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1.
Elife ; 112022 01 31.
Artículo en Inglés | MEDLINE | ID: mdl-35098925

RESUMEN

Although fossil evidence suggests that various animal groups were able to move actively through their environment in the early stages of their evolution, virtually no direct information is available on the nature of their muscle systems. The origin of jellyfish swimming, for example, is of great interest to biologists. Exceptionally preserved muscles are described here in benthic peridermal olivooid medusozoans from the basal Cambrian of China (Kuanchuanpu Formation, ca. 535 Ma) that have direct equivalent in modern medusozoans. They consist of circular fibers distributed over the bell surface (subumbrella) and most probably have a myoepithelial origin. This is the oldest record of a muscle system in cnidarians and more generally in animals. This basic system was probably co-opted by early Cambrian jellyfish to develop capacities for jet-propelled swimming within the water column. Additional lines of fossil evidence obtained from ecdysozoans (worms and panarthropods) show that the muscle systems of early animals underwent a rapid diversification through the early Cambrian and increased their capacity to colonize a wide range of habitats both within the water column and sediment at a critical time of their evolutionary radiation.


Asunto(s)
Evolución Biológica , Cnidarios/anatomía & histología , Cnidarios/fisiología , Músculos/fisiología , Animales , Ecosistema , Fósiles , Geografía , Filogenia , Escifozoos
2.
Sci Rep ; 10(1): 3574, 2020 02 27.
Artículo en Inglés | MEDLINE | ID: mdl-32107415

RESUMEN

Crustacean eggs are rare in the fossil record. Here we report the exquisite preservation of a fossil polychelidan embedded within an unbroken nodule from the Middle Jurassic La Voulte-sur-Rhône Lagerstätte (France) and found with hundreds of eggs attached to the pleon. This specimen belongs to a new species, Palaeopolycheles nantosueltae sp. nov. and offers unique clues to discuss the evolution of brooding behaviour in polychelidan lobsters. In contrast to their development, which now relies on a long-lived planktic larval stage that probably did not exist in the early evolutionary steps of the group, the brood size of polychelidan lobsters seems to have remained unchanged and comparatively small since the Jurassic. This finding is at odds with reproductive strategies in other lobster groups, in which a long-lived planktic larval stage is associated with a large brood size.


Asunto(s)
Nephropidae/clasificación , Óvulo/química , Animales , Evolución Biológica , Fósiles/anatomía & histología , Fósiles/historia , Francia , Historia Antigua , Nephropidae/anatomía & histología , Nephropidae/genética , Nephropidae/crecimiento & desarrollo , Óvulo/clasificación , Óvulo/crecimiento & desarrollo , Paleontología
3.
Blood Cells Mol Dis ; 66: 11-18, 2017 07.
Artículo en Inglés | MEDLINE | ID: mdl-28772256

RESUMEN

The most frequent germline mutations responsible for non syndromic congenital sideroblastic anemia are identified in ALAS2 and SLC25A38 genes. Iron overload is a key issue and optimal chelation therapy should be used to limit its adverse effects on the development of children. Our multicentre retrospective descriptive study compared the strategies for diagnosis and management of congenital sideroblastic anemia during the follow-up of six patients with an ALAS2 mutation and seven patients with an SLC25A38 mutation. We described in depth the clinical, biological and radiological phenotype of these patients at diagnosis and during follow-up and highlighted our results with a review of available evidence and data on the management strategies for congenital sideroblastic anemia. This report confirms the considerable variability in manifestations among patients with ALAS2 or SLC25A38 mutations and draws attention to differences in the assessment and the monitoring of iron overload and its complications. The use of an international registry would certainly help defining recommendations for the management of these rare disorders to improve patient outcome.


Asunto(s)
5-Aminolevulinato Sintetasa/genética , Anemia Sideroblástica/congénito , Proteínas de Transporte de Membrana Mitocondrial/genética , Anemia Sideroblástica/genética , Niño , Humanos , Sobrecarga de Hierro , Fenotipo , Estudios Retrospectivos
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