Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Chengqi Xin"'
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 14 (2024)
Rhino-orbital-cerebral mucormycosis (ROCM) is a rare, invasive, and fatal fungal disease that is often easily misdiagnosed in the early stages due to the lack of specific clinical manifestations and adequate auxiliary examinations. Early diagnosis an
Externí odkaz:
https://doaj.org/article/8621bcd22e1b45aa95c21601309c94e4
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-6 (2018)
Abstract Background Kabuki syndrome (KS) is a rare pediatric congenital disorder with multiple congenital anomalies and intellectual disabilities, which is inherited in an autosomal dominant manner. Mutations in KMT2D and KDM6A have been proven to be
Externí odkaz:
https://doaj.org/article/20b4aa02f5014200acf9517c3f6265b6
Autor:
Wei Xu, Chengqi Xin, Qiang Lin, Feng Ding, Wei Gong, Yuanyuan Zhou, Jun Yu, Peng Cui, Songnian Hu
Publikováno v:
Genomics, Proteomics & Bioinformatics, Vol 12, Iss 3, Pp 111-119 (2014)
Postnatal cerebral development is a complicated biological process precisely controlled by multiple genes. To understand the molecular mechanism of cerebral development, we compared dynamics of mouse cerebrum transcriptome through three developmental
Externí odkaz:
https://doaj.org/article/8471c33067d34485abf2deb3740593b2
Autor:
Peng Cui, Qiang Lin, Lingfang Zhang, Feng Ding, Chengqi Xin, Daoyong Zhang, Fanglin Sun, Songnian Hu, Jun Yu
Publikováno v:
PLoS ONE, Vol 6, Iss 8, p e23219 (2011)
To further understand the relationship between nucleosome-space occupancy (NO) and global transcriptional activity in mammals, we acquired a set of genome-wide nucleosome distribution and transcriptome data from the mouse cerebrum and testis based on
Externí odkaz:
https://doaj.org/article/162b80456bd5477db1c32136e8e5c56f
Autor:
Lin Kang, Shilin Jin, Jiayi Wang, Zhongyue Lv, Chengqi Xin, Chengcheng Tan, Mengke Zhao, Liang Wang, Jing Liu
Publikováno v:
Journal of Controlled Release. 355:458-473
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b4e831356ffa196dc6c3faf906ec1d0
https://doi.org/10.1016/j.jconrel.2023.01.067
https://doi.org/10.1016/j.jconrel.2023.01.067
Publikováno v:
Neurochemical research.
Cerebral palsy (CP) describes a heterogeneous group of non-progressive neurodevelopmental disorders affecting movement and posture. The etiology and diagnostic biomarkers of CP are a hot topic in clinical research. Recent advances in omics techniques
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bdb2389dca194088718891a02d62136
https://pubmed.ncbi.nlm.nih.gov/36512293
https://pubmed.ncbi.nlm.nih.gov/36512293
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-6 (2018)
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-6 (2018)
Background Kabuki syndrome (KS) is a rare pediatric congenital disorder with multiple congenital anomalies and intellectual disabilities, which is inherited in an autosomal dominant manner. Mutations in KMT2D and KDM6A have been proven to be the prim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d13d5a5c5783c2a339e15bb5126b7d1
http://europepmc.org/articles/PMC6389055
http://europepmc.org/articles/PMC6389055
Table S1. Summary of published mutations in KMT2D. (DOCX 64 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3005c05d0ceed4dab22fe5003ce09287
Autor:
Xiaoyan Li, Liang Wang, Runjie Li, Jing Liu, Ying Wang, Ying Li, Fan Song, Yang Jiao, Chengqi Xin, Wanming Cui
Publikováno v:
SSRN Electronic Journal.
Allan Herndon Dudley syndrome (AHDS), an X-linked condition, constitutes a rare, progressive, clinically heterogeneous disorder involving severe psychomotor retardation and peripheral thyrotoxicosis, consequent to thyroid hormone transporter SLC16A2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdb868662c8ed29a0d8a67b7e068349e
https://doi.org/10.2139/ssrn.3251496
https://doi.org/10.2139/ssrn.3251496
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1638
MicroRNAs (miRNAs) are small endogenous noncoding RNAs. Plant miRNAs are known to play important regulatory roles in homeostasis, stress response, and diverse developmental processes. Here, we describe the identification of conserved miRNAs in date p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::081476e909b9788c406e2d83d825628d
https://pubmed.ncbi.nlm.nih.gov/28755233
https://pubmed.ncbi.nlm.nih.gov/28755233