Ciclo XII de seleção entre e dentro de progênies de meios-irmãos na variedade de milho BR-5028 São Francisco.

1999

Evolução das exportações de manga e uva produzidas no Submédio do Vale do São Francisco no período de 2010-2014.

O objetivo deste trabalho foi analisar as estatísticas disponíveis para aferir a evolução, nos últimos 5 anos (2010-2014), das exportações das frutas de maior importância econômica para o Submédio do Vale do São Francisco, enfocando tanto o comportamento agregado quanto o mercado europeu e o americano. A base de dados usada foi a do sistema Aliceweb2, do Ministério do Desenvolvimento, Indústria e Comércio Exterior, (MDIC).

Vida de S. Francisco Xavier de la Compania de Iesvs primero Apostol del Iapon, y segundo de la India, y de otras Prouincias del Oriente

Van añadidas en esta impression muchas cosas, cuya tabla se pone despues del prologo.

Fortalecimiento de la actividad artesanal para familias vinculadas al programa de desarrollo alternativo - PDA en los Municipios de Sibundoy, Santiago, Colón y San Francisco en el Departamento de Putumayo y en el Municipio de Santa Marta en el Departamento del Magadalen : informe final.

286 hojas : ilustraciones, fotografías.

Fortalecimiento de la actividad artesanal para familias vinculadas al programa de desarrollo alternativo - PDA en los Municipios de Sibundoy, Santiago, Colón y San Francisco en el Departamento de Putumayo y en el Municipio de Santa Marta en el Departamento del Magdalena : informe Expoartesanías 2007.

12 hojas.

A miR-34a-Numb Feedforward Loop Triggered by Inflammation Regulates Asymmetric Stem Cell Division in Intestine and Colon Cancer.

Emerging evidence suggests that microRNAs can initiate asymmetric division, but whether microRNA and protein cell fate determinants coordinate with each other remains unclear. Here, we show that miR-34a directly suppresses Numb in early-stage colon cancer stem cells (CCSCs), forming an incoherent feedforward loop (IFFL) targeting Notch to separate stem and non-stem cell fates robustly. Perturbation of the IFFL leads to a new intermediate cell population with plastic and ambiguous identity. Lgr5+ mouse intestinal/colon stem cells (ISCs) predominantly undergo symmetric division but turn on asymmetric division to curb the number of ISCs when proinflammatory response causes excessive proliferation. Deletion of miR-34a inhibits asymmetric division and exacerbates Lgr5+ ISC proliferation under such stress. Collectively, our data indicate that microRNA and protein cell fate determinants coordinate to enhance robustness of cell fate decision, and they provide a safeguard mechanism against stem cell proliferation induced by inflammation or oncogenic mutation.

MiR-215 Is Induced Post-transcriptionally via HIF-Drosha Complex and Mediates Glioma-Initiating Cell Adaptation to Hypoxia by Targeting KDM1B.

The hypoxic tumor microenvironment serves as a niche for maintaining the glioma-initiating cells (GICs) that are critical for glioblastoma (GBM) occurrence and recurrence. Here, we report that hypoxia-induced miR-215 is vital for reprograming GICs to fit the hypoxic microenvironment via suppressing the expression of an epigenetic regulator KDM1B and modulating activities of multiple pathways. Interestingly, biogenesis of miR-215 and several miRNAs is accelerated post-transcriptionally by hypoxia-inducible factors (HIFs) through HIF-Drosha interaction. Moreover, miR-215 expression correlates inversely with KDM1B while correlating positively with HIF1α and GBM progression in patients. These findings reveal a direct role of HIF in regulating miRNA biogenesis and consequently activating the miR-215-KDM1B-mediated signaling required for GIC adaptation to hypoxia.

miR-7 and miR-214 are specifically expressed during neuroblastoma differentiation, cortical development and embryonic stem cells differentiation, and control neurite outgrowth in vitro

The mammalian nervous system exerts essential control on many physiological processes in the organism and is itself controlled extensively by a variety of genetic regulatory mechanisms. microRNA (miR), an abundant class of small non-coding RNA, are emerging as important post-transcriptional regulators of gene expression in the brain. Increasing evidence indicates that miR regulate both the development and function of the nervous system. Moreover, deficiency in miR function has also been implicated in a number of neurological disorders. Expression profile analysis of miR is necessary to understand their complex role in the regulation of gene expression during the development and differentiation of cells. Here we present a comparative study of miR expression profiles in neuroblastoma, in cortical development, and in neuronal differentiation of embryonic stem (ES) cells. By microarray profiling in combination with real time PCR we show that miR-7 and miR-214 are modulated in neuronal differentiation (as compared to miR-1, -16 and -133a), and control neurite outgrowth in vitro. These findings provide an important step toward further elucidation of miR function and miR-related gene regulatory networks in the mammalian central nervous system. (C) 2010 Elsevier Inc. All rights reserved.