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1دورية أكاديمية
المؤلفون: Macher, Hada, Suárez Artacho, Gonzalo, Guerrero Montávez, Juan Miguel, Gómez Bravo, Miguel Ángel, Álvarez Gómez, Sara, Bernal Bellido, Carmen, Domínguez Pascual, Inmaculada, Rubio Calvo, Amalia Macarena
المساهمون: Universidad de Sevilla. Departamento de Bioquímica Médica y Biología Molecular e Inmunología, Universidad de Sevilla. Departamento de Cirugía, Universidad de Sevilla. CTS160: Neuroendocrinología Molecular, Universidad de Sevilla. CTS664: Cirugía Avanzada y Trasplantes. Terapia Celular y Bioingeniería Aplicada a la Cirugía
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2دورية أكاديمية
المؤلفون: Guevara, Evelyn K., Palo, Jukka U., Oversti, Sanni, King, Jonathan L., Seidel, Maria, Stoljarova, Monika, Wendt, Frank R., Bus, Magdalena M., Guengerich, Anna, Church, Warren B., Guillen, Sonia, Roewer, Lutz, Budowle, Bruce, Sajantila, Antti
المصدر: PLoS One
مصطلحات موضوعية: Archaeology, Biodiversity, Chromosomes, Human, Y / genetics, DNA, Mitochondrial / genetics, Female, Gene Flow, Genetic Markers, Genetics, Population, History, Humans, Indians, South American / genetics, Male, Population Dynamics / history, Sex Factors, South America
الوقت: 15th Century, 16th Century
وصف الملف: application/pdf
العلاقة: https://doi.org/10.1371/journal.pone.0244497Test; Guevara, E. K., Palo, J. U., Översti, S., King, J. L., Seidel, M., Stoljarova, M., Wendt, F. R., Bus, M. M., Guengerich, A., Church, W. B., Guillén, S., Roewer, L., Budowle, B., & Sajantila, A. (2020). Genetic assessment reveals no population substructure and divergent regional and sex-specific histories in the Chachapoyas from northeast Peru. PloS one, 15(12), e0244497. https://doi.org/10.1371/journal.pone.0244497Test; https://hdl.handle.net/20.500.12503/31609Test; 15; 12
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3دورية أكاديمية
المؤلفون: Elkamel, S, Marques, SL, Alvarez, L, Gomes, V, Boussetta, S, Mourali-Chebil, S, Khodjet-El-Khil, H, Cherni, L, Benammar-Elgaaied, A, João Prata, M
المساهمون: Instituto de Investigação e Inovação em Saúde
مصطلحات موضوعية: Arabs / genetics, Chromosomes, Human, Y / genetics, Genetics, Population, Haplotypes, Humans, Male, Paternal Inheritance, Tunisia
وصف الملف: application/pdf
العلاقة: Scientific Reports, vol.11(1):15728; https://www.nature.com/articles/s41598-021-95144-xTest; https://hdl.handle.net/10216/153747Test
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4دورية أكاديمية
المؤلفون: Monteiro, B, Arenas, M, Prata, MJ, Amorim, A
المساهمون: Instituto de Investigação e Inovação em Saúde
مصطلحات موضوعية: Chromosome Mapping / methods, Chromosomes, Human, X / genetics, Y / genetics, Crossing Over, Genetic / genetics, Female, Gene Frequency / genetics, Genetic Linkage, Humans, Linkage Disequilibrium / genetics, Male, Meiosis / genetics, Pseudoautosomal Regions / genetics, Recombination
وصف الملف: application/pdf
العلاقة: info:eu-repo/grantAgreement/FCT/POR_NORTE/SFRH%2FBD%2F135612%2F2018/PT; PLoS Genetics, vol.17:e1009532; https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1009532Test; https://hdl.handle.net/10216/152483Test
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5دورية أكاديمية
المؤلفون: Ferragut, JF, Ramon, C, Castro, JA, Amorim, A, Alvarez, L, Picornell, A
المساهمون: Instituto de Investigação e Inovação em Saúde
مصطلحات موضوعية: Chromosomes, Human, Y / genetics, DNA, Mitochondrial / genetics, Gene Pool, Genetic Variation, Genetics, Population, Haplotypes, Humans, Jews / genetics, Male, Maternal Inheritance, Middle East / ethnology, Paternal Inheritance, Sequence Analysis, DNA / methods, Spain / ethnology
وصف الملف: application/pdf
العلاقة: info:eu-repo/grantAgreement/FCT/5876-PPCDTI/PTDC%2FATP-DEM%2F4545%2F2012/PT; Scientific Reports, vol.10(1):21428; https://www.nature.com/articles/s41598-020-78487-9Test; https://hdl.handle.net/10216/145245Test
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6دورية أكاديمية
المؤلفون: Kutanan, Wibhu, Shoocongdej, Rasmi, Srikummool, Metawee, Hübner, Alexander, Suttipai, Thanatip, Srithawong, Suparat, Kampuansai, Jatupol, Stoneking, Mark
المصدر: http://lobid.org/resources/99370671030206441Test#!, 28(11):1563-1579.
مصطلحات موضوعية: Female [MeSH], DNA, Mitochondrial/genetics [MeSH], Humans [MeSH], Inheritance Patterns [MeSH], Cultural Characteristics [MeSH], Evolution, Molecular [MeSH], Polymorphism, Genetic [MeSH], Article, Pedigree [MeSH], Male [MeSH], Ethnic Groups/genetics [MeSH], Evolutionary biology, Chromosomes, Human, Y/genetics [MeSH], Population genetics, Thailand [MeSH], Gene Frequency [MeSH]
العلاقة: https://repository.publisso.de/resource/frl:6472014Test; https://doi.org/10.1038/s41431-020-0693-xTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576213Test/
الإتاحة: https://doi.org/10.1038/s41431-020-0693-xTest
https://repository.publisso.de/resource/frl:6472014Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576213Test/ -
7دورية أكاديمية
المؤلفون: García-González, Pablo, de Rojas, Itziar, Heilmann-Heimbach, Stefanie, Gomez-Garre, Pilar, Periñán, María Teresa, Alvarez, Ignacio, Diez-Fairen, Monica, Nuñez Llaves, Raul, Olivé Roig, Claudia, Garcia-Ribas, Guillermo, Menéndez-González, Manuel, Martínez, Carmen, Moreno-Grau, Sonia, Aguilar, Miquel, Buongiorno, Mariateresa, Franco-Macías, Emilio, Saez, Maria Eugenia, Cano, Amanda, Bullido, Maria J, Real, Luis Miguel, Rodríguez-Rodríguez, Eloy, Royo, Jose Luís, Álvarez, Victoria, Montrreal, Laura, Pastor, Pau, Piñol-Ripoll, Gerard, Mir, Pablo, Lara, Miguel Calero, Padilla, Miguel Medina, Sánchez-Juan, Pascual, Carracedo, Angel, Valero, Sergi, Hernandez, Isabel, Tàrraga, Lluis, Puerta, Raquel, Ramirez, Alfredo, Boada, Mercé, Ruiz, Agustín, Alarcón-Martín, Emilio, Quintela, Inés, Orellana, Adela, Andrade, Victor, Adami, Pamela V Martino
المصدر: International journal of molecular sciences 24(2), 898 (2023). doi:10.3390/ijms24020898
مصطلحات موضوعية: info:eu-repo/classification/ddc/540, Humans, Male, Female, Alzheimer Disease: genetics, Chromosomes, Human, Y: genetics, Genome-Wide Association Study, Mosaicism, Risk Factors, Cognitive Dysfunction: genetics, tau Proteins: genetics, Biomarkers, Amyloid beta-Peptides: genetics, Alzheimer’s disease, CSF biomarkers, EADB, GR@ACE/DEGESCO, GWAS, Mendelian randomization, disease progression, mild cognitive impairment, mosaic loss of chromosome Y, polygenic risk score, tau Proteins, Amyloid beta-Peptides
جغرافية الموضوع: DE
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/pmid:36674414; info:eu-repo/semantics/altIdentifier/issn/1422-0067; info:eu-repo/semantics/altIdentifier/issn/1661-6596; https://pub.dzne.de/record/194981Test; https://pub.dzne.de/search?p=id:%22DZNE-2023-00168%22Test
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8دورية أكاديمية
المؤلفون: Thompson, Deborah J, Genovese, Giulio, Forsberg, Lars A, Perry, John R B, Boomsma, Dorret, Nivard, Michel, van Dongen, Jenny, Pool, Renée, Hottenga, Jouke Jan
المصدر: Thompson , D J , Genovese , G , Forsberg , L A , Perry , J R B , International Lung Cancer Consortium (INTEGRAL-ILCCO) , Boomsma , D , Nivard , M , van Dongen , J , Pool , R & Hottenga , J J 2019 , ' Genetic predisposition to mosaic Y chromosome loss in blood ' , Nature , vol. 575 , no. 7784 , pp. 652-657 . https://doi.org/10.1038/s41586-019-1765-3Test
مصطلحات موضوعية: Adult, Aged, Chromosome Deletion, Chromosomes, Human, Y/genetics, Computational Biology, Databases, Genetic, Female, Genetic Markers/genetics, Genetic Predisposition to Disease/genetics, Genomic Instability/genetics, Humans, Leukocytes/pathology, Male, Middle Aged, Mosaicism, Neoplasms/genetics, United Kingdom
وصف الملف: application/pdf
الإتاحة: https://doi.org/10.1038/s41586-019-1765-3Test
https://research.vu.nl/en/publications/84ac6a66-ace9-4347-bf9b-736ee2f37c13Test
https://hdl.handle.net/1871.1/84ac6a66-ace9-4347-bf9b-736ee2f37c13Test
https://research.vu.nl/ws/files/159685655/Genetic_predisposition_to_mosaic_Y_chromosome_loss_in_blood.pdfTest -
9دورية أكاديمية
المؤلفون: Dotto, G.P.
المصدر: EMBO molecular medicine, vol. 11, no. 5
مصطلحات موضوعية: Brain/growth & development, Chromosomes, Human, Y/genetics, Female, Health, Hormones/metabolism, Humans, Male, Sex Characteristics, Sex Factors
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30979711; info:eu-repo/semantics/altIdentifier/eissn/1757-4684; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_BE86C1AB94537; https://serval.unil.ch/notice/serval:BIB_BE86C1AB9453Test; urn:issn:1757-4676; https://serval.unil.ch/resource/serval:BIB_BE86C1AB9453.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_BE86C1AB94537Test
الإتاحة: https://doi.org/10.15252/emmm.201910668Test
https://serval.unil.ch/notice/serval:BIB_BE86C1AB9453Test
https://serval.unil.ch/resource/serval:BIB_BE86C1AB9453.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_BE86C1AB94537Test -
10
المؤلفون: Jögi, Annika, Øra, Ingrid, Nilsson, Helén, Lindeheim, Åsa, Makino, Yuichi, Poellinger, Lorenz, Axelson, Håkan, Påhlman, Sven
المصدر: Proceedings of the National Academy of Sciences. 99(10):7021-7026
مصطلحات موضوعية: Non-U.S. Gov't, Support, Phenotype, Chromaffin : cytology, Paraganglia, Oxygen : metabolism, Neuropeptide Y : genetics, Neuroblastoma, Neural Crest : cytology, Experimental, Neoplasms, Nude, Mice, Lymphokines : genetics, Insulin-Like Growth Factor II : genetics, Human, Helix-Loop-Helix Motifs, Hela Cells, Trans-Activators : genetics, Trans-Activators : metabolism, Transcription Factors : genetics, Transcription Factors : metabolism, Heterologous, Transplantation, Tumor Cells, Cultured, Tyrosine 3-Monooxygenase : genetics, Sympathetic Nervous System : metabolism, Gene Expression, Female, Endothelial Growth Factors : genetics, Down-Regulation, DNA-Binding Proteins : genetics, Cell Hypoxia, Biological Markers, Animal, Medicin och hälsovetenskap, Klinisk medicin, Pediatrik, Medical and Health Sciences, Clinical Medicine, Pediatrics, Cancer och onkologi, Cancer and Oncology
الوصول الحر: https://lup.lub.lu.se/record/108252Test
http://www.ncbi.nlm.nih.gov:80/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12011461&dopt=AbstractTest
http://dx.doi.org/10.1073/pnas.102660199Test