Full text: http://www.tesisenred.net/TESIS_UdL/AVAILABLE/TDX-0204105-125138//Tmrm01de04.pdf
CARACTERIZACIÓN Y ANÁLISIS FUNCIONAL DE UNA FAMILIADE GLUTAREDOXINAS MONOTIÓLICAS EN LA LEVADURA Saccharomyces cerevisiae
Teresa Rodríguez-Manzaneque Martínez Julio 2002
Cluster Fe-S-Frataxin
Thursday, April 23, 2009
Evolution based on domain combinations: the case of glutaredoxins
Full text: http://www.biomedcentral.com/content/pdf/1471-2148-9-66.pdf
Evolution based on domain combinations: the case of glutaredoxin
BMC Evolutionary Biology 2009, 9:66 doi:10.1186/1471-2148-9-66
Rui Alves (ralves@cmb.udl.es)
Ester Vilapinyo (evilaprinyo@cmb.udl.es)
Albert Sorribas (albert.sorribas@cmb.udl.es)
Enrique Herrero (enric.herrero@cmb.udl.es
Evolution based on domain combinations: the case of glutaredoxin
BMC Evolutionary Biology 2009, 9:66 doi:10.1186/1471-2148-9-66
Rui Alves (ralves@cmb.udl.es)
Ester Vilapinyo (evilaprinyo@cmb.udl.es)
Albert Sorribas (albert.sorribas@cmb.udl.es)
Enrique Herrero (enric.herrero@cmb.udl.es
PGC-1/β induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders
Human Molecular Genetics Advance Access originally published online on March 18, 2009
Human Molecular Genetics 2009 18(10):1805-1812; doi:10.1093/hmg/ddp093
PGC-1/β induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders
Sarika Srivastava1,,, Francisca Diaz1,, Luisa Iommarini1,3, Karine Aure4, Anne Lombes4 and Carlos T. Moraes1,2,*
1 Department of Neurology 2 Department of Cell Biology and Anatomy, University of Miami School of Medicine, 1095 NW 14th Terrace, Miami, FL 33136, USA 3 Dipartimento di Scienze Neurologiche, Università di Bologna, Bologna, Italy 4 Inserm 582; UPMC-Paris6; AP/HP, Paris F-75013, France
* To whom correspondence should be addressed. Tel: +1 3052435858; Fax: +1 3052433914; Email: cmoraes@med.miami.edu
Present address: Harvard Medical School, Boston, MA 02115, USA.
Human Molecular Genetics 2009 18(10):1805-1812; doi:10.1093/hmg/ddp093
PGC-1/β induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders
Sarika Srivastava1,,, Francisca Diaz1,, Luisa Iommarini1,3, Karine Aure4, Anne Lombes4 and Carlos T. Moraes1,2,*
1 Department of Neurology 2 Department of Cell Biology and Anatomy, University of Miami School of Medicine, 1095 NW 14th Terrace, Miami, FL 33136, USA 3 Dipartimento di Scienze Neurologiche, Università di Bologna, Bologna, Italy 4 Inserm 582; UPMC-Paris6; AP/HP, Paris F-75013, France
* To whom correspondence should be addressed. Tel: +1 3052435858; Fax: +1 3052433914; Email: cmoraes@med.miami.edu
Present address: Harvard Medical School, Boston, MA 02115, USA.
Wednesday, April 22, 2009
Resveratrol Highlights
http://www.lmcfood.dk/fileadmin/lmc_files/food/Kristensen-5_Resveratrol-Cell-2006.pdf
Lagouge et al., Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1a,
Cell (2006), doi:10.1016/j.cell.2006.11.013
Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1a
Marie Lagouge,8,1 Carmen Argmann,8,1 Zachary Gerhart-Hines,2 Hamid Meziane,3 Carles Lerin,2
Frederic Daussin,4 Nadia Messadeq,3 Jill Milne,5 Philip Lambert,5 Peter Elliott,5 Bernard Geny,4 Markku Laakso,6
Pere Puigserver,2 and Johan Auwerx1,3,7,* 1 Institut de Ge´ ne´ tique et de Biologie Mole´ culaire et Cellulaire, CNRS / INSERM / ULP, 67404 Illkirch, France
2Department of Cell Biology, John Hopkins University School of Medicine, Baltimore, MD 21205, USA
3 Institut Clinique de la Souris, BP10142, 67404, Illkirch, France
4Department of Respiratory, Cardiocirculatory and Exercise Physiology, Hoˆ pitaux Universitaires, 67000 Strasbourg, France
5 Sirtris Pharmaceutical, Cambridge, MA 02139, USA
6Department of Medicine, University of Kuopio, 70211 Kuopio, Finland
7IGBMC-ICS, 67404 Illkirch, France
8These authors contributed equally to this work.
*Contact: auwerx@igbmc.u-strasbg.fr
--------------------------------------------------------------
http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=85386&Ausgabe=230907&ProduktNr=224154&filename=85386.pdf
Neurosignals 2005;14:61–70
DOI: 10.1159/000085386
Received: December 6, 2004
Accepted after revision: March 1, 2005
Unique Properties of Polyphenol Stilbenes in the Brain: More than Direct Antioxidant Actions; Gene/Protein Regulatory Activity
Sylvain Doré
Johns Hopkins University, School of Medicine, Baltimore, Md. , USA
________________________________
http://www.ncbi.nlm.nih.gov/pubmed/18629638?dopt=Abstract
Neurochem Res. 2008 Dec;33(12):2444-71. Epub 2008 Jul 16.
Cellular stress response: a novel target for chemoprevention and nutritional neuroprotection in aging, neurodegenerative disorders and longevity.
Calabrese V, Cornelius C, Mancuso C, Pennisi G, Calafato S, Bellia F, Bates TE, Giuffrida Stella AM, Schapira T, Dinkova Kostova AT, Rizzarelli E.Section of Biochemistry and Molecular Biology, Department of Chemistry, Faculty of Medicine, University of Catania, Viale Andrea Doria 6, 95100, Catania, Italy. calabres@unict.it
_________________________________
http://www3.interscience.wiley.com/journal/121682622/abstract?CRETRY=1&SRETRY=0
Histone Deacetylase Inhibition Activity and Molecular Docking of (E )-Resveratrol: Its Therapeutic Potential in Spinal Muscular Atrophy
Didem Dayangaç-Erden 1,*, Gamze Bora 1 , Peruze Ayhan 2 , Çetin Kocaefe 1 , Sevim Dalkara 3 , Kemal Yelekçi 4 , Ayhan S. Demir 2 and Hayat Erdem-Yurter 1
1 Department of Medical Biology, Faculty of Medicine, Hacettepe University, Ankara, Turkey 2 Department of Chemistry, Middle East Technical University, Ankara, Turkey 3 Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Hacettepe University, Ankara, Turkey 4 Department of Statistics and Computer Sciences, Faculty of Arts and Science, Kadir Has University, Istanbul, Turkey
Correspondence to *Dr Didem Dayangaç-Erden, didayan@hacettepe.edu.tr
Copyright Journal compilation © 2009 Blackwell Munksgaard
KEYWORDS
(E )-resveratrol • molecular docking • SMN2 • spinal muscular atrophy
________________________________
http://ntp.niehs.nih.gov/ntp/htdocs/Chem_Background/ExSumPDF/resveratrol.pdf
Lagouge et al., Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1a,
Cell (2006), doi:10.1016/j.cell.2006.11.013
Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1a
Marie Lagouge,8,1 Carmen Argmann,8,1 Zachary Gerhart-Hines,2 Hamid Meziane,3 Carles Lerin,2
Frederic Daussin,4 Nadia Messadeq,3 Jill Milne,5 Philip Lambert,5 Peter Elliott,5 Bernard Geny,4 Markku Laakso,6
Pere Puigserver,2 and Johan Auwerx1,3,7,* 1 Institut de Ge´ ne´ tique et de Biologie Mole´ culaire et Cellulaire, CNRS / INSERM / ULP, 67404 Illkirch, France
2Department of Cell Biology, John Hopkins University School of Medicine, Baltimore, MD 21205, USA
3 Institut Clinique de la Souris, BP10142, 67404, Illkirch, France
4Department of Respiratory, Cardiocirculatory and Exercise Physiology, Hoˆ pitaux Universitaires, 67000 Strasbourg, France
5 Sirtris Pharmaceutical, Cambridge, MA 02139, USA
6Department of Medicine, University of Kuopio, 70211 Kuopio, Finland
7IGBMC-ICS, 67404 Illkirch, France
8These authors contributed equally to this work.
*Contact: auwerx@igbmc.u-strasbg.fr
--------------------------------------------------------------
http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=85386&Ausgabe=230907&ProduktNr=224154&filename=85386.pdf
Neurosignals 2005;14:61–70
DOI: 10.1159/000085386
Received: December 6, 2004
Accepted after revision: March 1, 2005
Unique Properties of Polyphenol Stilbenes in the Brain: More than Direct Antioxidant Actions; Gene/Protein Regulatory Activity
Sylvain Doré
Johns Hopkins University, School of Medicine, Baltimore, Md. , USA
________________________________
http://www.ncbi.nlm.nih.gov/pubmed/18629638?dopt=Abstract
Neurochem Res. 2008 Dec;33(12):2444-71. Epub 2008 Jul 16.
Cellular stress response: a novel target for chemoprevention and nutritional neuroprotection in aging, neurodegenerative disorders and longevity.
Calabrese V, Cornelius C, Mancuso C, Pennisi G, Calafato S, Bellia F, Bates TE, Giuffrida Stella AM, Schapira T, Dinkova Kostova AT, Rizzarelli E.Section of Biochemistry and Molecular Biology, Department of Chemistry, Faculty of Medicine, University of Catania, Viale Andrea Doria 6, 95100, Catania, Italy. calabres@unict.it
_________________________________
http://www3.interscience.wiley.com/journal/121682622/abstract?CRETRY=1&SRETRY=0
Histone Deacetylase Inhibition Activity and Molecular Docking of (E )-Resveratrol: Its Therapeutic Potential in Spinal Muscular Atrophy
Didem Dayangaç-Erden 1,*, Gamze Bora 1 , Peruze Ayhan 2 , Çetin Kocaefe 1 , Sevim Dalkara 3 , Kemal Yelekçi 4 , Ayhan S. Demir 2 and Hayat Erdem-Yurter 1
1 Department of Medical Biology, Faculty of Medicine, Hacettepe University, Ankara, Turkey 2 Department of Chemistry, Middle East Technical University, Ankara, Turkey 3 Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Hacettepe University, Ankara, Turkey 4 Department of Statistics and Computer Sciences, Faculty of Arts and Science, Kadir Has University, Istanbul, Turkey
Correspondence to *Dr Didem Dayangaç-Erden, didayan@hacettepe.edu.tr
Copyright Journal compilation © 2009 Blackwell Munksgaard
KEYWORDS
(E )-resveratrol • molecular docking • SMN2 • spinal muscular atrophy
________________________________
http://ntp.niehs.nih.gov/ntp/htdocs/Chem_Background/ExSumPDF/resveratrol.pdf
Tuesday, April 21, 2009
Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPAR{gamma} pathway as a therapeutic target
Hum Mol Genet. 2009 Apr 17. [Epub ahead of print]
Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPAR{gamma} pathway as a therapeutic target in Friedreich's ataxia.
Coppola G, Marmolino D, Lu D, Wang Q, Cnop M, Rai M, Acquaviva F, Cocozza S, Pandolfo M, Geschwind DH.
Program in Neurogenetics, Department of Neurology David Geffen School of Medicine, University of California at Los Angeles, CA 90095.
OPEN ACCESS:
http://hmg.oxfordjournals.org/cgi/content/full/18/13/2452
http://hmg.oxfordjournals.org/cgi/reprint/18/13/2452.pdf
Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPAR{gamma} pathway as a therapeutic target in Friedreich's ataxia.
Coppola G, Marmolino D, Lu D, Wang Q, Cnop M, Rai M, Acquaviva F, Cocozza S, Pandolfo M, Geschwind DH.
Program in Neurogenetics, Department of Neurology David Geffen School of Medicine, University of California at Los Angeles, CA 90095.
OPEN ACCESS:
http://hmg.oxfordjournals.org/cgi/content/full/18/13/2452
http://hmg.oxfordjournals.org/cgi/reprint/18/13/2452.pdf
Brain iron homeostasis and neurodegenerative disease
Citation:
Neurology, Vol. 72, Issue 16, 1436-1440, April 21, 2009
CLINICAL IMPLICATIONS OF NEUROSCIENCE RESEARCH
Brain iron homeostasis and neurodegenerative disease
Eduardo E. Benarroch
Article topics:
Physiology..Transferrin
Medicine..Genes
Medicine..Iron Metabolism
Cell Biology..Endothelial Cells
Physiology..Homeostasis
Medicine..Gene Expression
Medicine..Genetics
Medicine..Neurodegenerative Diseases
Medicine..Cardiovascular Genetics
Biochemistry..Ferritin
Medicine..Friedreich Ataxia
Biochemistry..Pantothenate Kinase
Cell Biology..Astrocytes
Biochemistry..Kinases
Medicine..Ataxia
http://www.neurology.org/cgi/content/citation/72/16/1436?rss=1
Neurology, Vol. 72, Issue 16, 1436-1440, April 21, 2009
CLINICAL IMPLICATIONS OF NEUROSCIENCE RESEARCH
Brain iron homeostasis and neurodegenerative disease
Eduardo E. Benarroch
Article topics:
Physiology..Transferrin
Medicine..Genes
Medicine..Iron Metabolism
Cell Biology..Endothelial Cells
Physiology..Homeostasis
Medicine..Gene Expression
Medicine..Genetics
Medicine..Neurodegenerative Diseases
Medicine..Cardiovascular Genetics
Biochemistry..Ferritin
Medicine..Friedreich Ataxia
Biochemistry..Pantothenate Kinase
Cell Biology..Astrocytes
Biochemistry..Kinases
Medicine..Ataxia
http://www.neurology.org/cgi/content/citation/72/16/1436?rss=1
Sunday, April 19, 2009
E. coli mismatch repair acts downstream of replication fork stalling to stabilize the expanded (GAA.TTC)(n) sequence.
Mutat Res.Author manuscript; available in PMC 2009 February 10.
Published in final edited form as:
Mutat Res. 2009 February 10; 661(1-2): 71–77.
Published online 2008 November 13. doi: 10.1016/j.mrfmmm.2008.11.003. PMCID: PMC2637364
NIHMSID: NIHMS83510
Copyright notice and Disclaimer
E. coli mismatch repair acts downstream of replication fork stalling to stabilize the expanded (GAA·TTC)n sequence
Rebecka L. Bourn,1 Paul M. Rindler,1 Laura M. Pollard,1 and Sanjay I. Bidichandani1,2
1Department of Biochemistry & Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA
2Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA
Address all correspondence and requests for reprints to: Sanjay I. Bidichandani, MBBS, PhD, 975 NE 10th St., BRC458, Oklahoma City, OK 73104, USA, Tel: (405) 271-1360, Fax: (405) 271-3910, Email: Sanjay-Bidichandani@ouhsc.edu
The publisher's final edited version of this article is available at Mutat Res.
Keywords: mismatch repair, triplet repeat instability, GAA triplet repeat, replication fork stalling
Published in final edited form as:
Mutat Res. 2009 February 10; 661(1-2): 71–77.
Published online 2008 November 13. doi: 10.1016/j.mrfmmm.2008.11.003. PMCID: PMC2637364
NIHMSID: NIHMS83510
Copyright notice and Disclaimer
E. coli mismatch repair acts downstream of replication fork stalling to stabilize the expanded (GAA·TTC)n sequence
Rebecka L. Bourn,1 Paul M. Rindler,1 Laura M. Pollard,1 and Sanjay I. Bidichandani1,2
1Department of Biochemistry & Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA
2Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA
Address all correspondence and requests for reprints to: Sanjay I. Bidichandani, MBBS, PhD, 975 NE 10th St., BRC458, Oklahoma City, OK 73104, USA, Tel: (405) 271-1360, Fax: (405) 271-3910, Email: Sanjay-Bidichandani@ouhsc.edu
The publisher's final edited version of this article is available at Mutat Res.
Keywords: mismatch repair, triplet repeat instability, GAA triplet repeat, replication fork stalling
Friday, April 17, 2009
SCA-LSVD: A repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.
http://www.ncbi.nlm.nih.gov/pubmed/19370769?dopt=Abstract
Hum Mutat. 2009 Mar 3. [Epub ahead of print]
SCA-LSVD: A repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.
Faruq M, Scaria V, Singh I, Tyagi S, Srivastava AK, Mukerji M.Genomics and Molecular Medicine, Institute of Genomics and Integrative Biology-Council of Scientific and Industrial Research (IGIB-CSIR), Delhi, India.
The database is accessible online at http://miracle.igib.res.in/ataxia. Hum Mutat 30:1-6, 2009. (c) 2009 Wiley-Liss, Inc.PMID: 19370769 [PubMed - as supplied by publisher]
NOTE: Direct link to FXN information (http://miracle.igib.res.in/ataxia/home.php?select_db=FXN )
Hum Mutat. 2009 Mar 3. [Epub ahead of print]
SCA-LSVD: A repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.
Faruq M, Scaria V, Singh I, Tyagi S, Srivastava AK, Mukerji M.Genomics and Molecular Medicine, Institute of Genomics and Integrative Biology-Council of Scientific and Industrial Research (IGIB-CSIR), Delhi, India.
The database is accessible online at http://miracle.igib.res.in/ataxia. Hum Mutat 30:1-6, 2009. (c) 2009 Wiley-Liss, Inc.PMID: 19370769 [PubMed - as supplied by publisher]
NOTE: Direct link to FXN information (http://miracle.igib.res.in/ataxia/home.php?select_db=FXN )
Infrared thermography as an access pathway for individuals with severe motor impairments
Infrared thermography as an access pathway for individuals with severe motor impairments
Negar Memarian , Anastasios N Venetsanopoulos and Tom Chau
Journal of NeuroEngineering and Rehabilitation 2009, 6:11doi:10.1186/1743-0003-6-11
http://www.jneuroengrehab.com/content/6/1/11
Published:
16 April 2009
The complete article is available as a provisional PDF. The fully formatted PDF and HTML versions are in production http://www.jneuroengrehab.com/content/pdf/1743-0003-6-11.pdf
Negar Memarian , Anastasios N Venetsanopoulos and Tom Chau
Journal of NeuroEngineering and Rehabilitation 2009, 6:11doi:10.1186/1743-0003-6-11
http://www.jneuroengrehab.com/content/6/1/11
Published:
16 April 2009
The complete article is available as a provisional PDF. The fully formatted PDF and HTML versions are in production http://www.jneuroengrehab.com/content/pdf/1743-0003-6-11.pdf
Thursday, April 16, 2009
Enfermedades raras-ANALES DEL SISTEMA SANITARIO DE NAVARRA
http://www.cfnavarra.es/salud/anales/textos/suple31_2.htm
ANALES DEL SISTEMA SANITARIO DE NAVARRA
Enfermedades raras
Vol. 31, suplemento 2, 2008
ANALES DEL SISTEMA SANITARIO DE NAVARRA
Enfermedades raras
Vol. 31, suplemento 2, 2008
Subscribe to:
Posts (Atom)
