Zobrazeno 1 - 10
of 245
pro vyhledávání: '"Meera, E."'
Autor:
Robert D. Latzman, Olivia Campagne, Meera E. Modi, Marta Karas, C. J. Malanga, David A. H. Whiteman
Publikováno v:
Clinical and Translational Science, Vol 17, Iss 4, Pp n/a-n/a (2024)
Abstract A quantitatively‐driven evaluation of existing clinical data and associated knowledge to accelerate drug discovery and development is a highly valuable approach across therapeutic areas, but remains underutilized. This is especially the ca
Externí odkaz:
https://doaj.org/article/d0d9a9afbe2c4a97808826c10d992575
Autor:
Sameer C. Dhamne, Meera E. Modi, Audrey Gray, Simone Bonazzi, Lucas Craig, Elizabeth Bainbridge, Lahin Lalani, Chloe E. Super, Samantha Schaeffer, Ketthsy Capre, Danuta Lubicka, Guiqing Liang, Doug Burdette, Stephanie M. McTighe, Sarika Gurnani, Sheryl Anne D. Vermudez, Daniel Curtis, Christopher J. Wilson, Mustafa Q. Hameed, Angelica D'Amore, Alexander Rotenberg, Mustafa Sahin
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 10, Pp 1790-1801 (2023)
Abstract Objective Tuberous sclerosis complex (TSC) is a neurodevelopmental disorder caused by autosomal‐dominant pathogenic variants in either the TSC1 or TSC2 gene, and it is characterized by hamartomas in multiple organs, such as skin, kidney, l
Externí odkaz:
https://doaj.org/article/5e6e60c1d4644ed1b4ab20f434f5f54a
Autor:
Meera E. Deo
This book is the first formal, empirical investigation into the law faculty experience using a distinctly intersectional lens, examining both the personal and professional lives of law faculty members. Comparing the professional and personal experien
Autor:
Maya Chopra, Meera E. Modi, Kira A. Dies, Nancy L. Chamberlin, Elizabeth D. Buttermore, Stephanie Jo Brewster, Lisa Prock, Mustafa Sahin
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 27, Iss , Pp 32-46 (2022)
Interest in gene-based therapies for neurodevelopmental disorders is increasing exponentially, driven by the rise in recognition of underlying genetic etiology, progress in genomic technology, and recent proof of concept in several disorders. The cur
Externí odkaz:
https://doaj.org/article/b06707dc5eda41d08b9202717d7435f6
Autor:
Dhamne, Sameer C.1 (AUTHOR), Modi, Meera E.1 (AUTHOR), Gray, Audrey2 (AUTHOR), Bonazzi, Simone2 (AUTHOR), Craig, Lucas2 (AUTHOR), Bainbridge, Elizabeth1 (AUTHOR), Lalani, Lahin1 (AUTHOR), Super, Chloe E.1 (AUTHOR), Schaeffer, Samantha1 (AUTHOR), Capre, Ketthsy2 (AUTHOR), Lubicka, Danuta2 (AUTHOR), Liang, Guiqing2 (AUTHOR), Burdette, Doug2 (AUTHOR), McTighe, Stephanie M.2 (AUTHOR), Gurnani, Sarika1 (AUTHOR), Vermudez, Sheryl Anne D.1 (AUTHOR), Curtis, Daniel2 (AUTHOR), Wilson, Christopher J.2 (AUTHOR), Hameed, Mustafa Q.1 (AUTHOR), D'Amore, Angelica1 (AUTHOR)
Publikováno v:
Annals of Clinical & Translational Neurology. Oct2023, Vol. 10 Issue 10, p1790-1801. 12p.
Akademický článek
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Autor:
Deo, Meera E.
Publikováno v:
Journal of Legal Education, 2020 Jan 01. 69(2), 396-401.
Externí odkaz:
https://www.jstor.org/stable/27073494
Autor:
Michael. G. Mariscal, Elizabeth Berry-Kravis, Joseph D. Buxbaum, Lauren E. Ethridge, Rajna Filip-Dhima, Jennifer H. Foss-Feig, Alexander Kolevzon, Meera. E. Modi, Matthew W. Mosconi, Charles A. Nelson, Craig M. Powell, Paige M. Siper, Latha Soorya, Andrew Thaliath, Audrey Thurm, Bo Zhang, Mustafa Sahin, April R. Levin, the Developmental Synaptopathies Consortium
Publikováno v:
Molecular Autism, Vol 12, Iss 1, Pp 1-12 (2021)
Abstract Background Phelan-McDermid Syndrome (PMS) is a rare condition caused by deletion or mutation of the SHANK3 gene. Individuals with PMS frequently present with intellectual disability, autism spectrum disorder, and other neurodevelopmental cha
Externí odkaz:
https://doaj.org/article/31f157c0ad1e4a1da7dc386b11384ca7