Transcriptome analysis unveils the intricate dynamics of senescence responses in Himalayan treeline species, Betula utilis [0.03%]
转录组分析揭示了喜马拉雅林线物种白桦的衰老响应复杂动态机制
Vikas Sharma,Hari Shankar Gadri,Asif Chowdhary et al.
Vikas Sharma et al.
High-altitude ecosystems in the Himalayas exhibit extreme seasonal variations in their vegetation, with summer and winter presenting the most pronounced environmental contrasts. As winter progresses, temperatures drop, and deciduous plant s...
Neuronal expressions of Taxi and Adar are crucial in maintaining the lifespan of Drosophila melanogaster [0.03%]
Taxi和Adar的神经元表达对于维持黑腹果蝇寿命至关重要
Upasana Gupta,Vanlalrinchhani Varte,Fathima M Ashraf et al.
Upasana Gupta et al.
Ageing involves deterioration in physiological processes, such as maintenance of neuronal health, muscle, fat bodies, and gut bacteria, which play a crucial role in the progression of ageing. In this study, we show that the expression of Ta...
Complete mitochondrial DNA genome of the Indian Chhattisgarh duck and its phylogenetic analysis [0.03%]
印度恰蒂斯加尔鸭的完整线粒体DNA基因组及系统进化分析
Rajni Kumari,Ratna Prabha,Tirupati Rao Golla et al.
Rajni Kumari et al.
The Chhattisgarh duck (Anas platyrhynchos L., 1758) is a native Indian germplasm that provides crucial support for the local food security and livelihoods in the eastern region of India. For sustainable use, preservation and conservation, i...
A novel partial mRNA-derived duplication of the DMD gene identified in NGS carrier screening [0.03%]
NGS携带者筛查中鉴定的一种新颖的部分mRNA衍生的DMD基因重复
Xue Zhang,Gang Wang,Yuan Wan et al.
Xue Zhang et al.
Duplications in the dystrophin gene (DMD) represent a common genetic variation associated with the onset of Duchenne and Becker muscular dystrophy. In this study, we reported a novel mRNA-derived DMD duplication identified by next-generatio...
Case Reports
Journal of genetics. 2025:104:24. DOI: 2025
Mitochondrial genome sequence of Hippichthys heptagonus Bleeker, 1849 (Syngnathiformes, Syngnathidae) and its phylogenetic placement [0.03%]
线纹海龙(Hippichthys heptagonus)的线粒体基因组序列及其系统发育地位
Cheng-He Sun,Xiao-Die Chen,Chang-Hu Lu
Cheng-He Sun
The family Syngnathidae includes seahorses, sea dragons, and pipefishes. We sequenced the complete mitochondrial DNA (mtDNA) genome of the belly pipefish, Hippichthys heptagonus Bleeker, 1849. The genome is 16,646-bp long, and includes the ...
Comparative analysis of the mitochondrial genome of whip scorpion, Typopeltis sinensis (Butler, 1872) (Arachnida: Thelyphonidae) with phylogenetic implication [0.03%]
中华鞭节虎线粒体基因组的比较分析及系统发育意义研究
Hongyi Liu,Wei Xu,Gaoji Zhang et al.
Hongyi Liu et al.
The complete mitogenome of the common Chinese whip scorpion, Typopeltis sinensis (Butler, 1872) was sequenced and compared with another Uropygid mitogenome of Mastigoproctus giganteus (Lucas, 1835). Structural divergences include the absenc...
Comparative Study
Journal of genetics. 2025:104:23. DOI: 2025
Characteristics of the MAPK gene family in Zizania latifolia and MAPK3 role in response to fungal pathogen infection [0.03%]
宽叶泽泻MAPK基因家族特征及MAPK3响应真菌侵染的调控作用
Lijun Xu,Pengfei Guo,Yong Kuang et al.
Lijun Xu et al.
The stems of Zizania latifolia, an important vegetable in China, are targeted by the pathogen Ustilago esculenta, triggering a response through the mitogen-activated protein kinase (MAPK) signalling pathway. To investigate the characteristi...
NGLY1-CDDG: report of two cases from India and brief review of literature [0.03%]
NGLY1缺乏症的印度病例报告及文献综述
Mihika B Dave,Vrajesh P Udani,Anaita U Hegde et al.
Mihika B Dave et al.
N-glycanase1 (NGLY1) deficiency, an autosomal recessive disorder identified a decade ago, is categorized as a congenital disorder of deglycosylation (CDDG). This disorder arises from bi-allelic variants in the NGLY1 gene, leading to impaire...
On the reversibility of RNA deamination versus RNA methylation: exploring the proximate and ultimate causes [0.03%]
关于RNA脱氨基作用与甲基化作用的可逆性：探究近因与终极原因
Yuange Duan,Qi Cao
Yuange Duan
RNA modifications play a crucial role in regulating gene expression, splicing, decoding, translation, and degradation. Among the most studied modifications are adenosine-to-inosine (A-to-I) RNA editing and N6-methyladenosine (m6A). While m6...
Genetic analysis in a consanguineous MCPH family revealed a refinement of the MCPH12 locus and a founder effect of the recurrent CDK6 variant [c.589G>A, p.(Ala197Thr)] in the Pakistani population [0.03%]
遗传分析揭示了近亲MCPH家系中MCPH12位点的精确定位以及巴基斯坦人群中CDK6反复变异[c.589G>A，p.(Ala197Thr)]的创始人效应
Muzammil Ahmad Khan,Jasmin Blatterer,Markus Kuster et al.
Muzammil Ahmad Khan et al.
Primary microcephaly (MCPH) is an autosomal recessive condition of reduced head circumference due to a small cerebral cortex. Genetic studies have reported 30 MCPH genes. The aim of this study was to investigate whether the genetic mapping ...