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Neuronal UBE3A substrates hold therapeutic potential for Angelman syndrome
JC Krzeski, MC Judson, BD Philpot - Current Opinion in Neurobiology, 2024 - Elsevier
Emerging therapies for Angelman syndrome, a severe neurodevelopmental disorder, are
focused on restoring UBE3A gene expression in the brain. Further therapeutic opportunities …
focused on restoring UBE3A gene expression in the brain. Further therapeutic opportunities …
Understanding ubiquitination in neurodevelopment by integrating insights across space and time
MC Ambrozkiewicz, S Lorenz - Nature Structural & Molecular Biology, 2025 - nature.com
Ubiquitination regulates a myriad of eukaryotic signaling cascades by modifying substrate
proteins, thereby determining their functions and fates. In this perspective, we discuss …
proteins, thereby determining their functions and fates. In this perspective, we discuss …
Transcriptional reprogramming restores UBE3A brain-wide and rescues behavioral phenotypes in an Angelman syndrome mouse model
Angelman syndrome (AS) is a neurogenetic disorder caused by the loss of ubiquitin ligase
E3A (UBE3A) gene expression in the brain. The UBE3A gene is paternally imprinted in brain …
E3A (UBE3A) gene expression in the brain. The UBE3A gene is paternally imprinted in brain …
Crosstalk between ubiquitination and translation in neurodevelopmental disorders
N Elu, S Subash, S R. Louros - Frontiers in Molecular Neuroscience, 2024 - frontiersin.org
Ubiquitination is one of the most conserved post-translational modifications and together
with mRNA translation contributes to cellular protein homeostasis (proteostasis). Temporal …
with mRNA translation contributes to cellular protein homeostasis (proteostasis). Temporal …
STING exerts antiviral innate immune response by activating pentose phosphate pathway
DH Wu, ZL Zhao, WT Yin, H Liu, XY **ang… - Cell Communication and …, 2024 - Springer
Background The innate immune system serves as the host's first line of defense against
invading pathogens. Stimulator of interferon genes (STING) is a key component of this …
invading pathogens. Stimulator of interferon genes (STING) is a key component of this …
Posttranslational acylations of the rat brain transketolase discriminate the enzyme responses to inhibitors of ThDP-dependent enzymes or thiamine transport
VA Aleshin, T Kaehne, MV Maslova, AV Graf… - International Journal of …, 2024 - mdpi.com
Transketolase (TKT) is an essential thiamine diphosphate (ThDP)-dependent enzyme of the
non-oxidative branch of the pentose phosphate pathway, with the glucose-6P flux through …
non-oxidative branch of the pentose phosphate pathway, with the glucose-6P flux through …
[HTML][HTML] Multiscale spatio-temporal dynamics of UBE3A gene in brain physiology and neurodevelopmental disorders
M Biagioni, F Baronchelli, M Fossati - Neurobiology of Disease, 2024 - Elsevier
The UBE3A gene, located in the chromosomal region 15q11-13, is subject to neuron-
specific genomic imprinting and it plays a critical role in brain development. Genetic defects …
specific genomic imprinting and it plays a critical role in brain development. Genetic defects …
Can technology turn us green? Promoting green consumer behavior under the lens of norms activation theory
M Boota, S Ali, WS Khan, M Ali - Journal of Marketing …, 2025 - Taylor & Francis
The primary goal of this study is to highlight human behavior toward green consumers,
which helps to improve the social environment. In this regard, digital transformation is taken …
which helps to improve the social environment. In this regard, digital transformation is taken …
Proteomic Profiling of Potential E6AP Substrates via Ubiquitin‐based Photo‐Crosslinking Assisted Affinity Enrichment
J Schuck, C Bernecker, M Scheffner, A Marx - ChemBioChem, 2025 - Wiley Online Library
The ubiquitin (Ub) ligase E6AP, which is encoded by the UBE3A gene, has been associated
with several human diseases including cervical cancer and Angelman syndrome, a …
with several human diseases including cervical cancer and Angelman syndrome, a …
The atrial and ventricular myocardial proteome of end-stage lamin heart disease
Lamins A/C (encoded by LMNA gene) can lead to dilated cardiomyopathy (DCM). This pilot
study sought to explore the postgenomic phenotype of end-stage lamin heart disease …
study sought to explore the postgenomic phenotype of end-stage lamin heart disease …