Turnitin
降AI改写
早检测系统
早降重系统
Turnitin-UK版
万方检测-期刊版
维普编辑部版
Grammarly检测
Paperpass检测
checkpass检测
PaperYY检测
Introduction to exosome and its role in brain disorders
H Sharma, HK Rachamalla, N Mishra… - Exosomes Based Drug …, 2024 - Springer
Exosomes, which are small extracellular vehicles produced by a variety of cell types, have
emerged as key actors in intercellular communication due to their ability to transport a …
emerged as key actors in intercellular communication due to their ability to transport a …
[HTML][HTML] Small-molecule inhibition of the METTL3/METTL14 complex suppresses neuroblastoma tumor growth and promotes differentiation
M Pomaville, M Chennakesavalu, P Wang, Z Jiang… - Cell reports, 2024 - cell.com
Summary The N 6-methyladenosine (m 6 A) RNA modification is an important regulator of
gene expression. m 6 A is deposited by a methyltransferase complex that includes …
gene expression. m 6 A is deposited by a methyltransferase complex that includes …
The molecular basis of p21-activated kinase-associated neurodevelopmental disorders: from genotype to phenotype
M Dobrigna, S Poëa-Guyon, V Rousseau… - Frontiers in …, 2023 - frontiersin.org
Although the identification of numerous genes involved in neurodevelopmental disorders
(NDDs) has reshaped our understanding of their etiology, there are still major obstacles in …
(NDDs) has reshaped our understanding of their etiology, there are still major obstacles in …
Exome sequencing and the identification of new genes and shared mechanisms in polymicrogyria
Importance Polymicrogyria is the most commonly diagnosed cortical malformation and is
associated with neurodevelopmental sequelae including epilepsy, motor abnormalities, and …
associated with neurodevelopmental sequelae including epilepsy, motor abnormalities, and …
[HTML][HTML] The power of human stem cell-based systems in the study of neurodevelopmental disorders
M Jhanji, EM York, SB Lizarraga - Current Opinion in Neurobiology, 2024 - Elsevier
Highlights•Overview of convergent disease mechanisms across NDDs identified in 2D & 3D
models.•Discuss therapeutic implications for various ASOs and gene editing …
models.•Discuss therapeutic implications for various ASOs and gene editing …
[HTML][HTML] Functional genomics and small molecules in mitochondrial neurodevelopmental disorders
DG Calame, LT Emrick - Neurotherapeutics, 2024 - Elsevier
Mitochondria are critical for brain development and homeostasis. Therefore, pathogenic
variation in the mitochondrial or nuclear genome which disrupts mitochondrial function …
variation in the mitochondrial or nuclear genome which disrupts mitochondrial function …
Unbiased phenotype and genotype matching maximizes gene discovery and diagnostic yield
J Rips, O Halstuk, A Fuchs, Z Lang, T Sido… - Genetics in …, 2024 - Elsevier
Purpose Widespread application of next-generation sequencing, combined with data
exchange platforms, has provided molecular diagnoses for countless families. To maximize …
exchange platforms, has provided molecular diagnoses for countless families. To maximize …
[HTML][HTML] Exploring the mechanisms of lithium neurotoxicity based on network toxicology and molecular docking
W Wei, S Pu, C Yan, H Yang, H Chen - Ecotoxicology and Environmental …, 2025 - Elsevier
The rapid growth of lithium (Li)-related industrial activities and the application of Li-
containing products have become an emerging human health concern. Li has been …
containing products have become an emerging human health concern. Li has been …
The kinesin Kif21b regulates radial migration of cortical projection neurons through a non-canonical function on actin cytoskeleton
JR Alvarez, L Asselin, P Tilly, R Benoit, C Batisse… - Cell Reports, 2023 - cell.com
Completion of neuronal migration is critical for brain development. Kif21b is a plus-end-
directed kinesin motor protein that promotes intracellular transport and controls microtubule …
directed kinesin motor protein that promotes intracellular transport and controls microtubule …
KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon
M Almannai, L AlAbdi, S Maddirevula, M Alotaibi… - Human Genetics, 2023 - Springer
Human disorders of the enteric nervous system (ENS), eg, Hirschsprung's disease, are
rarely associated with major central nervous system involvement. We describe two families …
rarely associated with major central nervous system involvement. We describe two families …