RFLP mapping of thymidine kinase mutants places D17S4 proximal to the human TK1 locus.
作者信息
Amundson S A, Benjamin M B, Little J B, Liber H L
机构信息
Harvard School of Public Health, Boston, MA 02115.
出版信息
Nucleic Acids Res. 1991 Jul 11;19(13):3748. doi: 10.1093/nar/19.13.3748.
Abstract
摘要
相似文献
1
RFLP mapping of thymidine kinase mutants places D17S4 proximal to the human TK1 locus.胸苷激酶突变体的限制性片段长度多态性图谱显示，D17S4 位于人 TK1 基因座附近。
Nucleic Acids Res. 1991 Jul 11;19(13):3748. doi: 10.1093/nar/19.13.3748.
2
A second useful polymorphism for the cytosolic thymidine kinase gene (TK1) with the enzyme BstEII which will allow haplotying at this locus on chromosome 17 (q21-q22).胞质胸苷激酶基因（TK1）的第二种有用的多态性，它与BstEII酶有关，这将有助于对17号染色体（q21-q22）上该位点进行单倍型分析。
Nucleic Acids Res. 1987 Sep 11;15(17):7212. doi: 10.1093/nar/15.17.7212.
3
A comparison of induced mutation at homologous alleles of the tk locus in human cells. II. Molecular analysis of mutants.人类细胞中 tk 基因座同源等位基因的诱导突变比较。II. 突变体的分子分析。
Mutat Res. 1992 May;267(1):89-95. doi: 10.1016/0027-5107(92)90113-g.
4
Localization and ordering of acid alpha-glucosidase (GAA) and thymidine kinase (TK1) by fluorescence in situ hybridization.通过荧光原位杂交对酸性α-葡萄糖苷酶（GAA）和胸苷激酶（TK1）进行定位和排序。
Hum Genet. 1996 Mar;97(3):404-6. doi: 10.1007/BF02185782.
5
Molecular genetic analysis of recessive mutations at a heterozygous autosomal locus in human cells.人类细胞中杂合常染色体位点隐性突变的分子遗传学分析。
Mutat Res. 1990 Mar;229(1):89-102. doi: 10.1016/0027-5107(90)90011-r.
6
FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumors.
Cytogenet Cell Genet. 1996;72(4):319-21. doi: 10.1159/000134213.
7
Characterization of multilocus lesions in human cells exposed to X radiation and radon.暴露于X射线和氡的人类细胞中多位点损伤的特征分析。
Radiat Res. 1996 Jan;145(1):31-8.
8
Molecular dissection of mutations at the heterozygous thymidine kinase locus in mouse lymphoma cells.小鼠淋巴瘤细胞中杂合胸苷激酶基因座突变的分子剖析
Proc Natl Acad Sci U S A. 1990 Jan;87(1):51-5. doi: 10.1073/pnas.87.1.51.
9
Isolation and mapping of a polymorphic DNA sequence (pTHH59) on chromosome 17q [D17S4].17号染色体q臂上一个多态性DNA序列（pTHH59）[D17S4]的分离与定位。
Nucleic Acids Res. 1988 Apr 25;16(8):3598. doi: 10.1093/nar/16.8.3598.
10
A KpnI RFLP at the human myeloperoxidase locus.人类髓过氧化物酶基因座处的一种KpnI限制性片段长度多态性。
Nucleic Acids Res. 1991 Jul 11;19(13):3763. doi: 10.1093/nar/19.13.3763-a.
本文引用的文献
1
Chromosome 14 marker appearance in a human B lymphoblastoid cell line of nonmalignant origin.14号染色体标记在非恶性起源的人B淋巴母细胞系中的表现。
Cancer Genet Cytogenet. 1986 Feb 15;20(3-4):231-9. doi: 10.1016/0165-4608(86)90078-6.
2
Somatic mutations at a heterozygous autosomal locus in human cells occur more frequently by allele loss than by intragenic structural alterations.在人类细胞中，杂合常染色体位点处的体细胞突变通过等位基因丢失发生的频率高于通过基因内结构改变发生的频率。
Somat Cell Mol Genet. 1986 May;12(3):255-63. doi: 10.1007/BF01570784.
3
A mapped set of DNA markers for human chromosome 17.一组人类17号染色体的DNA标记图谱。
Genomics. 1988 May;2(4):302-9. doi: 10.1016/0888-7543(88)90018-3.
4
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.
Cytogenet Cell Genet. 1989;51(1-4):622-947. doi: 10.1159/000132810.
5
A genetic linkage map of chromosome 17.
Genomics. 1990 Sep;8(1):1-6. doi: 10.1016/0888-7543(90)90218-j.
6
A comparison of induced mutation at homologous alleles of the tk locus in human cells.
Mutat Res. 1991 Mar;247(1):19-27. doi: 10.1016/0027-5107(91)90029-n.
Zotero 插件