Navigating the dementia landscape: Biomarkers and emerging therapies

S Maheshwari, A Singh, VA Ansari, T Mahmood… - Ageing Research …, 2024 - Elsevier
The field of dementia research has witnessed significant developments in our understanding
of neurodegenerative disorders, with a particular focus on Alzheimer's disease (AD) and …

Dendrimers in corneal drug delivery: recent developments and translational opportunities

A Dhull, C Yu, AH Wilmoth, M Chen, A Sharma, S Yiu - Pharmaceutics, 2023 - mdpi.com
Dendrimers are biocompatible organic nanomaterials with unique physicochemical
properties, making them the focus of recent research in drug delivery. The cornea of the …

A Review on Tau Targeting Biomimetics Nano Formulations: Novel Approach for Targeting Alzheimer's Diseases

A Singh, S Maheshwari, JP Yadav… - … System Agents in …, 2024 - benthamdirect.com
Central nervous system disorders are prevalent, profoundly debilitating, and poorly
managed. Developing innovative treatments for these conditions, including Alzheimer's …

Dendrimer-enabled targeted delivery attenuates glutamate excitotoxicity and improves motor function in a rabbit model of cerebral palsy

F Zhang, Z Zhang, J Alt, SP Kambhampati… - … Clinics and Research, 2023 - journals.lww.com
Glutamate carboxypeptidase II (GCPII), localized on the surface of astrocytes and activated
microglia, regulates extracellular glutamate concentration in the central nervous system …

Inorganic Nanoparticles for Brain Targeting Scope and Limitations

H Ahmed, S Singh, A Alexander - … of Nanocarriers in Brain Delivery of …, 2024 - Springer
The drug delivery to the brain on systemic administration creates hindrance because of the
presence of blood–brain barrier (BBB). The utilization of novel nanomaterials such as …

From gene to therapy: a review of deciphering the role of ABCD1 in combating X-Linked adrenoleukodystrophy

X Zuo, Z Chen - Lipids in Health and Disease, 2024 - Springer
Abstract X-linked adrenoleukodystrophy (X-ALD) is a severe genetic disorder caused by
ABCD1 mutations, resulting in the buildup of very-long-chain fatty acids, leading to …

Generation and characterization of a zebrafish gain-of-function ACOX1 Mitchell disease model

Q Raas, A Wood, TJ Stevenson, S Swartwood… - Frontiers in …, 2024 - frontiersin.org
Background Mitchell syndrome is a rare, neurodegenerative disease caused by an ACOX1
gain-of-function mutation (c. 710A> G; p. N237S), with fewer than 20 reported cases …

Cystic Fibrosis Modulator Therapies: Bridging Insights from CF to other Membrane Protein Misfolding Diseases

M Kim, L Plate - Israel Journal of Chemistry, 2024 - Wiley Online Library
Cystic Fibrosis (CF) is a genetic disorder resulting from mutations in the cystic fibrosis
transmembrane conductance regulator (CFTR) gene, leading to a faulty CFTR protein …

[HTML][HTML] MedLink®, LLC

DS Rajan, EA Ali - medlink.com
X-linked adrenoleukodystrophy is a progressive neurodegenerative peroxisomal disorder
caused by mutations in the ABCD1 gene, leading to accumulation of very long-chain fatty …