Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Sainan, Tan"'
Autor:
Hunjin Luo, Liu Ni, Yi-Qiong Yang, Xiao-Min Zhang, Hongping Huang, Sainan Tan, Chen Ling, Li Liang, Ling Wang, Tang Dan, Shu-Xiang Zhou, Chunliu Yang
Publikováno v:
Molecular Cytogenetics, Vol 15, Iss 1, Pp 1-6 (2022)
Abstract Background Ring chromosomes can be formed by terminal breaks of two arms of a chromosome and their rejoining, leading to a loss of genetic material. They may also be formed by telomere-telomere fusions with no deletion, resulting in the form
Externí odkaz:
https://doaj.org/article/8c62a3ff8cf74aceafeee42784a9cbe0
Autor:
hunjin Luo, Sainan Tan, Wenying Li, Shu-Xiang Zhou, Liu Ni, Yi-Qiong Yang, Xiao-Min Zhang, Pinghong Huang, Huijian Yi, Xiaodong Yang
Thalassemia is a well-understood genetic disorder, and routine genetic tests typically cover 95% of known genetic mutations. Discordance between the clinical phenotype and genotypes suggest that expanded genetic studies should be performed to look fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f55a5e9cc5766c34e38cdfb1c6a67c8b
https://doi.org/10.22541/au.165500141.10145919/v1
https://doi.org/10.22541/au.165500141.10145919/v1
Autor:
Yan Liu, Fengyu Wang, Yuan Wu, Sainan Tan, Qiaolian Wen, Jing Wang, Xiaomei Zhu, Xi Wang, Congmin Li, Xu Ma, Hong Pan
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e98157 (2014)
CITED2 was identified as a cardiac transcription factor which is essential to the heart development. Cited2-deficient mice showed cardiac malformations, adrenal agenesis and neural crest defects. To explore the potential impact of mutations in CITED2
Externí odkaz:
https://doaj.org/article/37a281a1331d46a4bc5d812ea5472145
Publikováno v:
Gene Reports. 24:101282
Metachromatic leukodystrophy (MLD) is a rare autosomal recessive lysosomal storage disease caused by a deficiency of the enzyme arylsulfatase A (ARSA), which is encoded by the ARSA gene. Mutations discovered in the ARSA gene continuously improve our
Autor:
Sainan Tan, Bin Ni, Zhaobing Su, Jianmin Xiao, Qiuhong Chen, Shiming Liu, Beihong Liu, Hong Pan, Jing Wang
Publikováno v:
Pediatric Cardiology. 38:1226-1231
CITED2 gene is an important cardiac transcription factor that plays a fundamental role in the formation and development of embryonic cardiovascular. Previous studies have showed that knock-out of CITED2 in mice might result in various cardiac malform
Autor:
Shuxiang, Zhou, Bingwen, Song, Ni, Liu, Sainan, Tan, Yiqiong, Yang, Xiaomin, Zhang, Hunjin, Luo
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 36(9)
To explore the genetic basis for a patient with autism.High-throughput sequencing was carried out to detect copy number variations in the patient.DNA sequencing found that the patient has carried a 0.11 Mb deletion in distal 2p16.3 spanning from geno
Publikováno v:
Chemotherapy. 55:6-10
Background: Quercetin is a flavonoid found ubiquitously in nature. Studies in vitroand in vivohave suggested that quercetin may have a protective role against colon cancer. Methods: We selected the human colon cancer cell line RKO to investigate the
Publikováno v:
Anti-Cancer Drugs. 19:487-494
In our study we use nordihydroguaiaretic acid (NDGA), the naturally occurring lignan, to investigate whether it plays a role in the prevention and treatment of cancer by epigenetic modifications. The growth inhibitory effect of NDGA on human breast c
Publikováno v:
Life Sciences. 82:247-255
Phytoestrogens, including the two major groups isoflavones and lignans, are chemicals with weak estrogenic activity which occur naturally in many foods and herbs. Recently, several intriguing studies reported that some isoflavones can affect DNA meth
Autor:
Sainan Tan, Qiaolian Wen, Xu Ma, Xiaomei Zhu, Congmin Li, Fengyu Wang, Yan Liu, Xi Wang, Jing Wang, Hong Pan, Yuan Wu
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 5, p e98157 (2014)
PLoS ONE, Vol 9, Iss 5, p e98157 (2014)
CITED2 was identified as a cardiac transcription factor which is essential to the heart development. Cited2-deficient mice showed cardiac malformations, adrenal agenesis and neural crest defects. To explore the potential impact of mutations in CITED2