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81.
腋动脉分支变异较多,笔者在解剖1具成人男尸时发现其变异程度大,较罕见,特此报道,为国人统计腋动脉分支变异积累资料,也为临床外科手术注意特例情况提供解剖学依据(图1)。 相似文献
82.
Pituitary Adenylate-Cyclase-Activating Polypeptide (PACAP) Binding Sites and PACAP/Vasoactive Intestinal Polypeptide Receptor Expression in Human Pituitary Adenomas 下载免费PDF全文
83.
通过特异引物扩增出去掉终止密码的mCCL19编码序列,经酶切、亚克隆、拼接构建了真核表达载体pcDNA3.1-CCL19Ig,酶切和测序鉴定插入序列;将重组质粒转染CHO细胞进行体外表达,通过RT—PCR、Western blot鉴定目的基因的表达,利用趋化小室法测趋化活性。结果测序证实重组表达载体含mCCL19编码序列和人IgGI Fc段序列,其序列分别与GenBank中公布序列比对一致,IgG1-Fc段读码框未发生改变;Western blot结果证实转染了pcDNA3.1-mCEL19Ig的CHO细胞培养上清中有相对分子质量为38000的融合蛋白mCCL19Ig表达;体外趋化实验表明融合蛋白mCCL19Ig对小鼠脾细胞有趋化活性,且呈剂量依耐关系。 相似文献
84.
A fastidious gram-negative bacterium was isolated from the blood of a 37-year-old man who had insidious endocarditis with a sudden rupture of a cerebral aneurysm. Characterization of the organism through phylogenetic and phenotypic analyses revealed a novel species of Cardiobacterium, for which the name Cardiobacterium valvarum sp. nov. is proposed. C. valvarum will supplement the current sole species Cardiobacterium hominis, a known cause of endocarditis. Surgeries and antibiotic treatment cured the patient's infection and associated complications. During cardiac surgery, a congenital bicuspid aortic valve was found to be the predisposing factor for his endocarditis. 相似文献
85.
86.
Age-dependent and iron-independent expression of two mRNA isoforms of divalent metal transporter 1 in rat brain 总被引:12,自引:0,他引:12
Ke Y Chang YZ Duan XL Du JR Zhu L Wang K Yang XD Ho KP Qian ZM 《Neurobiology of aging》2005,26(5):739-748
The DMT1(Nramp2/DCT1) is a newly discovered proton-coupled metal-ion transport protein. The cellular localization and functional characterization of DMT1 suggest that it might play a role in physiological iron transport in the brain. In the study, we evaluated effects of dietary iron and age on iron content and DMT1 expression in four brain regions: cortex, hippocampus, striatum, substantia nigra. Total iron content in all regions was significantly lower in the low-iron diet rats and higher in the high-iron diet rats than that in the control animals, showing that dietary iron treatment for 6-weeks can alter brain iron levels. Contrary to our expectation, there was no significant alternation in DMT1(+IRE) and (-IRE) mRNA expression and protein content in all brain regions examined in spite of the existence of the altered iron levels in these regions after 6-weeks' diet treatment although TfR mRNA expression and protein level were affected significantly, as was expected. The data demonstrates that expression of DMT1(+IRE) and (-IRE) was not regulated by iron in these regions of adult rats. The lack of response of DMT1 to iron status in the brain suggests that the IRE of brain DMT1 mRNA might be not really iron-responsive and that DMT1-mediated iron transport might be not the rate-limiting step in brain iron uptake in adult rats. Our findings also showed that development can significantly affect brain iron and DMT1(+IRE) and (-IRE) expression but the effect varies in different brain regions, indicating a regionally specific regulation in the brain. 相似文献
87.
本文对296例小儿热性惊厥脑电图进行分析。结果:小儿热性惊厥脑电图(EEG)异常率48.65%,主要以阵性高幅慢波为主(77.78%)。小儿癫痫脑电图异常率(89.61%)。主要以阵发性棘慢波和局灶性改变为主(62.78%)。二周后EEG复查热性惊厥EEG大部分恢复正常(83.35%)。而小儿癫痫EEG未有恢复正常的。热性惊厥发作次数愈多,发作持续时间愈长EEG改变愈明显,二周后脑电图恢复正常的愈少。这对小儿热性惊厥的诊断和预后判定有重要价值。 相似文献
88.
多种金属离子与单宁酸反应媒染微血管的对比研究 总被引:2,自引:0,他引:2
目的 镜下观察单宁酸与金属盐溶液中Ca2 + 、Au+ 、Ag+ 、Pb2 + 、Cu2 + 、Al3 + 、U6+ 、K+ 联用显示大脑微血管的效果。方法 用单宁酸媒染固定液灌流大鼠 ,取脑切片 ,入氯化钙、氯化金、硝酸银、硝酸铅、硫酸铜、硫酸铝钾、醋酸双氧铀、高锰酸钾和重铬酸钾等溶液中呈色。结果 单宁酸与Ca2 + 、Cu2 + 、Ag+ 、Al3 + 结合显示血管清晰 ,与Au+ 、U6+ 、Pb2 + 、K+ 联用媒染血管效果欠佳。结论 含Ca2 + 、Cu2 + 、Ag+ 、Al3 + 的金属盐类可替代氯化铁媒染微血管 ,氯化金、醋酸双氧铀、硝酸铅、重铬酸钾和高锰酸钾不宜与单宁酸联用来显示血管 相似文献
89.
90.
Mengshu Zhang Likui Lu Bin Wei Yingying Zhang Xiang Li Yajun Shi Wei Ge Miao Sun 《American journal of medical genetics. Part A》2020,182(10):2432-2436
Brachydactyly type A (BDA) is defined as short middle phalanges of the affected digits and is subdivided into four types (BDA1‐4). To date, the molecular cause is unknown. However, there is some evidence that pathogenic variants of HOXD13 could be associated with BDA3 and BDA4. Here, we report a Chinese autosomal dominant BDA3 pedigree with a novel HOXD13 mutation. The affected individuals presented with an obviously shorter fifth middle phalanx. The radial side of the middle phalanx was shorter than the ulnar side, and the terminal phalanx of the fifth finger inclined radially and formed classical clinodactyly. Interestingly, the index finger was normal. The initial diagnosis was BDA3. However, the distal third and fourth middle phalanges were also slightly affected, resulting in mild radial clinodactyly. Both feet showed shortening of the middle phalanges, which were fused to the distal phalanges of the second to the fifth toes, as reported in BDA4. Therefore, this pedigree had combined BDA3 and atypical BDA4. By direct sequencing, a 13 bp deletion within exon 1 of HOXD13 (NM_000523.4: c.708_720del13; NP_000514.2: p.Gly237fs) was identified. The 13 bp deletion resulted in a frameshift and premature termination of HOXD13. This study provides further evidences that variants in HOXD13 cause BDA3‐BDA4 phenotypes. 相似文献