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Alejandro Leal
Alejandro Leal
Sección de Genética, E. de Biología, Universidad de Costa Rica
Verified email at ucr.ac.cr - Homepage
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Cited by
Cited by
Year
Mesenchymal stem cells as anti-inflammatories: implications for treatment of Duchenne muscular dystrophy
TE Ichim, DT Alexandrescu, F Solano, F Lara, RDN Campion, E Paris, ...
Cellular immunology 260 (2), 75-82, 2010
2032010
The homeobox gene Gax inhibits angiogenesis through inhibition of nuclear factor-κb–dependent endothelial cell gene expression
S Patel, AD Leal, DH Gorski
Cancer research 65 (4), 1414-1424, 2005
1172005
A second locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 19q13. 3
A Leal, B Morera, G Del Valle, D Heuss, C Kayser, M Berghoff, R Villegas, ...
The American Journal of Human Genetics 68 (1), 269-274, 2001
1022001
Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type …
A Leal, K Huehne, F Bauer, H Sticht, P Berger, U Suter, B Morera, ...
neurogenetics 10 (4), 275-287, 2009
962009
A novel myosin heavy chain gene in human chromosome 19q13. 3
A Leal, S Endele, C Stengel, K Huehne, J Loetterle, R Barrantes, ...
Gene 312, 165-171, 2003
822003
Differential expression of vascular endothelial growth factor–A isoforms at different stages of melanoma progression
DH Gorski, AD Leal, JS Goydos
Journal of the American College of Surgeons 197 (3), 408-418, 2003
812003
Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13. 3
C Berghoff, M Berghoff, A Leal, B Morera, R Barrantes, A Reis, ...
Neuromuscular Disorders 14 (5), 301-306, 2004
462004
The homeobox gene GAX activates p21WAF1/CIP1 expression in vascular endothelial cells through direct interaction with upstream AT-rich sequences
Y Chen, AD Leal, S Patel, DH Gorski
Journal of Biological Chemistry 282 (1), 507-517, 2007
452007
Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum
M Smogavec, A Cleall, J Hoyer, D Lederer, MC Nassogne, EE Palmer, ...
Journal of medical genetics 53 (12), 820-827, 2016
402016
Utilização de medidas biométricas para estimar peso vivo em ovinos
ES Souza, A Leal, C Barioni, A Matos, J Morais, M Araújo, O Neto, ...
Archivos Latinoamericanos de Producción Animal 17 (3), 61-66, 2009
302009
The polynucleotide kinase 3′-phosphatase gene (PNKP) is involved in Charcot-Marie-Tooth disease (CMT2B2) previously related to MED25
A Leal, S Bogantes-Ledezma, AB Ekici, S Uebe, CT Thiel, H Sticht, ...
neurogenetics 19 (4), 215-225, 2018
292018
Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one …
A Leal, C Berghoff, M Berghoff, G Del Valle, C Contreras, O Montoya, ...
Neurogenetics 4 (4), 191-197, 2003
222003
Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one …
A Leal, C Berghoff, M Berghoff, G Del Valle, C Contreras, O Montoya, ...
Neurogenetics 4 (4), 191-197, 2003
222003
Pathological mutations in PNKP trigger defects in DNA single-strand break repair but not DNA double-strand break repair
I Kalasova, R Hailstone, J Bublitz, J Bogantes, W Hofmann, A Leal, ...
Nucleic Acids Research 48 (12), 6672-6684, 2020
212020
Immune effects of mesenchymal stem cells: Implications for Charcot–Marie–Tooth disease
A Leal, TE Ichim, AM Marleau, F Lara, S Kaushal, NH Riordan
Cellular Immunology 253 (1-2), 11-15, 2008
182008
A new species of dink frog (Anura: Eleutherodactylidae: Diasporus) from Cordillera de Talamanca, Costa Rica
G Chaves, A Garcia-Rodriguez, A Mora, A Leal
Zootaxa 2088 (1), 1–14-1–14, 2009
172009
DNA repair deficiency in neuropathogenesis: when all roads lead to mitochondria
L Bermúdez-Guzmán, A Leal
Translational Neurodegeneration 8 (1), 1-14, 2019
152019
A homozygous mutation in GPT2 associated with nonsyndromic intellectual disability in a consanguineous family from Costa Rica
T Lobo-Prada, H Sticht, S Bogantes-Ledezma, A Ekici, S Uebe, A Reis, ...
JIMD Reports, Volume 36, 59-66, 2017
92017
Correlates of longitudinal leukocyte telomere length in the Costa Rican Longevity Study of Healthy Aging (CRELES): On the importance of DNA collection and storage procedures
L Rosero-Bixby, DH Rehkopf, WH Dow, J Lin, ES Epel, J Azofeifa, A Leal
PloS one 14 (10), e0223766, 2019
82019
Mutational survivorship bias: The case of PNKP
L Bermudez-Guzman, G Jimenez-Huezo, A Arguedas, A Leal
Plos one 15 (12), e0237682, 2020
72020
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