DOI:10.1007/BF00225082 - Corpus ID: 902030
Assignment of the developmentally regulated gene NEDD1 to human chromosome 12q22 by fluorescence in situ hybridization
@article{Takai2004AssignmentOT,
title={Assignment of the developmentally regulated gene NEDD1 to human chromosome 12q22 by fluorescence in situ hybridization},
author={Setsuo Takai and Yoko Yoshida and Makoto Noda and K. Yamada and S. Kumar},
journal={Human Genetics},
year={2004},
volume={95},
pages={96-98},
url={https://api.semanticscholar.org/CorpusID:902030}
}- S. Takai, Y. Yoshida, S. Kumar
- Published in Human Genetics 2004
- Biology
The human homolog (NEDD1) of the mouse gene Nedd 1 is mapped to chromosome 12q22 by fluorescence in situ hybridization using R-banded human (pro)metaphase chromosomes.
5 Citations
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The potential tumour suppressor function of NEDD2 is discussed and cDNA clones for the human homologue of the mouse gene are isolated and mapped the human N EDD2 gene to 7q34-35 by fluorescence in situ hybridisation.
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This chapter has confirmed that NEDD1 can be regulated by its phosphorylation state.
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Human high-affinity FcγRI (CD64) gene mapped to chromosome 1q21.2-q21.3 by fluorescence in situ hybridization
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Fluorescence in situ hybridization analysis is used to localize the FcγRI gene to human chromosome 1.2-q21.3 using R-banded human (pro)metaphase chromosomes.
R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1)
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The MYC gene was mapped to R-banded human prometaphase chromosomes and to chromosomes expressing fra(8)(q 24.11) by fluorescence in situ hybridization by high-resolution banding analysis, and the precise localization of MYC was to the subband 8q24.13 of the long arm of chromosome 8.
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The mapping of a gene causing Holt–Oram syndrome to the distal long arm of chromosome 12 (12q21–qter) by linkage analysis in nine informative families will hopefully shed light on the molecular mechanisms that govern heart septation in the early stages of embryogenesis.
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