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1.
Phys Rev Lett ; 89(1): 015001, 2002 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-12097046

RESUMO

A promising new plasma operational regime on the Wendelstein stellarator W7-AS has been discovered. It is extant above a threshold density and characterized by flat density profiles, high energy and low impurity confinement times, and edge-localized radiation. Impurity accumulation is avoided. Quasistationary discharges with line-averaged densities n(e) to 4 x 10(20) m(-3), radiation levels to 90%, and partial plasma detachment at the divertor target plates can be simultaneously realized. Energy confinement is up to twice that of a standard scaling. At B(t) = 0.9 T, an average beta value of 3.1% is achieved. The high n(e) values allow demonstration of electron Bernstein wave heating using linear mode conversion.

2.
Nature ; 393(6683): 382-6, 1998 May 28.
Artigo em Inglês | MEDLINE | ID: mdl-9620803

RESUMO

Notch proteins are ligand-activated transmembrane receptors involved in cell-fate selection throughout development. No known enzymatic activity is contained within Notch and the molecular mechanism by which it transduces signals across the cell membrane is poorly understood. In many instances, Notch activation results in transcriptional changes in the nucleus through an association with members of the CSL family of DNA-binding proteins (where CSL stands for CBF1, Su(H), Lag-1). As Notch is located in the plasma membrane and CSL is a nuclear protein, two models have been proposed to explain how they interact. The first suggests that the two interact transiently at the membrane. The second postulates that Notch is cleaved by a protease, enabling the cleaved fragment to enter the nucleus. Here we show that signalling by a constitutively active membrane-bound Notch-1 protein requires the proteolytic release of the Notch intracellular domain (NICD), which interacts preferentially with CSL. Very small amounts of NICD are active, explaining why it is hard to detect in the nucleus in vivo. We also show that it is ligand binding that induces release of NICD.


Assuntos
Proteínas de Ligação a DNA/metabolismo , Proteínas de Membrana/metabolismo , Receptores de Superfície Celular , Transdução de Sinais , Fatores de Transcrição , Células 3T3 , Sequência de Aminoácidos , Animais , Fatores de Transcrição Hélice-Alça-Hélice Básicos , Brefeldina A , Linhagem Celular , Núcleo Celular/metabolismo , Ciclopentanos/farmacologia , Regulação da Expressão Gênica , Genes Reporter , Complexo de Golgi/metabolismo , Proteínas de Homeodomínio/genética , Ligantes , Camundongos , Dados de Sequência Molecular , Monensin/farmacologia , Mutagênese , Fragmentos de Peptídeos/metabolismo , Regiões Promotoras Genéticas , Processamento de Proteína Pós-Traducional/efeitos dos fármacos , Receptor Notch1 , Fatores de Transcrição HES-1 , Transfecção
3.
Dev Dyn ; 201(1): 63-70, 1994 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-7803848

RESUMO

The enteroendocrine cell system of the mammalian gastrointestinal tract is comprised of at least 16 different subpopulations. Each subpopulation shows a characteristic distribution along both the crypt-villus and cephalo-caudal axes. In both the small intestine and colon of adult mice, multilabel immunohistochemistry has demonstrated that two or more neuroendocrine products can be coexpressed in various combinations in single cells along the crypt-villus axis, suggesting that enteroendocrine phenotypes may be actively regulated. Using bromodeoxyuridine (BrdU) incorporation and multilabel immunohistochemistry, we have previously demonstrated an enteroendocrine cell differentiation pathway consisting of two subpopulations of cells in the mouse proximal small intestine--one involving the sequential expression of substance P, serotonin, and secretin in cells migrating out of the crypts into the villi, and a second involving the expression of substance P and serotonin in cells which remain in the crypts. In this report, we use double label immunohistochemistry and BrdU incorporation to define the temporal and spatial interrelationships between gastrin, cholecystokinin (CCK), glucagon-like peptide-1 (GLP-1), and gastric inhibitory peptide (GIP) immunoreactive cells in the mouse proximal small intestine. The expression of these products was compared with that of substance P, serotonin, and secretin. Minimal overlap of expression was found in cells immunoreactive for substance P or serotonin with gastrin, CCK, GLP-1, or GIP; however, secretin was found colocalized in villus-associated gastrin, CCK, and GLP-1 containing cells.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Glândulas Endócrinas/química , Hormônios Gastrointestinais/análise , Mucosa Intestinal/química , Intestino Delgado/química , Animais , Bromodesoxiuridina , Diferenciação Celular , Glândulas Endócrinas/citologia , Glândulas Endócrinas/metabolismo , Feminino , Hormônios Gastrointestinais/biossíntese , Imuno-Histoquímica , Mucosa Intestinal/citologia , Mucosa Intestinal/metabolismo , Intestino Delgado/citologia , Intestino Delgado/metabolismo , Camundongos
4.
Science ; 210(4476): 1343-5, 1980 Dec 19.
Artigo em Inglês | MEDLINE | ID: mdl-17817844

RESUMO

Historical documents indicate that great earthquakes ruptured at least a 500-kilometer-long segment of the plate boundary near the Alaska Peninsula in 1788 and 1847. At least half of a major seismic gap in the Shumagin Islands ruptured during those shocks but has not experienced a great earthquake for at least 77 years. Large shocks along this and other plate boundaries occur in bursts followed by several decades during which there is very little energy release.

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