المؤلفون: Marion A.L. Picard, Fiona Leblay, Cécile Cassan, Anouk Willemsen, Josquin Daron, Frédérique Bauffe, Mathilde Decourcelle, Antonin Demange, Ignacio G. Bravo

المساهمون: Virostyle (MIVEGEC-Virostyle), Perturbations, Evolution, Virulence (PEV), Maladies infectieuses et vecteurs : écologie, génétique, évolution et contrôle (MIVEGEC), Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [France-Sud])-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [France-Sud])-Université de Montpellier (UM)-Maladies infectieuses et vecteurs : écologie, génétique, évolution et contrôle (MIVEGEC), Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [France-Sud])-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [France-Sud])-Université de Montpellier (UM), Plateforme de Protéomique Fonctionnelle (FPP), Pôle Protéome de Montpellier (PPM), Université de Montpellier (UM)-Université de Montpellier (UM)

المصدر: Protein Science
Protein Science, 2023, ⟨10.1002/pro.4576⟩

مصطلحات موضوعية: Synonymous codon recoding, heterologous gene expression, translation, genotype to phenotype, mutation-selection, [SDV]Life Sciences [q-bio], Molecular Biology, Biochemistry

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73f979fe4637a71e05196a21beb2dd71Test
https://doi.org/10.1002/pro.4576Test

المؤلفون: John L. Rinn, Daniel Andergassen

المصدر: Nature Reviews Genetics. 23:229-243

مصطلحات موضوعية: Genetics, ved/biology, Transgene, ved/biology.organism_classification_rank.species, RNA, Biology, Genome editing, In vivo, Human genome, Genotype to phenotype, Model organism, Molecular Biology, Genetics (clinical), Function (biology)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::5ea8bd5e953438f29ac684869c7fe1d6Test
https://doi.org/10.1038/s41576-021-00427-8Test

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

المؤلفون: Diogo Reis‐Carneiro, Conceição Robalo, Mário Laço, Marie Vidailhet, Luísa Diogo

المصدر: Mov Disord Clin Pract

مصطلحات موضوعية: Neurology, Neurology (clinical), Letters: Genotype and Phenotype

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7836f4dc5e8f1457bf36f1671735fbeTest
https://doi.org/10.1002/mdc3.13450Test

المؤلفون: Bandari Mahesh, Varun Kumar Singh, Abhishek Pathak, Anand Kumar, Rameshwar Nath Chaurasia

المصدر: Mov Disord Clin Pract

مصطلحات موضوعية: Neurology, Neurology (clinical), Letters: Genotype and Phenotype

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9ab0ce611d576e37677210e51388e7cTest
https://doi.org/10.1002/mdc3.13419Test

المؤلفون: Yorck Hellenbroich, Norbert Brüggemann, Katja Lohmann, Martje G. Pauly, Kathrin Grundmann-Hauser, Frauke Hinrichs

المصدر: Mov Disord Clin Pract

مصطلحات موضوعية: Leukoencephalopathy, Pathology, medicine.medical_specialty, Neurology, business.industry, Hereditary spastic paraplegia, medicine, Neurology (clinical), business, medicine.disease, Compound heterozygosity, Letters: Genotype and Phenotype

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87d6d166dc5930ca21b068f4bd0b0525Test
https://doi.org/10.1002/mdc3.13258Test

المؤلفون: Yin Hoon Chew, Daniel D. Seaton, Virginie Mengin, Anna Flis, Sam T. Mugford, Gavin M. George, Michael Moulin, Alastair Hume, Samuel C. Zeeman, Teresa B. Fitzpatrick, Alison M. Smith, Mark Stitt, Andrew J. Millar

المصدر: in silico Plants, 4 (2)
Chew, Y H, Seaton, D D, Mengin, V, Flis, A, Mugford, S T, George, G M, Moulin, M, Hume, A, Zeeman, S C, Fitzpatrick, T B, Smith, A M, Stitt, M & Millar, A J 2022, ' The Arabidopsis Framework Model version 2 predicts the organism-level effects of circadian clock gene mis-regulation ', In Silico Plants, vol. 4, no. 2, diac010 . https://doi.org/10.1093/insilicoplants/diac010Test

مصطلحات موضوعية: 0106 biological sciences, Systems biology, data sharing, Circadian clock, ved/biology.organism_classification_rank.species, gene regulatory network, Plant Science, Biology, 01 natural sciences, Biochemistry, Genetics and Molecular Biology (miscellaneous), 03 medical and health sciences, Arabidopsis, Circadian rhythm, Allele, Data sharing, gene regulatory networks, genotype to phenotype, mathematical model, metabolism, open research, photosynthesis, Model organism, 030304 developmental biology, Genetics, 0303 health sciences, ved/biology, biology.organism_classification, Phenotype, CLOCK, Modeling and Simulation, Agronomy and Crop Science, 010606 plant biology & botany

وصف الملف: application/application/pdf; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55cba69fad9b9f229c730833c0cfcb0dTest
https://doi.org/10.1093/insilicoplants/diac010Test

المؤلفون: Arata Horii, Aiko Isami, Hironori Baba, Masahiro Uemura, Takeshi Ikeuchi, Osamu Onodera, Tomone Taneda, Yo Higuchi, Takuya Konno, Masato Kanazawa

المصدر: Mov Disord Clin Pract

مصطلحات موضوعية: NEURONAL INTRANUCLEAR INCLUSION DISEASE, Neurology, Voice tremor, business.industry, Medicine, Neurology (clinical), business, Neuroscience, Letters: Genotype and Phenotype

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb1035f9a365232bea21618ceefa7a2Test
https://doi.org/10.1002/mdc3.13382Test

المؤلفون: Annapurna Kuppa, Yuri V. Sergeev

المصدر: Journal of analytical & pharmaceutical research

مصطلحات موضوعية: Genetics, molecular modeling, MYO7A, computational mutagenesis, Usher syndrome, Genetic disorder, Mutagenesis (molecular biology technique), genetic mutations, Biology, medicine.disease, genotype-to-phenotype, Article, inherited eye disease, Protein structure, Usher syndrome type 1B, atomic structure, Myosin VIIa, Retinitis pigmentosa, otorhinolaryngologic diseases, medicine, Missense mutation, Homology modeling

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fde92047ffe4d5937178829fa1a1129bTest
https://doi.org/10.15406/japlr.2021.10.00364Test

المؤلفون: Caryn Babaian, Sudhir Kumar

المصدر: The American Biology Teacher. 83:138-146

مصطلحات موضوعية: 0301 basic medicine, Cognitive science, Ecology (disciplines), 05 social sciences, 050301 education, Variation (game tree), Mega, Agricultural and Biological Sciences (miscellaneous), Education, 03 medical and health sciences, 030104 developmental biology, Molecular evolution, Genotype to phenotype, General Agricultural and Biological Sciences, 0503 education, Apex predator

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::44572561defd11226967c9877ff8a53aTest
https://doi.org/10.1525/abt.2021.83.3.138Test