Manioc : Portail | resultats 1 - 20 pour la recherche: Alexander, Joseph G

Reports from committees : eighteen volumes. Sugar and coffee planting. Session 18 november 1847 - 5 september 1848, Part. 4
Auteur(s) : Grande Bretagne. House of commons. Library
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Almanach royal, année bissextile M.DCC.LXXXVIII présenté à sa majesté pour la première fois en 1699
Auteur(s) : Houry, Laurent d' (1644-1725)
Auteurs secondaires : Debure, François-Jean-Noël (1743-1802)
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Bulletin officiel de la Guyane française
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The colony of British Guyana and its labouring population
Auteur(s) : Bronkhurst, Rév. H.V.P.
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Rerum medicarum novae Hispaniae thesaurus seu plantarum animalium mineralium mexicanorum historia ex Francisci Hernandez novi orbi medici primarii relationibus in ipsa mexicana urbe conscriptis a Nardo Antonio Reccho monte corvinate Cath. Majest. medico et Neap. Regni archiatro generali jussu Philippi II Hisp. ind. etc. regis collecta ac in ordinem digesta a Joanne Terrentio Lynceo Constantiense Germ. Ph.o ac medico notis illustrata... Quibus jam excussis accessere demum alia quorum omnium synopsis sequenti pagina ponitur. Opus duobus voluminibus divisum Philippo IIII. regi catholico magno....
Auteur(s) : Hernandez, Francisco (1515-1587)
Auteurs secondaires : Greuter, Johann Friedrich (1590-1662) Faber, Johann (1570-1640) Recchi, Nardo Antonio (1540-1595) Terentius, Joannes (1576-1630) Cesi, Federico (1585-1630) Colonna, Fabio (1567-1650)
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Observaciones sobre la esclavitud y comercio de eslcavos
Auteur(s) : Alexander, Joseph G Madden, Richard Robert Madden, Richard Robert

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British philanthropy and Jamaica distress
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Surinaamsche almanak voor het jaar 1902
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M. Roosevelt, président des Etats-Unis, et la République d'Haïti
Auteur(s) : Firmin, Anténor (1850-1911)
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Guidelines for the use and interpretation of assays for monitoring autophagy.
Auteur(s) : Klionsky, Daniel J Abdalla, Fabio C Abeliovich, Hagai Abraham, Robert T Acevedo-Arozena, Abraham Adeli, Khosrow Agholme, Lotta Agnello, Maria
Auteurs secondaires : Molecular and Cellular Biology ; University of Leuven Laboratoire d'Epigénétique et Cancer ; CNRS - Université Paris-Sud - Paris 11 (UP11) Department of Pharmacology ; Department of Pharmacology Immunobiologie des Cellules Dendritiques ; INSERM - Institut Pasteur de Paris Franche-Comté Électronique Mécanique, Thermique et Optique - Sciences et Technologies (FEMTO-ST) ; CNRS - Université de Franche-Comté - Université de Technologie de Belfort-Montbeliard - Ecole Nationale Supérieure de Mécanique et des Microtechniques Telethon Institute for Genetics and Medicine ; Telethon Institute Medical Genetics ; Federico II University Department of Molecular and Human Genetics ; Baylor College of Medicine

Éditeur(s) : HAL CCSD Landes Bioscience
Résumé : International audience
In 2008 we published the first set of guidelines for standardizing research in autophagy. Since then, research on this topic has continued to accelerate, and many new scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Accordingly, it is important to update these guidelines for monitoring autophagy in different organisms. Various reviews have described the range of assays that have been used for this purpose. Nevertheless, there continues to be confusion regarding acceptable methods to measure autophagy, especially in multicellular eukaryotes. A key point that needs to be emphasized is that there is a difference between measurements that monitor the numbers or volume of autophagic elements (e.g., autophagosomes or autolysosomes) at any stage of the autophagic process vs. those that measure flux through the autophagy pathway (i.e., the complete process); thus, a block in macroautophagy that results in autophagosome accumulation needs to be differentiated from stimuli that result in increased autophagic activity, defined as increased autophagy induction coupled with increased delivery to, and degradation within, lysosomes (in most higher eukaryotes and some protists such as Dictyostelium) or the vacuole (in plants and fungi). In other words, it is especially important that investigators new to the field understand that the appearance of more autophagosomes does not necessarily equate with more autophagy. In fact, in many cases, autophagosomes accumulate because of a block in trafficking to lysosomes without a concomitant change in autophagosome biogenesis, whereas an increase in autolysosomes may reflect a reduction in degradative activity. Here, we present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes. These guidelines are not meant to be a formulaic set of rules, because the appropriate assays depend in part on the question being asked and the system being used. In addition, we emphasize that no individual assay is guaranteed to be the most appropriate one in every situation, and we strongly recommend the use of multiple assays to monitor autophagy. In these guidelines, we consider these various methods of assessing autophagy and what information can, or cannot, be obtained from them. Finally, by discussing the merits and limits of particular autophagy assays, we hope to encourage technical innovation in the field.
Autophagy

hal-00735751
https://hal.archives-ouvertes.fr/hal-00735751
PUBMED : 22966490

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