Yonghong Xie,Yunmin Wei,Rongrong Han et al.
Yonghong Xie et al.
The formate dehydrogenase (FDH) is regarded as a universal stress protein involved in various plant abiotic stress responses. This study aims to ascertain GmFDH function in conferring tolerance to aluminum (Al) stress. The bioinformatics an...
AICRF: ancestry inference of admixed population with deep conditional random field [0.03%]
具有深度条件随机场的混合体祖源推断(AICRF)
Farhad Alizadeh,Hamid Jazayeriy,Omid Jazayeri et al.
Farhad Alizadeh et al.
Ancestry inference of admixed populations is an important issue in anthropology and studies of gene discovery, and characterization. Usually, local ancestor inference (LAI) methods use fixed-length windows to divide chromosomes into smaller...
David Curtis
David Curtis
Modern genetics research increasingly reveals that what is commonly termed Mendelian genetics occurs rarely in nature, especially with regard to the effects that genetic variation exerts on human characteristics. It has been argued that an ...
Serum exosomal hsa_circRNA_0001842 is the potential biomarker for diagnosing lower limb vascular disease in type 2 diabetes mellitus [0.03%]
外泌体hsa_circRNA_0001842可作为2型糖尿病下肢血管病变诊断的潜在标志物
Qian-Qian Liu,Xing-Hui Liu,Hai-Ming Wang et al.
Qian-Qian Liu et al.
This study aimed to identify the potential circular RNAs (circRNAs) in exosomes isolated from serum as biomarkers of lower limb vascular disease (LLVD) in patients with type 2 diabetes mellitus (T2DM). This research collected circRNAs from ...
Indigenous population genome databases for India and South Asia: emerging need for health and social applications [0.03%]
印度和南亚的土著人口基因组数据库：健康和社会应用的新兴需求
Dhavendra Kumar
Dhavendra Kumar
With increased technological sophistication and rapidly reducing costs, currently, a huge amount of personal and populationlevel human genomic data and information is generated globally. There is an urgent need for an adequately curated and...
Review
Journal of genetics. 2023:102:46. DOI: 2023
A novel METTL5 variant disrupting a donor splice site leads to primary microcephaly-related intellectual disability in an Iranian family: clinical features and literature review [0.03%]
伊朗一个家族中的新生METTL5突变导致与原发性小头畸形相关的智力障碍：临床特征和文献综述
Fatemeh Shakarami,Zahra Nouri,Hossein Khanahmad et al.
Fatemeh Shakarami et al.
Intellectual disability (ID) is a highly heterogeneous disorder, affecting 1-3% of the world's population, which is associated with a significant disorder in cognitive development, adaptive functioning and behavioural problems in human life...
Review
Journal of genetics. 2023:102:45. DOI: 2023
Molecular characterization of de novo ring chromosome 21 in a child with seizures, growth retardation, and multiple congenital anomalies [0.03%]
新生儿21号环状染色体的分子表征：一名患有癫痫、生长迟缓和多种先天性畸形的儿童案例研究
Prafulla S Ambulkar,Thomas Liehr,Manish Jain et al.
Prafulla S Ambulkar et al.
The ring chromosome 21[r(21)] syndrome is a rare disorder, and mainly occurs as a de novo event. However, a wide variation of the phenotype has been reported in r(21) cases depending on breakpoints, loss of genetic material, and mosaicism o...
Population genetic analysis and scans for adaptation and contemporary selection footprints provide genomic insight into aus, indica and japonica rice cultivars diversification [0.03%]
基于群体遗传分析和适应性及当代选择印记扫描的水稻亚种基因组研究
Seyed Milad Vahedi,Moslem Momen,Seyedeh Fatemeh Mousavi et al.
Seyed Milad Vahedi et al.
Following domestication, rice cultivars have been spread worldwide to different climates and have experienced selection pressures to improve desirable traits. This has resulted in diverse cultivars that display variations in phenotypic trai...
In silico genotyping of blood group alleles using WGS data: a comparative study of the Orang Asli in Peninsular Malaysia [0.03%]
基于WGS数据的血型基因座群体基因分型研究——以马来西亚半岛的orang asli群体为例
Mercy Rophina,Teh Lay Kek,Sridhar Sivasubbu et al.
Mercy Rophina et al.
Differences in the distribution of RBC antigens defining the blood group types among different populations have been well established. Fewer studies exist that have explored the blood group profiles of indigenous populations worldwide. With...
Overexpression of microRNA-130a-3p suppresses glucose lipid levels and oxidative damage in diabetic retinopathy mice via modulating cell division cycle 42 [0.03%]
microRNA-130a-3p过表达通过调控细胞周期蛋白42抑制糖尿病视网膜病变小鼠的糖脂水平及氧化损伤
Hui Wang,Xu Dong,Jing Zhou et al.
Hui Wang et al.
MicroRNA (miR)-130a-3p has been unraveled to exert effects on diabetes. However, the research for probing its role in diabetic retinopathy (DR) is limited. Our study intends to unravel the regulatory effects of miR-130a-3p on DR development...