المؤلفون: Douglas R. Storts, Roderick A.F. MacLeod, Christine Alston-Roberts, J. N. Butler, Arihiro Kohara, Steven R. Bauer, Wilhelm G. Dirks, Manohar R. Furtado, Gregory Sykes, Yvonne Reid, Anton F. Steuer, Roland M. Nardone, Liz Kerrigan, James A. Thomson, John R. W. Masters, Margaret C. Kline, Amanda Capes-Davis, Raymond W. Nims, Zenobia Taraporewala, Paul J. Price, Rita Barallon, Mark Nardone, Georgyi V. Los, Elmore E, Jaiprakash G. Shewale

المصدر: In Vitro Cellular & Developmental Biology. Animal
Barallon, Rita; Bauer, Steven R.; Butler, John; Capes-Davis, Amanda; Dirks, Wilhelm G.; Elmore, Eugene; et al.(2010). Recommendation of short tandem repeat profiling for authenticating human cell lines, stem cells, and tissues. In Vitro Cellular & Developmental Biology-Animal, 46(9), pp 727-732. doi: 10.1007/s11626-010-9333-z. Retrieved from: http://www.escholarship.org/uc/item/0g29152jTest

مصطلحات موضوعية: education, Tissue Banks, Identity testing, Biology, Cell Line, Specimen Handling, Profiling (information science), Consensus standard, Humans, National standard, Authentication, Invited Review, Cell authentication, business.industry, Cell Culture, Gene Expression Profiling, Stem Cells, Animal Genetics and Genomics, Life Sciences, STR profiling, Quality control, General Medicine, Cell Biology, Human cell, Data science, United States, Str profiling, Biotechnology, STR Profile, Stem cell, business, Microsatellite Repeats, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb3c590ab66a14de2747d73c1c9abcd8Test

المؤلفون: Evan Elliott, Stefano Nardone, Michal Mor, Dev Sharan Sams

المصدر: Molecular Autism

مصطلحات موضوعية: Genetics, Small RNA, DNA methylation, Research, Autism, MicroRNA, Biology, medicine.disease, Oxytocin receptor, Psychiatry and Mental health, Developmental Neuroscience, microRNA, Gene expression, medicine, Epigenetics, Molecular Biology, Gene, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e46004feee5b3c41a1299f834620480Test

المؤلفون: Giampiero Palmieri, Anna Maria Nardone, Barbara Testa, D. Minella, Livia Biancone, Antonio Novelli, Francesco Pallone, Marina Frontali, Caterina Tanzarella, Michela Biancolella, Alessandra di Masi, Giuseppe Novelli, Emma Calabrese, Antonio Antoccia, Maria Rosaria D'Apice, Norma Licata, Federica Sangiuolo, Francesca Gullotta

المصدر: BMC medical genetics (Online) 16 (2015): 1. doi:10.1186/s12881-015-0164-3
info:cnr-pdr/source/autori:D'Apice M.R.; Novelli A.; di Masi A.; Biancolella M.; Antoccia A.; Gullotta F.; Licata N.; Minella D.; Testa B.; Nardone A.M.; Palmieri G.; Calabrese E.; Biancone L.; Tanzarella C.; Frontali M.; Sangiuolo F.; Novelli G.; Pallone F./titolo:Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: A novel recognizable microdeletion syndrome?/doi:10.1186%2Fs12881-015-0164-3/rivista:BMC medical genetics (Online)/anno:2015/pagina_da:1/pagina_a:/intervallo_pagine:1/volume:16

مصطلحات موضوعية: Male, Letter, Adolescent, Apraxias, Pseudogene, Developmental Disabilities, Locus (genetics), Hemizygosity, Biology, Young Adult, Malabsorption Syndromes, Genetics, Humans, Child, Preschool, Gene Expression Regulation, Genetic Loci, Multigene Family, Phenotype, Pseudogenes, Sequence Deletion, Genetics(clinical), Copy-number variation, Allele, Child, Preschool, Gene, Genetics (clinical), cromosoma 8, Microdeletion syndrome, Human genetics, dismorfismo, Settore MED/03 - Genetica Medica, microdelezione

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::249e481b7cd6f1707c467ca2dadc13deTest