標(biāo)題: Titlebook: Chromosome 12 Aberrations in Human Solid Tumors; Cytogenetics and Mol J. Bullerdiek,S. Bartnitzke Conference proceedings 1994 Springer-Verl [打印本頁(yè)] 作者: 搖尾乞憐 時(shí)間: 2025-3-21 18:36
書(shū)目名稱(chēng)Chromosome 12 Aberrations in Human Solid Tumors影響因子(影響力)
書(shū)目名稱(chēng)Chromosome 12 Aberrations in Human Solid Tumors影響因子(影響力)學(xué)科排名
書(shū)目名稱(chēng)Chromosome 12 Aberrations in Human Solid Tumors網(wǎng)絡(luò)公開(kāi)度
書(shū)目名稱(chēng)Chromosome 12 Aberrations in Human Solid Tumors網(wǎng)絡(luò)公開(kāi)度學(xué)科排名
書(shū)目名稱(chēng)Chromosome 12 Aberrations in Human Solid Tumors被引頻次
書(shū)目名稱(chēng)Chromosome 12 Aberrations in Human Solid Tumors被引頻次學(xué)科排名
書(shū)目名稱(chēng)Chromosome 12 Aberrations in Human Solid Tumors年度引用
書(shū)目名稱(chēng)Chromosome 12 Aberrations in Human Solid Tumors年度引用學(xué)科排名
書(shū)目名稱(chēng)Chromosome 12 Aberrations in Human Solid Tumors讀者反饋
書(shū)目名稱(chēng)Chromosome 12 Aberrations in Human Solid Tumors讀者反饋學(xué)科排名
作者: 勉強(qiáng) 時(shí)間: 2025-3-21 22:56 作者: Pandemic 時(shí)間: 2025-3-22 03:17
978-3-662-06257-9Springer-Verlag Berlin Heidelberg 1994作者: septicemia 時(shí)間: 2025-3-22 07:35
Do Most Americans Believe in Redemption?, percent of these tumors are found in the parotid gland, 10% in the minor salivary glands, and 5% in the submandibular gland (Seifert et al. 1986). The pleomorphic adenoma is the most common type of salivary gland tumor, accounting for almost 50% of all neoplasms in these organs (Seifert et al. 1986作者: 大炮 時(shí)間: 2025-3-22 08:46 作者: Allodynia 時(shí)間: 2025-3-22 14:09
Schriften der Universit?t Heidelberg). It should, however, be stressed that the data are heavily biased in favor of hematologic neoplasms; of the total data base comprising 14141 human tumors reported to have clonal chromosome aberrations, 68% involve hematologic disorders, 11%, lymphomas, and 21%, solid tumors (Mitelman 1991). This i作者: Allodynia 時(shí)間: 2025-3-22 18:34
Hermann Hoepke,Curt Elze,Hans Bluntschli pin a label on about 10% of sarcomas”(Fletcher 1990). In this context, the characterization of new tumor markers is of paramount interest for the diagnosis, prognosis, and classification of soft tissue tumors (Sandberg and Turc-Carel 1987; Molenaar et al. 1989; Fletcher et al. 1991).作者: 繁榮中國(guó) 時(shí)間: 2025-3-22 23:14
https://doi.org/10.1007/978-3-663-04177-1ng 12q13–15. The currently best investigated examples are pleomorphic adenomas (Mark et al. 1980, 1988; Bullerdiek et al. 1987a,b), lipomas (Heim et al. 1986; Turc-Carel et al. 1986a; Mandahl et al. 1988), myxoid liposarcomas (Turc-Carel et al. 1986b), and uterine leiomyomas (Heim et al. 1988; Turc-作者: 廢止 時(shí)間: 2025-3-23 03:10
Wiederherstellung der Rechtseinheitmary change in these tumors [1]. It has also been sporadically described in some non-Hodgkin’s lymphomas [2]. In nonlymphatic solid tumors, however, an extra chromosome 12, especially as the only cytogenetic deviation, has been rarely observed. During our cytogenetic studies on solid tumors of the f作者: Communicate 時(shí)間: 2025-3-23 07:12
Für eine radikale liberale Politik 1989; Giwercman et al. 1990; Vos et al. 1990) — the so-called carcinoma in situ (CIS) (Skakkeb?k et al. 1987). Therefore questions about the early chromosomal events in the pathogenesis of TGCTs still remain to be answered. In addition, possible chromosomal heterogeneity of CIS, in itself and in re作者: craven 時(shí)間: 2025-3-23 10:08 作者: Colonnade 時(shí)間: 2025-3-23 16:02 作者: 損壞 時(shí)間: 2025-3-23 21:59
Frankophone Literatur aus dem Maghreb,he breakpoints and the chromosomal localization of oncogenes or suppressor genes has been of particular interest. In this region, four oncogenes (.) and two putative suppressor genes (., CHOP) have been localized (Fig. 1). The main results obtained concerning the function of these genes during norma作者: 易彎曲 時(shí)間: 2025-3-24 00:55
https://doi.org/10.1007/978-3-322-97042-8rcomas stop proliferation after 3–4 in vitro passages, not allowing sufficient material for molecular analyses by in vitro preparation to be obtained (for PSA, see Stern et al. 1990), One alternative to overcome the problem of replicative senescence (Hayflick and Moorhead 1961) of tumor cells in cul作者: nitric-oxide 時(shí)間: 2025-3-24 05:56 作者: Pamphlet 時(shí)間: 2025-3-24 07:07 作者: 表兩個(gè) 時(shí)間: 2025-3-24 13:59
Redeploying Urban Infrastructuretics to the more detailed description and understanding of oncogenesis (Sandberg 1990; Mitelman 1991; Solomon et al. 1991). Although fundamental genetic analysis of leukaemias and lymphomas has advanced more rapidly in the past than that of solid tumours, extensive knowledge about solid tumours has 作者: consolidate 時(shí)間: 2025-3-24 18:42 作者: Conflagration 時(shí)間: 2025-3-24 21:26
Shifting the State from Left to Right,liposarcoma, for instance, the primary cytogenetic change is mostly the highly consistent reciprocal translocation t(12;16)(q13;p11) or the more complex three-way translocation also involving chromosome 1 (Turc-Carel et al. 1986a; Ohjimi et al. 1992). Cytogenetic analysis of lipomas, a subgroup of b作者: Malaise 時(shí)間: 2025-3-25 01:40
http://image.papertrans.cn/c/image/226338.jpg作者: Merited 時(shí)間: 2025-3-25 05:27 作者: tooth-decay 時(shí)間: 2025-3-25 09:48 作者: Kernel 時(shí)間: 2025-3-25 15:11
https://doi.org/10.1007/978-3-642-94585-4e in size during pregnancy or after administration of oral contraceptives (Buttramn and Reiter 1981) and regress after menopause and under luteinizing hormone-releasing hormone agonist treatment (Benagiano 1989).作者: 同時(shí)發(fā)生 時(shí)間: 2025-3-25 19:13 作者: mendacity 時(shí)間: 2025-3-25 22:14 作者: 雄偉 時(shí)間: 2025-3-26 04:10
Involvement of Chromosome 12 in Uterine Leiomyomae in size during pregnancy or after administration of oral contraceptives (Buttramn and Reiter 1981) and regress after menopause and under luteinizing hormone-releasing hormone agonist treatment (Benagiano 1989).作者: 保守黨 時(shí)間: 2025-3-26 07:46 作者: 書(shū)法 時(shí)間: 2025-3-26 10:08 作者: 價(jià)值在貶值 時(shí)間: 2025-3-26 14:44 作者: 軍械庫(kù) 時(shí)間: 2025-3-26 17:02
Wiederherstellung der Rechtseinheitemale genital tract we made the observation that trisomy 12 is frequently found in these tumors. The karyotype of a recently analyzed cystadenofibroma of the ovary is shown in Fig. 1. Moreover, trisomy 12 appears to be a feature almost restricted to neoplasms originating from the female genital organs.作者: RAFF 時(shí)間: 2025-3-26 23:05
Für eine radikale liberale Politiklation to the histology of invasive tumors — seminomas (SE) and nonseminomatous TGCTs (NS) — is unknown. The chromosomal basis of the heterogeneity found in some invasive TGCTs by ploidy analysis (Oosterhuis et al. 1989; Foss? et al. 1991a,b; Ky Sela and Matoska 1991) is also not understood.作者: 豎琴 時(shí)間: 2025-3-27 04:45
Reden, die die Republik bewegtens et al. 1990). Testicular GCTs (TGCTs) themselves are also heterogeneous (Atkin 1973; De Jong et al. 1990) and can epidemiologically be subdivided into three groups: infantile tumors, tumors in adults, and tumors in elderly men.作者: 形容詞 時(shí)間: 2025-3-27 08:24 作者: Hirsutism 時(shí)間: 2025-3-27 12:36 作者: 柔聲地說(shuō) 時(shí)間: 2025-3-27 13:53
Amplification of the , and , Loci in Tumor Cells: Is , only by Chance Coamplified Together with Anotal. 1987; Heim et al. 1988). The most specific of these rearrangements are those found in the myxoid liposarcomas, where the distal part of chromosome 12 (ql3-qter) is reciprocally translocated to 16pll. Several putative oncogenes have been localized to this chromosomal region and thus could be candidate target genes for the rearrangements.作者: 反復(fù)拉緊 時(shí)間: 2025-3-27 21:50 作者: acclimate 時(shí)間: 2025-3-27 22:47
Trisomy 12 Clusters to Tumors of the Female Genital Tractemale genital tract we made the observation that trisomy 12 is frequently found in these tumors. The karyotype of a recently analyzed cystadenofibroma of the ovary is shown in Fig. 1. Moreover, trisomy 12 appears to be a feature almost restricted to neoplasms originating from the female genital organs.作者: 檔案 時(shí)間: 2025-3-28 02:57
Numerical Chromosome 12 Analysis of Carcinoma In Situ and Invasive Germ Cell Tumors of the Adult Teslation to the histology of invasive tumors — seminomas (SE) and nonseminomatous TGCTs (NS) — is unknown. The chromosomal basis of the heterogeneity found in some invasive TGCTs by ploidy analysis (Oosterhuis et al. 1989; Foss? et al. 1991a,b; Ky Sela and Matoska 1991) is also not understood.作者: 施魔法 時(shí)間: 2025-3-28 07:51 作者: BOAST 時(shí)間: 2025-3-28 14:29 作者: glomeruli 時(shí)間: 2025-3-28 15:51 作者: Canyon 時(shí)間: 2025-3-28 22:07
https://doi.org/10.1007/978-3-322-97042-8 expression of several EBV genes, and (3) indefinite proliferation leading to lymphoblastoid cell lines. For the establishment and maintenance of the immortal state of the host cells, continuous expression of a subset of the EBV viral genes is necessary.作者: arabesque 時(shí)間: 2025-3-29 01:15
Zur Genealogie der theoretischen Klammer,een completely sequenced, comprises only about 122 kb (Sulston et al. 1992). Thus it becomes clear that we are far from the goal of systematically analyzing the human genome. It may become possible in the not too distant future to systematically analyze a selected chromosome band or a chromosome seg作者: 陪審團(tuán) 時(shí)間: 2025-3-29 05:45 作者: aggressor 時(shí)間: 2025-3-29 11:02
Shifting the State from Left to Right,s et al. 1991) and pleomorphic adenomas of the salivary gland (Sandros et al. 1990). Comparison of available cytogenetic data suggests that the chromosome 12 breakpoint in myxoid liposarcoma is proximal to those in the three benign tumours; this might point towards the implication of different genet作者: 過(guò)份艷麗 時(shí)間: 2025-3-29 11:42 作者: misshapen 時(shí)間: 2025-3-29 16:16
Cytogenetic and Molecular Studies of Clear-Cell Sarcoma of Tendons and Aponeurosesof CCS, including electron microscopy, immuno-cytochemistry and cytochemistry, indicates that this entity is of neural crest origin presenting variable degrees of differentiation along melanocytic and Schwann’s cell lines.作者: 詩(shī)集 時(shí)間: 2025-3-29 22:22
Comparative Gene Mapping: Human Chromosome 12 and Mouse Chromosome 15chromosomal translocations. One breakpoint which is most common to these tumors is localized in the region 12q13–15 (see Sreekantaiah et al. 1991, for overview). It was therefore of interest to map the gene GPD1 as exactly as possible in the human karyotype. Figure 2 shows the results of an in situ 作者: pantomime 時(shí)間: 2025-3-30 01:27
Cell Lines from Tumors Showing 12q13–15 Aberrations expression of several EBV genes, and (3) indefinite proliferation leading to lymphoblastoid cell lines. For the establishment and maintenance of the immortal state of the host cells, continuous expression of a subset of the EBV viral genes is necessary.作者: 名字 時(shí)間: 2025-3-30 06:29
Analysis of DNA from a Specific Chromosome Regioneen completely sequenced, comprises only about 122 kb (Sulston et al. 1992). Thus it becomes clear that we are far from the goal of systematically analyzing the human genome. It may become possible in the not too distant future to systematically analyze a selected chromosome band or a chromosome seg作者: 似少年 時(shí)間: 2025-3-30 09:24
Development and Characterization of Cell Lines from a Myxoid Liposarcoma with t(12;16)(q13;p11.2) antween chromosomes 12 and 16, t(12;16)(q13;p11), or a three-way translocation also involving chromosome 1 (Turc-Carel et al. 1986a; Ohjimi et al. 1992). Interestingly, in cytogenetically abnormal lipomas the same cytogenetic region of chromosome 12 is frequently implicated in translocations; in contr作者: Orchiectomy 時(shí)間: 2025-3-30 16:05
Analysis of Solid Tumours with Recurrent Breakpoints in Chromosome Region 12q13–15 by Fluorescence Is et al. 1991) and pleomorphic adenomas of the salivary gland (Sandros et al. 1990). Comparison of available cytogenetic data suggests that the chromosome 12 breakpoint in myxoid liposarcoma is proximal to those in the three benign tumours; this might point towards the implication of different genet作者: 危機(jī) 時(shí)間: 2025-3-30 17:04 作者: Permanent 時(shí)間: 2025-3-30 21:04
Involvement of Chromosome 12 in Uterine Leiomyomae, and very rarely below the age of 18. Their pathogenesis is not clearly understood, but a role for sex steroid hormones is likely since they increase in size during pregnancy or after administration of oral contraceptives (Buttramn and Reiter 1981) and regress after menopause and under luteinizing作者: refraction 時(shí)間: 2025-3-31 02:12
Lipoma Cytogenetics). It should, however, be stressed that the data are heavily biased in favor of hematologic neoplasms; of the total data base comprising 14141 human tumors reported to have clonal chromosome aberrations, 68% involve hematologic disorders, 11%, lymphomas, and 21%, solid tumors (Mitelman 1991). This i作者: BLAND 時(shí)間: 2025-3-31 06:23 作者: 威脅你 時(shí)間: 2025-3-31 12:32
Breakpoints and Recipient Chromosomes in Pleomorphic Adenomas, Lipomas, and Uterine Leiomyomas — Whang 12q13–15. The currently best investigated examples are pleomorphic adenomas (Mark et al. 1980, 1988; Bullerdiek et al. 1987a,b), lipomas (Heim et al. 1986; Turc-Carel et al. 1986a; Mandahl et al. 1988), myxoid liposarcomas (Turc-Carel et al. 1986b), and uterine leiomyomas (Heim et al. 1988; Turc-作者: myocardium 時(shí)間: 2025-3-31 16:44 作者: 廣告 時(shí)間: 2025-3-31 17:32 作者: Tinea-Capitis 時(shí)間: 2025-3-31 22:14
Cytogenetic and Molecular Studies of Clear-Cell Sarcoma of Tendons and Aponeurosest clinicopathologic entity among soft tissue sarcomas. Originally it was suspected that there was a relationship between CCS and synovial sarcoma (Enzinger 1965; Kubo 1969; Hajdu et al. 1977). The light-microscopic similarity to malignant melanoma, the occurrence of melanin in some cases (Enzinger 1作者: Hamper 時(shí)間: 2025-4-1 05:40
Comparative Gene Mapping: Human Chromosome 12 and Mouse Chromosome 158, 1989). The combined data of these studies are shown in Fig. 1. Most of mouse chromosome 15 is conserved in three linkage groups in the human genome. These linkage groups reside on human chromosomes 8q24, 22ql3.3-qter and 12cen-ql5 (Fig. 1). The linkage group common to mouse chromosome 15 and huma
