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Assignment of the developmentally regulated gene NEDD1 to human chromosome 12q22 by fluorescence in situ hybridization.

作者信息

Takai S, Yoshida Y, Noda M, Yamada K, Kumar S

机构信息

Department of Genetics, International Medical Center of Japan, Tokyo.

出版信息

Hum Genet. 1995 Jan;95(1):96-8. doi: 10.1007/BF00225082.

DOI:10.1007/BF00225082
PMID:7814034
Abstract

The developmentally regulated mouse gene Nedd 1 encodes a protein showing similarities with the beta-subunit of heterotrimeric GTP-binding proteins and has growth suppressing activity when overexpressed in various cultured cell types. We have mapped the human homolog (NEDD1) of the mouse gene to chromosome 12q22 by fluorescence in situ hybridization using R-banded human (pro)metaphase chromosomes.

摘要

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本文引用的文献

1
Mapping of the KREV1 transformation suppressor gene and its pseudogene (KREV1P) to human chromosome 1p13.3 and 14q24.3, respectively, by fluorescence in situ hybridization.通过荧光原位杂交技术，分别将KREV1转化抑制基因及其假基因（KREV1P）定位到人类染色体1p13.3和14q24.3上。
Cytogenet Cell Genet. 1993;63(1):59-61. doi: 10.1159/000133503.
2
Human high-affinity Fc gamma RI (CD64) gene mapped to chromosome 1q21.2-q21.3 by fluorescence in situ hybridization.通过荧光原位杂交技术，将人类高亲和力FcγRI（CD64）基因定位于染色体1q21.2-q21.3。
Hum Genet. 1994 Jan;93(1):13-5. doi: 10.1007/BF00218905.
3
Molecular cloning and biological activity of a novel developmentally regulated gene encoding a protein with beta-transducin-like structure.
J Biol Chem. 1994 Apr 15;269(15):11318-26.
4
Mapping of the human gene encoding the mutual signal-transducing subunit (beta-chain) of granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-3 (IL-3), and interleukin-5 (IL-5) receptor complexes to chromosome 22q13.1.
Hum Genet. 1994 Feb;93(2):198-200. doi: 10.1007/BF00210610.
5
A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12.Holt-Oram综合征的一个基因定位于12号染色体长臂末端。
Nat Genet. 1994 Apr;6(4):405-8. doi: 10.1038/ng0494-405.
6
Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q.Holt-Oram综合征是一种基因异质性疾病，其中一个基因座定位于人类12号染色体长臂。
Nat Genet. 1994 Apr;6(4):401-4. doi: 10.1038/ng0494-401.
7
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.使用定量、高灵敏度荧光杂交技术的细胞遗传学分析。
Proc Natl Acad Sci U S A. 1986 May;83(9):2934-8. doi: 10.1073/pnas.83.9.2934.
8
Sensitive, high-resolution chromatin and chromosome mapping in situ: presence and orientation of two closely integrated copies of EBV in a lymphoma line.敏感、高分辨率的染色质和染色体原位图谱：淋巴瘤细胞系中两个紧密整合的EBV拷贝的存在及方向
Cell. 1988 Jan 15;52(1):51-61. doi: 10.1016/0092-8674(88)90530-2.
9
R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1).R带和非同位素原位杂交：人类Ⅱ型胶原基因（COL2A1）的精确定位
Hum Genet. 1990 Nov;86(1):14-6. doi: 10.1007/BF00205165.
10
Cytogenetic and molecular analysis of human male germ cell tumors: chromosome 12 abnormalities and gene amplification.人类男性生殖细胞肿瘤的细胞遗传学和分子分析：12号染色体异常与基因扩增
Genes Chromosomes Cancer. 1990 Mar;1(4):289-300. doi: 10.1002/gcc.2870010406.