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性母细胞

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There were 29 cases of osteogenic sarcoma, 18 chondroma sarcomatosum, 7 maligant enchondroma with pathological fracture, 20 maligant giant cell tumor,and 4 maligant inflammatory myofibroblastoma of the bone.

成骨肉瘤29例,软骨肉瘤18例,潜在恶性内生软骨瘤伴有病理性骨折7例,恶性骨巨细胞瘤20例,恶性炎症性肌纤维母细胞瘤4例。

The pathological outcomes were as following: pulmonary blastoma in 6, leiomyosarcoma in 3, fibrosarcoma in 2, carcinosarcoma in 2, and pantmorphic sarcoma in 1 patient.

术后病理诊断:肺母细胞瘤6例,平滑肌肉瘤3例,纤维肉瘤2例,癌肉瘤2例(胶冻样物质癌肉瘤1例,结节状癌肉瘤1例),伴有巨细胞的未分化多形性肉瘤1例。

Aim To study the mutual influence of membrane current induced by receptors with diverse coupling modes in Xenopus oocytes .

目的研究不同偶联模式的兴奋性氨基酸受体所介导非洲爪蟾卵母细胞跨膜电流的相互影响。

Objective To investigate the expression of P53 protein and DNA content in angioimmunoblastic lymphadenopathy and discuss the nature and pathogenesis of AIL.

目的 研究P53蛋白在血管免疫母细胞性淋巴结病中的表达及DNA含量,探讨AIL的发生发展规律、病变性质。

In conclusion, fibroblastic rheumatism is a rare rheumatologic entity of unknown etiology.

总结来说,纤维母细胞性风湿病为罕见的风湿性疾病,目前病因仍不清楚。

We described the occurrence of fibroblastic rheumatism in a female patient with systemic lupus erythematosus.

吾人在此报告-纤维母细胞性风湿病发生在一患有红斑性狼疮的女性患者。

2N gametes are the result of meiotic mutation during micro- and mega-sporogenesis that bear the sporophytic rather than the gametophytic chromosome number. This paper reviewed the genetic markers including the morphologic, cytological, isozymes and DNA markers, which have been employed in the generation, inheritance, heterozygosity and marker-assisted breeding of 2n gametes based on the frequency of large pollen grains, cytological analyses, unexpected occurrence of polyploidy progeny and the associations between parents and progenies.

文章综述了植物2n配子发生及其遗传标记研究现状,论述涉及有关形态学标记、细胞学标记、同工酶标记乃至DNA标记等遗传标记在2n配子研究中的应用,指出通过花粉形态观察、大小孢子母细胞减数分裂行为观察、杂种后代倍性鉴定以及亲子分子标记相关分析等,对2n配子发生、2n配子遗传类型与杂合性以及2n配子在育种实践中的有效性等进行研究。

Our results demonstrate that (1) the lipogenic tumor markers CDK4 and MDM2 can be used as surrogate immunohistochemical markers for the diagnosis of malignant lipomatous tumors with high sensitivity;(2) approximately 26% of retroperitoneal/thigh UHGPS cases that were positive for PPAR-γ, CDK4, or MDM2 by immunohistochemistry showed characteristic CDK4 and MDM2 gene amplification, suggesting that a subset of UHGPS cases represent DDL despite lacking histologic evidence of lipoblasts.

我们的结果表明:(1)脂肪源性肿瘤标记CDK4和MDM2可以作为诊断恶性脂肪肿瘤的免疫标记物,且敏感性高;(2)腹膜后/大腿UHGPS免疫表达PPAR-γ, CDK4或MDM2的病例中,约有26%例显示特征性的CDK4和MDM2基因扩增,这表明部分UHGPS病例表现为DDL,虽然组织学上找不到脂母细胞。

Objective The nature of myoid/myofibroblastic differentiation in dermatofibrosarcoma protuberans and its clinical and pathological significance were studied.

目的 探讨隆突性皮纤维肉瘤中肌样/肌纤维母细胞性分化的本质及其临床病理学意义。

MNSFP was a previously identified novel implantation-related factor that needed to be further investigated in our lab, and is a lymphokine produced by suppressor T cell.

MNSFD是本实验室正在研究的另一个新发现的着床相关因子,它是一种由抑制性T细胞合成的具有非特异性免疫抑制作用的淋巴因子,因其能抑制IL-4的分泌和Th2细胞的产生,所以推测其可能与母胎间免疫耐受的形成有关,但有待于研究证实。

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