A higher far-red intensity promotes the transition to flowering in triticale grown under speed breeding conditions [0.03%]
高远红光强度促进速生育种条件下小黑麦的开花转变
A O Blinkov,V М Nagamova,Y V Minkova et al.
A O Blinkov et al.
It typically takes 12 to 15 years to develop a new promising variety. One of the ways to reduce this time is through speed breeding. This method allows for up to six consecutive generations of spring cereals in a single year. Although far-r...
On the genetic structure and origin of the little ground squirrel Spermophilus pygmaeus (Pallas, 1778) in the North Caucasus [0.03%]
北高加索小旱獭的遗传结构及起源研究
F A Tembotova,A Kh Amshokova,M S Gudova
F A Tembotova
Little ground squirrel Spermophilus pygmaeus (Pallas, 1778) is a polytypic species of significant interest for the study of taxonomic diversity, genetic structure, gene flow and genetic diversity. Despite the long history of study, the taxo...
Metabolic effects of trehalose in mice of the C57BL/6 strain with obesity induced by a high carbohydrate-fat diet [0.03%]
蔗糖八硫酸钠对高碳脂肪饮食诱导的C57BL/6肥胖小鼠的代谢效应
A B Pupyshev,N M Bazhan,A Yu Kazantseva et al.
A B Pupyshev et al.
The ability of trehalose to improve metabolic parameters in mice with experimental obesity has been shown to depend on the type of obesity model. In db/db mice, it reduced body weight, insulin, blood glucose, and cholesterol levels. In mice...
A new combination of 5'- and 3'-untranslated regions increases the expression of mRNAs in vitro and in vivo [0.03%]
一个新的5'-和3'-非翻译区组合在体外和体内均增加了mRNA的表达
D N Antropov,O V Markov,A S Dome et al.
D N Antropov et al.
mRNA vaccine technologies have been actively developing since the beginning of the 21st century and have received a major boost from new findings about the functioning of the immune system and the development of efficient vehicles for nucle...
A V Kazantseva,D V Yakovleva,Yu D Davydova et al.
A V Kazantseva et al.
To date, several genome-wide association studies (GWAS) of antisocial behavior (ASB) have been conducted in Europeans, which promoted research aimed at evaluating liability to ASB-related phenotypes in independent samples. Such studies impl...
HOXB13 interactome in prostate cancer cells: biochemical and functional interactions between the transcription factors HOXB13 and TBX3 [0.03%]
前列腺癌细胞中HOXB13互作蛋白及其与转录因子TBX3的生化及功能互作研究
М M Erokhin,N Y Kozelchuk,R H Ziganshin et al.
М M Erokhin et al.
Transcription factors represent one of the major groups of proteins, whose suppression leads to tumor growth arrest. Different types of cancer express a specific set of transcription factors that create and maintain unique patterns of gene ...
Association of the rs823144 variant of the RAB29 gene with the activity of lysosomal hydrolases in blood cells and risk of Parkinson's disease [0.03%]
RAB29基因rs823144多态性与血液细胞溶酶体水解酶活性及其帕金森病易感性的相关性研究
K S Basharova,A I Bezrukova,K A Senkevich et al.
K S Basharova et al.
Recent genome-wide association studies have identified a link between the RAB29 gene and Parkinson's disease (PD). The Rab29 protein encoded by RAB29 regulates leucine-rich repeat kinase 2 (LRRK2). Mutations in the LRRK2 gene increase its k...
The сontribution of FOXO family transcription factor genes (FOXO1, FOXO3) to chronic obstructive pulmonary disease [0.03%]
FOXO家族转录因子基因（FOXO1，FOXO3）在慢性阻塞性肺疾病中的作用研究进展
V A Markelov,L Z Akhmadishina,T R Nasibullin et al.
V A Markelov et al.
Chronic obstructive pulmonary disease (COPD) is a multifactorial disease of the respiratory system and is the third leading cause of death worldwide. In the framework of the most relevant concepts of COPD pathogenesis, the key focus is on a...
Molecular genetic study of triploidy and the hydatidiform mole in pregnancy loss: analysis of 10,000 consecutive cases [0.03%]
万例连续妊娠丢失标本的染色体倍性及葡萄胎分子遗传学研究
V P Pushkarev,A S Masycheva,E A Glazyrina et al.
V P Pushkarev et al.
Approximately 10-15 % of clinically recognized pregnancies result in miscarriage, with chromosomal abnormalities identified in about 50 % of early pregnancy losses (PL). Triploidy accounts for approximately 12 % of all chromosomal abnormali...
A E Kopytova,E N Tolmacheva,D A Emelina et al.
A E Kopytova et al.
Genetic factors contribute to the etiology of intellectual disability in 25-50 % of cases. Chromosomal abnormalities, such as microdeletions and microduplications, are the most significant genetic causes. We examined a family where two boys...