Results 221 to 230 of about 97,673 (295)

EU Policy‐Making in the Digital Age: Major Trends and Insights From Public Policy Research

European Policy Analysis, EarlyView.
ABSTRACT Has digitalization changed policy‐making dynamics at the European Union (EU) level? To investigate this issue, this article presents a scoping review of the literature on EU digital policy‐making. While much scholarship adopts a ‘Governance’ approach, two conceptually rich strands emerge: critical approaches, and digital sovereignty.
Chloé Bérut
wiley   +1 more source

Cell type diversification and phenotype convergence underlying white fin-ornamentation of cyprinid fishes. [PDF]

Proc Natl Acad Sci U S A
Huang D, Liu T, Carr AA, de Mello PH, Liang Y, Shriver LP, Chauvigné F, Johnson SL, Cerdà J, Patti GJ, Parichy DM.   +10 more
europepmc   +1 more source

Mechanisms of SCN2A loss of function do not predict presence or phenotype of epilepsy

Epilepsia, EarlyView.
Abstract Objective SCN2A loss‐of‐function (LoF) variants are associated with epilepsy (onset age ≥ 3 months), intellectual disability (ID), and autism spectrum disorder (ASD). Despite numerous identified variants and the description of phenotypic subgroups, relationships between Nav1.2 channel dysfunction and clinical phenotypes remain unclear.
Marsha Tan, Beatrice Southby Goad, Meagan Allen, Jill Rodda, Kay L. Richards, Simone L. Ardern‐Holmes, Daniel Bamborschke, Daniel Fritzen, Inna Hughes, Kate Riney, Ana Roche Martinez, Angelo Russo, Adriane Sinclair, Stefano Sartori, Marina Trivisano, Angela De Dominicis, Nicola Specchio, Rikke S. Møller, Ingrid E. Scheffer, Walid Fazeli, Markus Wolff, Steven Petrou, Katherine B. Howell, Géza Berecki   +23 more
wiley   +1 more source

Spectrum of Various Mosaicism Types According to Female Age: An Analysis of 36,506 Blastocysts Using Preimplantation Genetic Testing for Aneuploidy. [PDF]

Biomedicines
Jeon MS, Kim MJ, Choi N, Hong J, Choi R, Jeong Y, Lee HS, Lee KA, Yu EJ, Kang IS.   +9 more
europepmc   +1 more source

Genetic testing for familial epilepsies: Diagnostic yield and genetic findings

Epilepsia, EarlyView.
Abstract Objective Genetic testing has become a routine part of clinical epilepsy care. Family history is an indication for genetic testing, but the diagnostic yield, predictors of a genetic diagnosis, and association with familial patterns are not well understood.
Colin A. Ellis, Juliette Copeland, Isabella Velez, Karen L. Oliver, Hannah Shalaby, Aaron Baldwin, Caren Armstrong, Amanda Back, Brianna Berlin, Stacey Cohen, Vishnu Anand Cuddapah, Danielle deCampo, Holly Dubbs, Natalie Ginn, Alicia G. Harrison, Naomi Lewin, Laina Lusk, Eric D. Marsh, Shavonne L. Massey, Pamela Pojomovsky McDonnell, Jillian L. McKee, Xilma Ortiz‐Gonzalez, Anna J. Prentice, Katie Rose Sullivan, Sarah M. Ruggiero, Mark P. Fitzgerald, Ethan M. Goldberg, Ingo Helbig   +27 more
wiley   +1 more source

Impact of the war on forest ecosystem in Ukraine based on Sentinel-2 data. [PDF]

Sci Rep
Waśniewski A, Rynkiewicz A, Hościło A, Havryliuk S, Chaskovskyy O.   +4 more
europepmc   +1 more source

A comprehensive study of c-Kit-expressing amacrine cells in the mammalian retina. [PDF]

Sci Rep
Jiang Z, Shen W.
europepmc   +1 more source

Integrative Advances in Pig Genomics: From Reference Assemblies and Evolutionary History to the Mechanistic Dissection of Key Traits. [PDF]

Biology (Basel)
Tang S, Li D, Lu Y, Gao Z, Wang B, Liu X, Wei H, Wu J.   +7 more
europepmc   +1 more source

Optimization-Based Pairwise Interaction Point Process (O-PIPP): A Precise and Universal Retinal Mosaic Modeling Approach. [PDF]

Invest Ophthalmol Vis Sci
He L, Wang W, Ma L, Huang T.
europepmc   +1 more source