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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2017/03/31 21:03:17」(JST)

English Journal

A dual amplification fluorescent strategy for sensitive detection of DNA methyltransferase activity based on strand displacement amplification and DNAzyme amplification.

Cui W1, Wang L2, Jiang W3.
Biosensors & bioelectronics.Biosens Bioelectron.2016 Mar 15;77:650-5. doi: 10.1016/j.bios.2015.10.040. Epub 2015 Oct 22.
DNA methyltransferase (MTase) plays a critical role in many biological processes and has been regarded as a predictive cancer biomarker and a therapeutic target in cancer treatment. Sensitive detection of DNA MTase activity is essential for early cancer diagnosis and therapeutics. Here, we developed
PMID 26492469

Wang W1, Zhu H2, Wang J1, Wang S1, Wang D3, Zhao J2, Zhu H4.
Human pathology.Hum Pathol.2016 Feb;48:88-94. doi: 10.1016/j.humpath.2015.09.032. Epub 2015 Oct 23.
Adenomatoid tumor is a relatively rare disease that predominantly involves male and female internal genital tracts. Although its clinical and pathologic features are well characterized, there is still controversy regarding its nature as a true neoplasm or a variant of mesothelial hyperplasia of a re
PMID 26772404

Haemophilia A and cardiovascular morbidity in a female SHAM syndrome carrier due to skewed X chromosome inactivation.

Janczar S1, Kosinska J2, Ploski R2, Pastorczak A1, Wegner O1, Zalewska-Szewczyk B1, Paige AJ3, Borowiec M1, Mlynarski W4.
European journal of medical genetics.Eur J Med Genet.2016 Jan;59(1):43-7. doi: 10.1016/j.ejmg.2015.12.004. Epub 2015 Dec 10.
We have recently described a severe haemophilia A and moyamoya (SHAM) syndrome caused by Xq28 deletions encompassing F8 and the BRCC3 familial moyamoya gene. The phenotype includes haemophilia A, moyamoya angiopathy, dysmorphia and hypertension. The genetic analysis of the family of our SHAM patient
PMID 26691666