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Linkage analyses of multiple endocrine neoplasia, type 2A (MEN-2A) with 20 DNA polymorphisms: 5% of the genome excluded.

作者信息

Kidd K K, Kidd J R, Castiglione C M, Genel M, Darby J, Cavalli-Sforza L L, Gusella J F

出版信息

Hum Hered. 1986;36(4):243-9. doi: 10.1159/000153634.

DOI:10.1159/000153634
PMID:2875939
Abstract

Pairwise linkage analyses are reported between the locus for multiple endocrine neoplasia type 2A (MEN-2A) and 20 restriction fragment length polymorphisms (RFLPs) in a single large kindred which was previously screened for linkage with this form of cancer using 23 blood group and serum protein polymorphisms. No significant, positive lod scores have been obtained so far. These 20 RFLPs have excluded the MEN2 locus from about as much of the genome as did the 23 classical markers previously reported. This is a clear demonstration of the value of RFLPs for linkage studies since these 20 RFLPs were not selected for being the most polymorphic of those available. Over 10% of the human genome has been excluded from linkage with the MEN2 locus in this particular family.

摘要

相似文献

1
Linkage analyses of multiple endocrine neoplasia, type 2A (MEN-2A) with 20 DNA polymorphisms: 5% of the genome excluded.
Hum Hered. 1986;36(4):243-9. doi: 10.1159/000153634.
2
Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.定位于20p12的DNA标记与2A型多发性内分泌腺瘤的连锁分析。
Am J Hum Genet. 1985 Sep;37(5):890-7.
3
Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group-specific loci: use of restriction fragment length polymorphisms extends exclusion region.
Genet Epidemiol. 1986;3(3):195-200. doi: 10.1002/gepi.1370030306.
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The beta subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies.人纤连蛋白受体β亚基基因座:DNA限制性片段长度多态性及连锁图谱研究。
Hum Genet. 1989 Nov;83(4):383-90. doi: 10.1007/BF00291386.
5
Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A.家族性甲状腺髓样癌和2B型多发性内分泌肿瘤与2A型多发性内分泌肿瘤定位于10号染色体的同一区域。
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6
One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map.
Henry Ford Hosp Med J. 1987;35(2-3):164-7.
7
Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: evidence against synteny.2A型多发性内分泌腺瘤(MEN-2A)与20号染色体上三个DNA标记的连锁分析:反对同线性的证据
Cancer Genet Cytogenet. 1987 Aug;27(2):327-34. doi: 10.1016/0165-4608(87)90015-x.
8
A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus.一个与2A型多发性内分泌肿瘤(MEN2A)基因座紧密连锁的新的多态性标记(D10S97)。
Hum Genet. 1993 Jan;90(5):516-20. doi: 10.1007/BF00217451.
9
Linkage analyses of multiple endocrine neoplasia, type 2 (MEN-2) with 23 classical genetic polymorphisms.
Hum Hered. 1986;36(1):6-11. doi: 10.1159/000153592.
10
Screening for multiple endocrine neoplasia type 2a with DNA-polymorphism analysis.通过DNA多态性分析筛查2a型多发性内分泌腺瘤病
N Engl J Med. 1989 Oct 12;321(15):996-1001. doi: 10.1056/NEJM198910123211502.

引用本文的文献

1
Diagnosis of genetic disease using recombinant DNA. Supplement.使用重组DNA进行遗传病诊断。增刊。
Hum Genet. 1987 Sep;77(1):66-75. doi: 10.1007/BF00284717.
2
An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.一种使用多点连锁分析进行基因定位的有效策略:将多发性内分泌腺瘤病2A(MEN2A)基因座排除在13号染色体之外。
Am J Hum Genet. 1987 Apr;40(4):329-37.
3
The beta subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies.
人纤连蛋白受体β亚基基因座:DNA限制性片段长度多态性及连锁图谱研究。
Hum Genet. 1989 Nov;83(4):383-90. doi: 10.1007/BF00291386.
4
Progress in the search for genetic linkage with Tourette syndrome: an exclusion map covering more than 50% of the autosomal genome.抽动秽语综合征基因连锁研究进展:一张覆盖超过50%常染色体基因组的排除图谱。
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