Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Jin‐Lan Chen"'
Autor:
Yi Yu, Ming Ding, Jin-Lan Chen, Ting Wang, Yu-Han Chen, Xiao-Min Yang, Su-Yun Chen, Yue-Peng Wang, Yi-Gang Li
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundLipomatous atrial septal hypertrophy (LASH) with atrial septal defect (ASD) is a rare congenital anomaly. Although LASH is a histologically benign cardiac lesion characterized by excessive fat deposition in the interatrial septum that spare
Externí odkaz:
https://doaj.org/article/660f62b87a6e48ffbb5ec0c916d27e69
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 4, Pp n/a-n/a (2021)
Abstract Background Leigh syndrome, the most common mitochondrial syndrome in pediatrics, has diverse clinical manifestations and is genetically heterogeneous. Pathogenic mutations in more than 75 genes of two genomes (mitochondrial and nuclear) have
Externí odkaz:
https://doaj.org/article/91c8df8b3dd44beca770510e79b98950
Autor:
Li Xie, Jin-Lan Chen, Wei-Zhi Zhang, Shou-Zheng Wang, Tian-Li Zhao, Can Huang, Jian Wang, Jin-Fu Yang, Yi-Feng Yang, Zhi-Ping Tan
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e96471 (2014)
BACKGROUND: Ongoing studies using genomic microarrays and next-generation sequencing have demonstrated that the genetic contributions to cardiovascular diseases have been significantly ignored in the past. The aim of this study was to identify rare c
Externí odkaz:
https://doaj.org/article/2fef8ba0f8e2432ca3f8025ad0b901b6
Autor:
Ting Xie, Zhi-Ping Tan, Huiling Zhou, Hui Guo, Haidan Liu, Li Xie, Ke Gong, Jin-Lan Chen, Yifeng Yang, Yong Luo
Publikováno v:
Technology in Cancer Research & Treatment
Technology in Cancer Research & Treatment, Vol 20 (2021)
Technology in Cancer Research & Treatment, Vol 20 (2021)
Background: Non-small cell lung cancer (NSCLC) is the most common type of lung cancer affecting humans. However, appropriate biomarkers for diagnosis and prognosis have not yet been established. Here, we evaluated the gene expression profiles of pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c838d0da54761eb7eaf0dfb8a8fff54d
http://europepmc.org/articles/PMC8649439
http://europepmc.org/articles/PMC8649439
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 4, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 4, Pp n/a-n/a (2021)
Background Leigh syndrome, the most common mitochondrial syndrome in pediatrics, has diverse clinical manifestations and is genetically heterogeneous. Pathogenic mutations in more than 75 genes of two genomes (mitochondrial and nuclear) have been ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdae2b1469ac038f5ac6117733a36da5
https://pubmed.ncbi.nlm.nih.gov/33661577
https://pubmed.ncbi.nlm.nih.gov/33661577
Publikováno v:
PLoS ONE, Vol 16, Iss 6, p e0252452 (2021)
PLoS ONE
PLoS ONE
Introduction Kidney renal clear cell carcinoma (KIRC) has a high incidence globally, and its pathogenesis remains unclear. Long non-coding RNA (lncRNA), as a molecular sponge, participates in the regulation of competitive endogenous RNA (ceRNA). We a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8076efb311468927300a51b127c7c24b
https://doaj.org/article/949c972639cd48e6847245fad13ff3f3
https://doaj.org/article/949c972639cd48e6847245fad13ff3f3
Publikováno v:
Journal of Cardiothoracic Surgery
Journal of Cardiothoracic Surgery, Vol 16, Iss 1, Pp 1-8 (2021)
Journal of Cardiothoracic Surgery, Vol 16, Iss 1, Pp 1-8 (2021)
Background The outcomes of mitral valve replacement (MVR) in pediatrics especially in the patients weighing less than 10 kg are not always favorable. This study aimed to measure long-term outcomes of MVR in our institution. Methods Nine young childre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7b7defe606d9ba5ac0d7ee1eda942f5
https://pubmed.ncbi.nlm.nih.gov/33789713
https://pubmed.ncbi.nlm.nih.gov/33789713
Autor:
Jinfu Yang, Tianli Zhao, Li Xie, Zhi-Ping Tan, Jian Wang, Mi Tang, Yifeng Yang, Jin-Lan Chen, Weizhi Zhang
Publikováno v:
American Journal of Medical Genetics Part A. 167:3174-3179
Chromosome region 10q22.3-q23.3 contains several low copy repeats (LCRs) and is prone to recombination. Deletions with breakpoints within LCR3 and LCR4 have been described to be associated with intellectual disability and dysmorphic features, while t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::004d36738ea6f20d51b8ae277ea7918b
https://doi.org/10.1002/ajmg.a.37347
https://doi.org/10.1002/ajmg.a.37347
Autor:
Jin-Lan Chen1 chenjinlanmm@sina.com, Xin Zhu2 zhuxin2000@gmail.com, Tian-Li Zhao1 zhaotianli69@126.com, Jian Wang1,3 wangjian.19860820@163.com, Yi-Feng Yang1,3 yyf627@163.com, Zhi-Ping Tan1,3 tanzhiping@gmail.com
Publikováno v:
Molecular Cytogenetics (17558166). 2014, Vol. 7 Issue 1, p1-13. 13p.