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1دورية أكاديمية
المؤلفون: Megan Li, Yi-Lee Ting, Trevor Williams, Jackie Tahiliani, Brandon Bunker, Daniel Pineda-Alvarez, Swaroop Aradhya
المصدر: Genetics in Medicine Open, Vol 2, Iss , Pp 101478- (2024)
وصف الملف: electronic resource
العلاقة: http://www.sciencedirect.com/science/article/pii/S2949774424006241Test; https://doaj.org/toc/2949-7744Test
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2دورية أكاديمية
المؤلفون: Sherin Bakhashab, Megan Li Yuen Yeoh, David J. Coulson, Samuel Christian Steel, Sabina L. Ray, Jolanta U. Weaver
المصدر: International Journal of Molecular Sciences, Vol 23, Iss 24, p 15659 (2022)
مصطلحات موضوعية: cardiovascular disease, circulating endothelial progenitor cells, miR-200c-3p, inflammation, proangiogenic cells, type 1 diabetes mellitus, Biology (General), QH301-705.5, Chemistry, QD1-999
وصف الملف: electronic resource
العلاقة: https://www.mdpi.com/1422-0067/23/24/15659Test; https://doaj.org/toc/1661-6596Test; https://doaj.org/toc/1422-0067Test
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3دورية أكاديمية
المؤلفون: Sabina L. Ray, David J. Coulson, Megan Li Yuen Yeoh, Alice Tamara, Jevi Septyani Latief, Sherin Bakhashab, Jolanta U. Weaver
المصدر: International Journal of Molecular Sciences, Vol 21, Iss 19, p 7217 (2020)
مصطلحات موضوعية: CXCR1/2, PANX2, TNF-α, inflammation, miR-342-3p/-5p, therapeutic targets, Biology (General), QH301-705.5, Chemistry, QD1-999
وصف الملف: electronic resource
العلاقة: https://www.mdpi.com/1422-0067/21/19/7217Test; https://doaj.org/toc/1661-6596Test; https://doaj.org/toc/1422-0067Test
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4دورية أكاديمية
المؤلفون: Dalga D Surofchy, PharmD (c), Sam Oh, PhD, MPH, Joshua Galanter, MD, MAS, Pin Xiang, PharmD, Megan Li, PhD (c), Su Guo, PhD, Tejal Desai, PhD, B Joseph Guglielmo, PharmD, Kathy Giacomini, PhD, Janel Long-Boyle, PharmD, PhD, Alan HB Wu, PhD, Esteban Burchard, MD, MPH
المصدر: INNOVATIONS in Pharmacy, Vol 8, Iss 1 (2017)
مصطلحات موضوعية: pharmacogenomics, genotyping, pharmacy curriculum, pharmacogenetics, personal pharmacogenetics, Pharmacy and materia medica, RS1-441
وصف الملف: electronic resource
العلاقة: https://pubs.lib.umn.edu/index.php/innovations/article/view/482Test; https://doaj.org/toc/2155-0417Test
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5دورية أكاديمية
المؤلفون: Elisa Calì, Mohnish Suri, Marcello Scala, Matteo P. Ferla, Shahryar Alavi, Eissa Faqeih, Emilia K. Bijlsma, Kristen Wigby, Diana Baralle, Mohammad Yahya Vahidi Mehrjardi, Jennifer Schwab, Konrad Platzer, Katharina Steindl, Mais Hashem, Marilyn C. Jones, Dmitriy Niyazov, Jennifer Jacober, Rebecca O. Littlejohn, Denisa Weis, Neda Zadeh, Lance H. Rodan, Alice Goldenberg, François Lecoquierre, Marina Dutra‐Clarke, Gabriella Horváth, Dana Young, Naama Orenstein, Shahad Bawazeer, Anneke T. Vulto‐van Silfhout, Yvan Herenger, Mohammadreza Dehghani, Seyed Mohammad Seyedhassani, Amir Bahreini, Mahya Ebrahimi Nasab, A. Gulhan Ercan‐Sencicek, Zahra Firoozfar, Mojtaba Movahedinia, Stéphanie Efthymiou, Pasquale Striano, Ehsan Ghayoor Karimiani, Vincenzo Salpietro, Jenny C. Taylor, Melody Redman, Alexander P.A. Stegmann, Andreas Laner, Ghada M.H. Abdel‐Salam, Megan Li, Mario Bengala, Amelie J. Müller, María Cristina Digilio
مصطلحات موضوعية: Protein Arginine Methylation in Mammals, Molecular Biology, Biochemistry, Genetics and Molecular Biology, Life Sciences, Epigenetic Modifications and Their Functional Implications, Protein Arginine Methyltransferases, Brachydactyly, Short stature, Autism spectrum disorder, Hypotonia, Global developmental delay, Neurodevelopmental disorder, Intellectual disability, Craniofacial, Craniofacial abnormality, Medicine, Genetics, FOS Biological sciences, Pediatrics, Psychology, FOS Psychology, Phenotype, Autism, Biology, Psychiatry, Gene
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6
المؤلفون: Elijah Robert Bouma-Sims, Megan Li, Yanzi Lin, Adia Sakura-Lemessy, Alexandra Nisenoff, Ellie Young, Eleanor Birrell, Lorrie Faith Cranor, Hana Habib
المصدر: Proceedings of the 2023 CHI Conference on Human Factors in Computing Systems.
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::8457fd71d665dade14c1189ed16ed2deTest
https://doi.org/10.1145/3544548.3580725Test -
7
المؤلفون: Deanna L. Kroetz, Kouros Owzar, Alan P. Venook, Mark J. Ratain, Federico Innocenti, Howard L. McLeod, William Kevin Kelly, Susan Halabi, Hope S. Rugo, James N. Atkins, Heinz-Josef Lenz, Howard S. Hochster, Donna Niedzwiecki, Michiaki Kubo, Yukihide Momozawa, Paula N. Friedman, Fei Shen, Bryan P. Schneider, Bert H. O’Neil, Chen Jiang, Flora Mulkey, Megan Li
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e99a814a31f502415951927ae4a4f7eTest
https://doi.org/10.1158/1078-0432.c.6525887Test -
8
المؤلفون: Deanna L. Kroetz, Kouros Owzar, Alan P. Venook, Mark J. Ratain, Federico Innocenti, Howard L. McLeod, William Kevin Kelly, Susan Halabi, Hope S. Rugo, James N. Atkins, Heinz-Josef Lenz, Howard S. Hochster, Donna Niedzwiecki, Michiaki Kubo, Yukihide Momozawa, Paula N. Friedman, Fei Shen, Bryan P. Schneider, Bert H. O’Neil, Chen Jiang, Flora Mulkey, Megan Li
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d7f6e43ffa601f9d5a68422bda7d13aTest
https://doi.org/10.1158/1078-0432.22464992Test -
9دورية أكاديمية
المؤلفون: Dong Li, Qin Wang, Allan Bayat, Mark Battig, Yijing Zhou, Daniëlle G. M. Bosch, Gijs van Haaften, Leslie Granger, Andrea K. Petersen, Luis Perez-Jurado, Gemma Aznar-Laín, Anushree Aneja, Miroslava Hancarova, Sarka Bendova, Martin Schwarz, Radka Kremlíková Pourová, Zdenek Sedlacek, Beth A. Keena, Michael E. March, Cuiping Hou, Nora O'Connor, Elizabeth J. Bhoj, Margaret H. Harr, Gabrielle Lemire, Kym M. Boycott, Meghan C. Towne, Megan Li, mark tarnopolsky, Lauren Brady, Michael J. Parker, Hanna Faghfoury, Lea Kristin Parsley, Emanuele Agolini, Maria Lisa Dentici, Antonio Novelli, Meredith S. Wright, Rachel Palmquist, Khanh Lai, Marcello Scala, Pasquale Striano, Michele Iacomino, Federico Zara, Annina Cooper, Timothy J. Maarup, Melissa Byler, Robert Roger Lebel, Tugce B. Balci, Raymond J. Louie, Michael J. Lyons, Jessica Douglas, Catherine B. Nowak
المساهمون: Li, Dong, Wang, Qin, Bayat, Allan, Battig, Mark, Zhou, Yijing, Bosch, Daniëlle G. M., van Haaften, Gij, Granger, Leslie, Petersen, Andrea K., Perez-Jurado, Lui, Aznar-Laín, Gemma, Aneja, Anushree, Hancarova, Miroslava, Bendova, Sarka, Schwarz, Martin, Kremlíková Pourová, Radka, Sedlacek, Zdenek, Keena, Beth A., March, Michael E., Hou, Cuiping, O'Connor, Nora, Bhoj, Elizabeth J., Harr, Margaret H., Lemire, Gabrielle, Boycott, Kym M., Towne, Meghan C., Li, Megan, Tarnopolsky, Mark, Brady, Lauren, Parker, Michael J., Faghfoury, Hanna, Kristin Parsley, Lea, Agolini, Emanuele, Lisa Dentici, Maria, Novelli, Antonio, Wright, Meredith S., Palmquist, Rachel, Lai, Khanh, Scala, Marcello, Striano, Pasquale, Iacomino, Michele, Zara, Federico, Cooper, Annina, Maarup, Timothy J., Byler, Melissa, Roger Lebel, Robert, Balci, Tugce B., Louie, Raymond J., Lyons, Michael J., Douglas, Jessica, Nowak, Catherine B.
مصطلحات موضوعية: Development, Genetic disease, Genetic, Neurodevelopment, iPS cells
وصف الملف: ELETTRONICO
العلاقة: firstpage:N/A; lastpage:N/A; journal:THE JOURNAL OF CLINICAL INVESTIGATION; https://hdl.handle.net/11567/1158036Test
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10
المؤلفون: Elisa Cali, Mohnish Suri, Marcello Scala, Matteo P. Ferla, Shahryar Alavi, Eissa Ali Faqeih, Emilia K. Bijlsma, Kristen M. Wigby, Diana Baralle, Mohammad Y.V. Mehrjardi, Jennifer Schwab, Konrad Platzer, Katharina Steindl, Mais Hashem, Marilyn Jones, Dmitriy M. Niyazov, Jennifer Jacober, Rebecca Okashah Littlejohn, Denisa Weis, Neda Zadeh, Lance Rodan, Alice Goldenberg, François Lecoquierre, Marina Dutra-Clarke, Gabriella Horvath, Dana Young, Naama Orenstein, Shahad Bawazeer, Anneke T. Vulto-van Silfhout, Yvan Herenger, Mohammadreza Dehghani, Seyed Mohammad Seyedhassani, Amir Bahreini, Mahya E. Nasab, A. Gulhan Ercan-Sencicek, Zahra Firoozfar, Mojtaba Movahedinia, Stephanie Efthymiou, Pasquale Striano, Ehsan Ghayoor Karimiani, Vincenzo Salpietro, Jenny C. Taylor, Melody Redman, Alexander P.A. Stegmann, Andreas Laner, Ghada Abdel-Salam, Megan Li, Mario Bengala, Amelie Johanna Müller, Maria C. Digilio, Anita Rauch, Murat Gunel, Hannah Titheradge, Daniela N. Schweitzer, Alison Kraus, Irene Valenzuela, Scott D. McLean, Chanika Phornphutkul, Mustafa Salih, Amber Begtrup, Rhonda E. Schnur, Erin Torti, Tobias B. Haack, Carlos E. Prada, Fowzan S. Alkuraya, Henry Houlden, Reza Maroofian
المساهمون: MUMC+: DA KG Lab Specialisten (9), RS: FHML non-thematic output, Institut Català de la Salut, [Cali E] Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom. [Suri M] Nottingham Clinical Genetics Service, Nottingham University Hospitals NHS Trust, City Hospital Campus, Nottingham, United Kingdom. [Scala M] Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy. Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy. [Ferla MP] Genomic Medicine theme, Oxford Biomedical Research Centre, NIHR, Oxford, Oxfordshire, United Kingdom. Wellcome Centre for Human Genetics, Oxford University, Oxford, Oxfordshire, United Kingdom. [Alavi S] Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom. Department of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran. Palindrome, Isfahan, Iran. [Faqeih EA] Section of Medical Genetics, Children’s Specialist Hospital, King Fahad Medical, City, Riyadh, Saudi Arabia. [Valenzuela I] Àrea de Genètica Clínica i Molecular, Vall d'Hebron Hospital Universitari, Barcelona, Spain. Grup de Recerca de Medicina Genètica, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus
المصدر: Genetics in Medicine, 25(1), 135-142. Nature Publishing Group
Genetics in Medicine, 25, 1, pp. 135-142
Scientia
Genetics in Medicine, 25, 135-142مصطلحات موضوعية: Neurobiologia del desenvolupament, Discapacitat intel·lectual - Aspectes genètics, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Otros calificadores::Otros calificadores::/genética [Otros calificadores], enfermedades y anomalías neonatales congénitas y hereditarias::enfermedades genéticas congénitas::enanismo [ENFERMEDADES], trastornos mentales::trastornos del desarrollo neurológico [PSIQUIATRÍA Y PSICOLOGÍA], Nanisme, Nervous System Diseases::Neurologic Manifestations::Neurobehavioral Manifestations::Intellectual Disability [DISEASES], All institutes and research themes of the Radboud University Medical Center, Other subheadings::Other subheadings::/genetics [Other subheadings], Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Genetic Diseases, Inborn::Dwarfism [DISEASES], enfermedades del sistema nervioso::manifestaciones neurológicas::manifestaciones neuroconductuales::discapacidad intelectual [ENFERMEDADES], Genetics (clinical), Mental Disorders::Neurodevelopmental Disorders [PSYCHIATRY AND PSYCHOLOGY]
وصف الملف: application/pdf; image/jpeg; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet; text
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ceace68f22e9fddfec1c6fe140b0167Test
https://cris.maastrichtuniversity.nl/en/publications/81d27084-ec1f-4ef6-a38c-5c73866a5a8eTest