Showing results (3271-3280 of 16,029) with videos related to

Sort By:
Pageof 1,603
Frontiers in Genetics|December 15, 2025
Type 1 Bartter syndrome presenting as primary diabetes insipidus: a rare Case Report with 8-year follow-upHuijuan Lu, Shaojun Liu, Jia Sun, et al.
Frontiers in Genetics|December 23, 2025
Sex-specific circRNA-miRNA-mRNA networks in peripheral blood mononuclear cells of patients with idiopathic pulmonary arterial hypertension: a pilot studyYuan Li, Yuanyuan Sun, Yuxia Huang, et al.
Frontiers in Genetics|December 22, 2025
Integrating GWAS and machine learning for disease risk prediction in the Taiwanese Hakka populationJing-Hong Xiao, Hsiao-Yen Kang, Li-Ching Wu, et al.
Frontiers in Genetics|December 16, 2025
Correction: MAPT mutation-induced behavioral variant frontotemporal dementia in an Asian patient: a multimodal biomarker case report resolving diagnostic challenges with Alzheimer's diseaseYan Zhang, Siwei Chen, Guiying Yan, et al.
Frontiers in Genetics|December 16, 2025
FusDRM-m5C: a hybrid model for accurate prediction of 5-methylcytosine modification sites based on feature fusion and attention mechanismHui Huang, Fenglin Zhou, Jianhua Jia
Frontiers in Genetics|December 16, 2025
Case Report: Pitfalls in CF screening - targeted variant analysis can cause misleading results and therapy recommendationsMaike Karnstedt, Simone Ahting, Sophie Behrendt, et al.
Frontiers in Genetics|December 10, 2025
Mechanistic study of TFE3 breakage in TFE3-rearranged renal cell carcinoma: the perspective of non-canonical DNA structures and their stabilityXiaopo Zhang, Qinshuang Dang, Xinghe Pan, et al.
Frontiers in Genetics|December 10, 2025
Application of trio-based whole-exome sequencing in fetal ultrasound anomalies: a single-center retrospective study of 454 casesDongyi Yu, Dairong Feng, Jiangbo Qu, et al.
Frontiers in Genetics|December 2, 2025
Single-cell RNA-seq combined with bulk RNA-seq explores shared gene signatures between thyroid and breast cancersZhiping Feng, Liang He, Xin Yang, et al.
Frontiers in Genetics|December 1, 2025
Case Report: Identification and functional characterization of a novel heterozygous splice-donor (c.647+1G>A) site mutation in the SPTB gene that causes hereditary spherocytosis with hemolytic anemiaKe Cao, Xiaojuan Luo, Lianlian Liu, et al.
Pageof 1,603