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1دورية أكاديمية
مصطلحات موضوعية: Medicine, Microbiology, Genetics, Evolutionary Biology, Ecology, Infectious Diseases, Biological Sciences not elsewhere classified, non-identical environments, Pseudomonas species, Pel exopolysaccharide, Mutated regions, SBW 25, Pseudomonas protegens Pf -5, promoter regions, adaptive phenotype, evolution, testable predictions, genotype-to-phenotype map, wrinkly spreader system, mutation, diguanylate cyclases, gene, forecasting, Pseudomonas protegens, non-identical environment, Pseudomonas fluorescens SBW 25, influence outcomes, SBW 25 system, mutant, air-liquid interface
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2
المؤلفون: Libby, Eric, Lind, Peter A.
المصدر: Bio-protocol. 9(20)
مصطلحات موضوعية: Evolutionary forecasting, Mathematical modeling, Adaptation, Mutation, Evolution, Genotype-to-phenotype map, evolutionär genetik, evolutionary genetics, Mathematics, matematik
وصف الملف: electronic
الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-164303Test
https://doi.org/10.21769/BioProtoc.3407Test
https://umu.diva-portal.org/smash/get/diva2:1362757/FULLTEXT01.pdfTest -
3
المؤلفون: Emine Kartal Baykan, Ceren Alavanda, Erdal Kurnaz, Pinar Ata, Oguzhan Yarali, Ayberk Turkyilmaz, Atilla Cayir, Dilek Gogas Yavuz
المصدر: Metabolic Syndrome and Related Disorders. 19:340-346
مصطلحات موضوعية: Adult, medicine.medical_specialty, Turkey, Endocrinology, Diabetes and Metabolism, Familial hypercholesterolemia, Cohort Studies, Hyperlipoproteinemia Type II, symbols.namesake, Internal medicine, Internal Medicine, Humans, Medicine, Child, Lipoprotein cholesterol, Heterogeneous group, business.industry, medicine.disease, Endocrinology, Receptors, LDL, Mutation, Cohort, LDL receptor, Mendelian inheritance, symbols, lipids (amino acids, peptides, and proteins), Genotype to phenotype, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::917e09b90c2cae45765ca6925d4185d8Test
https://doi.org/10.1089/met.2021.0004Test -
4
المؤلفون: Bin Wang, Xia Fang, Yu An, Ruiji Guo, Jiateng Zhou, Hailei Mao, Bin Sun
المصدر: Frontiers in Genetics, Vol 12 (2021)
Frontiers in Geneticsمصطلحات موضوعية: Genetics, Mutation, synpolydactyly, Brachydactyly, Biology, QH426-470, medicine.disease_cause, medicine.disease, genotype and phenotype, Synpolydactyly, Genotype-phenotype distinction, HOXD13, polyalanine extension, embryonic structures, medicine, Molecular Medicine, Missense mutation, HoxD13, Syndactyly, transcription regulation, Genetics (clinical), Exome sequencing, Original Research
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5b436b364517f4ab94ce6d2dd7adb40Test
https://www.frontiersin.org/articles/10.3389/fgene.2021.731278/fullTest -
5
المؤلفون: Hamid Alinejad-Rokny, Amir Mohseni, Abdollah Dehzangi, Amin Beheshti, Hamid R. Rabiee, Amin Ghareyazi, Hamed Dashti
المصدر: Cancers, Vol 13, Iss 4376, p 4376 (2021)
Cancers
Volume 13
Issue 17مصطلحات موضوعية: Genetics, Cancer Research, Mutation, biology, Point mutation, pancreatic cancer, Cancer, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, personalized medicine, medicine.disease_cause, medicine.disease, therapeutic targets, Genome, Phenotype, Article, Oncology, Pancreatic cancer, medicine, biology.protein, somatic point mutations, Epidermal growth factor receptor, cancer subtype identification, Gene, RC254-282, genotype and phenotype characterization
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fea22cd644b0cee2f2d22563f37b7c8bTest
https://www.mdpi.com/2072-6694/13/17/4376Test -
6
المؤلفون: Daniela Ricci, Filippo Amore, Marco Tartaglia, Eugenio Mercuri, Annabella Salerni, Daniela Chieffo, Giuseppe Zampino, Lorenzo Orazi, Chiara Leoni, Simona Leone, Cristiana Agazzi, Roberta Onesimo, Maria Petrianni
المصدر: Genes
Genes, Vol 12, Iss 972, p 972 (2021)
Volume 12
Issue 7مصطلحات موضوعية: 0301 basic medicine, Male, Pediatrics, genetic structures, Disease, QH426-470, Correlation, CHD7, Cohort Studies, CHARGE syndrome, 0302 clinical medicine, genotype–ocular-phenotype, Prospective Studies, Child, Genetics (clinical), media_common, Coloboma, VISIOCHARGE, rare diseases, DNA-Binding Proteins, Phenotype, Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA, Child, Preschool, Female, Cohort study, Adult, medicine.medical_specialty, Adolescent, Genotype, media_common.quotation_subject, Nonsense, Affect (psychology), Article, Frameshift mutation, 03 medical and health sciences, Young Adult, medicine, Genetics, visual function, Humans, Genetic Predisposition to Disease, Genetic Association Studies, business.industry, DNA Helicases, medicine.disease, eye diseases, Ophthalmology, 030104 developmental biology, Mutation, business, 030217 neurology & neurosurgery
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ce16ee769ac3f67f364c41949448dd6Test
http://europepmc.org/articles/PMC8303791Test -
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المؤلفون: Marc Corral-Juan, Jon Infante, Ana L. Pelayo-Negro, Antonio Sánchez-Rodríguez, Leire Manrique, Antoni Matilla-Dueñas
المساهمون: Universidad de Cantabria
المصدر: Movement Disorders, 2021; Volume8, Issue6; Pages 969-971
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Mov Disord Clin Practمصطلحات موضوعية: Genetics, Myoclonus, Ataxia, Atp13a2 gene, business.industry, Action myoclonus, Kufor-Rakeb, Letters: Genotype and Phenotype, Neurology, Mutation (genetic algorithm), Mutation, medicine, Neurology (clinical), medicine.symptom, ATP13A2, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ea006da174546988fc95156c1b2762eTest
http://hdl.handle.net/10902/24021Test -
8
المؤلفون: Darren G. Monckton
المصدر: Journal of Huntington's Disease
مصطلحات موضوعية: 0301 basic medicine, DNA Repair, DNA mismatch repair, Disease, Review, Biology, medicine.disease_cause, History, 21st Century, Germline, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Huntington's disease, Somatic expansion, medicine, Genetics, Animals, Humans, CAG repeat, Mutation, Mechanism (biology), Anticipation, Genetic, History, 19th Century, History, 20th Century, genotype to phenotype, medicine.disease, Human genetics, 030104 developmental biology, Huntington Disease, Anticipation (genetics), anticipation, Neurology (clinical), mutation, Trinucleotide Repeat Expansion, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a01c960813043cee777c7ad2936c25fTest
https://pubmed.ncbi.nlm.nih.gov/33579863Test -
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المؤلفون: Ruth Nussinov, Lang Li, Feixiong Cheng, Timothy A. Chan, Junfei Zhao, William R. Martin, Yadi Zhou, Jiansong Fang, Charis Eng
المصدر: Genome Biology
Genome Biology, Vol 22, Iss 1, Pp 1-18 (2021)مصطلحات موضوعية: lcsh:QH426-470, Genotype, Computational biology, Biology, DNA sequencing, Database, Nodetic, Protein-protein interaction, Somatic mutations, Neoplasms, Drug Discovery, medicine, Humans, Genomic medicine, Exome, Protein Interaction Domains and Motifs, Allele, lcsh:QH301-705.5, Alleles, Exome sequencing, Drug discovery, Computational Biology, Cancer, Genomics, medicine.disease, Human genetics, lcsh:Genetics, Phenotype, lcsh:Biology (General), Mutanome, Mutation, Edgetic, Genotype to phenotype, Protein Processing, Post-Translational, Precision cancer medicine
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::915fae2758d9fe5171c2978ca58f19a9Test
https://doi.org/10.1186/s13059-021-02269-3Test -
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مصطلحات موضوعية: Medicine, Microbiology, Genetics, Evolutionary Biology, Ecology, Infectious Diseases, Biological Sciences not elsewhere classified, non-identical environments, Pseudomonas species, Pel exopolysaccharide, Mutated regions, SBW 25, Pseudomonas protegens Pf -5, promoter regions, adaptive phenotype, evolution, testable predictions, genotype-to-phenotype map, wrinkly spreader system, mutation, diguanylate cyclases, gene, forecasting, Pseudomonas protegens, non-identical environment, Pseudomonas fluorescens SBW 25, influence outcomes, SBW 25 system, mutant, air-liquid interface