Genomic Instability in Pluripotent Stem Cells: Implications for Clinical Applications. Suzanne E. Peterson and Jeanne F. Loring; The Journal of Biological Chemistry, 289, 4578-4584. 10.1074/jbc.R113.516419 February 21, 2014
FULL TEXT PDF
There are several examples of dramatic genomic changes that appear when cells are reprogrammed. Studies of some trinucleotide repeat diseases have reported changes in the repeat length following reprogramming. Specifically, in Friedreich ataxia, the GAA/TTC triplet repeat length in the FXN (frataxin) gene appeared to change following reprogramming of patient fibroblasts
Although the probability of an FDA-approved hPSC-derived cell therapy causing harm to a patient appears to be low, the consequences of adverse events are enormous. There is an important lesson from the failures in early gene therapy trials. If even one patient is harmed in an FDA-approved trial using hPSC derivatives, all further trials will be in serious jeopardy, and the promise of stem cell therapy will be put on indefinite hold.
Saturday, February 22, 2014
The Neuroprotective Role of Acupuncture and Activation of the BDNF Signaling Pathway
The Neuroprotective Role of Acupuncture and Activation of the BDNF Signaling Pathway. Lin, Dong; De La Pena, Ike; Lin, Lili; Zhou, Shu-Feng; Borlongan, Cesar V.; Cao, Chuanhai; International Journal of Molecular Sciences. 2014; 15(2):3234-3252.
OPEN ACCESS, FULL TEXT PDF
OPEN ACCESS, FULL TEXT PDF
Global Identification of Genes Affecting Iron-Sulfur Cluster Biogenesis and Iron Homeostasis
Global Identification of Genes Affecting Iron-Sulfur Cluster Biogenesis and Iron Homeostasis . Ryota Hidese, Hisaaki Mihara, Tatsuo Kurihara and Nobuyoshi Esaki; J. Bacteriol. March 2014 vol. 196 no. 6 1238-1249; Published ahead of print 10 January 2014, doi: 10.1128/JB.01160-13
Drosophila models for studying iron-related neurodegenerative diseases.
Drosophila models for studying iron-related neurodegenerative diseases. Zhu ZJ, Wu KC, Qian ZM, Yung WH, Ke Y.; Acta Physiologica Sinica, February 25, 2014, 66(1): 47–54; DOI: 10.13294/j.aps.2014.0007 http://www.actaps.com.cn
4.1 FRDA Drosophila models
Full text PDF
4.1 FRDA Drosophila models
Full text PDF
Friday, February 21, 2014
Poster: BDNF function in health and disease
Poster: BDNF function in health and disease
This poster is freely available thanks to support from EVER Neuro Pharma.
High-resolution PDF (167 KB)
This poster is freely available thanks to support from EVER Neuro Pharma.
High-resolution PDF (167 KB)
Thursday, February 20, 2014
Characterization of biometal - profiles in neurological disorders
Characterization of biometal - profiles in neurological disorders. Stefanie Pfaender and Andreas M Grabrucker; Metallomics, 2014,
DOI: 10.1039/C4MT00008K
DOI: 10.1039/C4MT00008K
Accelerating development, registration and access to medicines for rare diseases in the European Union through adaptive approaches: features and perspectives
Accelerating development, registration and access to medicines for rare diseases in the European Union through adaptive approaches: features and perspectives. David Uguen, Thomas Lönngren, Yann Le Cam, Sarah Garner, Emmanuelle Voisin, Carlo Incerti, Marc Dunoyer and Moncef Slaoui; Orphanet Journal of Rare Diseases 2014, 9:20 doi:10.1186/1750-1172-9-20
OPEN ACCESS, FULL TEXT PDF
OPEN ACCESS, FULL TEXT PDF
Sunday, February 16, 2014
Nucleoside 5’-phosphorothioate derivatives are highly effective neuroprotectants
Nucleoside 5’-phosphorothioate derivatives are highly effective neuroprotectants. O. Danino, N. Giladi,S. Grossman, B. Fischer; Biochemical Pharmacology. Available online 15 February 2014. http://dx.doi.org/10.1016/j.bcp.2014.02.001
Saturday, February 15, 2014
Voyager Lifts Off With $45M From Third Rock Ventures
Voyager Lifts Off With $45M From Third Rock Ventures. By Paul Bonanos, The pink Sheet, February 12 2014
Voyager hopes to have three programs in the clinic by early 2017, targeting Parkinson’s, ALS and Friedreich’s ataxia.
Voyager hopes to have three programs in the clinic by early 2017, targeting Parkinson’s, ALS and Friedreich’s ataxia.
Wednesday, February 12, 2014
Voyager Therapeutics, a new gene therapy company focused on CNS diseases, including Friedreich's Ataxia (FA), is launched
Voyager Therapeutics, a new gene therapy company focused on CNS diseases, including Friedreich's Ataxia (FA), is launched. FARA Press Release, February 12, 2014
Downingtown, PA- February 12, 2014- FARA is pleased to recognize today's launch of Voyager Therapeutics and its commitment to developing gene therapies for central nervous system disorders, including FA. Voyager is backed by leading life sciences investor Third Rock Ventures, and the company has assembled leaders in adeno-associated virus (AAV) gene therapy to develop life-changing treatments with the goal of dramatically improving patients’ lives. See press release from Voyager Therapeutics: http://www.voyagertherapeutics.com/pdfs/Voyager_02.11.14.pdf
Downingtown, PA- February 12, 2014- FARA is pleased to recognize today's launch of Voyager Therapeutics and its commitment to developing gene therapies for central nervous system disorders, including FA. Voyager is backed by leading life sciences investor Third Rock Ventures, and the company has assembled leaders in adeno-associated virus (AAV) gene therapy to develop life-changing treatments with the goal of dramatically improving patients’ lives. See press release from Voyager Therapeutics: http://www.voyagertherapeutics.com/pdfs/Voyager_02.11.14.pdf
Subscribe to:
Posts (Atom)
