المؤلفون: R. А. Yakymchuk, V. F. Valyuk, L. Y. Sobolenko, S. І. Sorokina

المصدر: Regulatory Mechanisms in Biosystems, Vol 12, Iss 3, Pp 506-512 (2021)

مصطلحات موضوعية: ionizing radiation, induced mutagenesis, frequency of mutations, spectrum of mutations, Science

وصف الملف: electronic resource

Relation: https://medicine.dp.ua/index.php/med/article/view/751; https://doaj.org/toc/2519-8521; https://doaj.org/toc/2520-2588

URL الوصول: https://doaj.org/article/fe3f16ae940a4bf7a58305c533ebf2f8

المؤلفون: N. N. Chakova, S. M. Komissarova, E. A. Zasim, T. V. Dolmatovich, E. S. Rebeko, S. S. Niyazova, E. V. Zaklyazminskaya, L. I. Plashchinskaya, M. V. Dudko

المصدر: Российский кардиологический журнал, Vol 26, Iss 10 (2021)

مصطلحات موضوعية: long qt interval syndrome, spectrum of mutations, kcnq1 gene, kcnh2 gene, scn5a gene, cacna1c gene, ank2 gene, risk stratification, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://russjcardiol.elpub.ru/jour/article/view/4704; https://doaj.org/toc/1560-4071; https://doaj.org/toc/2618-7620

URL الوصول: https://doaj.org/article/08e052b84a794d2093f9296e42b2ee93

المؤلفون: Sakaeva, D. D., Danilova, D. V., Gordiev, M. G., Сакаева, Д. Д., Данилова, Д. В., Гордиев, М. Г.

مصطلحات موضوعية: METASTATIC COLORECTAL CANCER, TARGETED THERAPY, GENE RAS VALUE, THE FREQUENCY AND SPECTRUM OF MUTATIONS IN KRAS AND NRAS GENE, МЕТАСТАТИЧЕСКИЙ КОЛОРЕКТАЛЬНЫЙ РАК, ТАРГЕТНАЯ ТЕРАПИЯ, ЧАСТОТА И СПЕКТР МУТАЦИИ ГЕНА KRAS И NRAS

وصف الملف: application/pdf

Relation: Уральский медицинский журнал. 2016. T. 144, № 11.; Сакаева, Д. Д. Предсказательное значение молекулярно-генетических маркеров в противоопухолевой лекарственной терапии метастатического колоректального рака / Д. Д. Сакаева, Д. В. Данилова, М. Г. Гордиев. – Текст: электронный // Уральский медицинский журнал. - 2016. – T. 144, № 11. – С. 103-107.; http://elib.usma.ru/handle/usma/13375

الاتاحة: http://elib.usma.ru/handle/usma/13375

المؤلفون: Changshuo Wei, Ke-Jia Shan, Weiguang Wang, Shuya Zhang, Qing Huan, Wenfeng Qian

المصدر: Journal of Genetics and Genomics

مصطلحات موضوعية: Binding Sites, Spike-ACE2 interaction, SARS-CoV-2, Omicron, COVID-19, Host Specificity, Receptor-binding domain, Evolution, Molecular, Mice, Evolutionary origins, Host-Pathogen Interactions, Mutation, Spike Glycoprotein, Coronavirus, Genetics, Animals, Humans, Molecular spectrum of mutations, Molecular Biology, Original Research

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b22f6555600746538f8792efa6085fe3
https://pubmed.ncbi.nlm.nih.gov/34954396

المؤلفون: Моргун, Владимир, Катеринчук, Александр, Чугункова, Татьяна

مصطلحات موضوعية: ПШЕНИЦА,ХИРАЛЬНЫЕ МУТАГЕНЫ,ОПТИМАЛЬНЫЕ КОНЦЕНТРАЦИИ,ХРОМОСОМНЫЕ АБЕРРАЦИИ,ЧАСТОТА И СПЕКТР МУТАЦИЙ,WHEAT,CHIRAL MUTAGENS,OPTIMAL CONCENTRATION,CHROMOSOMAL ABERRATIONS,THE FREQUENCY AND SPECTRUM OF MUTATIONS

وصف الملف: text/html

الاتاحة: http://cyberleninka.ru/article/n/ispolzovanie-novyh-stereoizomerov-nitrozoalkilmocheviny-v-selektsii-ozimoy-pshenitsy
http://cyberleninka.ru/article_covers/15610682.png

المؤلفون: Uffan Zafar, Muhammad Usman Baig, Fariha Zafar, Zain Ali Khan, Kamran Naseem, Saba Akram

المصدر: Cureus

مصطلحات موضوعية: 0301 basic medicine, chorionic villus sampling, medicine.medical_specialty, Thalassemia, Population, Ethnic group, Chorionic villus sampling, Prenatal diagnosis, 030105 genetics & heredity, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, education, education.field_of_study, beta thalassemia, prenatal diagnosis, medicine.diagnostic_test, business.industry, Obstetrics, General Engineering, Gestational age, Beta thalassemia, medicine.disease, Mutation (genetic algorithm), Obstetrics/Gynecology, spectrum of mutations, Radiology, business, 030215 immunology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9195f983061339271075cb49c2603d3e
https://doi.org/10.7759/cureus.3265

المؤلفون: Heyden, Benita Von

مصطلحات موضوعية: APOE-gene, Wilson´s Disease, HFE-gene, 3402delC-mutation, spectrum of mutations, Kayser-Fleischer-Ring, H1069Q-mutation, genotype-phenotype-correlation, L708P-mutation, 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6632552b07235ab3d4b4544a668f4c65
https://doi.org/10.17169/refubium-17498

المؤلفون: David, D., Ventura, C., Moreira, I., Diniz, M., Antunes, M., Tavares, A., Araújo, F., Morais, S., Campos, M., Lavinha, J., Kemball-Cook, G.

المساهمون: Repositório Científico da Unidade Local de Saúde de Santo António

مصطلحات موضوعية: hemophilia A, molecular modeling, spectrum of mutations, splicing mutations, vWF

وصف الملف: application/pdf

الاتاحة: http://hdl.handle.net/10400.16/692

المؤلفون: David, D., Ventura, C., Moreira, I., Diniz, M. J., Antunes, M., Tavares, A., Araújo, F., Morais, S., Campos, M., João Lavinha, Kemball-Cook, G.

المصدر: Europe PubMed Central
Scopus-Elsevier
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

مصطلحات موضوعية: Polimorfismo de Conformação de Filamento Único, Factor VIII, Portugal, molecular modeling, Mapeamento por Restrição, Códon Sem Sentido, Polimorfismo Genético, Inversão Cromossômica, Hemofilia A, Mutação de Sentido Incorrecto, Factor VII, splicing mutations, Processamento Alternativo, spectrum of mutations, hemophilia A, vWF, Família, Mutação, Sequência de Bases

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3be9e545ceaccc9ecdbf4e569e877cff
http://europepmc.org/abstract/med/16769589

المؤلفون: Loçlar, İlayda, Bademci, G.; Cengiz, F. B.; Foster, J., II; Duman, D.; Sennaroğlu, L.; Diaz-Horta, O.; Atik, T.; Kirazlı, T.; Olgun, L.; Alper, H.; Menendez, I.; Sennaroğlu, G.; Tokgöz-Yılmaz, S.; Guo, S.; Olgun, Y.; Mahdieh, N.; Bonyadi, M.; Bozan, N.; Ayral, A.; Özkınay, F.; Yıldırım-Baylan, M.; Blanton, S. H.; Tekin, M., School of Medicine

المصدر: Scientific Reports

مصطلحات الفهرس: Multidisciplinary sciences, Copy-number variation; Charge syndrome; Noonan syndrome; Pendred-syndrome; Hypertrophic cardiomyopathy; Waardenburg syndrome; Diagnostic-criteria; Mutation spectrum; Slc26a4 mutations; Kallmann-syndrome, Journal article, text/academic publication

URL: http://libdigitalcollections.ku.edu.tr/cdm/ref/collection/IR/id/861
http://worldcat.org/oclc/1200730091/viewonline
Publisher version
Koç University Institutional Repository