Regional localization of rat peripheral myelin protein 22 (Pmp22) gene to chromosome 10q22 by FISH.

Suppr

超能文献

作者信息

Liehr T, Rautenstrauss B

出版信息

Mamm Genome. 1995 Jul;6(7):489. doi: 10.1007/BF00360665.

DOI:10.1007/BF00360665

PMID:7579898

Abstract

摘要

相似文献

Regional localization of rat peripheral myelin protein 22 (Pmp22) gene to chromosome 10q22 by FISH.

Mamm Genome. 1995 Jul;6(7):489. doi: 10.1007/BF00360665.

cDNA cloning, genomic structure, and chromosome mapping of the human epithelial membrane protein CL-20 gene (EMP1), a member of the PMP22 family.人上皮膜蛋白CL-20基因（EMP1）的cDNA克隆、基因组结构及染色体定位，EMP1是外周髓鞘蛋白22家族的成员之一。

Genomics. 1997 Apr 1;41(1):40-8. doi: 10.1006/geno.1997.4524.

Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathy.17号染色体短臂部分三体合并遗传性运动感觉神经病1型患者中周围髓鞘蛋白22基因的重复

Hum Genet. 1996 May;97(5):642-9.

Localization of PMP-22 gene (candidate gene for the Charcot-Marie-Tooth disease 1A) to band 17p11.2 by direct R-banding fluorescence in situ hybridization.

Jpn J Hum Genet. 1992 Dec;37(4):303-6. doi: 10.1007/BF01883321.

Structure and localization of the gene encoding human peripheral myelin protein 2 (PMP2).

Genomics. 1993 Nov;18(2):244-8. doi: 10.1006/geno.1993.1462.

Four frequently observed polymorphisms in the 3'-UTR of human peripheral myelin protein 22 (PMP22): identification of different haplotypes.人外周髓鞘蛋白22（PMP22）3'-非翻译区的四种常见多态性：不同单倍型的鉴定

Clin Genet. 1996 Jun;49(6):321-2. doi: 10.1111/j.1399-0004.1996.tb03799.x.

Charcot-Marie-Tooth phenotype produced by a duplicated PMP22 gene as part of a 17p trisomy-translocation to the X chromosome.由重复的PMP22基因产生的夏科-马里-图思表型，该基因是17号染色体三体易位至X染色体的一部分。

Clin Genet. 1998 Nov;54(5):413-6. doi: 10.1111/j.1399-0004.1998.tb03755.x.

Regional localization of rat myelin protein zero Mpz gene to chromosome 13q24-25 by means of FISH.

Mamm Genome. 1995 Nov;6(11):824-5. doi: 10.1007/BF00539016.

Human nerve pathology caused by different mutational mechanisms of the PMP22 gene.

Ann N Y Acad Sci. 1999 Sep 14;883:336-43.

Regional localization of rat microvascular endothelial differentiation gene 1 (Mdg1) to chromosome 6q16-23 by means of FISH.

Mamm Genome. 1996 Nov;7(11):867-8. doi: 10.1007/s003359900301.

引用本文的文献

Regional localization of Flic1, a calcyclin/S100A6-like gene, to rat chromosome 7q22-31 by means of FISH.

Mamm Genome. 1998 Jan;9(1):94-5.

Mapping of two different alpha-1,2-fucosyltransferase genes to rat chromosome 1q22-q31.两个不同的α-1,2-岩藻糖基转移酶基因定位于大鼠染色体1q22-q31。

Mamm Genome. 1997 Apr;8(4):297-8. doi: 10.1007/s003359900422.

The Tage4 gene maps to rat chromosome 1q22.Tage4基因定位于大鼠1号染色体1q22区域。

Mamm Genome. 1997 Feb;8(2):157-8. doi: 10.1007/s003359900636.

Regional localization of rat microvascular endothelial differentiation gene 1 (Mdg1) to chromosome 6q16-23 by means of FISH.

Mamm Genome. 1996 Nov;7(11):867-8. doi: 10.1007/s003359900301.

Regional localization of rat myelin protein zero Mpz gene to chromosome 13q24-25 by means of FISH.

Mamm Genome. 1995 Nov;6(11):824-5. doi: 10.1007/BF00539016.

本文引用的文献

Assignment of 22 loci in the rat by somatic hybrid and linkage analysis.

Mamm Genome. 1993;4(10):585-8. doi: 10.1007/BF00361389.

Localization of the human beta-catenin gene (CTNNB1) to 3p21: a region implicated in tumor development.

Genomics. 1994 Sep 1;23(1):272-4. doi: 10.1006/geno.1994.1493.

Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease.夏科-马里-图思病：遗传性疾病机制的新范例。

Trends Genet. 1994 Apr;10(4):128-33. doi: 10.1016/0168-9525(94)90214-3.

Effect of 3-methylcholanthrene and dimethylnitrosamine on anchorage dependence of rat fibroblasts chronically infected with Rauscher leukemia virus.3-甲基胆蒽和二甲基亚硝胺对长期感染劳斯氏白血病病毒的大鼠成纤维细胞贴壁依赖性的影响。

Int J Cancer. 1973 Jan 15;11(1):123-30. doi: 10.1002/ijc.2910110114.

Axon-regulated expression of a Schwann cell transcript that is homologous to a 'growth arrest-specific' gene.

EMBO J. 1991 Dec;10(12):3661-8. doi: 10.1002/j.1460-2075.1991.tb04933.x.

Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

Genomics. 1991 Apr;9(4):623-8. doi: 10.1016/0888-7543(91)90355-i.

A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse.颤抖-J小鼠中22 kDa外周髓鞘蛋白假定的第一个跨膜结构域中的亮氨酸到脯氨酸突变。

Proc Natl Acad Sci U S A. 1992 May 15;89(10):4382-6. doi: 10.1073/pnas.89.10.4382.

Localization of growth arrest-specific genes on mouse chromosomes 1, 7, 8, 11, 13, and 16.生长停滞特异性基因在小鼠1号、7号、8号、11号、13号和16号染色体上的定位。

Mamm Genome. 1992;2(2):130-4. doi: 10.1007/BF00353861.

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