发布求助
文献互助 智能选刊 最新文献

Cytogenetics最新文献

筛选
英文 中文
Cytogenetic effects of measles virus fusion factor (FF) on human leukocytes. 麻疹病毒融合因子(FF)对人白细胞的细胞遗传学影响。
Cytogenetics Pub Date : 1971-01-01 DOI: 10.1159/000130155
S Henry, M M Cohen, D T Karzon
{"title":"Cytogenetic effects of measles virus fusion factor (FF) on human leukocytes.","authors":"S Henry, M M Cohen, D T Karzon","doi":"10.1159/000130155","DOIUrl":"https://doi.org/10.1159/000130155","url":null,"abstract":"In human leukocyte cultures, extensive chromosome changes (pulverization, uncoiling, or a combination of these) induced by UV-inactivated measles virus (fusion factor or FF) (1) wer","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"10 5","pages":"367-76"},"PeriodicalIF":0.0,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000130155","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"16242951","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Unusually large sex chromosomes: new methods of measuring and description of karyotypes of six rodents (Myomorpha and Hystricomorpha) and one lagomorph (Ochontonidae). 异常大的性染色体:六种啮齿类动物(肌形目和水形目)和一种鼠形目动物(鼠形目)核型测量和描述的新方法。
Cytogenetics Pub Date : 1971-01-01 DOI: 10.1159/000130136
D H Wurster, J R Snapper, K Benirschke
{"title":"Unusually large sex chromosomes: new methods of measuring and description of karyotypes of six rodents (Myomorpha and Hystricomorpha) and one lagomorph (Ochontonidae).","authors":"D H Wurster, J R Snapper, K Benirschke","doi":"10.1159/000130136","DOIUrl":"https://doi.org/10.1159/000130136","url":null,"abstract":"Chromosome studies of six rodents, of which three have unusually large X chromosomes, and one lagomorph have been made. Two new methods of measuring unusually large sex chromosomes are presented. Comp","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"10 3","pages":"153-76"},"PeriodicalIF":0.0,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000130136","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"16242988","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 33
The association pattern of the Ph chromosome. Ph染色体的结合模式。
Cytogenetics Pub Date : 1971-01-01 DOI: 10.1159/000130143
R M Kitchin, M W Shaw
{"title":"The association pattern of the Ph chromosome.","authors":"R M Kitchin, M W Shaw","doi":"10.1159/000130143","DOIUrl":"https://doi.org/10.1159/000130143","url":null,"abstract":"A total of 951 Ph1+ cells and 364 Ph1–cells from a female patient with chronic myelogenous leukemia was scored for acrocentric associations. The Ph1+ and Ph1-cells differed significantly in their association patterns. The average number of association groups per cell, the average size of the groups, and the total number of chromosomes involved in associations per cell were significantly lower in the Ph1+ cells. Although the Ph1 chromosome itself tended to be found in association more often than expected by chance, it appeared to associate at random with the other acrocentrics.","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"10 4","pages":"235-43"},"PeriodicalIF":0.0,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000130143","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"16375273","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
[Autoradiographic studies on X-autosomal translocation in man: 45,X.15-,tan(15qZq+)+]. [男性x常染色体易位的放射自显影研究:45,X.15-，tan(15qZq+)+]。
Cytogenetics Pub Date : 1971-01-01 DOI: 10.1159/000130131
W. Engel, W. Vogel, H. Reinwein
{"title":"[Autoradiographic studies on X-autosomal translocation in man: 45,X.15-,tan(15qZq+)+].","authors":"W. Engel, W. Vogel, H. Reinwein","doi":"10.1159/000130131","DOIUrl":"https://doi.org/10.1159/000130131","url":null,"abstract":"In a female infant exhibiting cleft palate, hydrocephalus communicans, vitium cordis congenitum, and other anomalies, chromosome analysis revealed a C/D translocation. According to its replication pat","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"10 2 1","pages":"87-98"},"PeriodicalIF":0.0,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000130131","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"64617019","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 25
Further studies on a Robertsonian translocation in the Saanen dairy goat. 萨宁奶山羊罗伯逊易位的进一步研究。
Cytogenetics Pub Date : 1971-01-01 DOI: 10.1159/000130127
B Padeh, M Wyskoki, M Soller
{"title":"Further studies on a Robertsonian translocation in the Saanen dairy goat.","authors":"B Padeh, M Wyskoki, M Soller","doi":"10.1159/000130127","DOIUrl":"https://doi.org/10.1159/000130127","url":null,"abstract":"Additional observations on a Robertsonian translocation segregating in the Saanen goat are reported. All of the animals born in this series of matings had balanced karyotypes, and all were phenotypica","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"10 1","pages":"61-9"},"PeriodicalIF":0.0,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000130127","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"16196558","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 20
Sex-chromosome mosaicism in pouch young of marsupials Perameles and Isoodon. 有袋动物幼崽的性染色体嵌合现象。
Cytogenetics Pub Date : 1971-01-01
S M Walton
{"title":"Sex-chromosome mosaicism in pouch young of marsupials Perameles and Isoodon.","authors":"S M Walton","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"10 2","pages":"115-20"},"PeriodicalIF":0.0,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"16185107","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+). 一例因易位而出现明显单体21的患者的研究:45,XX,21-，t(18q+)。
Cytogenetics Pub Date : 1971-01-01 DOI: 10.1159/000130162
H E Wyandt, F Hecht, E W Lovrien, R E Stewart
{"title":"Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).","authors":"H E Wyandt, F Hecht, E W Lovrien, R E Stewart","doi":"10.1159/000130162","DOIUrl":"https://doi.org/10.1159/000130162","url":null,"abstract":"A five-year-old girl with mild mental retardation and dyschondrosteosis was found to have 45 chromosomes. A G (21-22) chromosome was missing. The parents were chromosomally normal. Measurements confirmed the presence of an unusually long chromosome No. 17 or 18 in the girl’s karyotypes. Late labeling with 3H-thymidine and autoradiography showed it to be No. 18. By quinacrine fluoromicroscopy the apparently missing G chromosome proved to be No. 21. Thus, the apparent autosomal monosomy was the result of a de novo 18/21 translocation with loss of the short arm and centromere of No. 21 and of material from the long arms of No. 18 or No. 21 or both equivalent to two thirds of a G long arm. Although no evidence was found for deletion of a genetic marker, heterozygosity at five gene loci (MNSs, Jk, Hp, PGM, and AcP) excluded their deletion. We suggest that other instances of apparent autosomal monosomy may on careful study be found to be the result of similarly subtle chromosome rearrangements.","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"10 6","pages":"413-26"},"PeriodicalIF":0.0,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000130162","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"16233339","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 16
Autoradiographic study of DNA synthesis in homologous chromosomes distinguishable by morphology. 形态学上可区分的同源染色体DNA合成的放射自显影研究。
Cytogenetics Pub Date : 1971-01-01 DOI: 10.1159/000130163
A De Capoa, A Rocchi, D A Miller, O J Miller
{"title":"Autoradiographic study of DNA synthesis in homologous chromosomes distinguishable by morphology.","authors":"A De Capoa, A Rocchi, D A Miller, O J Miller","doi":"10.1159/000130163","DOIUrl":"https://doi.org/10.1159/000130163","url":null,"abstract":"Autoradiographic terminal labeling studies performed on leukocyte cultures of a man (A. de J.) and his son (H. de J.), both carriers of an enlarged satellite on a D-group chromosome, demonstrated that the morphological marker was a No. 15. Counts of grains on the long arms of the two chromosomes 15 showed that the marker chromosome was less heavily labeled than its normal homolog. This difference was highly significant in both cases. The marker chromosome was also shorter than its homolog, though not significantly so in one case. Possible interpretations of these findings, i.e., chromosomal polymorphism or autosomal lyonization, were discussed.","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"10 6","pages":"427-35"},"PeriodicalIF":0.0,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000130163","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"16233340","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Chromosomal abnormality in a phenotypically and clinically normal dog. 表型和临床正常犬的染色体异常。
Cytogenetics Pub Date : 1971-01-01 DOI: 10.1159/000130145
N S Ma, C E Gilmore
{"title":"Chromosomal abnormality in a phenotypically and clinically normal dog.","authors":"N S Ma, C E Gilmore","doi":"10.1159/000130145","DOIUrl":"https://doi.org/10.1159/000130145","url":null,"abstract":"A seven-month-old black female setter-retriever cross was found to have a modal chromosome number of 77 and an apparent centric fusion of two autosomes. Extensive clinical examinations were performed,","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"10 4","pages":"254-9"},"PeriodicalIF":0.0,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000130145","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"16252594","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Observations on human somatic chromosomes treated with hyaluronidase. 透明质酸酶处理人类体细胞染色体的观察。
Cytogenetics Pub Date : 1971-01-01 DOI: 10.1159/000130148
A Iino
{"title":"Observations on human somatic chromosomes treated with hyaluronidase.","authors":"A Iino","doi":"10.1159/000130148","DOIUrl":"https://doi.org/10.1159/000130148","url":null,"abstract":"By means of hyaluronidase (1 mg in 100 ml of distilled water), the spiral structure of human somatic chromsomes was studied in cultured leukocytes. The number of chromonemata forming a chromatid is tw","PeriodicalId":78202,"journal":{"name":"Cytogenetics","volume":"10 4","pages":"286-94"},"PeriodicalIF":0.0,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000130148","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"16213872","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 16
首页 上一页 下一页 尾页
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整，为了账户安全，请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们：info@booksci.cn Book学术提供免费学术资源搜索服务，方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号：604180095
Book学术官方微信
小红书