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1.
Nat Commun ; 6: 7361, 2015 Jun 10.
Artigo em Inglês | MEDLINE | ID: mdl-26059779

RESUMO

For over a decade, controlling domain-wall injection, motion and annihilation along nanowires has been the preserve of the nanomagnetics research community. Revolutionary technologies have resulted, like racetrack memory and domain-wall logic. Until recently, equivalent research in analogous ferroic materials did not seem important. However, with the discovery of sheet conduction, the control of domain walls in ferroelectrics has become vital for the future of what has been termed 'domain-wall electronics'. Here we report the creation of a ferroelectric domain-wall diode, which allows a single direction of motion for all domain walls, irrespective of their polarity, under a series of alternating electric field pulses. The diode's sawtooth morphology is central to its function. Domain walls can move readily in the direction in which thickness increases gradually, but are prevented from moving in the other direction by the sudden thickness increase at the sawtooth edge.

2.
Cells Tissues Organs ; 171(4): 241-9, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12169821

RESUMO

OBJECTIVES: To obtain further knowledge on the morphogenesis of the articulations in the tympanic ossicular chain in humans. MATERIAL AND METHODS: In 25 temporal bones of human fetuses the structural development of incudomallear, incudostapedial and stapediovestibular articulations was studied. The chronological ages were between the 7th week (21 mm) and the 29th week (270 mm). RESULTS AND DISCUSSION: Incudomallear articulation showed diarthrosis and sellar joint characteristics. It showed a homogenous interzone in the 7th week of development, a three-layered interzone in the 8th week, the first cavitation signs in the 9th week and the presence of an articular cavity in the 10th week. The presence of a hyaline cartilage covering articular surfaces was observed starting in the 20th week of development. Incudostapedial articulation showed typical characteristics of a diarthrosis and spheroidal joint with a homogenous interzone at the 7th week, showing similar characteristics for 12 weeks, and completed its cavitation at the 16th week. We observed hyaline cartilage on articular surfaces from 29 weeks. Stapediovestibular articulation showed typical characteristics of syndesmosis. The annular ligament primordium derived from cartilage differentiation, both from stapedial footplate and from the surrounding otic capsule, into mesenchyme and its subsequent transformation into fibrous tissue, reaching definitive characteristics from the 12th week.


Assuntos
Ossículos da Orelha/embriologia , Padronização Corporal/fisiologia , Diferenciação Celular/fisiologia , Feto , Idade Gestacional , Humanos , Bigorna/embriologia , Martelo/embriologia , Janela do Vestíbulo/embriologia , Estribo/embriologia
3.
Dev Cell ; 1(4): 527-37, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11703943

RESUMO

The specificity of intracellular vesicle transport is mediated in part by tethering factors that attach the vesicle to the destination organelle prior to fusion. We have identified a protein, Dor1p, that is involved in vesicle targeting to the yeast Golgi apparatus and found it to be associated with seven further proteins. Identification of these revealed that they include Sec34p and Sec35p, the two known components of the Sec34/35 complex previously proposed to tether vesicles to the Golgi. Of the six previously uncharacterized components, four have homologs in higher eukaryotes, including a subunit of a mammalian Golgi transport complex. Furthermore, several of the proteins show distant homology to components of two other putative tethering complexes, the exocyst and the Vps52/53/54 complex, revealing that tethering factors involved in different membrane traffic steps are structurally related.


Assuntos
Proteínas Adaptadoras de Transporte Vesicular , Proteínas de Transporte/metabolismo , Proteínas Fúngicas/genética , Complexo de Golgi/metabolismo , Proteínas de Membrana/genética , Proteínas de Membrana/metabolismo , Transporte Proteico/fisiologia , Proteínas de Saccharomyces cerevisiae , Proteínas de Transporte Vesicular , Animais , Células COS , Proteínas Fúngicas/metabolismo , Humanos , Dados de Sequência Molecular , Mutação/fisiologia , Fenótipo , Homologia de Sequência de Aminoácidos , Leveduras
4.
Curr Biol ; 11(13): 1074-8, 2001 Jul 10.
Artigo em Inglês | MEDLINE | ID: mdl-11470415

RESUMO

The soluble hydrolases of the mammalian lysosome are marked for delivery to this organelle by the addition of mannose 6-phosphate to their N-glycans. Two related mannose 6-phosphate receptors (MPRs) recognize this feature in the trans Golgi network (TGN) and deliver the hydrolases to the late endosome. In contrast, the vacuolar hydrolases of the yeast Saccharomyces cerevisiae do not contain 6-phosphate monoesters on their N-glycans, and the only sorting receptor so far identified in this organism is the product of the VPS10 gene. This protein also cycles between the Golgi and the late endosome, but is unrelated to the vertebrate MPRs, and recognizes a specific amino acid sequence of carboxypeptidase Y (CPY). This has led to the notion that although yeast and mammals share many components in Golgi to endosome traffic, they use unrelated receptor systems to sort their abundant soluble hydrolases. In this paper, we report that the yeast genome does in fact contain an uncharacterized ORF (YPR079w) that encodes a membrane protein that is distantly related to mammalian MPRs. The protein encoded by this gene (which we term MRL1) cycles through the late endosome. Moreover, there is a strong synergistic effect on the maturation of proteinases A and B when both MRL1 and VPS10 are deleted, which suggests that Mrl1p may serve as a sorting receptor in the delivery of vacuolar hydrolases.


Assuntos
Endopeptidases/metabolismo , Proteínas de Membrana/fisiologia , Receptor IGF Tipo 2/fisiologia , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/enzimologia , Vacúolos/enzimologia , Proteínas de Transporte Vesicular , Sequência de Aminoácidos , Endossomos/enzimologia , Proteínas Fúngicas/genética , Deleção de Genes , Complexo de Golgi/metabolismo , Humanos , Proteínas de Membrana/genética , Dados de Sequência Molecular , Transporte Proteico , Receptor IGF Tipo 2/genética , Receptores de Superfície Celular/genética , Homologia de Sequência de Aminoácidos , Serina Endopeptidases/metabolismo
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