Hum Brain Mapp. 2011 Jun 14. doi: 10.1002/hbm.21319. [Epub ahead of print]
Ginestroni A, Diciotti S, Cecchi P, Pesaresi I, Tessa C, Giannelli M, Nave RD, Salvatore E, Salvi F, Dotti MT, Piacentini S, Soricelli A, Cosottini M, De Stefano N, Mascalchi M.
Department of Clinical Physiopathology, Radiodiagnostic Section, University of Florence, Florence, Italy.
Keywords: Friedreich's ataxia (FRDA), neurodegeneration, spinal cord, brain, MR Imaging (fMRI), left primary sensory-motor cortex, right cerebellum, left thalamus, right dorsolateral prefrontal cortex, globus pallidus, anterior cingulum, globus pallidus, regional neuronal damage, compensatory significance.
Thursday, June 16, 2011
Tuesday, June 14, 2011
Friedreich’s ataxia variants I154F and W155R diminish frataxin-based activation of the iron-sulfur cluster assembly complex
Biochemistry, Just Accepted Manuscript, DOI: 10.1021/bi200666h
Publication Date (Web): June 14, 2011
Chi-Lin Tsai , Jennifer Bridwell-Rabb , and David P. Barondeau
Keywords: Friedreich’s ataxia (FRDA), frataxin (Fxn), GAA expansion, missense mutation, FRDA I154F, W155R variants, Nfs1, Isd11, Isu2, Fe-S cluster assembly machine, Fxn triggers sulfur transfer from Nfs1 to Isu.
Publication Date (Web): June 14, 2011
Chi-Lin Tsai , Jennifer Bridwell-Rabb , and David P. Barondeau
Keywords: Friedreich’s ataxia (FRDA), frataxin (Fxn), GAA expansion, missense mutation, FRDA I154F, W155R variants, Nfs1, Isd11, Isu2, Fe-S cluster assembly machine, Fxn triggers sulfur transfer from Nfs1 to Isu.
Sunday, June 12, 2011
New project: Identification of the E3 ligase that ubiquitinates frataxin
Principal researcher: Dr Roberto Testi, Department of Experimental Medicine,
University of Rome, ‘Tor Vergata,’ Italy
Keywods: frataxin, ubiquitin-proteasome system, ubiquitination, E3 ligase.
University of Rome, ‘Tor Vergata,’ Italy
Keywods: frataxin, ubiquitin-proteasome system, ubiquitination, E3 ligase.
Saturday, June 11, 2011
Sherman ku PhD working with friedreich's ataxia and induced pluripotent stem cells (iPSC)
Sigma bioblogs (3 Jun 2011)
Sherman Ku PhD interview
The Scripps Research Institute, Member of the Gottesfeld Lab
What is the focus of your research?
My research has focused on developing an induced pluripotent stem cell (iPSC) model of Friedreich’s ataxia (FRDA), which is ..... read more....
Sherman Ku PhD interview
The Scripps Research Institute, Member of the Gottesfeld Lab
What is the focus of your research?
My research has focused on developing an induced pluripotent stem cell (iPSC) model of Friedreich’s ataxia (FRDA), which is ..... read more....
Edison Pharmaceuticals Announces Results of EPI-A0001 Phase 2A Double Blind Placebo Controlled 28-Day Clinical Trial in the Mitochondrial Disease- Friedreich's Ataxia
10th of June 2011
MOUNTAIN VIEW, Calif., June 10, 2011 /PRNewswire/ -- Edison Pharmaceuticals, Inc. announced today preliminary results obtained on a 28-day phase 2A clinical trial in Friedreich's ataxia.
EPI-A0001 did significantly improve neurological function as assessed by the Friedreich's Ataxia Rating Scale (FARS).
Read more
MOUNTAIN VIEW, Calif., June 10, 2011 /PRNewswire/ -- Edison Pharmaceuticals, Inc. announced today preliminary results obtained on a 28-day phase 2A clinical trial in Friedreich's ataxia.
EPI-A0001 did significantly improve neurological function as assessed by the Friedreich's Ataxia Rating Scale (FARS).
Read more
Friday, June 10, 2011
Emergency Use Protocol for EPI-743 in Acutely Ill Patients With Inherited Mitochondrial Respiratory Chain Disease Within 90 Days of End-of-Life Care
This study is currently recruiting participants.
First Received on June 7, 2011. Last Updated on June 9, 2011
Sponsor: Edison Pharmaceuticals Inc
Information provided by: Edison Pharmaceuticals Inc
ClinicalTrials.gov Identifier: NCT01370447
Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
First Received on June 7, 2011. Last Updated on June 9, 2011
Sponsor: Edison Pharmaceuticals Inc
Information provided by: Edison Pharmaceuticals Inc
ClinicalTrials.gov Identifier: NCT01370447
Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Transcranial Sonography Reveals Cerebellar, Nigral, and Forebrain Abnormalities in Friedreich’s Ataxia
Neurodegenerative Dis, (DOI: 10.1159/000327751)
Matthis Synofzik, Jana Godau, Tobias Lindig, Ludger Schöls, Daniela Berg
Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, and German Research Center for Neurodegenerative Diseases, University of Tübingen, Tübingen, Germany
Keywords: Ataxia, Transcranial sonography, Friedreich’s ataxia, Imaging, Substantia nigra, Dentate nucleus, Iron, Cerebellum
Matthis Synofzik, Jana Godau, Tobias Lindig, Ludger Schöls, Daniela Berg
Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, and German Research Center for Neurodegenerative Diseases, University of Tübingen, Tübingen, Germany
Keywords: Ataxia, Transcranial sonography, Friedreich’s ataxia, Imaging, Substantia nigra, Dentate nucleus, Iron, Cerebellum
Mortality in Friedreich Ataxia
Journal of the Neurological Sciences,Article in Press,
doi:10.1016/j.jns.2011.05.023
(J Neurol Sci. 2011 Aug 15;307(1-2):46-9. Epub 2011 Jun 8.)
Amy Y. Tsoua, Erin K. Paulsena, b, c, d, Sarah J. Lagedrosta, b, c, d, Susan L. Perlmane, Katherine D. Mathewsf, George R. Wilmotg, Bernard Ravinah, Arnulf H. Koeppeni, j and David R. Lyncha, b, c, d,
a Department of Neurology, University of Pennsylvania Medical School, United States
b Department of Pediatrics, University of Pennsylvania Medical School, United States
c Children's Hospital of Philadelphia, United States
d University of Pennsylvania Medical School, United States
e University of California Los Angeles, Los Angeles, CA, United States
f University of Iowa, Iowa City, IA, United States
g Emory University, Atlanta, GA, United States
h University of Rochester, Rochester, NY, United States
i VA Hospital, Albany, NY, United States
Keywords: Cerebellum; Sensory; Cardiomyopathy; Echocardiogram; Arrhythmia; Neurodegenerative disease
doi:10.1016/j.jns.2011.05.023
(J Neurol Sci. 2011 Aug 15;307(1-2):46-9. Epub 2011 Jun 8.)
Amy Y. Tsoua, Erin K. Paulsena, b, c, d, Sarah J. Lagedrosta, b, c, d, Susan L. Perlmane, Katherine D. Mathewsf, George R. Wilmotg, Bernard Ravinah, Arnulf H. Koeppeni, j and David R. Lyncha, b, c, d,
a Department of Neurology, University of Pennsylvania Medical School, United States
b Department of Pediatrics, University of Pennsylvania Medical School, United States
c Children's Hospital of Philadelphia, United States
d University of Pennsylvania Medical School, United States
e University of California Los Angeles, Los Angeles, CA, United States
f University of Iowa, Iowa City, IA, United States
g Emory University, Atlanta, GA, United States
h University of Rochester, Rochester, NY, United States
i VA Hospital, Albany, NY, United States
Keywords: Cerebellum; Sensory; Cardiomyopathy; Echocardiogram; Arrhythmia; Neurodegenerative disease
Thursday, June 9, 2011
Repligen Reports Fourth Quarter ........ "RG2833 for Friedreich’s Ataxia"
9th of June 2011
RG2833 for Friedreich’s Ataxia
We are currently developing histone deacetylase class 1 inhibitors for the treatment of inherited neurodegenerative diseases such as Friedreich's ataxia. Friedreich's ataxia is caused by inadequate production of the protein frataxin which leads to degeneration of the nerves controlling muscle movements. Pending regulatory approval, we plan to initiate a Phase 1 study of RG2833 in Friedreich's ataxia patients in Europe by the end of the year. We are currently engaged in discussions with potential
pharmaceutical partners to evaluate whether partnering this program would increase the trajectory for global development and ultimately maximize the commercial potential of the asset.
RG2833 for Friedreich’s Ataxia
We are currently developing histone deacetylase class 1 inhibitors for the treatment of inherited neurodegenerative diseases such as Friedreich's ataxia. Friedreich's ataxia is caused by inadequate production of the protein frataxin which leads to degeneration of the nerves controlling muscle movements. Pending regulatory approval, we plan to initiate a Phase 1 study of RG2833 in Friedreich's ataxia patients in Europe by the end of the year. We are currently engaged in discussions with potential
pharmaceutical partners to evaluate whether partnering this program would increase the trajectory for global development and ultimately maximize the commercial potential of the asset.
Stem Cell Transplantation Offers 'Sea Of Opportunity' For Treating Debilitating Diseases
Medical News Today, Article Date: 09 Jun 2011
An article in the current issue of Technology & Innovation, Proceedings of the National Academy of Inventors ™ reports on the bright future and enormous need for stem cell therapeutics that may offer hope for those suffering from debilitating and deadly diseases. read more...
An article in the current issue of Technology & Innovation, Proceedings of the National Academy of Inventors ™ reports on the bright future and enormous need for stem cell therapeutics that may offer hope for those suffering from debilitating and deadly diseases. read more...
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