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Morphometric Analysis of Hepatocellular carcinomaLaiMao-de(来茂德);ChenPei-hui(陈培辉)andZhouShui-yun(周水云)(DepartmentofPathology,Zh... 相似文献
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Ronald K. Wetherington 《American journal of physical anthropology》1982,57(1):117-121
Cone-shaped epiphyses (CSE) are reported in left-hand radiographs of a sample of 1,399 otherwise normal Japanese children aged 5–11 years. CSE occurred in only three centers: distal thumb, mid-index finger, and mid-fifth finger. The overall frequency of 23% shows a female bias (32% to 16%), which disappears when mid-5 cones are excluded. Chi-squared analyses show significant gender bias for mid-5 cones alone or in combination with the other phalanges, and show significant center associations: CSE in distal-1 and/or mid-2 are more common in association with mid-5 cones than they are without mid-5 cones. The CSE female bias in mid-5 is essentially unchanged across age-cohorts when bone-age is controlled for precocity, and no significant trends in CSE frequency with age are noted for either gender. 相似文献
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Matthew B. Greenblatt Jung-Min Kim Hwanhee Oh Kwang Hwan Park Min-Kyung Choo Yasuyo Sano Coralee E. Tye Ziedonis Skobe Roger J. Davis Jin Mo Park Marianna Bei Laurie H. Glimcher Jae-Hyuck Shim 《The Journal of biological chemistry》2015,290(1):284-295
An improved understanding of the molecular pathways that drive tooth morphogenesis and enamel secretion is needed to generate teeth from organ cultures for therapeutic implantation or to determine the pathogenesis of primary disorders of dentition (Abdollah, S., Macias-Silva, M., Tsukazaki, T., Hayashi, H., Attisano, L., and Wrana, J. L. (1997) J. Biol. Chem. 272, 27678–27685). Here we present a novel ectodermal dysplasia phenotype associated with conditional deletion of p38α MAPK in ectodermal appendages using K14-cre mice (p38αK14 mice). These mice display impaired patterning of dental cusps and a profound defect in the production and biomechanical strength of dental enamel because of defects in ameloblast differentiation and activity. In the absence of p38α, expression of amelogenin and β4-integrin in ameloblasts and p21 in the enamel knot was significantly reduced. Mice lacking the MAP2K MKK6, but not mice lacking MAP2K MKK3, also show the enamel defects, implying that MKK6 functions as an upstream kinase of p38α in ectodermal appendages. Lastly, stimulation with BMP2/7 in both explant culture and an ameloblast cell line confirm that p38α functions downstream of BMPs in this context. Thus, BMP-induced activation of the p38α MAPK pathway is critical for the morphogenesis of tooth cusps and the secretion of dental enamel. 相似文献
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应用抗人结肠癌单克隆抗体CL-2,CL-4,对205例大肠癌及癌旁病变进行了免疫组化研究。CL-2相应抗原在移行粘膜,轻、中、重度非腺瘤异型增生,大肠癌的阳性率分别为37.6%、63.2%、86.7%、90.9%及86.8%,阳性率呈递增趋势;CL-4相应抗原的阳性率依次是39.1%、57.9%、73.3%、81.8%及77.6%;40例正常大肠粘膜均阴性。结果表明,CL-2、CL-4都是对大肠癌阳性率较高的标记物,但用来鉴别癌与异型增生意义不大;一部分大肠癌可能来源于非腺瘤途径;移行粘膜不同程度的肿瘤相关抗原的表达,反映了其潜在的恶性性质,但其程度低于异型增生,文中,对其临床意义进行了讨论。 相似文献
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WISP-3 (Wnt1 inducible secreted protein-3) mutations have been linked to the connective tissue diseases progressive pseudorheumatoid dysplasia and polyarticular juvenile idiopathic arthritis, both of which are accompanied by disorders in cartilage maintenance/homeostasis. The molecular mechanism of WISP-3 mediated effects in the sustenance of cartilage has not been described in detail. Our previous study illustrates the potential role of WISP-3 in regulating the expression of cartilage-specific molecules that sustain chondrocyte growth and cartilage integrity. The present study was conducted to investigate the mode of action of WISP-3 in greater detail. Experimental results depicted here suggest that WISP-3 can function as a ligand and signal via autocrine and/or paracrine modes upon being secreted by chondrocytes. Furthermore, apart from regulating collagen II and aggrecan expression, WISP-3 may also promote superoxide dismutase expression and activity in chondrocytes. 相似文献
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Kim SD Pahuja KB Ravazzola M Yoon J Boyadjiev SA Hammamoto S Schekman R Orci L Kim J 《The Journal of biological chemistry》2012,287(13):10134-10144
COPII proteins are essential for exporting most cargo molecules from the endoplasmic reticulum. The membrane-facing surface of the COPII proteins (especially SEC23-SEC24) interacts directly or indirectly with the cargo molecules destined for exit. As we characterized the SEC23A mutations at the SEC31 binding site identified from patients with cranio-lenticulo-sutural dysplasia, we discovered that the SEC23-SEC31 interface can also influence cargo selection. Remarkably, M702V SEC23A does not compromise COPII assembly, vesicle size, and packaging of cargo molecules into COPII vesicles that we have tested but induces accumulation of procollagen in the endoplasmic reticulum when expressed in normal fibroblasts. We observed that M702V SEC23A activates SAR1B GTPase more than wild-type SEC23A when SEC13-SEC31 is present, indicating that M702V SEC23A causes premature dissociation of COPII from the membrane. Our results indicate that a longer stay of COPII proteins on the membrane is required to cargo procollagen than other molecules and suggest that the SEC23-SEC31 interface plays a critical role in capturing various cargo molecules. 相似文献