المؤلفون: Alessandra Renieri, Diego Lopergolo, Anna Maria Pinto, Carla Battisti, A. Russo

مصطلحات موضوعية: Epilepsy, business.industry, COL4A1 gene, MEDLINE, Headache, Bioinformatics, medicine.disease, Small vessel disease, Leukoencephalopathy, Stroke, Neurology, New mutation, medicine, Fundus oculi, Neurology (clinical), business, Gene

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c984db40b269f738529441a07187928aTest
http://hdl.handle.net/11365/1133689Test

المؤلفون: Raghav Prasad Parouha, Kedar Nath Das

المصدر: Advances in Intelligent Systems and Computing ISBN: 9789811532894
SocProS (1)

مصطلحات موضوعية: 0209 industrial biotechnology, Mathematical optimization, Computer science, Crossover, MathematicsofComputing_NUMERICALANALYSIS, Economic dispatch, Particle swarm optimization, 02 engineering and technology, Mechanism (engineering), 020901 industrial engineering & automation, Differential evolution, Mutation (genetic algorithm), New mutation, 0202 electrical engineering, electronic engineering, information engineering, Benchmark (computing), 020201 artificial intelligence & image processing

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::dbad77b91acad4c3ca8572b5ee7ac248Test
https://doi.org/10.1007/978-981-15-3290-0_5Test

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

المؤلفون: Wei-Min Zheng, Zhenyu Meng, Jeng-Shyang Pan

المصدر: Enterprise Information Systems. 14:221-242

مصطلحات موضوعية: Mathematical optimization, Information Systems and Management, Computer science, 05 social sciences, Population structure, Structure (category theory), 02 engineering and technology, Computer Science Applications, Local optimum, Differential evolution, 0502 economics and business, New mutation, 0202 electrical engineering, electronic engineering, information engineering, 020201 artificial intelligence & image processing, Overall performance, Global optimization, 050203 business & management

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::2c2c942302203f49d87183d84c5a0320Test
https://doi.org/10.1080/17517575.2018.1491064Test

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

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 Medicine

مصطلحات 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

المؤلفون: Stefan Kramer, Sayantan Mitra, Sriparna Saha

المصدر: ACM Transactions on Knowledge Discovery from Data. 12:1-30

مصطلحات موضوعية: General Computer Science, Computer science, 02 engineering and technology, computer.software_genre, Multi-objective optimization, Cluster validity index, 020204 information systems, Simulated annealing, New mutation, 0202 electrical engineering, electronic engineering, information engineering, A priori and a posteriori, 020201 artificial intelligence & image processing, Data mining, Cluster analysis, Multiple view, computer

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::458611e61f1556640c03a96e3d52e2d1Test
https://doi.org/10.1145/3182181Test

المؤلفون: Rudolf Happle

المصدر: Journal of the European Academy of Dermatology and Venereology. 32:1075-1088

مصطلحات موضوعية: medicine.medical_specialty, Skin Neoplasms, Genetic counseling, Dermatology, Loss of heterozygosity, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, Neoplastic Syndromes, Hereditary, Genetic etiology, Humans, Medicine, Vascular Diseases, Allele, Connective Tissue Diseases, Paraganglioma, Extra-Adrenal, Mosaicism, business.industry, Skin Diseases, Genetic, Glomus Tumor, Molecular analysis, Infectious Diseases, Clinical evidence, 030220 oncology & carcinogenesis, New mutation, Bone Diseases, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a79842b2afad2c2e7161ec12bf4e87b2Test
https://doi.org/10.1111/jdv.14838Test

المؤلفون: Ana Maria Reis Ferreira, Felipe Gomes Ferreira Padilha, Liane de Castro, Kênia Balbi El-Jaick, Aline dos Santos Moreira

المصدر: Journal of Equine Science. 29:21-24

مصطلحات موضوعية: 0106 biological sciences, 0301 basic medicine, Genetics, biology, Equine, Myostatin, 01 natural sciences, Genomic databases, Breed, Genetic profile, 03 medical and health sciences, 030104 developmental biology, New mutation, biology.protein, Gene, Selection (genetic algorithm), 010606 plant biology & botany, Genetic association

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::3438d16df79d9d65c8843f228ba4261eTest
https://doi.org/10.1294/jes.29.21Test

المؤلفون: Atsushi Watanabe, Yasuo Kitamura, Keiki Yokoo, Naoki Hirokawa, Masahiro Miyajima, Sayaka Kudoh, Aki Ishikawa, Gen Yamada, Hiroshi Saijo, Hiroki Takahashi, Hiroko Morisaki, Hirofumi Chiba

المصدر: Respiratory Medicine Case Reports
Respiratory Medicine Case Reports, Vol 25, Iss, Pp 73-77 (2018)

مصطلحات موضوعية: Pulmonary and Respiratory Medicine, medicine.medical_specialty, Osler-Weber-Rendu Disease, Case Report, Endovascular occlusion, Pulmonary arteriovenous malformation, 030218 nuclear medicine & medical imaging, 03 medical and health sciences, 0302 clinical medicine, medicine, Telangiectasia, Genetic testing, lcsh:RC705-779, medicine.diagnostic_test, business.industry, lcsh:Diseases of the respiratory system, Partial resection, Hereditary hemorrhagic telangiectasia, 030228 respiratory system, Mutation (genetic algorithm), New mutation, Radiology, medicine.symptom, business, Osler-Weber-Rendu disease

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e4e80833bb1bef44c1f409b4db3ba6aTest
https://doi.org/10.1016/j.rmcr.2018.07.001Test