Press Releases

Image
Map of gene expression levels in a sample of human brain tissue.
Friday, June 21, 2024
NIH-funded study shines light on disease mechanisms, pointing to possible therapeutic targets
Image
cryptic peptide shown in red
Wednesday, January 31, 2024

Proteins could serve as biomarkers that improve diagnosis and guide the development of novel therapies 

Image
Cell types found in the spinal cord
Thursday, February 2, 2023
Human spinal cord cell atlas provides foundation to study neurodegeneration, chronic pain, and other diseases.
Image
NIH Logo
Wednesday, September 14, 2022
Today, the U.S. Food and Drug Administration and the National Institutes of Health (NIH) announced the launch of the Critical Path for Rare Neurodegenerative Diseases (CP-RND)—a public-private partnership aimed at advancing the understanding of neurodegenerative diseases and fostering the development of treatments for amyotrophic lateral sclerosis (ALS) and other rare neurodegenerative diseases.
Image
NIH Logo
Tuesday, August 30, 2022
Researchers have published two papers describing how they identified a potential new pathway for treating a sporadic form of amyotrophic lateral sclerosis (ALS). The studies were published as part of a cooperative research agreement between the National Institute of Neurological Disorders and Stroke (NINDS), part of the National Institutes of Health, and the Switzerland-based biotechnology company GeNeuro Inc.
Image
Illustration of brain cell firing an action potential.
Monday, February 28, 2022
Researchers from two independent research teams have discovered how the mislocalization of a protein, known as TDP-43, alters the genetic instructions for UNC13A, providing a possible therapeutic target that could also have implications in treating amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), and other forms of dementia.
Image
Picture of two neurons from a mouse spinal cord.
Monday, January 24, 2022
Using an experimental drug, researchers were able to suppress a mutated amyotrophic lateral sclerosis (ALS) gene.
Image
oligodendrocyte wrapping around axon and providing SIRT to boost ATP levels
Thursday, September 30, 2021

NIH study identifies possible target for certain neurodegenerative disorders

Image
Picture of patient examination. Patient in wheelchair is on the left. The examining doctor is on the right. In the middle of the picture is another doctor sitting and observing the examination.
Monday, May 31, 2021

In a study of 11 medical-mystery patients, an international team of researchers led by scientists at the National Institutes of Health and the Uniformed Services University (USU) discovered a new and unique form of amyotrophic lateral sclerosis (ALS).

Export to:
A maximum of 400 records can be exported.