Sex chromosome-encoded protein homologs: current progress and open questions

MC Owens, A Yanas, KF Liu - Nature Structural & Molecular Biology, 2024 - nature.com
The complexity of biological sex differences is markedly evident in human physiology and
pathology. Although many of these differences can be ascribed to the expression of sex …

Autism spectrum disorder and various mechanisms behind it

P Rajabi, AS Noori, J Sargolzaei - Pharmacology Biochemistry and …, 2024 - Elsevier
Abstract Autism Spectrum Disorder (ASD) is a complex and heterogeneous
neurodevelopmental condition characterized by a range of social, communicative, and …

Late stage melanoma is hallmarked by low NLGN4X expression leading to HIF1A accumulation

D Schörghofer, L Vock, MA Mirea, O Eckel… - British Journal of …, 2024 - nature.com
Background Despite ongoing research and recent advances in therapy, metastatic
melanoma remains one of the cancers with the worst prognosis. Here we studied the …

Genetic etiology of autism spectrum disorder in the African population: a scoping review

O Hakizimana, J Hitayezu, JP Uyisenga… - Frontiers in …, 2024 - frontiersin.org
Background Autism spectrum disorder (ASD) is a neurodevelopmental disorder (NDD)
characterized by significant impairments in social, communicative, and behavioral abilities …

Neuroplasticity of children in autism spectrum disorder

Z Chen, X Wang, S Zhang, F Han - Frontiers in Psychiatry, 2024 - frontiersin.org
Autism spectrum disorder (ASD) is a neurodevelopmental disorder that encompasses a
range of symptoms including difficulties in verbal communication, social interaction, limited …

[HTML][HTML] Key Synaptic Pathology in Autism Spectrum Disorder: Genetic Mechanisms and Recent Advances

Y Zhang, R Tang, ZM Hu, XH Wang, X Gao… - Journal of Integrative …, 2024 - imrpress.com
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by
impaired social interactions and verbal communication, accompanied by symptoms of …

Micro-Scale Control of Oligodendrocyte Morphology and Myelination by the Intellectual Disability-Linked Protein Acyltransferase ZDHHC9

HK Jeong, E Gonzalez-Fernandez, I Crawley, J Hwang… - bioRxiv, 2023 - biorxiv.org
Mutations in the X-linked ZDHHC9 gene cause cognitive deficits in humans, with a subset of
patients suffering from epilepsy. X-linked intellectual disability (XLID) is often ascribed to …

Otizm spektrum bozukluğu tanısı olan çocuklar ile kardeşlerinin periferik dolaşımda NCAM-1, NRXN-1, NLGN-4, CDH2 düzeylerinin değerlendirilmesi

ATH Selen - 2024 - acikerisim.erbakan.edu.tr
Amaç: Otizm spektrum bozukluğu (OSB), sinaptik fonksiyon ve plastisite ile bağlantılı olduğu
ve bu süreçlerde hücre adezyon moleküllerinin (CAM) önemli bir rol oynadığı …

A influência dos níveis de ocitocina e expressão de seus receptores no desenvolvimento de crianças com Transtorno do Espectro Autista (TEA): uma revisão …

ACM Bandeira, MLC de Souza… - Revista …, 2024 - revistas2.unievangelica.edu.br
Resumo O Transtorno do Espectro Autista (TEA) é um distúrbio do desenvolvimento
marcado por dificuldades na interação social e na comunicação, tanto verbal quanto não …

[引用][C] Physiological and lifestyle-related cardiovascular risk factors for vessels, ventricle, and valve

P Sarajlic - 2024 - Inst för medicin, Solna/Dept of …