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排序方式: 共有10000条查询结果,搜索用时 78 毫秒
991.
Vivian E. von Gruenigen M.D. Joseph T. Santoso M.D. Robert L. Coleman M.D. Carolyn Y. Muller M.D. David Scott Miller M.D. J.Michael Mathis Ph.D. 《Gynecologic oncology》1998,69(3):197-204
Objectives.To test the safety, efficacy, and toxicity of gene therapy using wild-type p53-expressing adenovirus (Ad-CMV-p53) in a nude mouse model with intraperitoneal (ip) 2774 human ovarian cancer cell line that contains a p53 mutation.Study design.An initial study of adenovirus tolerance was determined in nude mice by a single ip injection of increasing doses of Ad-CMV-p53. Nude mice were implanted with an LD100dose of 1 × 107cells. To study the efficacy and specificity of Ad-CMV-p53 treatment, the mice received treatment with different adenovirus constructs. One group received Ad-CMV-p53 and another group received a control adenovirus construct, Ad-CMV-βgal. To study the treatment response to Ad-CMV-p53, the mice were divided into groups and received various treatment schedules of 1 × 108pfu of Ad-CMV-p53.Results.The mice tolerated Ad-CMV-p53 without adverse effects at doses of 1 × 108pfu. The response to Ad-CMV-p53 showed significant survival duration in each dose regimen, with a survival time greater than that of untreated animals (P= 0.0173). However, no statistically significant survival advantage was observed between Ad-CMV-p53- and Ad-CMV-βgal-treated mice.Conclusions.These studies show that at the adenovirus dose and administration regimen used, there is effective but not specific 2774 tumor growth inhibitionin vivo.Efficient introduction of biologically active genes into tumor cells would greatly facilitate cancer therapy. Thus, although promising, these results caution that much effort will be required to realize the potential for clinical application of adenovirus-based ovarian cancer gene therapy. 相似文献
992.
993.
Sofikitis N; Miyagawa I; Yamamoto Y; Loutradis D; Mantzavinos T; Tarlatzis V 《Human reproduction update》1998,4(3):197-212
This review refers to the evolution of ooplasmic injectionsof round spermatid nuclei ROSNI) or intact round spermatidsROSI). Conclusions from their preliminary application in thehamster, rabbit, mouse and human are discussed. Criteria foridentification of round spermatids and guidelines/quality controlfor application of ROSNI/ROSI techniques are emphasized. Althoughall the animal offspring and the human newborns delivered afterROSNI/ROSI are healthy additional research efforts are necessaryto confirm the safety of these procedures and improve theiroutcome 相似文献
994.
采用高效液相色谱法测定双氯芬酸钠滴眼液的含量,方法简便,准确,能将药与杂质峰完全分离。应用化学动力学原理以恒温加试验预测双氯芬酸钠滴眼液稳定性及有效期,室温下有效期t^25℃0.9约为2.57年,与留样观察结果相符。 相似文献
995.
Pituitary stalk meningioma: case report 总被引:1,自引:0,他引:1
We report a 45-year-old woman with a meningioma which was in contact with only the pituitary stalk on MRI. As the pituitary
stalk has no dura mater, we suggest this tumour may have originated from the arachnoid membrane of the pituitary stalk. Though
some reports have shown that meningiomas can arise from sites lacking a dural component, this is the first report of a meningioma
originating from the pituitary stalk.
Received: 21 December 1995 Accepted: 26 February 1996 相似文献
996.
997.
M. Emoto H. Iwasaki K. Oshima M. Kikuchi Y. Kaneko T. Kawarabayashi 《Virchows Archiv : an international journal of pathology》1997,431(4):249-256
Rhabdomyosarcoma (RMS) is occasionally found in the female genital tract, and mostly appears as one of the heterologous mesenchymal
components in uterine carcinosarcoma designated as malignant mixed müllerian tumour (MMMT). We examined the biological properties
of a pure rhabdomyosarcoma (RMS) cell line designated FU-MMT-3, which was newly established from a surgical specimen taken
from a patient with uterine MMMT. We also evaluated c-myc and MYCN gene amplification in three RMS cell lines (including FU-MMT-3) derived from three MMMTs by Southern blot analysis.
FU-MMT-3 cells were propagated continuously for 57 serial passages over a 2-year period in vitro. FU-MMT-3 was able to produce
tumours demonstrating pure RMS in athymic nude mice. Cytogenetically, FU-MMT-3 showed a triploidy pattern, with complex karyotypic
abnormalities including trisomy of chromosome 8. All three RMS cell lines, including FU-MMT-3, showed amplification of the
c-myc gene (approximately fourfold to eightfold), while no cell lines demonstrated MYCN gene amplification. FU-MMT-3 is considered
to provide a useful system for the study of the biological behaviour of RMS in MMMTs. Extra copies of chromosome 8 and c-myc gene amplification may be associated with the rhabdomyoblastic differentiation in MMMT.
Received: 7 January 1997 / Accepted: 2 May 1997 相似文献
998.
999.
1000.
Y. Kajiya M. Nakajo N. Ichinari Y. Kajiya K. Yamazumi T. Otuji T. Tanaka 《Abdominal imaging》1997,22(1):111-113
A foregut cyst is formed as a result of abnormal budding and pinching of the tracheobronchial tree when bronchial buds develop
to form the primitive respiratory tree. Foregut cysts are clinically classified as bronchogenic, esophageal, enterogastric,
or ciliated hepatic. We present a foregut cyst that occurred in the retroperitoneum and was difficult to distinguish from
other retroperitoneal cystic mass lesions. Magnetic resonance imaging was useful in revealing the cyst's continuity to adjacent
organs.
Received: 19 June 1995/Accepted: 23 July 1995 相似文献