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1号和9号染色体C带在复发性流产中的相互作用。

Interactions between C-bands of chromosomes 1 and 9 in recurrent reproductive loss.

作者信息

Ford J H, Callen D F, Roberts C G, Jahnke A B

出版信息

Hum Genet. 1983;63(1):58-62. doi: 10.1007/BF00285399.

DOI:10.1007/BF00285399
PMID:6832780
Abstract

The size of the heterochromatic regions of chromosomes 1 and 16 was measured in a Test group of women with histories of recurrent spontaneous abortion and a Control group of fertile women. Measurements were made on Giemsa banded preparations and the euchromatic regions of 1q and 16q were used to correct for between-cell contraction. For each chromosome pair, the larger and smaller chromosome was identified and populations of each were compared between the two subject groups. For chromosome 1, the smaller chromosome of the Test group was significantly smaller than that of the Control group (P less than 0.001) and the size of the pair difference was larger in the Test than in the Control group (P less than 0.01). For chromosome 16, the smaller chromosome of the Test group was smaller than that of the Control group (5% level). The interaction of chromosome 1 and chromosome 9 heterochromatin in each individual has been analyzed. The combined score for the smaller chromosome 1 and the larger chromosome 9 shows a bimodal distribution and allows discrimination between the two subject groups. Various possible ways in which this interaction might affect reproductive outcome are discussed.

摘要

在一组有反复自然流产史的女性试验组和一组可育女性对照组中,测量了1号和16号染色体异染色质区域的大小。测量在吉姆萨染色带标本上进行,1q和16q的常染色质区域用于校正细胞间收缩。对于每对染色体,确定较大和较小的染色体,并比较两个受试组中每组的数量。对于1号染色体,试验组中较小的染色体明显小于对照组(P小于0.001),试验组中染色体对差异的大小大于对照组(P小于0.01)。对于16号染色体,试验组中较小的染色体小于对照组(5%水平)。分析了每个个体中1号染色体和9号染色体异染色质的相互作用。较小的1号染色体和较大的9号染色体的综合评分显示出双峰分布,并且能够区分两个受试组。讨论了这种相互作用可能影响生殖结果的各种可能方式。

相似文献

1
Interactions between C-bands of chromosomes 1 and 9 in recurrent reproductive loss.1号和9号染色体C带在复发性流产中的相互作用。
Hum Genet. 1983;63(1):58-62. doi: 10.1007/BF00285399.
2
Heterochromatic polymorphism in spontaneous abortions.自然流产中的异染色质多态性。
J Med Genet. 1979 Oct;16(5):358-62. doi: 10.1136/jmg.16.5.358.
3
Within pair differences of human chromosome 9 C-bands associated with reproductive loss.与生殖损失相关的人类9号染色体C带的配对差异之内。
Hum Genet. 1982;61(4):360-3. doi: 10.1007/BF00276601.
4
[Human chromosome polymorphism and disordered reproductive function. II. C-variant chromosomes].[人类染色体多态性与生殖功能紊乱。II. C变异染色体]
Genetika. 1979;15(10):1870-9.
5
Chromatin of h regions of human chromosomes at high resolution.人类染色体h区域的高分辨率染色质。
Experientia. 1984 Aug 15;40(8):878-9. doi: 10.1007/BF01952006.
6
A rapid method for identification of constitutive heterochromatin of secondary constriction regions of human chromosomes 1, 9, and 16.一种快速鉴定人类1号、9号和16号染色体次缢痕区组成型异染色质的方法。
J Hered. 1982 Jan-Feb;73(1):74-6. doi: 10.1093/oxfordjournals.jhered.a109582.
7
NOR associations with heterochromatin.核仁组织区与异染色质的关联。
Cytogenet Cell Genet. 1984;38(3):165-70. doi: 10.1159/000132054.
8
[Human chromosome polymorphism and disordered reproductive function. I. Routine chromosome variants].[人类染色体多态性与生殖功能紊乱。I. 常规染色体变异]
Genetika. 1979;15(10):1858-69.
9
Heteromorphism of constitutive heterochromatin in carcinoma and dysplasia of the uterine cervix.子宫颈癌和发育异常中组成型异染色质的异质性
Eur J Obstet Gynecol Reprod Biol. 1980 Mar;10(3):173-82. doi: 10.1016/0028-2243(80)90058-1.
10
Cytogenetic findings in 122 couples with recurrent abortions.122对复发性流产夫妇的细胞遗传学研究结果
Hum Genet. 1981;57(1):101-3. doi: 10.1007/BF00271179.

引用本文的文献

1
C-band length variability and reproductive wastage.C波段长度变异性与生殖损耗
Hum Genet. 1987 Jan;75(1):56-61. doi: 10.1007/BF00273840.
2
A new variant of chromosome 16.
Hum Genet. 1987 May;76(1):100-1. doi: 10.1007/BF00283058.
3
Organization and chromosomal specificity of autosomal homologs of human Y chromosome repeated DNA.人类Y染色体重复DNA常染色体同源物的组织和染色体特异性
Chromosoma. 1985;92(3):225-33. doi: 10.1007/BF00348698.

本文引用的文献

1
Within pair differences of human chromosome 9 C-bands associated with reproductive loss.与生殖损失相关的人类9号染色体C带的配对差异之内。
Hum Genet. 1982;61(4):360-3. doi: 10.1007/BF00276601.
2
Heterochromatin polymorphism and human cancer.异染色质多态性与人类癌症。
Cancer Genet Cytogenet. 1981 Apr;3(3):261-72. doi: 10.1016/0165-4608(81)90093-5.
3
Chromosomal analysis of two consecutive abortuses in each of 43 women.对43名女性中的每一位的两次连续流产胎儿进行染色体分析。
Humangenetik. 1973 Sep 20;19(3):275-80. doi: 10.1007/BF00278402.
4
Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families.十个非亲缘家庭中9号染色体臂间倒位与生殖功能衰竭的关联
Humangenetik. 1975 Sep 20;30(3):217-24. doi: 10.1007/BF00279187.
5
Chromosomal variants and nondisjunction.染色体变异与不分离。
Cytogenet Cell Genet. 1978;21(5):300-3. doi: 10.1159/000130906.
6
C-Band polymorphisms of chromosomes 1, 9, and 16 in four subgroups of mentally retarded patients and a normal control population.智障患者四个亚组及正常对照人群中1号、9号和16号染色体的C波段多态性
Hum Genet. 1979 Oct 2;51(3):269-75. doi: 10.1007/BF00283393.