Maria L Arbones

Maria L Arbones

UNVERIFIED PROFILE

Are you Maria L Arbones?   Register this Author

Register author
Maria L Arbones

Maria L Arbones

Publications by authors named "Maria L Arbones"

Are you Maria L Arbones?   Register this Author

26Publications

438Reads

30Profile Views

Impaired development of neocortical circuits contributes to the neurological alterations in DYRK1A haploinsufficiency syndrome.

Neurobiol Dis 2019 07 1;127:210-222. Epub 2019 Mar 1.

Instituto de Biología Molecular de Barcelona (IBMB), CSIC, 08028 Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, Spain. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nbd.2019.02.022DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753933PMC
July 2019

DYRK1A and cognition: A lifelong relationship.

Pharmacol Ther 2019 02 28;194:199-221. Epub 2018 Sep 28.

INSERM U1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMRS 1127, Institut du Cerveau et de la Moelle épinière, ICM, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.pharmthera.2018.09.010DOI Listing
February 2019

Automated Macro Approach to Quantify Synapse Density in 2D Confocal Images from Fixed Immunolabeled Neural Tissue Sections.

Methods Mol Biol 2019 ;2040:71-97

Molecular Biology Institute of Barcelona (IBMB-CSIC), Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/978-1-4939-9686-5_5DOI Listing
January 2019

DYRK1A Kinase Positively Regulates Angiogenic Responses in Endothelial Cells.

Cell Rep 2018 05;23(6):1867-1878

Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, 08003 Barcelona, Spain; Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER), Spain; Institució Catalana de Recerca i Estudis Avançats (ICREA), 08010 Barcelona, Spain. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.celrep.2018.04.008DOI Listing
May 2018

DYRK1A-mediated Cyclin D1 Degradation in Neural Stem Cells Contributes to the Neurogenic Cortical Defects in Down Syndrome.

EBioMedicine 2015 17;2(2):120-34. Epub 2015 Jan 17.

Department of Developmental Biology, Instituto de Biología Molecular de Barcelona, CSIC, and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), 08028 Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ebiom.2015.01.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484814PMC
December 2016

Abnormal mineralization of the Ts65Dn Down syndrome mouse appendicular skeleton begins during embryonic development in a Dyrk1a-independent manner.

Mech Dev 2015 May 30;136:133-42. Epub 2014 Dec 30.

Department of Biology, Indiana University-Purdue University Indianapolis and Indiana University Center for Regenerative Biology and Medicine, 723 W. Michigan Street, SL306, Indianapolis, IN 46202, USA. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.mod.2014.12.004DOI Listing
May 2015

Dyrk1a haploinsufficiency induces diabetes in mice through decreased pancreatic beta cell mass.

Diabetologia 2014 May 30;57(5):960-9. Epub 2014 Jan 30.

INSERM U1016, Institut Cochin, Faculté de Médecine Cochin, Université Paris Descartes, 24 Rue du Faubourg St Jacques, 75014, Paris, France,

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00125-014-3174-3DOI Listing
May 2014

Triplication of DYRK1A causes retinal structural and functional alterations in Down syndrome.

Hum Mol Genet 2013 Jul 19;22(14):2775-84. Epub 2013 Mar 19.

Department of Developmental Biology, Institut de Biologia Molecular de Barcelona IBMB-CSIC, Barcelona 08028, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddt125DOI Listing
July 2013

Upregulation of RCAN1 causes Down syndrome-like immune dysfunction.

J Med Genet 2013 Jul 3;50(7):444-54. Epub 2013 May 3.

Department Biochemistry and Molecular Biology, Monash University, Wellington Rd, Clayton, VIC 3800, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1136/jmedgenet-2013-101522DOI Listing
July 2013

Over-expression of RCAN1 causes Down syndrome-like hippocampal deficits that alter learning and memory.

Hum Mol Genet 2012 Jul 17;21(13):3025-41. Epub 2012 Apr 17.

Department of Biochemistry and Molecular Biology, Monash University, Clayton, 3168 Victoria, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/dds134DOI Listing
July 2012

Gene expression analysis of the embryonic subplate.

Cereb Cortex 2012 Jun 22;22(6):1343-59. Epub 2011 Aug 22.

Department of Physiology, Anatomy and Genetics, Oxford University, Oxford OX1 3QX, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/cercor/bhr197DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972418PMC
June 2012

Regulator of calcineurin 1 mediates pathological vascular wall remodeling.

J Exp Med 2011 Sep 19;208(10):2125-39. Epub 2011 Sep 19.

Department of Vascular Biology and Inflammation, Centro Nacional de Investigaciones Cardiovasculares (CNIC), E-28029 Madrid, Spain.

View Article

Download full-text PDF

Source
http://www.jem.org/lookup/doi/10.1084/jem.20110503
Publisher Site
http://dx.doi.org/10.1084/jem.20110503DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182048PMC
September 2011

Regulated segregation of kinase Dyrk1A during asymmetric neural stem cell division is critical for EGFR-mediated biased signaling.

Cell Stem Cell 2010 Sep;7(3):367-79

Departamento de Biología Celular and Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED), Universidad de Valencia, 46100 Burjassot, Spain.

View Article

Download full-text PDF

Source
http://linkinghub.elsevier.com/retrieve/pii/S193459091000345
Publisher Site
http://dx.doi.org/10.1016/j.stem.2010.06.021DOI Listing
September 2010

Age-associated motor and visuo-spatial learning phenotype in Dyrk1A heterozygous mutant mice.

Neurobiol Dis 2009 Nov 4;36(2):312-9. Epub 2009 Aug 4.

Genes and Disease Program, Center for Genomic Regulation (CRG), Pompeu Fabra University, Barcelona Biomedical Research Park (PRBB) and CIBER de Enfermedades Raras (CIBERER), Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nbd.2009.07.027DOI Listing
November 2009

Efficient and specific transduction of cochlear supporting cells by adeno-associated virus serotype 5.

Neurosci Lett 2008 Sep 26;442(2):134-9. Epub 2008 Jun 26.

Genes and Disease Programme, Center for Genomic Regulation (CRG), UPF, Barcelona, Catalonia, Spain.

View Article

Download full-text PDF

Source
http://linkinghub.elsevier.com/retrieve/pii/S030439400800891
Publisher Site
http://dx.doi.org/10.1016/j.neulet.2008.06.060DOI Listing
September 2008

DSCR1/RCAN1 regulates vesicle exocytosis and fusion pore kinetics: implications for Down syndrome and Alzheimer's disease.

Hum Mol Genet 2008 Apr 7;17(7):1020-30. Epub 2008 Jan 7.

Molecular and Cellular Neuroscience Group, Department of Human Physiology and Centre for Neuroscience, Flinders University, Adelaide, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddm374DOI Listing
April 2008

Differential expression of members of the RCAN family of calcineurin regulators suggests selective functions for these proteins in the brain.

Eur J Neurosci 2007 Sep;26(5):1213-26

Center for Genomic Regulation (CRG), UPF, Dr Aiguader 88, E-08003 Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1460-9568.2007.05749.xDOI Listing
September 2007

RCAN1 (DSCR1) increases neuronal susceptibility to oxidative stress: a potential pathogenic process in neurodegeneration.

Hum Mol Genet 2007 May 6;16(9):1039-50. Epub 2007 Mar 6.

Genes and Disease Program, Center for Genomic Regulation (CRG-UPF), Biomedical Research Park Building, E-08003 Barcelona, Catalonia, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddm049DOI Listing
May 2007

Expression profiles of the connexin genes, Gjb1 and Gjb3, in the developing mouse cochlea.

Mech Dev 2002 Dec;119 Suppl 1:S111-5

Genes and Disease Program, Centre de Regulació Genòmica, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0925-4773(03)00102-3DOI Listing
December 2002

Expression profiles of the connexin genes, Gjb1 and Gjb3, in the developing mouse cochlea.

Gene Expr Patterns 2002 Nov;2(1-2):113-7

Genes and Disease Program, Centre de Regulació Genòmica, Barcelona, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0925-4773(02)00299-xDOI Listing
November 2002