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A tightly organized, conserved gene cluster on mouse chromosome 3 (E3-F1).

作者信息

Vos H L, Mockensturm-Wilson M, Rood P M, Maas A M, Duhig T, Gendler S J, Bornstein P

机构信息

Department of Tumor Biology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

出版信息

Mamm Genome. 1995 Nov;6(11):820-2. doi: 10.1007/BF00539013.

DOI:10.1007/BF00539013
PMID:8597643
Abstract
摘要

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本文引用的文献

1
Isolation and characterization of the mouse thrombospondin 3 (Thbs3) gene.小鼠血小板反应蛋白3（Thbs3）基因的分离与鉴定
Genomics. 1993 Mar;15(3):607-13. doi: 10.1006/geno.1993.1114.
2
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 3.《小鼠基因组百科全书III》。1993年10月。小鼠3号染色体。
Mamm Genome. 1993;4 Spec No:S47-57. doi: 10.1007/BF00360829.
3
Direct evidence for homologous sequences on the paracentric regions of human chromosome 1.人类1号染色体臂内倒位区域同源序列的直接证据。
Mmu-miR-1894-3p 通过靶向 Trim46 抑制乳腺癌细胞的增殖和迁移。
Int J Mol Sci. 2016 Apr 22;17(4):609. doi: 10.3390/ijms17040609.
4
Mice with a disruption of the thrombospondin 3 gene differ in geometric and biomechanical properties of bone and have accelerated development of the femoral head.血小板反应蛋白3基因缺失的小鼠在骨骼的几何和生物力学特性方面存在差异，且股骨头发育加速。
Mol Cell Biol. 2005 Jul;25(13):5599-606. doi: 10.1128/MCB.25.13.5599-5606.2005.
5
Identification of three additional genes contiguous to the glucocerebrosidase locus on chromosome 1q21: implications for Gaucher disease.在1号染色体1q21上鉴定出另外三个与葡萄糖脑苷脂酶基因座相邻的基因：对戈谢病的意义。
Genome Res. 1997 Oct;7(10):1020-6. doi: 10.1101/gr.7.10.1020.
Genomics. 1994 May 15;21(2):359-63. doi: 10.1006/geno.1994.1277.
4
Report and abstracts of the First International Workshop on Human Chromosome 1 Mapping 1994. Bethesda, Maryland, March 25-27, 1994.1994年第一届人类1号染色体图谱绘制国际研讨会报告及摘要。1994年3月25日至27日于马里兰州贝塞斯达。
Cytogenet Cell Genet. 1994;67(3):144-65.
5
A genetic map of the mouse with 4,006 simple sequence length polymorphisms.一张具有4006个简单序列长度多态性的小鼠遗传图谱。
Nat Genet. 1994 Jun;7(2 Spec No):220-45. doi: 10.1038/ng0694supp-220.
6
Isolation of a YAC clone covering a cluster of nine S100 genes on human chromosome 1q21: rationale for a new nomenclature of the S100 calcium-binding protein family.一个覆盖人类染色体1q21上9个S100基因簇的酵母人工染色体（YAC）克隆的分离：S100钙结合蛋白家族新命名法的基本原理
Genomics. 1995 Feb 10;25(3):638-43. doi: 10.1016/0888-7543(95)80005-7.
7
Metaxin, a gene contiguous to both thrombospondin 3 and glucocerebrosidase, is required for embryonic development in the mouse: implications for Gaucher disease.
Proc Natl Acad Sci U S A. 1995 May 9;92(10):4547-51. doi: 10.1073/pnas.92.10.4547.
8
Mouse chromosome 3.
Mamm Genome. 1994;5 Spec No:S40-50.
9
A glucocerebrosidase fusion gene in Gaucher disease. Implications for the molecular anatomy, pathogenesis, and diagnosis of this disorder.戈谢病中的葡萄糖脑苷脂酶融合基因。对该疾病分子解剖学、发病机制及诊断的意义。
J Clin Invest. 1990 Jan;85(1):219-22. doi: 10.1172/JCI114415.
10
Structure and expression of the human polymorphic epithelial mucin gene: an expressed VNTR unit.
Biochem Biophys Res Commun. 1990 Dec 31;173(3):1019-29. doi: 10.1016/s0006-291x(05)80888-5.