A somatic cell hybrid panel for mouse gene mapping characterized by PCR and FISH.

Suppr

超能文献

作者信息

Williamson P, Holt S, Townsend S, Boyd Y

机构信息

MRC Radiobiology Unit, Chilton, Didcot, Oxon, UK.

出版信息

Mamm Genome. 1995 Jun;6(6):429-32. doi: 10.1007/BF00355646.

DOI:10.1007/BF00355646

PMID:7647467

Abstract

摘要

相似文献

A somatic cell hybrid panel for mouse gene mapping characterized by PCR and FISH.

Mamm Genome. 1995 Jun;6(6):429-32. doi: 10.1007/BF00355646.

Localization of the human glucosidase I gene to chromosome 2p12-p13 by fluorescence in situ hybridization and PCR analysis of somatic cell hybrids.通过荧光原位杂交和体细胞杂种的PCR分析将人葡糖苷酶I基因定位于染色体2p12 - p13。

Genomics. 1996 Jun 15;34(3):442-3. doi: 10.1006/geno.1996.0313.

Mapping of acidic epididymal glycoprotein (Aeg) genes to mouse chromosome 17.酸性附睾糖蛋白（Aeg）基因在小鼠17号染色体上的定位。

Mamm Genome. 1995 Jan;6(1):52-4. doi: 10.1007/BF00350895.

Assignment of human B2-1 gene (D17S811E) to chromosome 17qter by PCR analysis of somatic cell hybrids and fluorescence in situ hybridization.

Cytogenet Cell Genet. 1993;63(1):42-4. doi: 10.1159/000133498.

Isolation and characterization of somatic cell hybrids with breakpoints spanning 17q22-->q24.具有跨越17q22至q24断点的体细胞杂种的分离与鉴定

Cytogenet Cell Genet. 1993;64(3-4):222-3. doi: 10.1159/000133581.

The oxytocin receptor gene (OXTR) localizes to human chromosome 3p25 by fluorescence in situ hybridization and PCR analysis of somatic cell hybrids.通过荧光原位杂交以及对体细胞杂种进行PCR分析，催产素受体基因（OXTR）定位于人类染色体3p25。

Genomics. 1995 Apr 10;26(3):623-5. doi: 10.1016/0888-7543(95)80188-r.

Fibrillin genes map to regions of conserved mouse/human synteny on mouse chromosomes 2 and 18.原纤蛋白基因定位于小鼠2号和18号染色体上小鼠/人类同源保守区域。

Genomics. 1993 Dec;18(3):667-72. doi: 10.1016/s0888-7543(05)80371-4.

Characterization of mouse-hamster somatic cell hybrids by PCR: a panel of mouse-specific primers for each chromosome.

Mamm Genome. 1992;2(2):106-9. doi: 10.1007/BF00353858.

Chromosomal localization of the gamma-glutamyl carboxylase gene at 2p12.γ-谷氨酰羧化酶基因在2p12的染色体定位。

Genomics. 1995 Feb 10;25(3):746-8. doi: 10.1016/0888-7543(95)80024-g.

Assignment of the human macrophage mannose receptor gene (MRC1) to 10p13 by in situ hybridization and PCR-based somatic cell hybrid mapping.

Genomics. 1994 Aug;22(3):656-8. doi: 10.1006/geno.1994.1445.

引用本文的文献

Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease.在显性巨结肠（一种人类先天性巨结肠病的小鼠模型）中，与性别决定基因Sry相关的Sox10基因发生突变。

Proc Natl Acad Sci U S A. 1998 Apr 28;95(9):5161-5. doi: 10.1073/pnas.95.9.5161.

The mouse homologs of human GIF, DDB1, and CFL1 genes are located on chromosome 19.人类GIF、DDB1和CFL1基因的小鼠同源基因位于19号染色体上。

Mamm Genome. 1998 Apr;9(4):339. doi: 10.1007/s003359900763.

A gene spans the pseudoautosomal boundary in mice.一个基因跨越小鼠的假常染色体边界。

Proc Natl Acad Sci U S A. 1997 Oct 28;94(22):12030-5. doi: 10.1073/pnas.94.22.12030.

The mouse homologs of RELA and MLK3 are located within a 120-kb fragment on chromosome 19.RELA和MLK3的小鼠同源基因位于19号染色体上一个120千碱基对的片段内。

Mamm Genome. 1997 Jul;8(7):513-5. doi: 10.1007/s003359900487.

The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.

Mamm Genome. 1997 Jun;8(6):394-8. doi: 10.1007/s003359900454.

Fath, the murine homolog of the Drosophila fat tumor suppressor gene, maps to chromosome 8.

Mamm Genome. 1997 May;8(5):383-4. doi: 10.1007/s003359900450.

Isolation and mapping of three STSs on mouse chromosome 19.

Mamm Genome. 1996 Jun;7(6):464. doi: 10.1007/s003359900282.

本文引用的文献

Mapping on human and mouse chromosomes of the gene for the beta-galactoside-binding protein, an autocrine-negative growth factor.β-半乳糖苷结合蛋白基因在人类和小鼠染色体上的定位，β-半乳糖苷结合蛋白是一种自分泌负生长因子。

Genomics. 1993 Jan;15(1):216-8. doi: 10.1006/geno.1993.1039.

A genetic linkage map of the mouse: current applications and future prospects.小鼠的遗传连锁图谱：当前应用与未来前景

Science. 1993 Oct 1;262(5130):57-66. doi: 10.1126/science.8211130.

Complex Y chromosome aberrations are a recurrent secondary event in radiation-induced murine acute myeloid leukaemia.复杂的Y染色体畸变是辐射诱导的小鼠急性髓系白血病中反复出现的继发事件。

Leukemia. 1995 Mar;9(3):506-12.

Structure and genomic organization of the mouse dihydrofolate reductase gene.小鼠二氢叶酸还原酶基因的结构与基因组组织

Cell. 1980 Feb;19(2):355-64. doi: 10.1016/0092-8674(80)90510-3.

Molecular cloning and sequence analysis of a haploid expressed gene encoding t complex polypeptide 1.编码t复合多肽1的单倍体表达基因的分子克隆及序列分析

Cell. 1986 Mar 14;44(5):727-38. doi: 10.1016/0092-8674(86)90839-1.

Towards construction of a high resolution map of the mouse genome using PCR-analysed microsatellites.利用PCR分析的微卫星构建小鼠基因组高分辨率图谱。

Nucleic Acids Res. 1990 Jul 25;18(14):4123-30. doi: 10.1093/nar/18.14.4123.

A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes.一个定位于小鼠Y染色体性别决定区域的基因是一个胚胎期表达的新基因家族的成员。

Nature. 1990 Jul 19;346(6281):245-50. doi: 10.1038/346245a0.

The generation of a library of PCR-analyzed microsatellite variants for genetic mapping of the mouse genome.用于小鼠基因组遗传图谱绘制的经聚合酶链反应分析的微卫星变体文库的构建。

Genomics. 1991 Aug;10(4):874-81. doi: 10.1016/0888-7543(91)90175-e.

The molecular characterization of an A:T to G:C transition in the Hbb-b1 gene of the murine homologue of hemoglobin Rainier.

Biochem Genet. 1991 Dec;29(11-12):617-26. doi: 10.1007/BF02426875.

Additional microsatellite markers for mouse genome mapping.用于小鼠基因组图谱绘制的额外微卫星标记。

Mamm Genome. 1991;1(4):273-82. doi: 10.1007/BF00352339.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验