Results 201 to 210 of about 5,276,450 (332)

Navigating international academic collaboration: The Arabic translation and cultural adaptation of the Quality Maternal and Newborn Care Framework index. [PDF]

PLoS One
Zaza K, Symon A, Hassan S, Ali-Masri H, McNeill J, Stockdale J, Alhulaibi W, Mortensen B.   +7 more
europepmc   +1 more source

Aging Is a Key Driver for Adult Acute Myeloid Leukemia

Aging and Cancer, EarlyView.
Acute myeloid leukemia (AML) is a classical age‐related hematologic malignancy, and a key driver of AML is aging, which profoundly regulates intrinsic factors such as genomic instability, epigenetic reprogramming, and metabolic dysregulation, and alters bone marrow microenvironment.
Rong Yin, Haojian Zhang
wiley   +1 more source

Circular RNA as emerging precision therapeutics: from RNA regulation to peptide translation. [PDF]

Precis Clin Med
Wu N, Amalraj J, Yang BB.
europepmc   +1 more source

Mutant NPM1 in Acute Myeloid Leukemia Initiation and Maintenance

Aging and Cancer, EarlyView.
NPM1 mutations drive acute myeloid leukemia by acting as neomorphic transcriptional regulators that cooperate with Menin–MLL and XPO1 to sustain HOX/MEIS1 expression and block differentiation. Targeting these mutant‐specific transcriptional dependencies provides a rational therapeutic strategy for NPM1‐mutated AML.
Yanan Jiang, Zhong Fan, Runmeng Liu, Xiaotian Zhang   +3 more
wiley   +1 more source

Exploring the use of translation technologies to overcome language barriers in mental healthcare: a qualitative cross-country study. [PDF]

Int J Equity Health
Kreienbrinck A, Hanft-Robert S, Topçu MT, Peters L, Oltean O, Nozewu A, Al-Kalaf H, Liem A, Forray AI, Madzamba R, Swartz L, Anthonissen C, Sanders T, Hall B, Schouten B, Jenks C, Cherecheș R, Mösko M.   +17 more
europepmc   +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

Bridging single-molecule and genome-wide studies of cellular mRNA translation. [PDF]

RNA
Koch A, Tomuro K, Wakigawa T, Morisaki T, Iwasaki S, Stasevich TJ.   +5 more
europepmc   +1 more source

Translatress, Translator, Translation

, 2009
I still manage to surprise a few scholars from other fields when they hear that there is such a thing as research of gender issues within the field of translation studies. It may seem as such a narrow niche – but only deceivingly so. It is language, linguistics, pragmatics, culture, history, literature, anthropology, gender metaphorics, communication ...
openaire   +1 more source

Regulation of translation initiation in eukaryotes: mechanisms and biological targets.

Cell, 2009
N. Sonenberg, A. Hinnebusch
semanticscholar   +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