Lou Gehrig's Disease News and Research

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Lou Gehrig's Disease or Amyotrophic Lateral Sclerosis (ALS) is a neurological disorder characterized by progressive degeneration of motor neuron cells in the spinal cord and brain, which ultimately results in paralysis and death. The disease takes its less-scientific name from Lou Gehrig, a baseball player with the New York Yankees in the late 1920s and 1930s, who was forced to retire in 1939 as a result of the loss of motor control caused by the disease.

In 1991, a team of researchers linked familial ALS to chromosome 21. Two years later, the SOD1 gene was identified as being associated with many cases of familial ALS. The enzyme coded for by SOD1 carries out a very important function in cells: it removes dangerous superoxide radicals by converting them into non-harmful substances. Defects in the action of this enzyme mean that the superoxide radicals attack cells from the inside, causing their death. Several different mutations in this enzyme all result in ALS, making the exact molecular cause of the disease difficult to ascertain.

Recent research has suggested that treatment with drugs called antioxidants may benefit ALS patients. However, since the molecular genetics of the disease are still unclear, a significant amount of research is still required to design other promising treatments for ALS.
Scientists determine structure of Ltn1 protein

Scientists determine structure of Ltn1 protein

ARHGEF28 gene mutations present in amyotrophic lateral sclerosis: Research

ARHGEF28 gene mutations present in amyotrophic lateral sclerosis: Research

Repression of PTB protein in fibroblasts can convert pluripotent stem cells into functional neurons

Repression of PTB protein in fibroblasts can convert pluripotent stem cells into functional neurons

Apparent stem cell transplant success in mice may hold promise for people with ALS

Apparent stem cell transplant success in mice may hold promise for people with ALS

FUS RNA binding ability essential for development of Amyotrophic Lateral Sclerosis

FUS RNA binding ability essential for development of Amyotrophic Lateral Sclerosis

Scientists uncover TDP-43 protein as possible target for treatment of ALS, FTD

Scientists uncover TDP-43 protein as possible target for treatment of ALS, FTD

Lou Gehrig's disease may be treatable using neural stem cells

Lou Gehrig's disease may be treatable using neural stem cells

Lack of TDP-43 protein can lead to frontotemporal dementia/ALS

Lack of TDP-43 protein can lead to frontotemporal dementia/ALS

FoxP3 gene expression identifies ALS disease progression in 80% of patients

FoxP3 gene expression identifies ALS disease progression in 80% of patients

Novel test reveals rate of progression of amyotrophic lateral sclerosis in patients

Novel test reveals rate of progression of amyotrophic lateral sclerosis in patients

Facts about Homecare

Facts about Homecare

Top-line results from Neuraltus’ NP001 Phase 2 study on amyotrophic lateral sclerosis

Top-line results from Neuraltus’ NP001 Phase 2 study on amyotrophic lateral sclerosis

STAT3 transcription factor remains in the axon of nerve cells to help prevent neurodegeneration

STAT3 transcription factor remains in the axon of nerve cells to help prevent neurodegeneration

Researchers use baker's yeast to identify new therapies for Lou Gehrig's disease

Researchers use baker's yeast to identify new therapies for Lou Gehrig's disease

Study describes how Dbr1 gene halts toxic buildup of TDP-43-a protein

Study describes how Dbr1 gene halts toxic buildup of TDP-43-a protein

First Edition: October 16, 2012

First Edition: October 16, 2012

Animal research shows promise in treating AD, brain damage and heart problems resulting from SCIs

Animal research shows promise in treating AD, brain damage and heart problems resulting from SCIs

Scripps scientists to study several compounds with potential to improve QOL for ALS patients

Scripps scientists to study several compounds with potential to improve QOL for ALS patients

New mouse model could foster ALS, Paget's and dementia breakthroughs

New mouse model could foster ALS, Paget's and dementia breakthroughs

Common RNA pathway links frontotemporal lobar dementia with ALS

Common RNA pathway links frontotemporal lobar dementia with ALS

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