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Profil bibliographique

Changmi Deng

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

48Publications signalées
511Citations signalées
5Affiliations récentes

Les institutions déclarées

Les domaines associés

Viral-associated cancers and disordersRenal and related cancersHead and Neck Cancer StudiesRNA modifications and cancerNeuroblastoma Research and Treatments

Les publications récentes

Accès ouvert 2025 article OpenAlex

ALKBH1 Gene rs6494 T>A Polymorphism Decreases Wilms Tumour Risk in Chinese Children

Changmi Deng, Haixia Zhou, Na Zhang, Min Chen et autres

Wilms tumour (WT) is the most predominant renal carcinoma that affects children, and the understanding of the genetic mechanisms underlying WT development is continually evolving. The role of the demethylase ALKBH1, which is known for its association with diverse cancers, in WT …

cn (code pays fourni par la source)

1 citation Journal of Cellular and Molecular Medicine
Accès ouvert 2025 article OpenAlex

A genome-wide association study integrated with single-cell and bulk profiles uncovers susceptibility genes for nasopharyngeal carcinoma involved in tumorigenesis via regulation of T cells

Tong‐Min Wang, Wenli Zhang, Jin-Ru Xie, Yong‐Qiao He et autres

Nasopharyngeal carcinoma is an aggressive malignancy originating from the nasopharyngeal mucosa and associated with genetic factors. Many nasopharyngeal carcinoma susceptibility loci have been identified by genome-wide association studies (GWASs), but their underlying functional insights are largely unexplained. A meta-GWAS including 5073 nasopharyngeal …

cn, us, hk, sg, no, se (code pays fourni par la source)

5 citations Genome biology
Accès ouvert 2025 article OpenAlex

Association between NAT10 gene rs8187 G > A polymorphism and Wilms tumor susceptibility in Chinese Han children: a five-center case-control study

Changmi Deng, Jinhong Zhu, Fei Duan, Wenli Zhang et autres

BACKGROUND: Wilms tumor, a prevalent pediatric kidney cancer, has been extensively studied to elucidate its genetic mechanisms. NAT10 (N-acetyltransferase 10) is a gene encoding acetyltransferase, which is involved in various cellular processes, including RNA modification, DNA repair, and protein acetylation. The oncogenic …

cn (code pays fourni par la source)

1 citation BMC Cancer
Accès ouvert 2025 article OpenAlex

Association between TRMT61B gene polymorphism and Wilms tumor susceptibility in Chinese children

Xiaokai Huang, Jinyu Lu, Changmi Deng, Weixian Tang et autres

BACKGROUND: A methyltransferase TRMT61B gene polymorphisms and Wilms tumor susceptibility is unclear. METHODS: We examined the relationship between TRMT61B gene rs4563180 G > C polymorphism (detected by TaqMan probe method) in 414 children with Wilms tumor and 1199 healthy controls. The relationship …

cn (code pays fourni par la source)

0 citations BMC Cancer
Accès ouvert 2025 article OpenAlex

TRMT10C polymorphisms confer Wilms tumor predisposition: a five-center study

Changmi Deng, Jinhong Zhu, Fei Duan, Min Chen et autres

Wilms tumor is a prevalent childhood kidney cancer, which is known to be influenced by genetic predisposition. TRMT10C plays a role in RNA modification and mitochondrial function. This study explored the associations of four TRMT10C variants with susceptibility to Wilms tumor in …

cn (code pays fourni par la source)

5 citations Epigenetics Insights
Accès ouvert 2024 article OpenAlex

Absence of Association Between the miR-27a rs895819 T>C Polymorphism and Susceptibility to Wilms Tumor

Shuang Wu, Changmi Deng, Yufeng Han, Wen Fu et autres

Wilms tumor is the most common kidney tumor in children aged 0-14 years. MicroRNAs are small, noncoding RNAs linked to the development of malignant tumors. Several studies have shown the association between single nucleotide polymorphism in miR-27a and cancer risk. This study …

cn (code pays fourni par la source)

0 citations Cancer Screening and Prevention
2024 article OpenAlex

Genetic variations in NER pathway gene polymorphisms and Wilms tumor risk: A six‐center case–control study in East China

Xueli Zhan, Haixia Zhou, Changmi Deng, Rui‐Xi Hua et autres

The nucleotide excision repair (NER) system is one of the main ways to protect organisms from DNA damage caused by endogenous and exogenous carcinogens. NER deficiency increases genome mutations, chromosomal aberrations, and cancer viability. However, the genetic association between Wilms tumor and …

cn (code pays fourni par la source)

0 citations IUBMB Life
Accès ouvert 2024 article OpenAlex

RETRACTED ARTICLE: N6-methyladenosine modification of circMARK2 enhances cytoplasmic export and stabilizes LIN28B, contributing to the progression of Wilms tumor

Guannan Shu, Zhao Zhang, Tianxin Zhao, Changmi Deng et autres

Abstract Background The potential involvement of circular RNAs (circRNAs) and N6-methyladenosine (m6A) modification in the progression of Wilms tumor (WT) has not been fully elucidated. This study investigates the regulatory mechanisms and clinical significance of m6A-modified circMARK2 and its role in WT …

cn (code pays fourni par la source)

5 citations Journal of Experimental & Clinical Cancer Research
Accès ouvert 2024 article OpenAlex

LMO family gene polymorphisms and Wilms tumor susceptibility in Chinese children: a five-center case-control study

Wen Fu, Linqing Deng, Xiaosong Yan, Rui‐Xi Hua et autres

BACKGROUND: Wilms tumor is the most prevalent embryonal kidney malignancy in children worldwide. Previous genome-wide association study (GWAS) identified that LIM domain only 1 (LMO1) gene polymorphisms affected the susceptibility to develop certain tumor types. Apart from LMO1, the LMO gene family …

cn (code pays fourni par la source)

0 citations BMC Cancer
Accès ouvert 2024 article OpenAlex

EBV DNA methylation profiles and its application in distinguishing nasopharyngeal carcinoma and nasal NK/T-cell lymphoma

Cao‐Li Tang, Xi‐Zhao Li, Ting Zhou, Changmi Deng et autres

BACKGROUND: As an oncovirus, EBV is associated with multiple cancers, including solid tumors and hematological malignancies. EBV methylation plays an important role in regulating tumor occurrence. However, the EBV methylation profiles in EBV-associated tumor tissues are poorly understood. RESULTS: In this study, …

cn (code pays fourni par la source)

10 citations Clinical Epigenetics
Accès ouvert 2024 article OpenAlex

YTHDF3 gene polymorphisms increase Wilms tumor risk in Chinese girls

Changmi Deng, Yufeng Han, Haixia Zhou, Jiao Zhang et autres

Wilms tumor is a prevalent pediatric tumor influenced by various genetic factors.m 6 A modification is a common nucleotide modification that plays a role in a variety of cancers.As a "reader", YTHDF3 is essential for recognizing m 6 A modifications.However, the association …

cn (code pays fourni par la source)

0 citations Journal of Cancer

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