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Localization of the human melanocortin-5 receptor gene (MC5R) to chromosome band 18p11.2 by fluorescence in situ hybridization.

作者信息

Chowdhary B P, Gustavsson I, Wikberg J E, Chhajlani V

机构信息

Department of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, Uppsala.

出版信息

Cytogenet Cell Genet. 1995;68(1-2):79-81. doi: 10.1159/000133895.

DOI:10.1159/000133895
PMID:7956366
Abstract

The recently cloned novel MC5R gene is suggested to be a mediator of neural functions of the melanocortic peptides, such as melanocyte-stimulating hormone (MSH) and adrenocorticotropic hormone (ACTH). We now report the localization of the human MC5R locus to chromosome 18p11.2.

摘要

相似文献

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引用本文的文献

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Melanocortin 5 receptor signaling pathway in health and disease.黑素皮质素 5 受体信号通路在健康和疾病中的作用。
Cell Mol Life Sci. 2020 Oct;77(19):3831-3840. doi: 10.1007/s00018-020-03511-0. Epub 2020 Apr 4.
3
γ₂-Melanocyte stimulation hormone (γ₂-MSH) truncation studies results in the cautionary note that γ₂-MSH is not selective for the mouse MC3R over the mouse MC5R.
γ₂-促黑素细胞激素(γ₂-MSH)截短研究的结果告诫人们,γ₂-MSH 对小鼠 MC3R 的选择性并不优于对小鼠 MC5R。
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4
Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency.人类和小鼠的促甲状腺激素释放激素(TPIT)基因突变会导致早发性垂体促肾上腺皮质激素(ACTH)缺乏。
Genes Dev. 2003 Mar 15;17(6):711-6. doi: 10.1101/gad.1065603.
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Linkage and association studies between the melanocortin receptors 4 and 5 genes and obesity-related phenotypes in the Québec Family Study.魁北克家族研究中黑皮质素受体4和5基因与肥胖相关表型之间的连锁和关联研究。
Mol Med. 1997 Oct;3(10):663-73.
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