Methylation at the D4S95 locus and predictive testing.
作者信息
Theilmann J L, Robbins C A, Hayden M R
出版信息
Am J Hum Genet. 1989 Sep;45(3):477-9.
Abstract
摘要
相似文献
1
Methylation at the D4S95 locus and predictive testing.D4S95基因座的甲基化与预测性检测。
Am J Hum Genet. 1989 Sep;45(3):477-9.
2
Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.家族研究的证据表明，导致亨廷顿舞蹈症的基因位于D4S95和D4S90的端粒位置。
Am J Hum Genet. 1989 Mar;44(3):422-5.
3
Methylation at the Huntington disease-linked D4S95 locus.亨廷顿病相关的D4S95基因座的甲基化
Am J Hum Genet. 1989 Aug;45(2):335-6.
4
5
Clustering of multiallele DNA markers near the Huntington's disease gene.亨廷顿舞蹈症基因附近多等位基因DNA标记的聚类
J Clin Invest. 1989 Sep;84(3):1013-6. doi: 10.1172/JCI114222.
6
Linkage disequilibrium and modification of risk for Huntington disease.亨廷顿病的连锁不平衡与风险修饰
Am J Hum Genet. 1991 Mar;48(3):595-603.
7
Genetic analysis of Huntington disease in Italy.
Am J Med Genet. 1991 May 1;39(2):211-4. doi: 10.1002/ajmg.1320390219.
8
Significant linkage disequilibrium between the Huntington's disease locus and markers at loci D4S10, D4S95, and D4S111 in Northern Ireland.在北爱尔兰，亨廷顿舞蹈症基因座与位于D4S10、D4S95和D4S111基因座的标记之间存在显著的连锁不平衡。
J Med Genet. 1993 Dec;30(12):1018-9. doi: 10.1136/jmg.30.12.1018.
9
Improved predictive testing for Huntington disease by using three linked DNA markers.通过使用三个连锁DNA标记改进亨廷顿病的预测性检测。
Am J Hum Genet. 1988 Nov;43(5):689-94.
10
Dinucleotide repeat polymorphism in the Huntington's disease region at the D4S182 locus.位于D4S182位点的亨廷顿病区域中的二核苷酸重复多态性
Hum Mol Genet. 1993 Apr;2(4):489. doi: 10.1093/hmg/2.4.489.
引用本文的文献
1
Identification of restriction endonucleases sensitive to 5-cytosine methylation at non-CpG sites, including expanded (CAG)n/(CTG)n repeats.鉴定可识别非 CpG 位点 5-胞嘧啶甲基化的限制内切酶，包括扩展（CAG）n/（CTG）n 重复序列。
Epigenetics. 2011 Apr;6(4):416-20. doi: 10.4161/epi.6.4.14953. Epub 2011 Apr 1.
2
Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues.扩展的 CTG 重复序列划定了肌强直性营养不良患者组织中异常 CpG 甲基化的边界。
Hum Mol Genet. 2011 Jan 1;20(1):1-15. doi: 10.1093/hmg/ddq427. Epub 2010 Nov 1.
3
Age at onset in Huntington's disease and methylation at D4S95.亨廷顿舞蹈症的发病年龄与D4S95位点的甲基化
J Med Genet. 1993 Mar;30(3):185-8. doi: 10.1136/jmg.30.3.185.
4
Linkage disequilibrium and modification of risk for Huntington disease.亨廷顿病的连锁不平衡与风险修饰
Am J Hum Genet. 1991 Mar;48(3):595-603.
本文引用的文献
1
Maternal age-specific rates of 47,+21 and other cytogenetic abnormalities diagnosed in the first trimester of pregnancy in chorionic villus biopsy specimens: comparison with rates expected from observations at amniocentesis.在绒毛取样标本中于妊娠早期诊断出的47，+21及其他细胞遗传学异常的特定孕产妇年龄发生率：与羊膜穿刺术观察预期发生率的比较
Am J Hum Genet. 1988 Jun;42(6):797-807.
2
A highly polymorphic locus very tightly linked to the Huntington's disease gene.一个与亨廷顿舞蹈症基因紧密连锁的高度多态性位点。
Nature. 1988 Apr 21;332(6166):734-6. doi: 10.1038/332734a0.
3
Methylation at the Huntington disease-linked D4S95 locus.亨廷顿病相关的D4S95基因座的甲基化
Am J Hum Genet. 1989 Aug;45(2):335-6.
4
Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.家族研究的证据表明，导致亨廷顿舞蹈症的基因位于D4S95和D4S90的端粒位置。
Am J Hum Genet. 1989 Mar;44(3):422-5.
Zotero 插件