The extracellular matrix in development

DAC Walma, KM Yamada - Development, 2020 - journals.biologists.com
As the crucial non-cellular component of tissues, the extracellular matrix (ECM) provides
both physical support and signaling regulation to cells. Some ECM molecules provide a …

The intercalated disc: a unique organelle for electromechanical synchrony in cardiomyocytes

MS Nielsen, CJM van Opbergen… - Physiological …, 2023 - journals.physiology.org
The intercalated disc (ID) is a highly specialized structure that connects cardiomyocytes via
mechanical and electrical junctions. Although described in some detail by light microscopy …

The genetic architecture of depression in individuals of East Asian ancestry: a genome-wide association study

O Giannakopoulou, K Lin, X Meng, MH Su… - JAMA …, 2021 - jamanetwork.com
Importance Most previous genome-wide association studies (GWAS) of depression have
used data from individuals of European descent. This limits the understanding of the …

[HTML][HTML] CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice

D Halperin, A Stavsky, R Kadir, M Drabkin… - Nature …, 2021 - nature.com
Attention-deficit hyperactivity disorder (ADHD) is a common childhood-onset psychiatric
disorder characterized by inattention, impulsivity and hyperactivity. ADHD exhibits …

[HTML][HTML] Excess ribosomal protein production unbalances translation in a model of Fragile X Syndrome

SS Seo, SR Louros, N Anstey… - Nature …, 2022 - nature.com
Dysregulated protein synthesis is a core pathogenic mechanism in Fragile X Syndrome (FX).
The mGluR Theory of FX predicts that pathological synaptic changes arise from the …

[HTML][HTML] Flying under the radar: CDH2 (N-cadherin), an important hub molecule in neurodevelopmental and neurodegenerative diseases

ZI László, Z Lele - Frontiers in Neuroscience, 2022 - frontiersin.org
CDH2 belongs to the classic cadherin family of Ca2+-dependent cell adhesion molecules
with a meticulously described dual role in cell adhesion and β-catenin signaling. During …

Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defects

L AlAbdi, M Desbois, DV Rusnac, RA Sulaiman… - Brain, 2023 - academic.oup.com
The corpus callosum is a bundle of axon fibres that connects the two hemispheres of the
brain. Neurodevelopmental disorders that feature dysgenesis of the corpus callosum as a …

Cadherin 2-related arrhythmogenic cardiomyopathy: prevalence and clinical features

A Ghidoni, PM Elliott, P Syrris, H Calkins… - Circulation: Genomic …, 2021 - Am Heart Assoc
Background: Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiac disease
characterized by fibrofatty replacement of the right and left ventricle, often causing …

[HTML][HTML] Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

SN Kobren, D Baldridge, M Velinder, JB Krier… - Genetics in …, 2021 - nature.com
Purpose Genomic sequencing has become an increasingly powerful and relevant tool to be
leveraged for the discovery of genetic aberrations underlying rare, Mendelian conditions …

[HTML][HTML] Stick around: cell–cell adhesion molecules during neocortical development

D de Agustín-Durán, I Mateos-White, J Fabra-Beser… - Cells, 2021 - mdpi.com
The neocortex is an exquisitely organized structure achieved through complex cellular
processes from the generation of neural cells to their integration into cortical circuits after …