Yong Shi,Ran Xue,Qi Zheng et al.
Yong Shi et al.
Heterotrimeric G-proteins are multifunctional modulators that participate in a wide range of growth and developmental processes in eukaryotic species, including yeast, plants, and animals. In this study, we characterized a maize mutant, ct2...
Understanding the prevalence of germline oncogenic biomarker variants across the Indian population [0.03%]
了解遗传性致癌生物标志物变异在印度人群中的流行率
Aastha Vatsyayan,Rahul C Bhoyar,Mohamed Imran et al.
Aastha Vatsyayan et al.
Genomic biomarkers are essential aspects of personalized medicine. They offer an opportunity for early detection and appropriate intervention, thereby leading to improved patient outcomes and cost-effective treatment. However, different pop...
A fine balancer: commemorating 40 years of the Journal of Genetics's revival [0.03%]
一丝不苟的平衡者——纪念Journal of Genetics杂志复刊四十周年
Durgadas P Kasbekar
Durgadas P Kasbekar
The Journal of Genetics, started by William Bateson in 1910, played a distinguished role in the early years of genetics. However, it stopped publishing in 1978. The Indian Academy of Sciences revived it in 1985, and has published it regular...
Analysis of tandem repeats in seven telomere-to-telomere primate genomes [0.03%]
七个端对端完整组装的灵长类基因组中的串联重复序列分析
Anukrati Sharma,Divya Tej Sowpati
Anukrati Sharma
Tandem repeats (TRs) are highly polymorphic low complexity regions present in all the genomes. The length variation in TRs, particularly that of short TRs (STRs), is associated with several cellular functions such as gene expression and gen...
Mapping and gene cloning of a wheat mutant dsc with dwarf and compacted spikes [0.03%]
小麦矮密穗突变体dsc的图位克隆
Ying Xue,Junchang Li,Yumei Jiang et al.
Ying Xue et al.
Plant height and spikelet density are two important traits for wheat (Triticum aestivum L.) yield. The development of wheat mutants not only provides new genetic resources for wheat improvement but also facilitates our understanding of the ...
Deletion of RAI1 noncoding exons 1-2 causes Smith-Magenis syndrome [0.03%]
RAI1非编码外显子1-2的缺失导致史密斯-马格尼斯综合征
Uri Hamiel,Alina Kurolap,Chofit Chai Gadot et al.
Uri Hamiel et al.
Smith-Magenis syndrome (SMS) is a complex genetic disorder characterized by developmental delay and a typical behavioral phenotype. Interstitial 17p11.2 deletions, which include the RAI1 gene are detected in >90% of patients, while single n...
Case Reports
Journal of genetics. 2025:104:9. DOI: 2025
Correction to: Assessment of the contribution of VDR and VDBP/GC genes in the pathogenesis of celiac disease [0.03%]
Correction to: 维生素D受体和VDBP/GC基因在乳糜泻发病机制中的作用评估
Pratibha Banerjee,Harinder Singh,Priyanka Tiwari et al.
Pratibha Banerjee et al.
THPO promoter mutation: a familial study on congenital amegakaryocytic thrombocytopenia [0.03%]
THPO启动子突变：先天性特发性血小板减少性巨核细胞缺乏症的家族研究
Reyhaneh Dehghanzad,Roghayeh Rahbar Parvaneh,Maryam Jamshidifar et al.
Reyhaneh Dehghanzad et al.
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare inherited bone marrow failure syndrome, which is characterized by a severe thrombocytopenia at birth without predictive stigmata and by a risk for progression into aplastic anaemi...
Case Reports
Journal of genetics. 2025:104:12. DOI: 2025
Analysis of whole-exome data of nonobese NAFLD patients from India reveals association with new markers on functionally relevant genes and pathways [0.03%]
对印度非肥胖NAFLD患者外显子组数据的分析揭示了与功能相关基因和途径的新标志物之间的关联
Arnab Ghosh,Anamita Barik,Rajesh K Rai et al.
Arnab Ghosh et al.
Nonalcoholic fatty liver disease (NAFLD) occurs in a significant number of nonobese individuals, especially in Asian populations. Many genetic loci are associated with NAFLD. However, no exome-wide analysis of polymorphism data to identify ...
Wenlan Li,Xinwei Hou,Zhaodong Meng et al.
Wenlan Li et al.
The nonexpressor of pathogenesis-related 1 (NPR1) is the salicylic acid (SA) receptor, which plays an important regulatory role in plant immunity. However, the NPR1-like gene family in maize has not been comprehensively identified and analy...