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[阿尔茨海默病与编码超氧化物歧化酶1的多态性探针之间不存在紧密连锁关系]

[Absence of a close linkage between Alzheimer's disease and the polymorphic probe coding for superoxide dismutase 1].

作者信息

David F, Intrator S, Foncin J F, Salmon D, Lucotte G

机构信息

Centre national de Transfusion sanguine, Institut, Laboratoire de Génétique moléculaire, Paris.

出版信息

C R Acad Sci III. 1988;306(1):1-4.

PMID:3126980
Abstract

The hypothesis of a tight linkage between Alzheimer's disease (AD), a presenile dementia, and the probe coding for superoxide dismutase 1 (SOD 1), located on chromosome 21 at 21q22, has been investigated in a large family originating from Calabria, in which AD is transmitted as an autosomal dominant mendelian trait. Analysis of the Msp I restriction polymorphism, after molecular hybridization with the probe of DNAs coming from 22 subjects of the pedigree, allowed to the demonstrate that there wasn't any tight linkage between AD and the marker studied.

摘要

阿尔茨海默病(AD,一种早老性痴呆)与位于21号染色体21q22的超氧化物歧化酶1(SOD 1)编码探针之间存在紧密连锁的假说,已在一个来自卡拉布里亚的大家庭中进行了研究,在这个家族中,AD作为常染色体显性孟德尔性状遗传。在用来自该家系22名受试者的DNA探针进行分子杂交后,对Msp I限制性多态性进行分析,结果表明AD与所研究的标记之间不存在紧密连锁。

相似文献

1
[Absence of a close linkage between Alzheimer's disease and the polymorphic probe coding for superoxide dismutase 1].[阿尔茨海默病与编码超氧化物歧化酶1的多态性探针之间不存在紧密连锁关系]
C R Acad Sci III. 1988;306(1):1-4.
2
[Absence of linkage between Alzheimer's disease and a polymorphic probe of the long arm of chromosome 21].[阿尔茨海默病与21号染色体长臂多态性探针之间不存在连锁关系]
C R Acad Sci III. 1987;305(2):21-4.
3
[Absence of a connection between Alzheimer's disease and complement markers].[阿尔茨海默病与补体标志物之间不存在关联]
C R Acad Sci III. 1986;303(5):149-54.
4
Absence of a close linkage between Alzheimer's disease susceptibility gene and a polymorphic DNA probe coding for beta-amyloid.阿尔茨海默病易感基因与编码β-淀粉样蛋白的多态性DNA探针之间不存在紧密连锁关系。
Biomed Pharmacother. 1988;42(9):575-7.
5
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families.在几个欧洲家族中,家族性阿尔茨海默病与A4淀粉样蛋白基因不连锁。
Nature. 1987;329(6135):153-5. doi: 10.1038/329153a0.
6
Linkage of an Alzheimer disease susceptibility locus to markers on human chromosome 21.
Am J Med Genet. 1991 Sep 15;40(4):449-53. doi: 10.1002/ajmg.1320400415.
7
Down syndrome--a gene dosage disease caused by trisomy of genes within a small segment of the long arm of chromosome 21, exemplified by the study of effects from the superoxide-dismutase type 1 (SOD-1) gene.唐氏综合征——一种由21号染色体长臂一小段内基因三体性导致的基因剂量疾病,以对1型超氧化物歧化酶(SOD-1)基因效应的研究为例。
APMIS Suppl. 1993;40:71-9.
8
Susceptibility genes for familial Alzheimer's disease on chromosomes 19 and 21: a reality check.19号和21号染色体上家族性阿尔茨海默病的易感基因:现状核查
Genet Epidemiol. 1993;10(6):425-30. doi: 10.1002/gepi.1370100616.
9
Allelic association at the D14S43 locus in early onset Alzheimer's disease. French Alzheimer's Disease Collaborative Study Group.早发性阿尔茨海默病中D14S43基因座的等位基因关联。法国阿尔茨海默病协作研究组。
Am J Med Genet. 1995 Apr 24;60(2):91-3. doi: 10.1002/ajmg.1320600202.
10
Clinical features of early onset, familial Alzheimer's disease linked to chromosome 14.与14号染色体相关的早发型家族性阿尔茨海默病的临床特征
Am J Med Genet. 1995 Feb 27;60(1):44-52. doi: 10.1002/ajmg.1320600109.

引用本文的文献

1
Familial Alzheimer's disease (FAD): co-segregation between alleles at the D21S11 DNA marker and the FAD gene in a particular pedigree.家族性阿尔茨海默病(FAD):在一个特定家系中,D21S11 DNA标记的等位基因与FAD基因之间的共分离。
J Neurol. 1988 Nov;235(8):485-6. doi: 10.1007/BF00314252.