A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder

M Ikeda, A Takahashi, Y Kamatani, Y Okahisa… - Molecular …, 2018 - nature.com
Genome-wide association studies (GWASs) have identified several susceptibility loci for
bipolar disorder (BD) and shown that the genetic architecture of BD can be explained by …

Schizophrenia-associated Mitotic Arrest Deficient-1 (MAD1) regulates the polarity of migrating neurons in the develo** neocortex

BS Goo, DJ Mun, S Kim, TTM Nhung, SB Lee… - Molecular …, 2023 - nature.com
Although large-scale genome-wide association studies (GWAS) have identified an
association between MAD1L1 (Mitotic Arrest Deficient-1 Like 1) and the pathology of …

Genome-wide investigation of VNTR motif polymorphisms in 8,222 genomes: Implications for biological regulation and human traits

S Zhang, Q Song, P Zhang, X Wang, R Guo, Y Li, S Liu… - Cell Genomics, 2024 - cell.com
Variable number tandem repeat (VNTR) is a pervasive and highly mutable genetic feature
that varies in both length and repeat sequence. Despite the well-studied copy-number …

Cortical thickness alterations are associated with astrocytes and excitatory neuron-specific transcriptome signatures in pediatric bipolar disorder

X Zhang, W Gao, W Cao, J Niu, Y Guo, D Cui… - Cerebral …, 2023 - academic.oup.com
Bipolar disorder (BD) is a heritable psychiatric disorder with a complex etiology that is often
associated with cortical alterations. Morphometric studies in adults with BD are well …

MAD2-p31comet axis deficiency reduces cell proliferation, migration and sensitivity of microtubule-interfering agents in glioma

D Wu, L Wang, Y Yang, J Huang, Y Hu, Y Shu… - Biochemical and …, 2018 - Elsevier
Abstract Mitotic arrest deficient-like-1 (MAD2, also known as MAD2L1) is thought to be an
important spindle assembly checkpoint protein, which ensures accurate chromosome …

Maternal genetic polymorphisms in the major mitotic checkpoint genes MAD1L1 and MAD2L1 associated with the risk of survival in abnormal chromosomal fetuses

Y Chan, Y Liu, Y Kong, W Xu, X Zeng, H Li… - Frontiers in …, 2023 - frontiersin.org
Background: The genetic etiology of fetal chromosome abnormalities remains unknown,
which brings about an enormous burden for patients, families, and society. The spindle …

Insight into the Structural Determinants of Imidazole Scaffold-Based Derivatives as TNF-α Release Inhibitors by in Silico Explorations

Y Wang, M Wu, C Ai, Y Wang - International Journal of Molecular …, 2015 - mdpi.com
Presently, 151 widely-diverse pyridinylimidazole-based compounds that show inhibitory
activities at the TNF-α release were investigated. By using the distance comparison …

[PDF][PDF] MAD1L1 (mitotic arrest deficient 1 like 1)

K Lima, JA Machado-Neto - DNA, 2018 - researchgate.net
MAD1L1 is coiled-coil protein that binds to improperly attached kinetochrore, what results in
recruitment and interaction with MAD2L1, activation of the mitotic checkpoint complex …

[PDF][PDF] Maestría y Doctorado en Ciencias Bioquímicas

LMR San Vicente - 2020 - ru.dgb.unam.mx
Los esfingolípidos tienen un papel importante en las vías de transducción de señales que
regulan tanto funciones fisiológicas como respuestas a estrés en eucariontes. En plantas …

[CYTOWANIE][C] Mining hub genes associated with late stage adrenocortical carcinoma.

KIF CCNB - Biomedical Research, 2019