ONE 16, nr 3 (31.03.2021): e0248956. http://dx.doi.org/10.1371/journal.pone.0248956.
Pełny tekst źródłade Koning-Tijssen, M. "One gene many phenotypes, one phenotype many genes". Journal of the Neurological Sciences 405 (październik 2019): 11. http://dx.doi.org/10.1016/j.jns.2019.10.028.
Pełny tekst źródłaXiromerisiou, Georgia, Henry Houlden, Nikolaos Scarmeas, Maria Stamelou, Eleanna Kara, John Hardy, Andrew J. Lees i in. "THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations". Movement Disorders 27, nr 10 (17.08.2012): 1290–94. http://dx.doi.org/10.1002/mds.25146.
Pełny tekst źródłaFerguson, Amy Christina, Sophie Thrippleton, David Henshall, Ed Whittaker, Bryan Conway, Malcolm MacLeod, Rainer Malik i in. "Frequency and Phenotype Associations of Rare Variants in 5 Monogenic Cerebral Small Vessel Disease Genes in 200,000 UK Biobank Participants". Neurology Genetics 8, nr 5 (24.08.2022): e200015. http://dx.doi.org/10.1212/nxg.0000000000200015.
Pełny tekst źródłaZhou, Xue, Keijiro Nakamura, Naohiko Sahara, Masako Asami, Yasutake Toyoda, Yoshinari Enomoto, Hidehiko Hara i in. "Exploring and Identifying Prognostic Phenotypes of Patients with Heart Failure Guided by Explainable Machine Learning". Life 12, nr 6 (24.05.2022): 776. http://dx.doi.org/10.3390/life12060776.
Pełny tekst źródłaSpring, Michele D., Jason C. Sousa, Qigui Li, Christian A. Darko, Meshell N. Morrison, Sean R. Marcsisin, Kristin T. Mills i in. "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, nr 11 (24.09.2019): 1761–70. http://dx.doi.org/10.1093/infdis/jiz386.
Pełny tekst źródłaRozprawy doktorskie na temat "Phenotype"
Moses, Lorraine. "Phenotypic factors influencing Mycobacterium tuberculosis phenotype". Thesis, Stellenbosch : Stellenbosch University, 2002. http://hdl.handle.net/10019.1/52997.
Pełny tekst źródłaSailer, Zachary. "Predicting Phenotypes in Sparsely Sampled Genotype-Phenotype Maps". Thesis, University of Oregon, 2019. http://hdl.handle.net/1794/24231.
Pełny tekst źródła2020-01-11
Arbon, Jed. "Phenotype-genotype correlation between the Hippo pathway and 3D craniofacial phenotypes". Thesis, University of Iowa, 2016. https://ir.uiowa.edu/etd/3042.
Pełny tekst źródłaHabib, Farhat Abbas. "Genotype-phenotype correlation using phylogenetic trees". Columbus, Ohio : Ohio State University, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1187297400.
Pełny tekst źródłaBloomfield, Kelly Louise, i 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.
Pełny tekst źródłaBloomfield, 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.
Pełny tekst źródłaThesis (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.
Pełny tekst źródłaAlsbou, Mohammed. "Dissecting phenotype-genoype relationships". Thesis, University of Liverpool, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.443925.
Pełny tekst źródłaARDISSONE, 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.
Pełny tekst źródłaMitochondrial 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.
Pełny tekst źródłaKsiążki na temat "Phenotype"
Zielonka, Stefan, i Simon Krah, red. Genotype Phenotype Coupling. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-4939-9853-1.
Pełny tekst źródłaZielonka, Stefan, i Simon Krah, red. Genotype Phenotype Coupling. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3279-6.
Pełny tekst źródłaSue, Malcolm, i Goodship Timothy H. J, red. Genotype to phenotype. Wyd. 2. Oxford: BIOS Scientific, 2001.
Znajdź pełny tekst źródłavan, Gils Jan A., red. The flexible phenotype: Towards a body-centred integration of ecology, physiology, and behaviour. Oxford: Oxford University Press, 2010.
Znajdź pełny tekst źródłaFeldbauer, Roman. Machine Learning for Microbial Phenotype Prediction. Wiesbaden: Springer Fachmedien Wiesbaden, 2016. http://dx.doi.org/10.1007/978-3-658-14319-0.
Pełny tekst źródłaSavagner, Pierre. Rise and Fall of Epithelial Phenotype. Boston, MA: Springer US, 2005. http://dx.doi.org/10.1007/0-387-28671-3.
Pełny tekst źródła1947-, Friedman J. M., i Riccardi Vincent M. 1940-, red. Neurofibromatosis: Phenotype, natural history, and pathogenesis. Wyd. 3. Baltimore: Johns Hopkins University Press, 1999.
Znajdź pełny tekst źródłaE, Eichner June, red. Neurofibromatosis: Phenotype, natural history, and pathogenesis. Baltimore: Johns Hopkins University Press, 1986.
Znajdź pełny tekst źródłaeditor, Fielding Roger A., Sieber Cornel editor, Vellas, B. J. (Bruno J.), editor i Nestlé Nutrition Institute, red. Frailty: Pathophysiology, phenotype and patient care. Basel, Switzerland: Karger, 2015.
Znajdź pełny tekst źródłaPontarotti, Pierre, red. Evolutionary Biology: Biodiversification from Genotype to Phenotype. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-19932-0.
Pełny tekst źródłaCzęści książek na temat "Phenotype"
Frank, J. Howard, J. Howard Frank, Michael C. Thomas, Allan A. Yousten, F. William Howard, Robin M. Giblin-davis, John B. Heppner i in. "Phenotype". W Encyclopedia of Entomology, 2841. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_2899.
Pełny tekst źródłaHahn, Martin, i Rohan Palmer. "Phenotype". W Encyclopedia of Clinical Neuropsychology, 2673. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_1861.
Pełny tekst źródłaManrubia, Susanna C. "Phenotype". W Encyclopedia of Astrobiology, 1224–25. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1179.
Pełny tekst źródłaHahn, Martin, i Rohan Palmer. "Phenotype". W Encyclopedia of Clinical Neuropsychology, 1934. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-79948-3_1861.
Pełny tekst źródłaMcCarthy, Jeanette. "Phenotype". W 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.
Pełny tekst źródłaNahler, Gerhard. "phenotype". W Dictionary of Pharmaceutical Medicine, 140. Vienna: Springer Vienna, 2009. http://dx.doi.org/10.1007/978-3-211-89836-9_1061.
Pełny tekst źródłaHahn, Martin, i Rohan Palmer. "Phenotype". W Encyclopedia of Clinical Neuropsychology, 1. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56782-2_1861-2.
Pełny tekst źródłaManrubia, Susanna. "Phenotype". W Encyclopedia of Astrobiology, 1851–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1179.
Pełny tekst źródłaTsui, Nancy B. Y., i Johnson Y. N. Lau. "Phenotype". W 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.
Pełny tekst źródłaSander, Jana. "Phenotype". W Encyclopedia of Child Behavior and Development, 1084. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-0-387-79061-9_2134.
Pełny tekst źródłaStreszczenia konferencji na temat "Phenotype"
Liu, Weizhen, Jiayu Tan, Guangyu Lan, Ao Li, Dongye Li, Le Zhao, Xiaohui Yuan i Nanqing Dong. "Benchmarking Fish Dataset and Evaluation Metric in Keypoint Detection - Towards Precise Fish Morphological Assessment in Aquaculture Breeding". W 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.
Pełny tekst źródłaHartmann, Morten, i Tim Goedeweeck. "Adapting a Genotype-phenotype Mapping to Phenotypic Complexity". W 2009 NASA/ESA Conference on Adaptive Hardware and Systems (AHS). IEEE, 2009. http://dx.doi.org/10.1109/ahs.2009.47.
Pełny tekst źródłaPeng, Jiajie, Weiwei Hui i Xuequn Shang. "Measuring phenotype-phenotype similarity through the interactome". W 2017 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2017. http://dx.doi.org/10.1109/bibm.2017.8217911.
Pełny tekst źródłaTsvelaya, V. A., M. M. Slotvitsky, A. A. Aitova, S. A. Romanova i K. I. Agladze. "TISSUE ENGINEERING AS A TOOL FOR RESEARCH AND DEVELOPMENT OF POTENTIAL THERAPIES FOR THE PROCESSES OF ARRHYTHMIAS". W 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.
Pełny tekst źródłaPeng, Jiajie, Hansheng Xue, Yukai Shao, Xuequn Shang, Yadong Wang i Jin Chen. "Measuring phenotype semantic similarity using Human Phenotype Ontology". W 2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2016. http://dx.doi.org/10.1109/bibm.2016.7822617.
Pełny tekst źródłaMorales, F. L., C. Gao, T. Stoeger, A. Pawlowski, P. Nannapaneni, D. H. Schneider, M. Kang i in. "Capturing Phenotypic Manifestations of Severe Pneumonia Through the Human Phenotype Ontology". W 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.
Pełny tekst źródłaOtter, Tim. "Genotype, phenotype and ontogeny". W the 2005 workshops. New York, New York, USA: ACM Press, 2005. http://dx.doi.org/10.1145/1102256.1102323.
Pełny tekst źródłaGKOUTOS, G. V., E. C. J. GREEN, A. M. MALLON, J. M. HANCOCK i D. DAVIDSON. "BUILDING MOUSE PHENOTYPE ONTOLOGIES". W Proceedings of the Pacific Symposium. WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812704856_0018.
Pełny tekst źródłaWATERS, DENNIS P. "LANGUAGE AS EXTENDED PHENOTYPE?" W Proceedings of the 8th International Conference (EVOLANG8). WORLD SCIENTIFIC, 2010. http://dx.doi.org/10.1142/9789814295222_0122.
Pełny tekst źródłaFerri, Sebastian, Ramona Sorrentino, Carlo Chessari, Giovanni Terranova, Teresa Augelletti, Raffaele Campisi, Enrico Heffler, Nunzio Crimi i Sabrina Genco. "Bronchiectasis: understanding the phenotype". W ERS International Congress 2017 abstracts. European Respiratory Society, 2017. http://dx.doi.org/10.1183/1393003.congress-2017.pa3594.
Pełny tekst źródłaRaporty organizacyjne na temat "Phenotype"
Daniel W McDonald i Ronald B Michaels. Plant Phenotype Characterization System. Office of Scientific and Technical Information (OSTI), wrzesień 2005. http://dx.doi.org/10.2172/850165.
Pełny tekst źródłaDubbin, K. R., D. R. Gray, K. A. Anderson i M. L. Moya. Metamaterials for Mechanically Directing Cell Phenotype. Office of Scientific and Technical Information (OSTI), kwiecień 2020. http://dx.doi.org/10.2172/1614964.
Pełny tekst źródłaKoutcher, Jason. Imaging Prostate Cancer (Pca) Phenotype and Evolution. Fort Belvoir, VA: Defense Technical Information Center, październik 2014. http://dx.doi.org/10.21236/ada612861.
Pełny tekst źródłaWalker, Cheryl. TSC2 Happloinsufficiency Leads to a Mutator Phenotype. Fort Belvoir, VA: Defense Technical Information Center, listopad 2007. http://dx.doi.org/10.21236/ada481229.
Pełny tekst źródłaLelievre, Sophie A. How Does Nuclear Organization Maintain Normal Mammary Phenotype? Fort Belvoir, VA: Defense Technical Information Center, marzec 2005. http://dx.doi.org/10.21236/ada436884.
Pełny tekst źródłaLeievre, Sophie A. How Does Nuclear Organization Maintain Normal Mammary Phenotype. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2001. http://dx.doi.org/10.21236/ada396710.
Pełny tekst źródłaMartin, Sandra L., i Hannah V. Carey. Translating the Hibernation Phenotype to Human Trauma Care. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 2008. http://dx.doi.org/10.21236/ada500737.
Pełny tekst źródłaLelievre, Sophie A. How Does Nuclear Organization Maintain Normal Mammary Phenotype. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2002. http://dx.doi.org/10.21236/ada408754.
Pełny tekst źródłaWilson, Sarah, Ingrid Scheffer, Valerie Yap, Alan Connelly i Neil McLachlan. Identifying Neurobiological Markers of the Broader Autism Phenotype. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 2013. http://dx.doi.org/10.21236/ada601230.
Pełny tekst źródłaWilson, Sarah, Ingrid Scheffer i Valerie Yap. Identifying Neurobiological Markers of the Broader Autism Phenotype. Fort Belvoir, VA: Defense Technical Information Center, styczeń 2015. http://dx.doi.org/10.21236/ada621217.
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