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المؤلفون: Dawei Jiang, Hongli Du, Shuhua Li, Meiling Hu, Jerome R Lon, Wei Liu, Binbin Xi, Yuting Huang, Yuhuan Meng, Yimo Qu, Shudai Lin, Lizhen Huang, Yunmeng Bai
المصدر: Computational and Structural Biotechnology Journal, Vol 19, Iss, Pp 1976-1985 (2021)
Computational and Structural Biotechnology Journalمصطلحات موضوعية: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Biophysics, Computational biology, Biology, Biochemistry, Genome, Article, 03 medical and health sciences, 0302 clinical medicine, Structural Biology, Epidemic trends, Genetics, Key mutations, 030304 developmental biology, ComputingMethodologies_COMPUTERGRAPHICS, 0303 health sciences, SARS-CoV-2, Haplotype, Automated tool, Pathogenicity, Computer Science Applications, Candidate key, 030220 oncology & carcinogenesis, New mutation, Mutation (genetic algorithm), Key (cryptography), TP248.13-248.65, Biotechnology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c22ad809cb934c122dd1cb5313719ea2Test
http://www.sciencedirect.com/science/article/pii/S2001037021001082Test -
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المؤلفون: Hongchun Xiong, Shirong Zhao, Lu-xiang Liu, Jiayu Gu, Hui-jun Guo, Linshu Zhao, Yongdun Xie
المصدر: Mutation breeding, genetic diversity and crop adaptation to climate change
مصطلحات موضوعية: Crop, Agronomy, New mutation, food and beverages, Biology, China
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::2b1625b944a20bee48a9c3632a1aa3bcTest
https://doi.org/10.1079/9781789249095.0005Test -
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المؤلفون: Elina Bychkova, E. A. Filippova, N. A. Golubeva, A. V. Markov, L. O. Sangina
المصدر: Russian Journal of Genetics. 56:108-111
مصطلحات موضوعية: 0106 biological sciences, Genetics, 0303 health sciences, CATS, engineering.material, Biology, Hair follicle, 01 natural sciences, Phenotype, Breed, Human genetics, 03 medical and health sciences, medicine.anatomical_structure, Carnelian, New mutation, engineering, medicine, Mc1r gene, 030304 developmental biology, 010606 plant biology & botany
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::ab439d6bcdbf16cb3dc087531623be89Test
https://doi.org/10.1134/s1022795420010020Test -
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المؤلفون: Sedeer El-Showk
المصدر: Nature Middle East.
مصطلحات موضوعية: Genetics, New mutation, Biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::2e8bb69f6fa96cf3e1977f8e98b1df61Test
https://doi.org/10.1038/nmiddleeast.2021.78Test -
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المؤلفون: Meiling Hu, Yuhuan Meng, Shudai Lin, Wei Liu, Jerome R Lon, Yunmeng Bai, Binbin Xi, Yuting Huang, Yimo Qu, Dawei Jiang, Shuhua Li, Hongli Du
مصطلحات موضوعية: Combinatorial analysis, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), New mutation, Haplotype, Mutation (genetic algorithm), Key (cryptography), Computational biology, Biology, Pathogenicity, Genome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::f8e205a811295c65dea45ec04d43dae2Test
https://doi.org/10.1101/2020.12.24.424271Test -
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المؤلفون: Charles Marques Lourenço, Jaime Eduardo Cecílio Hallak, Wilson Marques, Pedro J. Tomaselli, Silmara P. Gouvea, Fernanda Barbosa Figueiredo, Silvana Giuliatti, Wilson A. Silva, Anna Paula Paranhos Miranda Covaleski
المصدر: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USPمصطلحات موضوعية: 0301 basic medicine, Male, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Population, Prevalence, Nerve Tissue Proteins, Disease, Biology, Cohort Studies, 03 medical and health sciences, Tooth disease, Young Adult, 0302 clinical medicine, Recessive inheritance, Charcot-Marie-Tooth Disease, Humans, education, Child, Gene, Genetics (clinical), Likely pathogenic, Genetics, Guanine Deaminase, education.field_of_study, MUTAÇÃO GENÉTICA, Axons, nervous system diseases, Pedigree, 030104 developmental biology, Phenotype, Neurology, Pediatrics, Perinatology and Child Health, New mutation, Mutation, Female, Neurology (clinical), 030217 neurology & neurosurgery, Brazil
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef65dc156ae331e9a88bd20c1ef50efbTest
https://pubmed.ncbi.nlm.nih.gov/33903021Test -
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المصدر: IEEE/ACM transactions on computational biology and bioinformatics. 18(6)
مصطلحات موضوعية: Stochastic Processes, DNA Copy Number Variations, Somatic cell, Applied Mathematics, Computational Biology, Bayes Theorem, Computational biology, Biology, Tumor heterogeneity, Genetic Heterogeneity, Model parameter, Feature (computer vision), Neoplasms, Mutation (genetic algorithm), New mutation, Genotype, Mutation, Genetics, Humans, Gene, Monte Carlo Method, Algorithms, Biotechnology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20f8e5a5a48196d7ddf692bd4fa5965eTest
https://pubmed.ncbi.nlm.nih.gov/32070995Test -
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المؤلفون: Lavrentii G. Danilov, Andrew G. Matveenko, Varvara E. Ryzhkova, Mikhail V. Belousov, Olga I. Poleshchuk, Daria V. Likholetova, Petr A. Sokolov, Nina A. Kasyanenko, Andrey V. Kajava, Galina A. Zhouravleva, Stanislav A. Bondarev
المساهمون: Centre de recherche en Biologie Cellulaire (CRBM), Université Montpellier 2 - Sciences et Techniques (UM2)-Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM)-Université Montpellier 1 (UM1), St Petersburg State University (SPbU)
المصدر: Frontiers in Molecular Neuroscience
Frontiers in Molecular Neuroscience, Frontiers Media, 2019, 12, pp.274. ⟨10.3389/fnmol.2019.00274⟩
Frontiers in Molecular Neuroscience, Vol 12 (2019)مصطلحات موضوعية: 0301 basic medicine, Amyloid, In silico, [SDV]Life Sciences [q-bio], Saccharomyces cerevisiae, macromolecular substances, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, medicine.disease_cause, Fibril, lcsh:RC321-571, prion, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, medicine, Molecular Biology, Inhibitory effect, lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry, ArchCandy, ComputingMilieux_MISCELLANEOUS, chemistry.chemical_classification, Mutation, biology, Chemistry, [PSI+], amyloid, SUP35 mutation, biology.organism_classification, [SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM], Amino acid, 030104 developmental biology, New mutation, Biophysics, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40b4b2ce532f3775bb300419ae6b4acbTest
https://hal.umontpellier.fr/hal-02414139/file/fnmol-12-00274.pdfTest -
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المؤلفون: Alessandro Malandrini, Anna Rubegni, Maria Teresa Dotti, Teresa Anna Cantisani, Andrea Mignarri, Claudia Nesti, Antonio Federico, Niccola Funel, Elena Cardaioli, Filippo M. Santorelli
المصدر: Biochemical and Biophysical Research Communications. 500:158-162
مصطلحات موضوعية: Adult, 0301 basic medicine, Mitochondrial DNA, tRNATrp, Mitochondrial disease, Biophysics, Epilepsies, Myoclonic, Epilepsies, 030105 genetics & heredity, Biology, Trp, Biochemistry, Leukoencephalopathy, 03 medical and health sciences, 0302 clinical medicine, Leukoencephalopathies, Retinitis pigmentosa, medicine, Humans, Genetic Predisposition to Disease, Vascular Calcification, Tomography, Molecular Biology, Genetics, Base Sequence, mtDNA, MT-TW gene, New mutation, DNA, Sequence Analysis, DNA, Cell Biology, RNA, Transfer, Trp, medicine.disease, Female, Mutation, Retinitis Pigmentosa, Tomography, X-Ray Computed, MT-TW, Heteroplasmy, X-Ray Computed, Transfer, Mitochondrial respiratory chain, Mutation (genetic algorithm), RNA, Myoclonic, Sequence Analysis, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4908310ffbc2c194bdb0488778a5c4d4Test
https://doi.org/10.1016/j.bbrc.2018.04.009Test -
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المؤلفون: Panlai Shi, Conghui Wang, Rui Li, Xiangdong Kong
المصدر: Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicineمصطلحات موضوعية: Adult, Parents, copy number variations (CNVs), 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, DNA Copy Number Variations, lcsh:QH426-470, endocrine system diseases, 030105 genetics & heredity, Biology, CNV‐seq, Young Adult, 03 medical and health sciences, Fetus, Likely benign, Pregnancy, Gene Duplication, mental disorders, Gene duplication, Genetics, Humans, Clinical significance, Copy-number variation, Molecular Biology, Uncertain significance, Genetics (clinical), Likely pathogenic, parental origin, High-Throughput Nucleotide Sequencing, Sequence Analysis, DNA, Original Articles, clinical interpretation, lcsh:Genetics, 030104 developmental biology, New mutation, Amniocentesis, Female, Original Article, Gene Deletion
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acae10248934d7e1bd9aba8473dacba3Test
https://doi.org/10.1002/mgg3.944Test