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(S-dinitrophenyl)-6-mercaptopurine riboside triphosphate

structure given in first source

Also Known As:

DMRT; 9H-Purine, 6-((2,4-dinitrophenyl)thio)-9-(5-O-(hydroxy((hydroxy(phosphonooxy)phosphinyl)oxy)phosphinyl)-beta-D-ribofuranosyl)-

Networked: 16 relevant articles (0 outcomes, 3 trials/studies)

Bio-Agent Context: Research Results

Experts

1.	Chen, Yi-Lai: 1 article (01/2021)
2.	Griffin, Matthew D: 1 article (01/2021)
3.	Herrmann, Sandra M: 1 article (01/2021)
4.	Hickson, LaTonya J: 1 article (01/2021)
5.	Li, Jian-Wen: 1 article (01/2021)
6.	Luo, Jing-Yu: 1 article (01/2021)
7.	Ma, Wen-Ming: 1 article (01/2021)
8.	McNicholas, Bairbre A: 1 article (01/2021)
9.	Shen, Shuai-Qi: 1 article (01/2021)
10.	Wang, Yong-Mei: 1 article (01/2021)

Related Diseases

1.	Neoplasms (Cancer) 04/25/2023 - "This review summarizes the research progress about the mammalian DMRTs' structure, function and its critical role in cancer development, progression and therapy (mainly in human and mice), which suggests that DMRT gene could be a candidate gene in the study of tumor formation and therapeutic strategy." 06/18/2014 - "A total of 130 colon carcinoma samples were utilized to study the DMR at tumor sites (DMRT) and adjacent normal tissue (DMRN). "
2.	Kidney Diseases (Kidney Disease) 01/01/2021 - "Nonetheless, exciting progress in understanding the disease-specific mechanisms of action of MSCs and other DMRT, coupled with increasing knowledge of the pathophysiologic basis for renal-tissue injury and the experience gained from pioneering early-phase clinical trials provide optimism that influential, regenerative treatments for diverse kidney diseases will emerge in the years ahead."
3.	Carcinoma (Carcinomatosis) 06/18/2014 - "A total of 130 colon carcinoma samples were utilized to study the DMR at tumor sites (DMRT) and adjacent normal tissue (DMRN). "
4.	Gonadal Dysgenesis (Gonadal Agenesis) 03/01/2017 - "We hypothesized that in human the function of other DMRT genes clustered with DMRT1, namely DMRT3, might also be impaired by the chromosomal deletion, which leads to the gonadal dysgenesis phenotype. " 11/01/2009 - "Within this region the strongest candidates for the gonadal dysgenesis phenotype are the DMRT genes; however, the genetic mechanism is not clear yet. "
5.	Azoospermia 09/01/2015 - "In humans, the genomic region harboring the DMRT gene cluster has been implicated in disorders of sex development and recently DMRT1 deletions were shown to be associated with non-obstructive azoospermia (NOA). "

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