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The tight-skin (Tsk) mutation is closely linked to B2m on mouse chromosome 2.

作者信息

Everett E T, Pablos J L, Harris S E, LeRoy E C, Norris J S

机构信息

Department of Medicine, Medical University of South Carolina, Charleston 29425-2229.

出版信息

Mamm Genome. 1994 Jan;5(1):55-7. doi: 10.1007/BF00360571.

DOI:10.1007/BF00360571
PMID:8111131
Abstract
摘要

相似文献

1
The tight-skin (Tsk) mutation is closely linked to B2m on mouse chromosome 2.
Mamm Genome. 1994 Jan;5(1):55-7. doi: 10.1007/BF00360571.
2
The tight skin (Tsk) mutation in the mouse, a model for human fibrotic diseases, is tightly linked to the beta 2-microglobulin (B2m) gene on chromosome 2.
Genomics. 1993 Sep;17(3):748-51. doi: 10.1006/geno.1993.1398.
3
Tight-skin (Tsk) maps on mouse chromosome 2 within the region of linkage homology with human chromosome 15.紧皮（Tsk）基因定位于小鼠2号染色体上，与人类15号染色体存在连锁同源区域。
Genomics. 1994 Jul 1;22(1):223-5. doi: 10.1006/geno.1994.1368.
4
A tandem duplication within the fibrillin 1 gene is associated with the mouse tight skin mutation.原纤蛋白1基因内的串联重复与小鼠紧皮突变有关。
Genome Res. 1996 Apr;6(4):300-13. doi: 10.1101/gr.6.4.300.
5
Mapping of the agammaglobulinemia tyrosine kinase gene on the mouse X chromosome with interspecific crosses.
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6
Of mice and Marfan: genetic linkage analyses of the fibrillin genes, Fbn1 and Fbn2, in the mouse genome.小鼠与马凡氏综合征：小鼠基因组中纤连蛋白基因Fbn1和Fbn2的遗传连锁分析
Mamm Genome. 1994 Nov;5(11):696-700. doi: 10.1007/BF00426075.
7
Assignment of the gene for beta 2-microglobulin (B2m) to mouse chromosome 2.将β2-微球蛋白（B2m）基因定位到小鼠第2号染色体上。
Proc Natl Acad Sci U S A. 1982 Mar;79(6):1930-4. doi: 10.1073/pnas.79.6.1930.
8
Mouse chromosome 8.小鼠8号染色体。
Mamm Genome. 1992;3 Spec No:S121-35. doi: 10.1007/BF00648426.
9
The cardiac actin locus (Actc-1) is not on mouse chromosome 17 but is linked to beta 2-microglobulin on chromosome 2.
Genomics. 1989 Jul;5(1):19-23. doi: 10.1016/0888-7543(89)90081-5.
10
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.

引用本文的文献

1
Of mice and Marfan: genetic linkage analyses of the fibrillin genes, Fbn1 and Fbn2, in the mouse genome.小鼠与马凡氏综合征：小鼠基因组中纤连蛋白基因Fbn1和Fbn2的遗传连锁分析
Mamm Genome. 1994 Nov;5(11):696-700. doi: 10.1007/BF00426075.

本文引用的文献

1
Elastin and fibrillin mRNA and protein levels in the ontogeny of normal human aorta.
Connect Tissue Res. 1993;29(1):61-9. doi: 10.3109/03008209309061967.
2
Fibrillin delineates the primary axis of the early avian embryo.原纤维蛋白描绘了早期鸟类胚胎的主轴。
Dev Dyn. 1993 Jan;196(1):70-8. doi: 10.1002/aja.1001960109.
3
The ultrastructure of collagen in the dermis of tight-skin (Tsk) mutant mice.
J Invest Dermatol. 1980 Mar;74(3):139-47. doi: 10.1111/1523-1747.ep12535041.
4
Scleroderma-like alterations in collagen metabolism occurring in the TSK (tight skin) mouse.硬皮病样胶原代谢改变发生于TSK（紧皮）小鼠。
Arthritis Rheum. 1984 Feb;27(2):180-5. doi: 10.1002/art.1780270209.
5
The tight-skin mouse: physical and biochemical properties of the skin.
J Rheumatol. 1983 Oct;10(5):793-6.
6
Hereditary emphysema in the tight-skin mouse. Evaluation of pathogenesis.紧皮小鼠的遗传性肺气肿。发病机制评估。
Am Rev Respir Dis. 1984 May;129(5):850-5. doi: 10.1164/arrd.1984.129.5.850.
7
Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils.原纤蛋白是一种新的350千道尔顿糖蛋白，是细胞外微原纤维的一个组成部分。
J Cell Biol. 1986 Dec;103(6 Pt 1):2499-509. doi: 10.1083/jcb.103.6.2499.
8
A 16-month study of the development of genetic emphysema in tight-skin mice.对紧皮小鼠遗传性肺气肿发展情况的为期16个月的研究。
Am Rev Respir Dis. 1989 Jan;139(1):226-32. doi: 10.1164/ajrccm/139.1.226.
9
Interleukin-1 alpha and beta genes: linkage on chromosome 2 in the mouse.白细胞介素-1α和β基因：在小鼠2号染色体上的连锁关系。
Immunogenetics. 1987;26(6):339-43. doi: 10.1007/BF00343701.
10
Characterization of the mouse thrombospondin gene and evaluation of the role of the first intron in human gene expression.小鼠血小板反应蛋白基因的特征分析及首个内含子在人类基因表达中的作用评估。
J Biol Chem. 1990 Sep 25;265(27):16691-8.