Results 181 to 190 of about 61,218 (243)

Human iPSC-derived neural progenitor cells rescue motor function and brain pathology in symptomatic Canavan disease mice. [PDF]

open access: yesStem Cell Reports
Jackson N   +8 more
europepmc   +1 more source

Immunoaffinity‐Mimetic Assembly of Peptide‐Aptamer Conjugates and Stem Cell‐Derived Exosomes into Hierarchical Microgels for Spinal Cord Injury Repair

open access: yesAdvanced Science, Volume 13, Issue 16, 18 March 2026.
Inspired by antibody‐antigen binding, this study develops an unprecedented immunoaffinity‐mimetic assembly strategy, with Peptide‐AptCD63 conjugates acting as antibody surrogates binding CD63 epitopes on mesenchymal stem cell‐derived exosomes. This creates a hierarchical microstructure intended to synergistically integrate antioxidative and anti ...
Dantong Zheng   +8 more
wiley   +1 more source

Schwann Cell Synthesized Cholesterol Orchestrates Peripheral Nerve Regeneration via Structural and IGF1‐Dependent Signaling Mechanisms

open access: yesAdvanced Science, Volume 13, Issue 16, 18 March 2026.
This study reveals that Schwann cell FDFT1‐mediated cholesterol synthesis is essential for peripheral nerve regeneration via dual roles: as a structural component for myelin and as a metabolic signal that upregulates IGF1. IGF1 promotes axonal growth through paracrine action and enhances Schwann cell differentiation/ myelination via an intrinsic IGF1R ...
Shuyi Xu   +12 more
wiley   +1 more source

A metabolic switch for myelination. [PDF]

open access: yesCell Regen
Niu S, Zhao L, Jia D.
europepmc   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 661-672, March 2026.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim   +9 more
wiley   +1 more source

Specific Association Patterns Between Brain Glutathione Levels, Myelination, and Functional Connectivity in Adults With Autism Spectrum Disorder. [PDF]

open access: yesAutism Res
Iwabuchi T   +10 more
europepmc   +1 more source

From cradle to cortex: An exposome‐ and equity‐centered perspective of neurocognitive aging and dementia risk in the era of climate change

open access: yesAlzheimer's &Dementia, Volume 22, Issue 3, March 2026.
Abstract The convergence of climate change, adverse environmental exposures, and rapid population aging necessitates an equity‐based paradigm shift in safeguarding brain health across the life course. Older adults, especially those in marginalized and low‐resource settings, face disproportionate exposure to air pollution, toxicants, and climate‐related
Kelly E. Perry, Jenna Merenstein
wiley   +1 more source

Human Myelin Spheres for in Vitro Oligodendrocyte Maturation, Myelination and Neurological Disease Modeling. [PDF]

open access: yesStem Cell Rev Rep
Ahuja K   +23 more
europepmc   +1 more source

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