Hum. Mol. Genet. (10 May 2010), ddq183.
Juan A. Navarro, Elisabeth Ohmann, Diego Sanchez, Jose A. Botella, Gerhard Liebisch, Maria D. Molto, Maria D. Ganfornina, Gerd Schmitz, Stephan Schneuwly
Keywords: Friedreich's ataxia (FRDA), mitochondrial protein frataxin, Drosophila, lipid accumulation, peroxidation, oxidative stress, fatty acids, glial cells, lipid peroxidation.
Tuesday, May 11, 2010
The Lost Boys: Neglected Generation Of Young Men With Duchenne Muscular Dystrophy Demand More Support
Medicals News Today, Article Date: 11 May 2010
New research from the University of Bristol has found that the rights and needs of young men with Duchenne muscular dystrophy (DMD) - a life-limiting, inherited neuromuscular disease - are being severely restricted by the failure of many services to provide good planning and support.
New research from the University of Bristol has found that the rights and needs of young men with Duchenne muscular dystrophy (DMD) - a life-limiting, inherited neuromuscular disease - are being severely restricted by the failure of many services to provide good planning and support.
Thursday, May 6, 2010
CELLULAR STRESS RESPONSES, THE HORMESIS PARADIGM AND VITAGENES: NOVEL TARGETS FOR THERAPEUTIC INTERVENTION IN NEURODEGENERATIVE DISORDERS
http://www.liebertonline.com/doi/abs/10.1089/ars.2009.3074?mi=3b5d62&af=R&BeforeMonth=null&journalCode=null&issue=null&nh=20&AfterMonth=null&prevSearch=allfield%253A%2528%2522Friedreich%2527s%2522%2Bor%2B%2522Friedreich%2522%2Bor%2B%2522FRDA%2522%2529&discipline=null&group=null&restrict=all&result=true&filter=multiple&year=null&startPage=0&journal=null&AfterYear=null&favoriteJIds=null&sortBy=date&BeforeYear=null&doi=null&target=simple
Online Ahead of Editing: May 6, 2010
Online Ahead of Editing: May 6, 2010
Antioxidants & Redox Signaling. null, Vol. 0, No. ja
doi:10.1089/ars.2009.3074.
Prof. Vittorio Calabrese,University of Catania, Department of Chemistry, Catania, Italy; Dr. Carolin Cornelius,University of Catania, Department of Chemistry, Catania, Italy; Prof. Albena T. Dinkova-Kostova,University of Dundee, The Biomedical Research Institute, Dundee, United Kingdom; Prof. Edward J. Calabrese
University of Massachusetts, Environmental Health Sciences Division, School of Public Health, Amherst, Massachusetts, United States; Dr. Mark Mattson, National Institute on Aging, Intramural Research Program, Baltimore, Maryland, United States;
Keywords: chronic oxidative stress, metabolic and neurodegenerative diseases, hormesis, neuroprotection, biological plasticity, therapeutic dose, pharmaceutical agents, sirtuin, Nrfs, nitric oxide, carbon monoxide, H2S, mitochondrial redox signaling.
Tuesday, May 4, 2010
Mechanism elucidated for a rare disease
May 04 2010
Scientists at the Friedrich Miescher Institute for Biomedical Research (FMI, part of the Novartis Research Foundation) have dissected one of the molecular mechanisms underlying Friedreich's ataxia. In doing so, they have shed new light on the pathogenic mechanism of the disease. These findings could lead to the development of new therapeutic approaches for what is, as yet, an incurable condition. The results of the study were recently published in the journal EMBO Molecular Medicine.
FULL TEXT PDF
Scientists at the Friedrich Miescher Institute for Biomedical Research (FMI, part of the Novartis Research Foundation) have dissected one of the molecular mechanisms underlying Friedreich's ataxia. In doing so, they have shed new light on the pathogenic mechanism of the disease. These findings could lead to the development of new therapeutic approaches for what is, as yet, an incurable condition. The results of the study were recently published in the journal EMBO Molecular Medicine.
FULL TEXT PDF
Monday, May 3, 2010
Caenorhabditis elegans as a model system to study intercompartmental proteostasis: Interrelation of mitochondrial function, longevity, and neurodegenerative diseases
Dev Dyn. 2010 May;239(5):1529-38. DOI 10.1002/dvdy.22292
Janine Kirstein-Miles, Richard I. Morimoto *
Department of Biochemistry, Molecular Biology and Cell Biology, Rice Institute for Biomedical Research, Northwestern University, Evanston, Illinois
Keywords: proteostasis, eukaryotic cell, mitochondria, cellular metabolism, organismal development, lifespan, neurodegenerative diseases, Friedreich's ataxia, Parkinson's disease.
Janine Kirstein-Miles, Richard I. Morimoto *
Department of Biochemistry, Molecular Biology and Cell Biology, Rice Institute for Biomedical Research, Northwestern University, Evanston, Illinois
Keywords: proteostasis, eukaryotic cell, mitochondria, cellular metabolism, organismal development, lifespan, neurodegenerative diseases, Friedreich's ataxia, Parkinson's disease.
Sunday, May 2, 2010
Spinocerebellar ataxia: Patient and health professional perspectives on whether and how patents affect access to clinical genetic testing
Genetics in Medicine:
April 2010 - Volume 12 - Issue 4 - pp S83-S110
doi: 10.1097/GIM.0b013e3181d67e44
From the 1Center for Public Genomics, Center for Genome Ethics, Law and Policy, Institute of Genome Sciences and Policy, Duke University, Curriculum in Neurobiology, University of North at Carolina Chapel Hill, Center for Genomics and Society at the University of North Carolina at Chapel Hill, Chapel Hill, North Carolina; and 2Center for Genome Ethics, Law and Policy, Institute for Genome Sciences and Policy, Duke University, Durham, North Carolina.
Robert Cook-Deegan, MD, Center for Genome Ethics, Law and Policy, Institute for Genome Sciences and Policy, Duke University, Box 90141, Durham, NC 27708. Saturday, May 1, 2010
Friedreich's Ataxia Cardiomyopathy: Case Based Discussion and Management Issues
Irish Medical Journal, IMJ Online Paper.
A Hanley, R Corrigan, S Mohammad, B MacMahon
Monaghan General Hospital, Co Monaghan
Monaghan General Hospital, Co Monaghan
Keywords: Cardiac involvement, Friedreich’s Ataxia, The most common symptoms are shortness of breath at rest and palpitations, ejection systolic murmur, heart sound, ECG abnormalities, Echo abnormalities, idebenone, Beta blockers, ACE inhibitors.
Friday, April 30, 2010
Effects of Long-Term Pioglitazone Treatment on Peripheral and Central Markers of Aging
"Currently in France is running a trial with Pioglitazone . Although the subject matter of the article is not about the FA, get more information about this drug is interesting."
OPEN ACCES
PLoS ONE 5(4): e10405. doi:10.1371/journal.pone.0010405
OPEN ACCES
PLoS ONE 5(4): e10405. doi:10.1371/journal.pone.0010405
Eric M. Blalock1#, Jeremiah T. Phelps1#, Tristano Pancani1, James L. Searcy1, Katie L. Anderson1, John C. Gant1, Jelena Popovic1, Margarita G. Avdiushko2, Don A. Cohen2, Kuey-Chu Chen1, Nada M. Porter1, Olivier Thibault1*
1 Department of Molecular and Biomedical Pharmacology, University of Kentucky Medical Center, Lexington, Kentucky, United States of America, 2 Department of Microbiology and Immunology, University of Kentucky Medical Center, Lexington, Kentucky, United States of America
Abstract
Thiazolidinediones (TZDs) activate peroxisome proliferator-activated receptor gamma (PPARγ) and are used clinically to help restore peripheral insulin sensitivity in Type 2 diabetes (T2DM). Interestingly, long-term treatment of mouse models of Alzheimer's disease (AD) with TZDs also has been shown to reduce several well-established brain biomarkers of AD including inflammation, oxidative stress and Aβ accumulation. While TZD's actions in AD models help to elucidate the mechanisms underlying their potentially beneficial effects in AD patients, little is known about the functional consequences of TZDs in animal models of normal aging. Because aging is a common risk factor for both AD and T2DM, we investigated whether the TZD, pioglitazone could alter brain aging under non-pathological conditions.
FULL TEXT PDF
Thiazolidinediones (TZDs) activate peroxisome proliferator-activated receptor gamma (PPARγ) and are used clinically to help restore peripheral insulin sensitivity in Type 2 diabetes (T2DM). Interestingly, long-term treatment of mouse models of Alzheimer's disease (AD) with TZDs also has been shown to reduce several well-established brain biomarkers of AD including inflammation, oxidative stress and Aβ accumulation. While TZD's actions in AD models help to elucidate the mechanisms underlying their potentially beneficial effects in AD patients, little is known about the functional consequences of TZDs in animal models of normal aging. Because aging is a common risk factor for both AD and T2DM, we investigated whether the TZD, pioglitazone could alter brain aging under non-pathological conditions.
FULL TEXT PDF
Carbamylated erythropoietin increases frataxin independent from the erythropoietin receptor
European Journal of Clinical Investigation, Early View (Articles online in advance of print), Published Online: 28 Apr 2010
BRIEF COMMUNICATION
Brigitte Sturm*, Melissa Helminger*, Hannes Steinkellner*, Mohammad Mehdi Heidari*,†, Hans Goldenberg* and Barbara Scheiber-Mojdehkar*
*Medical University of Vienna, Vienna, Austria , † Yazd University, Yazd, Iran
KEYWORDS: Carbamylated erythropoietin • erythropoietin receptor • frataxin • Friedreich's ataxia • nonerythropoietic erythropoietin • recombinant human erythropoietin
BRIEF COMMUNICATION
Brigitte Sturm*, Melissa Helminger*, Hannes Steinkellner*, Mohammad Mehdi Heidari*,†, Hans Goldenberg* and Barbara Scheiber-Mojdehkar*
*Medical University of Vienna, Vienna, Austria , † Yazd University, Yazd, Iran
KEYWORDS: Carbamylated erythropoietin • erythropoietin receptor • frataxin • Friedreich's ataxia • nonerythropoietic erythropoietin • recombinant human erythropoietin
Thursday, April 29, 2010
Dysarthria in Friedreich's Ataxia: A Perceptual Analysis.
Folia Phoniatr Logop. 2010;62(3):97-103. Epub 2010 Apr 29.
The University of Queensland, Brisbane, Qld., Australia.
Keywords: speech intelligibility, dysarthria severity, Friedreich's ataxia (FRDA), clinical factors.
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