The GWAS-MAP|ovis platform for aggregation and analysis of genome-wide association study results in sheep [0.03%]
家养绵羊全基因组关联研究结果的汇总与分析平台GWAS-MAP|ovis
A V A V Kirichenko,A S Zlobin,T I Shashkova et al.
A V A V Kirichenko et al.
In recent years, the number of genome-wide association studies (GWAS) carried out for various economically important animal traits has been increasing. GWAS discoveries provide summary statistics that can be used both for targeted marker-or...
Characterization of demethylating DNA glycosylase ROS1 from Nicotiana tabacum L [0.03%]
烟草ROS1 DNA去甲基化酶的鉴定与功能分析
D V Petrova,N V Permyakova,I R Grin et al.
D V Petrova et al.
One of the main mechanisms of epigenetic regulation in higher eukaryotes is based on the methylation of cytosine at the C5 position with the formation of 5-methylcytosine (mC), which is further recognized by regulatory proteins. In mammals,...
Investigation of genetic polymorphism of Russian rape and turnip rape varieties using SSR and SRAP markers [0.03%]
利用SSR和SRAP标记研究俄罗斯甘蓝型油菜和芜青甘蓝种质的遗传多态性
I A Klimenko,V T Volovik,A A Antonov et al.
I A Klimenko et al.
Rapeseed (Brassica napus L.) and turnip rape (B. rapa L. subsp. campestris (L.)) are important agricultural plants widely used for food, fodder and technical purposes and as green manure. Over the past decades, a large number of perspective...
Design and assembly of plant-based COVID-19 candidate vaccines: reсent development and future prospects [0.03%]
基于植物的COVID-19候选疫苗的设计和组装：近期进展与未来前景
E A Uvarova,P A Belavin,E V Deineko
E A Uvarova
An outbreak of a new variant of the coronavirus infection, known as COVID-19, occurred at the end of 2019 in China, in the city of Wuhan. It was caused by the SARS-CoV-2 virus. This variant of the virus is characterized by a high degree of ...
R N Mustafin
R N Mustafin
Idiopathic pulmonary fibrosis (IPF) is a severe progressive interstitial lung disease with a prevalence of 2 to 29 per 100,000 of the world's population. Aging is a significant risk factor for IPF, and the mechanisms of aging (telomere depl...
Forecast for the zone of viticulture in European Russia under climate change [0.03%]
俄罗斯欧洲地区的葡萄种植气候带未来变化预测
L Yu Novikova,P V Ozerski
L Yu Novikova
Climate warming has turned out to be a significant factor in viticulture and winemaking in all grape-growing areas of the world. Many countries consider the advance of viticulture to the north and to mountainous areas as a possible way to a...
Transmission of potato spindle tuber viroid between Phytophthora infestans and host plants [0.03%]
Potato spindle tuber病毒小体在宿主植物和Phytophthora infestans之间的传播
O S Afanasenko,A V Khiutti,N V Mironenko et al.
O S Afanasenko et al.
Potato spindle tuber viroid (PSTVd) is a naked, circular, single-stranded RNA (356-363 nucleotides in length) which lacks any protein-coding sequences. It is an economically important pathogen and is classified as a high-risk plant quaranti...
Biochemical and technological properties of moose (Alces alces) recombinant chymosin [0.03%]
麋鹿(Alces alces)重组凝乳酶的生化及技术性质研究
D V Balabova,A P Rudometov,S V Belenkaya et al.
D V Balabova et al.
Recombinant chymosins (rСhns) of the cow and the camel are currently considered as standard milk coagulants for cheese-making. The search for a new type of milk-clotting enzymes that may exist in nature and can surpass the existing "cheese...
An experimental study of the effects of SNPs in the TATA boxes of the GRIN1, ASCL3 and NOS1 genes on interactions with the TATA-binding protein [0.03%]
TATA盒单核苷酸多态性对组蛋白甲基转移酶NSD1与TATA结合蛋白相互作用影响的实验研究
E B Sharypova,I A Drachkova,I V Chadaeva et al.
E B Sharypova et al.
The GRIN1, ASCL3, and NOS1 genes are associated with various phenotypes of neuropsychiatric disorders. For instance, these genes contribute to the development of schizophrenia, Alzheimer's and Parkinson's diseases, and epilepsy. These genes...
Analysis of the low density lipoprotein receptor gene (LDLR) mutation spectrum in Russian familial hypercholesterolemia [0.03%]
俄罗斯家族性高胆固醇血症低密度脂蛋白受体基因(LDLR)突变谱分析
V B Vasilyev,F M Zakharova,T Yu Bogoslovskaya et al.
V B Vasilyev et al.
Familial hypercholesterolemia (FH) is a very common human hereditary disease in Russia and in the whole world with most of mutations localized in the gene coding for the low density lipoprotein receptor (LDLR). The object of this review is ...