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Institution

Universidad Autónoma de la Ciudad de México

EducationMexico City, Mexico
About: Universidad Autónoma de la Ciudad de México is a education organization based out in Mexico City, Mexico. It is known for research contribution in the topics: Entamoeba histolytica & Gene. The organization has 604 authors who have published 1179 publications receiving 11285 citations. The organization is also known as: Universidad Autonoma de la Ciudad de Mexico.


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Journal ArticleDOI
TL;DR: In this paper, phase transitions and structural and magnetic properties of rapidly solidified Ni50Mn38Sn12 alloy ribbons have been studied and the coercivity values measured in both temperature intervals suggest a significant difference in the behavior of the two materials.
Abstract: Phase transitions and structural and magnetic properties of rapidly solidified Ni50Mn38Sn12 alloy ribbons have been studied. Ribbon samples crystallize as a single-phase, ten-layered modulated (10M) monoclinic martensite with a columnar-grain microstructure and a magnetic transition temperature of 308 K. By decreasing the temperature, martensite undergoes an intermartensitic phase transition around 195 K. Above room temperature, the high temperature martensite transforms into austenite. Below 100 K, magnetization hysteresis loops shift along the negative H-axis direction, confirming the occurrence of an exchange bias effect. On heating, the thermal dependence of the coercive field HC shows a continuous increase, reaching a maximum value of 1017 Oe around 50 K. Above this temperature, HC declines to zero around 195 K. But above this temperature, it increases again up to 20 Oe falling to zero close to 308 K. The coercivity values measured in both temperature intervals suggest a significant difference in the...

940 citations

Journal ArticleDOI
TL;DR: This review analyzes recent knowledge on MMPs and their participation in angiogenesis through the modulation of the balance between pro- and anti-angiogenic factors and concludes that Matrix metalloproteinases participate in the disruption, tumor neovascularization, and subsequent metastasis.
Abstract: During angiogenesis, new vessels emerge from existing endothelial lined vessels to promote the degradation of the vascular basement membrane and remodel the extracellular matrix (ECM), followed by endothelial cell migration, and proliferation and the new generation of matrix components. Matrix metalloproteinases (MMPs) participate in the disruption, tumor neovascularization, and subsequent metastasis while tissue inhibitors of metalloproteinases (TIMPs) downregulate the activity of these MMPs. Then, the angiogenic response can be directly or indirectly mediated by MMPs through the modulation of the balance between pro- and anti-angiogenic factors. This review analyzes recent knowledge on MMPs and their participation in angiogenesis.

488 citations

Journal ArticleDOI
TL;DR: An analysis of admixture in thirteen Mestizo populations from seven countries in Latin America based on data for 678 autosomal and 29 X-chromosome microsatellites found extensive variation in Native American and European ancestry among populations and individuals and evidence that admixture across Latin America has often involved predominantly European men and both Native and African women.
Abstract: The large and diverse population of Latin America is potentially a powerful resource for elucidating the genetic basis of complex traits through admixture mapping. However, no genome-wide characterization of admixture across Latin America has yet been attempted. Here, we report an analysis of admixture in thirteen Mestizo populations (i.e. in regions of mainly European and Native settlement) from seven countries in Latin America based on data for 678 autosomal and 29 X-chromosome microsatellites. We found extensive variation in Native American and European ancestry (and generally low levels of African ancestry) among populations and individuals, and evidence that admixture across Latin America has often involved predominantly European men and both Native and African women. An admixture analysis allowing for Native American population subdivision revealed a differentiation of the Native American ancestry amongst Mestizos. This observation is consistent with the genetic structure of pre-Columbian populations and with admixture having involved Natives from the area where the Mestizo examined are located. Our findings agree with available information on the demographic history of Latin America and have a number of implications for the design of association studies in population from the region.

431 citations

Journal ArticleDOI
Mandy Y.M. Ng1, Douglas F. Levinson2, Stephen V. Faraone3, Brian K. Suarez4, Lynn E. DeLisi5, Lynn E. DeLisi6, Tadao Arinami7, Brien P. Riley8, Tiina Paunio9, Tiina Paunio10, A. E. Pulver11, Irmansyah12, Peter Holmans13, Michael Escamilla14, Dieter B. Wildenauer15, Nigel Williams13, Claudine Laurent16, Bryan J. Mowry17, Linda M. Brzustowicz18, Michel Maziade19, Pamela Sklar20, D L Garver21, Gonçalo R. Abecasis22, Bernard Lerer, M D Fallin11, Hugh Gurling23, Pablo V. Gejman24, Eva Lindholm25, Hans W. Moises26, William Byerley27, Ellen M. Wijsman28, Paola Forabosco1, Ming T. Tsuang29, Ming T. Tsuang20, H-G Hwu30, Yuji Okazaki31, Kenneth S. Kendler8, Brandon Wormley8, Ayman H. Fanous32, Ayman H. Fanous21, Dermot Walsh, Francis A. O'Neill33, Leena Peltonen, Gerald Nestadt11, Virginia K. Lasseter11, Kung-Yee Liang11, G M Papadimitriou34, Dimitris Dikeos34, Sibylle G. Schwab15, Michael John Owen13, Michael Conlon O'Donovan13, Nadine Norton13, Elizabeth Hare14, Henriette Raventós35, Humberto Nicolini36, Margot Albus, Wolfgang Maier37, Vishwajit L. Nimgaonkar38, Lars Terenius39, J. Mallet40, Melanie Jay16, Stephanie Godard41, Deborah A. Nertney17, M. Alexander2, Raymond R. Crowe42, Jeremy M. Silverman43, Anne S. Bassett44, M-A Roy19, Chantal Mérette19, Carlos N. Pato45, Michele T. Pato45, J. Louw Roos46, Yoav Kohn, Daniela Amann-Zalcenstein47, Gursharan Kalsi23, Andrew McQuillin23, David Curtis48, Jon Brynjolfson, Thordur Sigmundsson, Hannes Petursson, Alan R. Sanders24, Jubao Duan24, Elena Jazin25, Marina Myles-Worsley3, Maria Karayiorgou49, Cathryn M. Lewis1 
King's College London1, Stanford University2, State University of New York Upstate Medical University3, Washington University in St. Louis4, New York University5, Nathan Kline Institute for Psychiatric Research6, University of Tsukuba7, Virginia Commonwealth University8, University of Helsinki9, National Institute for Health and Welfare10, Johns Hopkins University11, University of Indonesia12, Cardiff University13, University of Texas Health Science Center at San Antonio14, University of Western Australia15, Pierre-and-Marie-Curie University16, University of Queensland17, Rutgers University18, Laval University19, Harvard University20, Veterans Health Administration21, University of Michigan22, University College London23, NorthShore University HealthSystem24, Uppsala University25, University of Kiel26, University of California, San Francisco27, University of Washington28, University of California, San Diego29, National Taiwan University30, Tokyo Metropolitan Matsuzawa Hospital31, Georgetown University32, Queen's University Belfast33, National and Kapodistrian University of Athens34, University of Costa Rica35, Universidad Autónoma de la Ciudad de México36, University of Bonn37, University of Pittsburgh38, Karolinska Institutet39, University of Paris40, French Institute of Health and Medical Research41, University of Iowa42, Icahn School of Medicine at Mount Sinai43, University of Toronto44, University of Southern California45, University of Pretoria46, Weizmann Institute of Science47, Queen Mary University of London48, Columbia University49
TL;DR: The primary analysis met empirical criteria for ‘aggregate’ genome-wide significance, indicating that some or all of 10 bins are likely to contain loci linked to SCZ, including regions of chromosomes 1, 2q, 3q, 4q, 5q, 8p and 10q.
Abstract: A genome scan meta-analysis (GSMA) was carried out on 32 independent genome-wide linkage scan analyses that included 3255 pedigrees with 7413 genotyped cases affected with schizophrenia (SCZ) or related disorders. The primary GSMA divided the autosomes into 120 bins, rank-ordered the bins within each study according to the most positive linkage result in each bin, summed these ranks (weighted for study size) for each bin across studies and determined the empirical probability of a given summed rank (P(SR)) by simulation. Suggestive evidence for linkage was observed in two single bins, on chromosomes 5q (142-168 Mb) and 2q (103-134 Mb). Genome-wide evidence for linkage was detected on chromosome 2q (119-152 Mb) when bin boundaries were shifted to the middle of the previous bins. The primary analysis met empirical criteria for 'aggregate' genome-wide significance, indicating that some or all of 10 bins are likely to contain loci linked to SCZ, including regions of chromosomes 1, 2q, 3q, 4q, 5q, 8p and 10q. In a secondary analysis of 22 studies of European-ancestry samples, suggestive evidence for linkage was observed on chromosome 8p (16-33 Mb). Although the newer genome-wide association methodology has greater power to detect weak associations to single common DNA sequence variants, linkage analysis can detect diverse genetic effects that segregate in families, including multiple rare variants within one locus or several weakly associated loci in the same region. Therefore, the regions supported by this meta-analysis deserve close attention in future studies.

274 citations

Journal ArticleDOI
TL;DR: The role of hypoxia as a mechanism that drives the acquisition of tumor hallmarks that make certain cancers more aggressive is discussed and some combinations of therapies that inhibit the angiogenesis process and that may be a successful strategy for cancer patients are indicated.
Abstract: During carcinogenesis, advanced tumors are surrounded by both stromal and immune cells, which support tumor development. In addition, inflammation and angiogenesis are processes that play important roles in the development of cancer, from the initiation of carcinogenesis, tumor in situ and advanced stages of cancer. During acute inflammation, vascular hyperpermeability allows inflammatory mediators and immune response cells, including leukocytes and monocytes/macrophages, to infiltrate the site of damage. As a factor that regulates vascular permeability, vascular endothelial growth factor (VEGF) also plays a vital role as a multifunctional molecule and growth factor. Furthermore, stromal and immune cells secrete soluble factors that activate endothelial cells and favor their transmigration to eliminate the aggressive agent. In this review, we present a comprehensive view of both the relationship between chronic inflammation and angiogenesis during carcinogenesis and the participation of endothelial cells in the inflammatory process. In addition, the regulatory mechanisms that contribute to the endothelium returning to its basal permeability state after acute inflammation are discussed. Moreover, the manner in which immune cells participate in pathological angiogenesis release pro-angiogenic factors that contribute to early tumor vascularization, even before the angiogenic switch occurs, is also examined. Also, we discuss the role of hypoxia as a mechanism that drives the acquisition of tumor hallmarks that make certain cancers more aggressive. Finally, some combinations of therapies that inhibit the angiogenesis process and that may be a successful strategy for cancer patients are indicated.

169 citations


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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20234
202221
202168
202093
201999
201889