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1
Annotation: genetic effects of aneuploidy.注释：非整倍体的遗传效应。
Am J Hum Genet. 1973 May;25(3):332-9.
2
The cytogenetics of Neurospora.粗糙脉孢菌的细胞遗传学
Adv Genet. 1977;19:133-285. doi: 10.1016/s0065-2660(08)60246-1.
3
A new genetic concept: uniparental disomy and its potential effect, isodisomy.一个新的遗传学概念：单亲二体及其潜在影响——同二体。
Am J Med Genet. 1980;6(2):137-43. doi: 10.1002/ajmg.1320060207.
4
DISTRIBUTIVE PAIRING AND ANEUPLOIDY IN MAN.人类的分配配对与非整倍体
Science. 1964 Jul 3;145(3627):66-7. doi: 10.1126/science.145.3627.66.
5
[Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)].[母亲存在臂间倒位inv(10)，其儿子因重组出现inv(10)、rec(10)导致的染色体数目异常（作者译）]
Cytogenet Cell Genet. 1973;12(4):245-53. doi: 10.1159/000130460.
6
Cytogenetics: from aneuploidy to polymorphism.细胞遗传学：从非整倍体到多态性
Acta Paediatr Taiwan. 1999 Sep-Oct;40(5):297.
7
Aneusomie de recombinaison: rearrangement between paternal chromosomes 4 and 18 yielding offspring with features of the 18q- syndrome.
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8
The production of monosomic-trisomic individuals in Drosophila melanogaster by x-irradiation of immature oocytes.通过对未成熟卵母细胞进行X射线照射在黑腹果蝇中产生单体-三体个体。
Mutat Res. 1971 Dec;13(4):429-32. doi: 10.1016/0027-5107(71)90055-8.
9
Molecular studies of the 5S RNA genes of Drosophila melanogaster. I. Production of chromosomes containing duplications and deficiencies.黑腹果蝇5S RNA基因的分子研究。I. 产生含有重复和缺失的染色体。
Mol Gen Genet. 1973;120(4):309-18.
10
A model for somatic pairing derived from somatic crossing over with third chromosome rearrangements in Drosophila melanogaster.一种源自果蝇第三号染色体重排的体细胞交换的体细胞配对模型。
Mol Gen Genet. 1972;115(4):302-13. doi: 10.1007/BF00333169.

引用本文的文献

1
Viability and fertility of sex-linked autosomal duplications in Lucilia cuprina (wiedemann).性连锁常染色体重复在丽蝇蛹集金小蜂（Wiedemann）中的生存力和生育力。
Theor Appl Genet. 1983 Apr;65(1):9-16. doi: 10.1007/BF00276255.
2
Specific aneusomies in Chinese hamster cells at different stages of neoplastic transformation, initiated by nitrosomethylurea.由亚硝基甲基脲引发的中国仓鼠细胞在肿瘤转化不同阶段的特定染色体异常。
Proc Natl Acad Sci U S A. 2002 May 14;99(10):6778-83. doi: 10.1073/pnas.251670699. Epub 2002 May 7.
3
Auto-catalysed progression of aneuploidy explains the Hayflick limit of cultured cells, carcinogen-induced tumours in mice, and the age distribution of human cancer.非整倍体的自催化进展解释了培养细胞的海弗利克极限、小鼠致癌物诱导的肿瘤以及人类癌症的年龄分布。
Biochem J. 2000 Jun 15;348 Pt 3(Pt 3):497-506.
4
Aneuploidy vs. gene mutation hypothesis of cancer: recent study claims mutation but is found to support aneuploidy.癌症的非整倍体与基因突变假说：近期研究声称是突变，但结果却支持非整倍体。
Proc Natl Acad Sci U S A. 2000 Mar 28;97(7):3236-41. doi: 10.1073/pnas.97.7.3236.
5
How aneuploidy affects metabolic control and causes cancer.非整倍体如何影响代谢控制并引发癌症。
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6
A chromosomal duplication map of malformations: regions of suspected haplo- and triplolethality--and tolerance of segmental aneuploidy--in humans.畸形的染色体重复图谱：人类中疑似单倍体和三倍体致死区域以及节段性非整倍体耐受性区域
Am J Hum Genet. 1999 Jun;64(6):1702-8. doi: 10.1086/302410.
7
Genetic instability of cancer cells is proportional to their degree of aneuploidy.癌细胞的基因不稳定性与其非整倍体程度成正比。
Proc Natl Acad Sci U S A. 1998 Nov 10;95(23):13692-7. doi: 10.1073/pnas.95.23.13692.
8
Anatomic and chromosomal anomalies in 639 spontaneous abortuses.639例自然流产的解剖学和染色体异常情况。
Hum Genet. 1980;55(1):87-98. doi: 10.1007/BF00329132.
9
Trisomy of the long arm of human chromosome 1.人类1号染色体长臂三体性
Humangenetik. 1974;25(1):79-82. doi: 10.1007/BF00281010.
10
MHC-chromosome dosage effects: evidence for increased expression of Ia glycoprotein and alteration of B cell subpopulations in neonatal aneuploid chickens.MHC-染色体剂量效应：新生非整倍体鸡中Ia糖蛋白表达增加及B细胞亚群改变的证据。
Immunogenetics. 1988;27(1):24-30. doi: 10.1007/BF00404440.

本文引用的文献

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[PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].[小近端着丝粒染色体的部分单体性]
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2
A NOTE ON THE MEAN MEASUREMENTS OF HUMAN CHROMOSOMES.关于人类染色体平均测量的一则笔记。
Ann Hum Genet. 1964 Nov;28:195-6. doi: 10.1111/j.1469-1809.1964.tb00477.x.
3
Double autosomal trisomy (D trisomy plus mongolism).
Proc Staff Meet Mayo Clin. 1963 Jun 5;38:242-8.
4
[Double autosomal trisomy with 48 chromosomes (21 and 18)].48条染色体（21号和18号染色体）的双常染色体三体性
Union Med Can. 1961 Nov;90:1220-6.
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Three cases of triploidy in man.
Cytogenetics. 1967;6(2):81-104. doi: 10.1159/000129932.
6
Autosomal monosomy in man. Complete monosomy G (21-22) in a four-and-one-half-year-old mentally retarded girl.人类常染色体单体性。一名4岁半智力发育迟缓女孩的G组（21 - 22号染色体）完全单体性。
N Engl J Med. 1967 Oct 12;277(15):777-84. doi: 10.1056/NEJM196710122771502.
7
Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families.易位杂合性：三个家庭中五例猫叫综合征及两例5号染色体重复病例的病因。
Am J Hum Genet. 1967 Jul;19(4):586-603.
8
Probable assignment of the alpha locus of haptoglobin to chromome 16 in man.
Nature. 1969 Sep 13;223(5211):1163-5. doi: 10.1038/2231163a0.
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Asymmetry of chromosome number 1 pair in three generations of a phenotypically normal family.
Can J Genet Cytol. 1968 Sep;10(3):575-89. doi: 10.1139/g68-076.
10
Triploidy in man. Report of a case and a discussion on etiology.人类三倍体。一例报告及病因学讨论。
Cytogenetics. 1970;9(2):116-30.

Annotation: genetic effects of aneuploidy.

作者信息

Sandler L, Hecht F

出版信息

Am J Hum Genet. 1973 May;25(3):332-9.

PMID:4704865
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1762522/
Abstract
摘要