Caracterização dos macrófagos presentes nas lesões cutâneas da hanseníase: estudo por monoclonais

As lesões cutâneas de 16 pacientes com hanseníase foram estudadas por imunofluorescência com anticorpos monoclonais anti-monócitos (OKM1 e anti-MO) e anti-Ia (OKIa). Foi avaliada a atividade de fosfatase ácida utilizando-se naftol AS-B1 fosfato como substrato. Os macrófagos parecem constituir uma população heterogênea em relação aos antigenos estudados neste trabalho e quanto a atividade enzimática. Em todas as formas estudadas um grande número de células eram OKIa positivas.The skin lesions from 16 leprosy patients were studied by immunofluorescence technique using monoclonal antibodies against monocytes (OKM1 and Anti-Mo) and la-like antigen. Acid phosphatase activity was evaluated using naphthol AS-BI phosphate as substrate. The macrophages seem to be a heterogeneous population in concern with the antigens here studied as well as the enzimatic activity. Ia-like antigen was expressed in a great number of cells throughout the clinical spectrum

Caracterização dos macrófagos presentes nas lesões cutâneas da hanseníase: estudo por monoclonais

As lesões cutâneas de 16 pacientes com hanseníase foram estudadas por imunofluorescência com anticorpos monoclonais anti-monócitos (OKM1 e anti-MO) e anti-Ia (OKIa). Foi avaliada a atividade de fosfatase ácida utilizando-se naftol AS-B1 fosfato como substrato. Os macrófagos parecem constituir uma população heterogênea em relação aos antigenos estudados neste trabalho e quanto a atividade enzimática. Em todas as formas estudadas um grande número de células eram OKIa positivas

Caracterização dos macrófagos presentes nas lesões cutâneas da Hanseníase: estudo por monoclonais

Submitted by Sandra Infurna ([email protected]) on 2019-05-28T17:21:30Z No. of bitstreams: 1 euzenir nunessarno_etal_IOC_1988.pdf: 707578 bytes, checksum: d603c0bb32918e1411f3c6e220c4d63a (MD5)Approved for entry into archive by Sandra Infurna ([email protected]) on 2019-05-28T17:27:39Z (GMT) No. of bitstreams: 1 euzenir nunessarno_etal_IOC_1988.pdf: 707578 bytes, checksum: d603c0bb32918e1411f3c6e220c4d63a (MD5)Made available in DSpace on 2019-05-28T17:27:39Z (GMT). No. of bitstreams: 1 euzenir nunessarno_etal_IOC_1988.pdf: 707578 bytes, checksum: d603c0bb32918e1411f3c6e220c4d63a (MD5) Previous issue date: 1988Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hanseníase. Rio de Janeiro, RJ. Brasil.Universidade do estado do Rio de Janeiro. Disciplina de Patologia Geral. Rio de Janeiro, RJ, Brasil.Universidade do estado do Rio de Janeiro. Disciplina de Patologia Geral. Rio de Janeiro, RJ, Brasil.Hospital Geral de Bonsucesso. Serviço de Dermatololgia. Rio de Janeiro, RJ, Brasil.As lesões cutâneas de 16 pacientes com hanseníase foram estudadas por imunofluorescência com anticorpos monoclonais anti-monócitos (OKM1 e anti-MO) e anti-Ia (OKIa). Foi avaliada a atividade de fosfatase ácida utilizando-se naftol AS-B1 fosfato como substrato. Os macrófagos parecem constituir uma população heterogênea em relação aos antigenos estudados neste trabalho e quanto a atividade enzimática. Em todas as formas estudadas um grande número de células eram OKIa positivas

A Transcript Finishing Initiative for Closing Gaps in the Human Transcriptome

We report the results of a transcript finishing initiative, undertaken for the purpose of identifying and characterizing novel human transcripts, in which RT-PCR was used to bridge gaps between paired EST clusters, mapped against the genomic sequence. Each pair of EST clusters selected for experimental validation was designated a transcript finishing unit (TFU). A total of 489 TFUs were selected for validation, and an overall efficiency of 43.1% was achieved. We generated a total of 59,975 bp of transcribed sequences organized into 432 exons, contributing to the definition of the structure of 211 human transcripts. The structure of several transcripts reported here was confirmed during the course of this project, through the generation of their corresponding full-length cDNA sequences. Nevertheless, for 21% of the validated TFUs, a full-length cDNA sequence is not yet available in public databases, and the structure of 69.2% of these TFUs was not correctly predicted by computer programs. The TF strategy provides a significant contribution to the definition of the complete catalog of human genes and transcripts, because it appears to be particularly useful for identification of low abundance transcripts expressed in a restricted set of tissues as well as for the delineation of gene boundaries and alternatively spliced isoforms

Identification of human chromosome 22 transcribed sequences with ORF expressed sequence tags

Transcribed sequences in the human genome can be identified with confidence only by alignment with sequences derived from cDNAs synthesized from naturally occurring mRNAs. We constructed a set of 250,000 cDNAs that represent partial expressed gene sequences and that are biased toward the central coding regions of the resulting transcripts. They are termed ORF expressed sequence tags (ORESTES). The 250,000 ORESTES were assembled into 81,429 contigs. Of these, 1,181 (1.45%) were found to match sequences in chromosome 22 with at least one ORESTES contig for 162 (65.6%) of the 247 known genes, for 67 (44.6%) of the 150 related genes, and for 45 of the 148 (30.4%) EST-predicted genes on this chromosome. Using a set of stringent criteria to validate our sequences, we identified a further 219 previously unannotated transcribed sequences on chromosome 22. Of these, 171 were in fact also defined by EST or full length cDNA sequences available in GenBank but not utilized in the initial annotation of the first human chromosome sequence. Thus despite representing less than 15% of all expressed human sequences in the public databases at the time of the present analysis, ORESTES sequences defined 48 transcribed sequences on chromosome 22 not defined by other sequences. All of the transcribed sequences defined by ORESTES coincided with DNA regions predicted as encoding exons by genscan. (http://genes.mit.edu/GENSCAN.html)

NEOTROPICAL ALIEN MAMMALS: a data set of occurrence and abundance of alien mammals in the Neotropics

Biological invasion is one of the main threats to native biodiversity. For a species to become invasive, it must be voluntarily or involuntarily introduced by humans into a nonnative habitat. Mammals were among first taxa to be introduced worldwide for game, meat, and labor, yet the number of species introduced in the Neotropics remains unknown. In this data set, we make available occurrence and abundance data on mammal species that (1) transposed a geographical barrier and (2) were voluntarily or involuntarily introduced by humans into the Neotropics. Our data set is composed of 73,738 historical and current georeferenced records on alien mammal species of which around 96% correspond to occurrence data on 77 species belonging to eight orders and 26 families. Data cover 26 continental countries in the Neotropics, ranging from Mexico and its frontier regions (southern Florida and coastal-central Florida in the southeast United States) to Argentina, Paraguay, Chile, and Uruguay, and the 13 countries of Caribbean islands. Our data set also includes neotropical species (e.g., Callithrix sp., Myocastor coypus, Nasua nasua) considered alien in particular areas of Neotropics. The most numerous species in terms of records are from Bos sp. (n = 37,782), Sus scrofa (n = 6,730), and Canis familiaris (n = 10,084); 17 species were represented by only one record (e.g., Syncerus caffer, Cervus timorensis, Cervus unicolor, Canis latrans). Primates have the highest number of species in the data set (n = 20 species), partly because of uncertainties regarding taxonomic identification of the genera Callithrix, which includes the species Callithrix aurita, Callithrix flaviceps, Callithrix geoffroyi, Callithrix jacchus, Callithrix kuhlii, Callithrix penicillata, and their hybrids. This unique data set will be a valuable source of information on invasion risk assessments, biodiversity redistribution and conservation-related research. There are no copyright restrictions. Please cite this data paper when using the data in publications. We also request that researchers and teachers inform us on how they are using the data

Digital Modernism Heritage Lexicon

The book investigates the theme of Modernism (1920-1960 and its epigones) as an integral part of tangible and intangible cultural heritage which contains the result of a whole range of disciplines whose aim is to identify, document and preserve the memory of the past and the value of the future. Including several chapters, it contains research results relating to cultural heritage, more specifically Modernism, and current digital technologies. This makes it possible to record and evaluate the changes that both undergo: the first one, from a material point of view, the second one from the research point of view, which integrates the traditional approach with an innovative one. The purpose of the publication is to show the most recent studies on the modernist lexicon 100 years after its birth, moving through different fields of cultural heritage: from different forms of art to architecture, from design to engineering, from literature to history, representation and restoration. The book appeals to scholars and professionals who are involved in the process of understanding, reading and comprehension the transformation that the places have undergone within the period under examination. It will certainly foster the international exchange of knowledge that characterized Modernism