Results 251 to 260 of about 46,251,330 (370)

Biological functions of tsRNAs and research advances in human disease. [PDF]

Biochem Biophys Rep
Jiang Y, Liu S, Li G, Tang C, Zhang Y, Li J, Tan Z, Zhang S, Chen Z, Li S.   +9 more
europepmc   +1 more source

Depression, stress, and weight loss in individuals with metabolic syndrome in SHINE, a DPP translation study

, 2014
Paula M. Trief, Donald A. Cibula, Linda M. Delahanty, Ruth S. Weinstock   +3 more
openalex   +2 more sources

Amyotrophic Lateral Sclerosis Prevalence Projection in 2040: A Less Rare Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To project ALS prevalence across multiple countries through 2040, accounting for both population aging and increased survival. Methods Data from the Piemonte and Valle d'Aosta ALS register (PARALS) was used to estimate the trends in incidence and prevalence from 2005 to 2019. Survival trends over this period were also assessed.
Rosario Vasta, Stefano Callegaro, Antonio Canosa, Umberto Manera, Maurizio Grassano, Francesca Palumbo, Sara Cabras, Enrico Matteoni, Francesca Di Pede, Filippo De Mattei, Salvatore Tafaro, Neil M. Thakur, Ryan Grosenick, Fabiola De Marchi, Letizia Mazzini, Cristina Moglia, Andrea Calvo, Kuldip D. Dave, Adriano Chiò   +18 more
wiley   +1 more source

Sketching landscapes in translation studies: A bibliographic study

, 2015
F. Zanettin, G. Saldanha, S. Harding
semanticscholar   +1 more source

Translational Needs: Informing Tools to Close the Knowledge-to-Practice Gap in Suicide Prevention. [PDF]

Health Promot J Austr
Tran M, Stewart L, Cuenca J, Benson M, Reifels L.   +4 more
europepmc   +1 more source

A Study on the Definition of Ego-introspectionand Translation․Reverse Translation problem -Based on the study of Korean language and oriental origin-

, 2018
장만식
openalex   +1 more source

Exploratory Analysis of ELP1 Expression in Whole Blood From Patients With Familial Dysautonomia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Familial dysautonomia (FD) is a hereditary neurodevelopmental disorder caused by aberrant splicing of the ELP1 gene, leading to a tissue‐specific reduction in ELP1 protein expression. Preclinical models indicate that increasing ELP1 levels can mitigate disease manifestations.
Alejandra González‐Duarte, Lucy Norcliffe‐Kaufmann, Maria Luisa Cotrina, Zenith Khan, Kaia Dalamo, Patricio Millar Vernetti, Matthew Lawless, Elisabetta Morini, Monica Salani, Marla Weetall, Jana Narasimhan, Agostino G. Rocha, Susan A. Slaugenhaupt, Horacio Kaufmann   +13 more
wiley   +1 more source

Quality control and signaling pathways at stalled ribosomes. [PDF]

Exp Mol Med
Chang WD, Choe YJ.
europepmc   +1 more source

Age‐Related Characteristics of SYT1‐Associated Neurodevelopmental Disorder

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives We describe the clinical manifestations and developmental abilities of individuals with SYT1‐associated neurodevelopmental disorder (Baker‐Gordon syndrome) from infancy to adulthood. We further describe the neuroradiological and electrophysiological characteristics of the condition at different ages, and explore the associations ...
Sam G. Norwitz, Josefine Eck, Joel S. Winston, Kate Baker   +3 more
wiley   +1 more source

Integrating human-AI collaboration into translation education: A comprehensive protocol for assessment, diagnosis, and strategy development. [PDF]

PLoS One
Ren X, Wang R.
europepmc   +1 more source