Skip to main content

previous disabled Page of 54
and
  1. No Access

    Article

    Ethnic-specific genetic susceptibility loci for endometriosis in Taiwanese-Han population: a genome-wide association study

    Endometriosis is a common gynecological disorder affecting around 10% of reproductive-age women. Although many hypotheses were proposed, genetic alteration has been considered as one of the key factors promoti...

    Jim **n-Chyuan Sheu, Wei-Yong Lin, Ting-Yuan Liu in Journal of Human Genetics (2024)

  2. Article

    Open Access

    Genetic evidence for causal association between migraine and dementia: a mendelian randomization study

    There is an association between migraine and dementia, however, their causal relationship remains unclear. This study employed bidirectional two-sample Mendelian randomization (MR) to investigate the potential...

    Qiuyi Chen, Chengcheng Zhang, Shiyang Wu, Yiwei He, Yuhan Liu in BMC Medical Genomics (2024)

  3. No Access

    Article

    Stable inhibition of choroidal neovascularization by adeno-associated virus 2/8-vectored bispecific molecules

    Neovascular age-related macular degeneration (nAMD) causes severe visual impairment. Pigment epithelium-derived factor (PEDF), soluble CD59 (sCD59), and soluble fms-like tyrosine kinase-1 (sFLT-1) are potentia...

    Tinghui Bai, Bohao Cui, Man **ng, Siyue Chen, Yanfang Zhu, Dongxue Lin in Gene Therapy (2024)

  4. Article

    Open Access

    RNA-seq reveals differentially expressed lncRNAs and circRNAs and their associated functional network in HTR-8/Svneo cells under hypoxic conditions

    Placental hypoxia is hazardous to maternal health as well as fetal growth and development. Preeclampsia and intrauterine growth restriction are common pregnancy problems, and one of the causes is placental hyp...

    Jiaqing Zhou, YueHua Sheng, Zhezhan Chen, Huiqing Ding in BMC Medical Genomics (2024)

  5. No Access

    Article

    Anti-angiogenesis and anti-immunosuppression gene therapy through targeting COUP-TFII in an in situ glioblastoma mouse model

    Glioblastoma (GBM) is the most common and aggressive primary brain cancer; angiogenesis and immunosuppression exacerbate GBM progression. COUP-TFII demonstrates pro-angiogenesis activity; however, its role in gli...

    Fei Wang, Shuo Zhang, Fengjiao Sun, Weiwei Chen, Cuilan Liu in Cancer Gene Therapy (2024)

  6. Article

    Open Access

    Comprehensive analysis of the expression, prognostic, and immune infiltration for COL4s in stomach adenocarcinoma

    Collagen (COL) genes, play a key role in tumor invasion and metastasis, are involved in tumor extracellular matrix (ECM)-receptor interactions and focal adhesion pathways. However, studies focusing on the diag...

    Ying Xu, Hangbin **, Yan Chen, Zhen Yang, Dongchao Xu in BMC Medical Genomics (2024)

  7. Article

    Open Access

    Gut microbiota-mediated activation of GSDMD ignites colorectal tumorigenesis

    Activation of Gasdermin D (GSDMD) results in its cleavage, oligomerization, and subsequent formation of plasma membrane pores, leading to a form of inflammatory cell death denoted as pyroptosis. The roles of G...

    Ju Chen, Neha Singh, **aoyang Ye, Eileen Victoria Theune in Cancer Gene Therapy (2024)

  8. Article

    Open Access

    The prognostic significance of ubiquitination-related genes in multiple myeloma by bioinformatics analysis

    Immunoregulatory drugs regulate the ubiquitin-proteasome system, which is the main treatment for multiple myeloma (MM) at present. In this study, bioinformatics analysis was used to construct the risk model an...

    Feng zhang, **ao-Lei Chen, Hong-Fang Wang, Tao Guo, ** Yao in BMC Medical Genomics (2024)

  9. Article

    Open Access

    Identification of miRNA expression profile in middle ear cholesteatoma using small RNA-sequencing

    The present study aims to identify the differential miRNA expression profile in middle ear cholesteatoma and explore their potential roles in its pathogenesis.

    Mengyao **e, Qi Tang, Shu Wang, **aowu Huang, Zhiyuan Wu in BMC Medical Genomics (2024)

  10. No Access

    Article

    ScRNA-seq revealed the tumor microenvironment heterogeneity related to the occurrence and metastasis in upper urinary tract urothelial carcinoma

    Metastasis is the greatest clinical challenge for UTUCs, which may have distinct molecular and cellular characteristics from earlier cancers. Herein, we provide single-cell transcriptome profiles of UTUC para ...

    Shiyong **n, Yanwei Zhang, Zhenhua Zhang, Ziyao Li, **anchao Sun in Cancer Gene Therapy (2024)

  11. Article

    Open Access

    No causal relationship between glucose and inflammatory bowel disease: a bidirectional two-sample mendelian randomization study

    Association between glucose and inflammatory bowel disease (IBD) was found in previous observational studies and in cohort studies. However, it is not clear whether these associations reflect causality. Thus, ...

    JiePeng Cen, Kequan Chen, Ziyan Ni, QiJie Dai, Weipeng Lu in BMC Medical Genomics (2024)

  12. No Access

    Article

    Characteristics of tandem repeat inheritance and sympathetic nerve involvement in GAA-FGF14 ataxia

    Intronic GAA repeat expansion ([GAA] ≥250) in FGF14 is associated with the late-onset neurodegenerative disorder, spinocerebellar ataxia 27B (SCA27B, GAA-FGF14 ataxia). We aim to determine the prevalence of the G...

    Ze-Hong Zheng, Chun-Yan Cao, Bi Cheng, Ru-Ying Yuan in Journal of Human Genetics (2024)

  13. No Access

    Article

    PARP inhibitor and immune checkpoint inhibitor have synergism efficacy in gallbladder cancer

    Gallbladder cancer (GBC) is an aggressive cancer with poor prognosis. PARP inhibitors (PARPi) target PARP enzymes and have shown efficacy in patients with breast cancer gene (BRCA) mutations. Immunotherapy, es...

    Yu Chen, Xudong Fan, Ruohuang Lu, Shan Zeng, **** Gan in Genes & Immunity (2024)

  14. Article

    Open Access

    Clinical features and ALDH5A1 gene findings in 13 Chinese cases with succinic semialdehyde dehydrogenase deficiency

    To investigate the clinical features, ALDH5A1 gene variations, treatment, and prognosis of patients with succinic semialdehyde dehydrogenase (SSADH) deficiency.

    Hui Dong, Xue Ma, Zhehui Chen, Huiting Zhang, **qing Song in BMC Medical Genomics (2024)

  15. Article

    Open Access

    ZEB family is a prognostic biomarker and correlates with anoikis and immune infiltration in kidney renal clear cell carcinoma

    Zinc finger E-box binding homEeobox 1 (ZEB1) and ZEB2 are two anoikis-related transcription factors. The mRNA expressions of these two genes are significantly increased in kidney renal clear cell carcinoma (KI...

    Sheng Lin, Qi Chen, Canliang Tan, Manyi Su, Ling Min, Lv Ling in BMC Medical Genomics (2024)

  16. Article

    Open Access

    Increased risk of hearing loss associated with MT-RNR1 gene mutations: a real-world investigation among Han Taiwanese Population

    Previous studies have implicated inherited mutations in mitochondrial DNA (mtDNA) in sensorineural hearing loss (SNHL). However, the definitive association between mitochondrial 12S rRNA (MT-RNR1) variants and he...

    Hou-Kuang Chen, Yow-Wen Hsieh, Hsing-Yu Hsu, Ting-Yuan Liu in BMC Medical Genomics (2024)

  17. Article

    Open Access

    Deciphering the molecular nexus of BTG2 in periodontitis and diabetic kidney disease

    To investigate the role of BTG2 in periodontitis and diabetic kidney disease (DKD) and its potential underlying mechanism.

    Binhui Pan, Yangyang Teng, Renban Wang, Dan Chen, Hui Chen in BMC Medical Genomics (2024)

  18. Article

    Open Access

    Emerging role of RNA modification and long noncoding RNA interaction in cancer

    RNA modification, especially N6-methyladenosine, 5-methylcytosine, and N7-methylguanosine methylation, participates in the occurrence and progression of cancer through multiple pathways. The function and expre...

    Liqiong Yang, Lu Tang, Qi Min, Hua Tian, Linwei Li, Yueshui Zhao in Cancer Gene Therapy (2024)

  19. Article

    Open Access

    Genetic mutation patterns among glioblastoma patients in the Taiwanese population – insights from a single institution retrospective study

    This study utilized Next-Generation Sequencing (NGS) to explore genetic determinants of survival duration in Glioblastoma Multiforme (GBM) patients. We categorized 30 primary GBM patients into two groups based...

    Yu-Fen Huang, Ming-Tsang Chiao, Tzu-Hung Hsiao, Yong-**ang Zhan in Cancer Gene Therapy (2024)

  20. Article

    Open Access

    miR-124-3p and miR-194-5p regulation of the PI3K/AKT pathway via ROR2 in medulloblastoma progression

    Medulloblastoma (MB), a prevalent pediatric central nervous system tumor, is influenced by microRNAs (miRNAs) that impact tumor initiation and progression. However, the specific involvement of miRNAs in MB tum...

    Chen Wang, Runxi Fu, Yunkun Wang, Jia Wei, Ying Yu, Liuhua Hu in Cancer Gene Therapy (2024)

previous disabled Page of 54