English Journal
- Single-nucleotide polymorphisms in the TSPYL-4 and NT5DC1 genes are associated with susceptibility to chronic obstructive pulmonary disease.
- Guo Y1, Gong Y, Shi G, Yang K, Pan C, Li M, Li Q, Cheng Q, Dai R, Fan L, Wan H.
- Molecular medicine reports.Mol Med Rep.2012 Sep;6(3):631-8. doi: 10.3892/mmr.2012.964. Epub 2012 Jun 25.
- The risk of developing chronic obstructive pulmonary disease (COPD) is partially determined by genetic and environmental factors. Many published candidate gene studies show conflicting results due to ethnic differences and sample sizes. The number of these studies
- PMID 22736055
- Differentially expressed nucleolar transforming growth factor-beta1 target (DENTT) exhibits an inhibitory role on tumorigenesis.
- Kandalaft LE1, Zudaire E, Portal-Núñez S, Cuttitta F, Jakowlew SB.
- Carcinogenesis.Carcinogenesis.2008 Jun;29(6):1282-9. doi: 10.1093/carcin/bgn087. Epub 2008 Apr 1.
- Differentially expressed nucleolar transforming growth factor-beta1 target (DENTT), also known as testis-specific protein Y-encoded-like (TSPYL-2) and cell division autoantigen-1, is a member of the testis-specific protein Y-encoded (TSPY)/TSPY-L/SET/nucleosome assembly protein-1 superfamily. DENTT
- PMID 18381359
- Report of fertility in a woman with a predominantly 46,XY karyotype in a family with multiple disorders of sexual development.
- Dumic M1, Lin-Su K, Leibel NI, Ciglar S, Vinci G, Lasan R, Nimkarn S, Wilson JD, McElreavey K, New MI.
- The Journal of clinical endocrinology and metabolism.J Clin Endocrinol Metab.2008 Jan;93(1):182-9. Epub 2007 Nov 13.
- CONTEXT: We report herein a remarkable family in which the mother of a woman with 46,XY complete gonadal dysgenesis was found to have a 46,XY karyotype in peripheral lymphocytes, mosaicism in cultured skin fibroblasts (80% 46,XY and 20% 45,X) and a predominantly 46,XY karyotype in the ovary (93% 46,
- PMID 18000096
Japanese Journal
- Potential Mechanisms of Aberrant DNA Hypomethylation on the X Chromosome in Uterine Leiomyomas
- SATO Shun,MAEKAWA Ryo,YAMAGATA Yoshiaki,ASADA Hiromi,TAMURA Isao,LEE Lifa,OKADA Maki,TAMURA Hiroshi,SUGINO Norihiro
- Journal of Reproduction and Development 60(1), 47-54, 2014
- … However, one of them, TSPYL2, was hypomethylated in 68% of multiple leiomyoma specimens. … The incidence of aberrant hypomethylation of TSPYL2 was comparable to that of the MED12 mutation (68%), which is known to be detected at a high frequency in uterine leiomyomas. … TSPYL2 of the aberrantly hypomethylated genes on the X chromosome can be used as a biomarker of uterine leiomyomas. …
- NAID 130003381861
- Genes and proteins regarding radiation protection and sensitization
- KIM In Gyu
- 日本毒性学会学術年会 39.2(0), AS10-1, 2012
- … EFEMP1, ALDH1, TSPYL5, SM22α and TM4SF4 are representative genes and proteins that determine the characteristics of cancer stem cell like cells. …
- NAID 130005009271
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