Zobrazeno 1 - 10
of 52
pro vyhledávání: '"M. T Cho"'
Publikováno v:
Advanced Science Letters. 24:1991-1995
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ff1e1a4dc0b4c88cb9426c217e503cb
https://doi.org/10.1166/asl.2018.11828
https://doi.org/10.1166/asl.2018.11828
Characteristics of LED Air Guidance Light by Wavelength of Weather Change Using ESS of Hybrid System
Publikováno v:
Advanced Science Letters. 24:1996-2001
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5296e9b590ee18f7f4043598e3abdc81
https://doi.org/10.1166/asl.2018.11829
https://doi.org/10.1166/asl.2018.11829
Autor:
Ingrid M. Wentzensen, R. Colombo, L. Baker, L. Immken, T. Barbaro-Dieber, Cameron Mroske, Julie S. Cohen, H. Nagakura, Ali Fatemi, J.F. Reynolds, E.S. Jordan, Zöe Powis, Christopher Cunniff, M. T. Cho, Jennifer Burton, Kirsty McWalter, I. Petrik, Rebecca Willaert, Kevin R. Payne, Joseph H. Hersh, Robert Huether, K.A. Aleck, Karen W. Gripp, T. Stamper, K.D. Farwell Hagman, M.J. Guillen Sacoto, K.L. David, Alessandro Serretti, Sha Tang
Publikováno v:
Clinical Genetics. 93:752-761
Diagnostic exome sequencing (DES) has aided delineation of the phenotypic spectrum of rare genetic etiologies of intellectual disability (ID). A SET domain containing 5 gene (SETD5) phenotype of ID and dysmorphic features has been previously describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0d7bfc8125fa4102f14d75a6db7625f
https://doi.org/10.1111/cge.13132
https://doi.org/10.1111/cge.13132
Autor:
Laurent Guibaud, Kristin Lindstrom, F. Tran Mau-Them, Alice Masurel, John M. Graham, Yannis Duffourd, Renske Oegema, A. A. Sharkov, Markus Zweier, M. J. van den Boogaard, Thibaud Jouan, Ekaterina R. Lozier, Agnes Chen, M. T. Cho, Sergey Korostelev, Laurence Faivre, Henry J. Lin, F. A. Konovalov, Anaïs Begemann, Patricia I. Dickson, Jennifer Friedman, K.L.I. van Gassen, Boris Keren, Laurence Duplomb, C. Thauvin-Robinet, Moin Vera, Isabelle Marey, Margaret G. Au, Christophe Philippe, Thomas Schmitt-Mechelke, Floor E. Jansen, B. Urteaga, Caroline Nava, Stan F. Nelson, Julian A. Martinez-Agosto, Anita Rauch, Fanny Mochel, Antonio Vitobello
Publikováno v:
Genetics in Medicine, 21(4), 1008. Lippincott Williams and Wilkins
Purpose: Developmental and epileptic encephalopathies (DEEs) are severe clinical conditions characterized by stagnation or decline of cognitive and behavioral abilities preceded, accompanied or followed by seizures. Because DEEs are clinically and ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83b1b30225d1bce3f186d400623a2b18
https://dspace.library.uu.nl/handle/1874/392185
https://dspace.library.uu.nl/handle/1874/392185
Publikováno v:
Advanced Science Letters. 22:3209-3213
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::035cd9882f4426812b6bbdc05cc32105
https://doi.org/10.1166/asl.2016.7948
https://doi.org/10.1166/asl.2016.7948
Publikováno v:
Advanced Science Letters. 22:3269-3273
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ed9e67002e3ee2dd269eb5780222498
https://doi.org/10.1166/asl.2016.7949
https://doi.org/10.1166/asl.2016.7949
Autor:
M.J. Guillen Sacoto, Kyle Retterer, Rashmi Chikarmane, Berivan Baskin, Barbara K. Burton, Emma Bedoukian, S Hopkins, Brooke E. Spangler, Heather M. McLaughlin, Wendy K. Chung, Fran Kendall, Matthew A. Deardorff, David Kronn, M. T. Cho, Marie T. McDonald, Rebecca Willaert, N Oundjian, D Stern, Ingrid M. Wentzensen, Anne Slavotinek, Dianalee McKnight, Allyn McConkie-Rosell, S Schrier Vergano, Katherine H. Kim, N Chandy
Publikováno v:
Clinical Genetics. 92:221-223
Graphical abstract key: ADHD, attention deficit hyperactivity disorder; ASD, atrial septal defect; DD, developmental delay; EEG, electroencephalogram; Ht, height; ID, intellectual disability; OCD, obsessive-compulsive disorder; OFC, open fontanelle;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::581ee86a91c3e5561960d11be6b0ecf1
https://doi.org/10.1111/cge.12956
https://doi.org/10.1111/cge.12956
Publikováno v:
Engineering Design Applications ISBN: 9783319790046
Plant factory aim to achieve excellent productivity by automatically controlling plant growth in an enclosed environment. Because plant factories are very complex systems with various sensors and controls, an integrated operating system that controls
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::880e17e754492ec9efc8d5740334f3f6
https://doi.org/10.1007/978-3-319-79005-3_5
https://doi.org/10.1007/978-3-319-79005-3_5
Autor:
D, Stern, M T, Cho, R, Chikarmane, R, Willaert, K, Retterer, F, Kendall, M, Deardorff, S, Hopkins, E, Bedoukian, A, Slavotinek, S, Schrier Vergano, B, Spangler, M, McDonald, A, McConkie-Rosell, B K, Burton, K H, Kim, N, Oundjian, D, Kronn, N, Chandy, B, Baskin, M J, Guillen Sacoto, I M, Wentzensen, H M, McLaughlin, D, McKnight, W K, Chung
Publikováno v:
Clinical genetics. 92(2)
Graphical abstract key: ADHD, attention deficit hyperactivity disorder; ASD, atrial septal defect; DD, developmental delay; EEG, electroencephalogram; Ht, height; ID, intellectual disability; OCD, obsessive-compulsive disorder; OFC, open fontanelle;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8740338bfcd0e480a818899ca5d6c690
https://pubmed.ncbi.nlm.nih.gov/28111752
https://pubmed.ncbi.nlm.nih.gov/28111752
Autor:
R, Webster, M T, Cho, K, Retterer, F, Millan, C, Nowak, J, Douglas, A, Ahmad, G V, Raymond, M R, Johnson, A, Pujol, A, Begtrup, D, McKnight, O, Devinsky, W K, Chung
Publikováno v:
Clinical genetics. 91(5)
Intellectual disability (ID) affects about 3% of the population and has a male gender bias. Of at least 700 genes currently linked to ID, more than 100 have been identified on the X chromosome, including KIAA2022. KIAA2022 is located on Xq13.3 and is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::070ff9271c130a742ed8be39c127973c
https://pubmed.ncbi.nlm.nih.gov/27568816
https://pubmed.ncbi.nlm.nih.gov/27568816