SCI时时刷

search
+
Genetic characterization and linkage analysis of spotted leaf 6, liguleless and lax panicle traits in mutant rice
Genetic characterization and linkage analysis of spotted leaf 6, liguleless and lax panicle traits in mutant rice
Phenotypic mutants are valuable resources for elucidating the function of genes responsible for their expression. This stu...
Genetic analysis of a child with severe intellectual disability caused by a novel variant in the FERM domain of the FRMPD4 protein
Genetic analysis of a child with severe intellectual disability caused by a novel variant in the FERM domain of the FRMPD4 protein
Intellectual developmental disorder, X-linked 104 (XLID104), caused by the FRMPD4 gene variant, is a rare X-linked genetic...
Multiple mutations in BADH2 gene reveal the novel fragrance allele in indica rice (Oryza sativa L.)
Multiple mutations in BADH2 gene reveal the novel fragrance allele in indica rice (Oryza sativa L.)
The aroma in rice is the most appreciable quality trait, controlled by the loss of function of the betaine aldehyde dehydr...
Genomic determinants of antibody response to a typhoid vaccine in Indian recipients
Genomic determinants of antibody response to a typhoid vaccine in Indian recipients
Typhoid is endemic in India and has high global incidence. There were large outbreaks of typhoid in India between 1990 and...
Estimation of genetic diversity of the exotic Indian trout populations by using microsatellite markers
Estimation of genetic diversity of the exotic Indian trout populations by using microsatellite markers
Rainbow trout (Oncorhynchus mykiss) and brown trout (Salmo trutta fario) are popular salmonid species that are reared for ...
Characters of the MOCA family in wheat and TaMOCA1 function in salt stress tolerance
Characters of the MOCA family in wheat and TaMOCA1 function in salt stress tolerance
MOCA1 encodes the last key glucuronosyltransferase for ionic stress sensor glycosyl inositol phosphoryl-ceramide (GIPCs) b...
Efficient assembly of a synthetic attenuated SARS-CoV-2 genome in Saccharomyces cerevisiae using multi-copy yeast vectors
Efficient assembly of a synthetic attenuated SARS-CoV-2 genome in Saccharomyces cerevisiae using multi-copy yeast vectors
Saccharomyces cerevisiae has been demonstrated to be an excellent platform for the multi-fragment assembly of large DNA co...
Role of VDR gene polymorphisms and vitamin D levels in normal and overweight patients with PCOS
Role of VDR gene polymorphisms and vitamin D levels in normal and overweight patients with PCOS
Polycystic ovary syndrome (PCOS) is one of the most common endocrine diseases in women. In recent years, the effects of vi...
Genomewide architecture of adaptation in experimentally evolved Drosophila characterized by widespread pleiotropy
Genomewide architecture of adaptation in experimentally evolved Drosophila characterized by widespread pleiotropy
Dissecting the molecular basis of adaptation remains elusive despite our ability to sequence genomes and transcriptomes. A...
Two novel heterozygous ADCY10 variants identified in Chinese pediatric patients with absorptive hypercalciuria: case report and literature review
Two novel heterozygous ADCY10 variants identified in Chinese pediatric patients with absorptive hypercalciuria: case report and literature review
Absorptive hypercalciuria (AH) is a prevalent cause of kidney stones, and the adenylate cyclase 10 (ADCY10) gene is a rare...
Transferability of Nikita and Sukkula retrotransposons in domestic goose (Anser anser domesticus) genome
Transferability of Nikita and Sukkula retrotransposons in domestic goose (Anser anser domesticus) genome
This article aimed to detect the existence of barley-specific Nikita and Sukkula retrotransposons in domestic geese sample...
FSTest: an efficient tool for cross-population fixation index estimation on variant call format files
FSTest: an efficient tool for cross-population fixation index estimation on variant call format files
Fixation index (Fst) statistics provide critical insights into evolutionary processes affecting the structure of genetic v...
Molecular data reveals a new genus of blindsnakes within Asiatyphlopinae from India
Molecular data reveals a new genus of blindsnakes within Asiatyphlopinae from India
The genus Indotyphlops has a widespread distribution in the Indian landmass and Southeast Asia, with 20 reported species. ...
The effect of modification of DNA interference on myostatin gene expression in mice
The effect of modification of DNA interference on myostatin gene expression in mice
Myostatin is a known negative regulator of muscle tissue growth. Thus, an inhibitor of myostatin may be therapeutically us...
Fly clock, my clock, and lamin B receptor
Fly clock, my clock, and lamin B receptor
In the fruit fly Drosophila melanogaster, circadian rhythm was disrupted when the inn...
Genetic diversity analysis of volunteer wheat based on SSR markers
Genetic diversity analysis of volunteer wheat based on SSR markers
Volunteer wheat is a kind of wheat with weed characteristics, distributed widely in the main wheat-producing areas of Chin...
Why are you hitting yourself? Whole-exome sequencing diagnosis of monogenic autoimmunity
Why are you hitting yourself? Whole-exome sequencing diagnosis of monogenic autoimmunity
Inborn errors of immunity may present with autoimmunity and autoinflammation as hallmark clinical manifestations. We aimed...
Exploring the influences of geographical variation on sequence signatures in the human gut microbiome
Exploring the influences of geographical variation on sequence signatures in the human gut microbiome
Geography shapes the structure and function of human gut microbiomes. In this study, we have explored the available human ...
olf413, a putative octopamine biosynthesis pathway gene is required for negative geotactic motor function in Drosophila melanogaster
olf413, a putative octopamine biosynthesis pathway gene is required for negative geotactic motor function in Drosophila melanogaster
Olf413 gene annotated as CG12673 in the genome of Drosophila melanogaster has been predicted to code for a protein with pu...
AICRF: ancestry inference of admixed population with deep conditional random field
AICRF: ancestry inference of admixed population with deep conditional random field
Ancestry inference of admixed populations is an important issue in anthropology and studies of gene discovery, and charact...
The formate dehydrogenase enhances aluminum tolerance of tobacco
The formate dehydrogenase enhances aluminum tolerance of tobacco
The formate dehydrogenase (FDH) is regarded as a universal stress protein involved in various plant abiotic stress respons...
Mendel did not study common, naturally occurring phenotypes
Mendel did not study common, naturally occurring phenotypes
Modern genetics research increasingly reveals that what is commonly termed Mendelian genetics occurs rarely in nature, esp...
Serum exosomal hsa_circRNA_0001842 is the potential biomarker for diagnosing lower limb vascular disease in type 2 diabetes mellitus
Serum exosomal hsa_circRNA_0001842 is the potential biomarker for diagnosing lower limb vascular disease in type 2 diabetes mellitus
This study aimed to identify the potential circular RNAs (circRNAs) in exosomes isolated from serum as biomarkers of lower...
Indigenous population genome databases for India and South Asia: emerging need for health and social applications
Indigenous population genome databases for India and South Asia: emerging need for health and social applications
With increased technological sophistication and rapidly reducing costs, currently, a huge amount of personal and populatio...
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
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
Intellectual disability (ID) is a highly heterogeneous disorder, affecting 1–3% of the world’s population, whi...
Molecular characterization of de novo ring chromosome 21 in a child with seizures, growth retardation, and multiple congenital anomalies
Molecular characterization of de novo ring chromosome 21 in a child with seizures, growth retardation, and multiple congenital anomalies
The ring chromosome 21[r(21)] syndrome is a rare disorder, and mainly occurs as a de novo event. However, a wide variation...
In silico genotyping of blood group alleles using WGS data: a comparative study of the Orang Asli in Peninsular Malaysia with major global populations
In silico genotyping of blood group alleles using WGS data: a comparative study of the Orang Asli in Peninsular Malaysia with major global populations
Differences in the distribution of RBC antigens defining the blood group types among different populations have been well ...
Population genetic analysis and scans for adaptation and contemporary selection footprints provide genomic insight into aus, indica and japonica rice cultivars diversification
Population genetic analysis and scans for adaptation and contemporary selection footprints provide genomic insight into aus, indica and japonica rice cultivars diversification
Following domestication, rice cultivars have been spread worldwide to different climates and have experienced selection pr...
Overexpression of microRNA-130a-3p suppresses glucose lipid levels and oxidative damage in diabetic retinopathy mice via modulating cell division cycle 42
Overexpression of microRNA-130a-3p suppresses glucose lipid levels and oxidative damage in diabetic retinopathy mice via modulating cell division cycle 42
MicroRNA (miR)-130a-3p has been unraveled to exert effects on diabetes. However, the research for probing its role in diab...
A novel missense variant in EIF2B5 identified in a consanguineous Iranian family with vanishing white matter disease and a brief review of the literature
A novel missense variant in EIF2B5 identified in a consanguineous Iranian family with vanishing white matter disease and a brief review of the literature
Vanishing of white matter (VWM) is a hereditary heterogeneous brain disorder that most often affects children. However, th...
阅读更多
format_indent_increase