Top Links

Articles Related to genetic

Prevalence and Genetic Profile of β-Thalassemia Associated Mutations in a Mauritanian Population

Although common in the Mediterranean populations, β-thalassemia are present in various other parts of the world including south Asia and Africa. This study was aimed to re-evaluate the prevalence of β thalassemia, the specific underlying β globin gene mutations and their associated haplotypes in the Mauritanian population.
View complete article: PDF  |  Full-text

Behavior and Genetics: Confounding Effects on Adolescent BMI

Despite persistently high rates of obesity among American children and adults, the complex interplay between behavior, genetics and weight outcomes is not well understood.
View complete article: PDF  |  Full-text

Democratization of Genomic Tools to Improve Autochthonous Sheep Breeds Productivity in Developing Countries

While the gap is widening between developed and developing countries in the field of classical animal genetics and breeding, genomic tools are becoming the method of choice in developed countries. The objectives of this study were to 1) demonstrate by a real case how the lack of suitable breeding strategies can be a major threat to autochthonous sheep breeds improvement and 2) show how genomic tools could be an efficient alternative tool to reverse the decrease of native breed productivity. A total of 54,476 fat tail Barabrine lambs from 77 flocks recorded during the period 2010-2014 were used in this study.
View complete article: PDF  |  Full-text

Ingredients and Pathways for Sustainable Sheep Breeding Strategies under Low Input Production Systems: The Example of Two Distinct Sheep Breeds

Near East and North Africa have 90 percent of their territory classified as arid or semi-arid rangelands. Increasing importation of animals and animal products are still followed due to an increasing consumers’ demand and poor producing abilities of existing native breeds. The objectives of this paper were to: 1) underline major genetic constraints for improving native sheep breeds productivities under low input production systems, 2) identify main ingredients and pathways for sustainable sheep breeding strategies under low input production systems.
View complete article: PDF  |  Full-text

Diversity of Foliicolous Fungi in Kashmir

The fungus kingdom encompasses an enormous diversity of taxa with varied ecologies, life cycle strategies, and morphologies ranging from unicellular aquatic chytrids to large mushrooms. Studying fungal diversity is vital if we want to shed light on terrestrial ecosystem functioning. However, there is still poor understanding of fungal diversity and variation given that fungi are highly diversified and that most of fungal species remain uncultured.
View complete article: PDF  |  Full-text

Variability of Morphological Markers of Cone and Seeds in Natural Populations and Artificial Plantations of the Scots Pine (Pinus sylvestris L.)

The variability of morphological markers of the reproductive organs in seven natural populations and nine artificial plantations of the Scots pine of Ukrainian Polissya (Volyn, Rivne and Kyiv regions) was studied. The colour of cones, seeds, winged seeds, and the apophysis of the cones of the trees were used as morphological markers.
View complete article: PDF  |  Full-text

Veterinary Considerations for the Theoretical Resurrection of Extinct Species

The de-extinction of the dinosaur is a dubious possibility but its consideration brings forth some issues that are at least worthy of scientific discussion. In this review, we discuss two distinct issues that have implications for a de-extinct species such as a dinosaur: the ability, or lack thereof, to safely sedate a rare and potentially fractious animal capable of harming the veterinary staff tasked with its care; and, disease risks associated with a species that has been extinct for millions of years. To identify potential sedatives, comparative pharmacology will be needed to uncover the links between receptor pharmacology and the desired clinical outcomes of activating established alpha-2 adrenergic, opioid, and benzodiazepine receptors. Specific to disease control, it will be necessary to understand the unique susceptibility of the new species to current diseases as well as predicting their reservoir capacity for potential human and veterinary pandemic diseases. While the topics presented herein are not exhaustive, this review highlights some of the foremost research that should be conducted in order to serve the unique veterinary needs of a de-extinct species using the dinosaur as a paradigm. Addressing these issues should be considered if an intact dinosaur genome becomes available, regardless of the feasibility of dinosaur resurrection.
View complete article: PDF  |  Full-text

Clinical Significance of microRNA Polymorphisms and Expression Profiles in Oral Cancer Development

MicroRNAs (miRNA) are potent regulators, controlling multiple biological processes, including cell growth, differentiation, cell death, development and immune responses. With emerging data supporting that miRNAs play a central role in gene dysregulation in human malignancies, unraveling the miRNA genetic variations in cancer is essential and critical if we want to develop better diagnostic and prognostic system for our patients.
View complete article: PDF  |  Full-text

Analysis of antibody by Real-Valued Special Functions

Along with the rapid development of genetic engineering technology and antibody engineering technology, the humanized monoclonal antibody has been rapidly developed and gradually replaces the rat sourced monoclonal antibody. In this paper, we establish two new logarithmically completely monotonic functions involving the real-valued special functions according to two preferred interaction geometries, necessary and sufficient conditions are presented for one of them to be logarithmically completely monotonic. As a consequence, a sharp inequality involving the real-valued special functions is deduced to solve the problems of genetically engineered antibody.
View complete article: PDF  |  Full-text

Genetic Polymorphisms Associated with Risk of Developing Age-Related Macular Degeneration in Patients with Chronic Aspirin Usage

Age-related macular degeneration (AMD) is the leading cause of blindness in the elderly population. Aspirin usage has been reported to be associated with an increased risk of developing this disease. This study aims to determine whether the increased risk of AMD with chronic aspirin usage is related to genetic polymorphisms in the Vascular Endothelial Growth Factor A (VEGFA) and Catechol-O-Methyltransferase (COMT) genes.
View complete article: PDF  |  Full-text

Computing intrinsic noise of the genetic regulation modeled by Hill functions

Intrinsic noise embedded in stochastic gene regulation due to low copy number of species has been studied using the approach of theoretical modeling and computational simulation, including the standard methods of stochastic simulation algorithm (SSA) and linear noise approximation (LNA). At average cell level, Hill functions are widely used as a compact format to represent gene regulation involving multi-transcription-factor binding and cooperativity. Heuristic SSA and LNA methods (hSSA and hLNA) have been applied to study stochastic models employing Hill functions. It is however unclear which modeling and simulation method is suitable to characterize intrinsic noise of Hill-type gene regulation with sufficient accuracy and computational efficiency. In this work, we perform noise analysis of two gene regulatory models represented by second-order activating and inhibitory Hill functions, seeking to evaluate the performance of five existing noise modeling methods.
View complete article: PDF  |  Full-text

Envisioning Molecular Network of Obesity by Omics Stratification

To date, Obesity is considered prime concern of public health with multi-dimensional factors engaged in metabolic discrepancy that is rooted from multifactorial causes (i.e., environmental intoxication or genetic abnormality), and the unmet landscape of health care system seeks for therapeutic or preventive measures. Compelling evidence support Omics as strategic tool of systemic biology is benefit to define wiring of molecular circuit in metabolic malfunction and evaluation of metabolic modulator such as synthetic drugs, stem cell replacement, and natural secondary metabolites from various resources.
View complete article: PDF  |  Full-text

Genetic Characterization and Sequence Variations in 12S rRNA of Mitochondrial Gene in Three Indian Civets (Viverridae) Species: Implication in Wildlife Forensics

Comparative genomics of 12S and 16S rRNAs, cytochrome b (Cyt b) and the control region (CR) of mtDNA genome are commonly used in phylogenetics and wildlife forensics. We document the genetic characteristics and sequence variations of 12S rRNA (384 bp) in Indian civets, viz., the common palm civet (Paradoxurus hermaphroditus) (n=9), small Indian civet (Viverricula indica) (n=7) and Himalayan palm civet (Paguma larvata) (n=5). The nucleotide compositions vary from 17.6% to 36.3%, and found one to two haplotypes in all three civet species. Observed sequence divergence was 0.001 to 0.002 and 0.057 to 0.110 within and between species respectively. The nucleotide diversity was 0.00102 to 0.00184. Tajima’s D value was negative (-0.097256 to -1.36240) but statistically non-significant in all three species. Based on genetic characteristics, we discuss the use of observed forensically informative nucleotide sequencing (FINS) and topology in species identification for forensic purposes among these three civet species.
View complete article: PDF  |  Full-text

Responses and Survival under Pegylated Interferon α2a Treatment for Patients with Post-MPN Acute Myeloid Leukemia and Acute Panmyelosis with Myelofibrosis

We report here for the first time the efficacy of pegylated interferon α2a (Peg-Ifn) as a therapy for patients with myelofibrosis and high blast counts. We treated four patients who were in an accelerated phase of myeloproliferative neoplasms or acute panmyelosis with myelofibrosis using only this drug.
View complete article: PDF  |  Full-text

Parry Romberg Syndrome: A Case Report

Parry-Romberg syndrome is a rare disorder characterized by slowly progressive deterioration of the skin and soft tissues of half of the face. The syndrome presents with characteristic skeletal, dental, and soft tissue changes in the affected half of the face, with or without neurological signs and symptoms.
View complete article: PDF  |  Full-text


Editorial Board Members Related to genetic

Binquan Huang

Research Innovation Fellow of BBSRC
UK.

Alessia Giannetto

Researcher
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences
University of Messina
Italy

HONGWEI HOLLY YIN

Assistant Professor
Cancer and Cell Biology Division
Translational Genomics Research Institute
United States

Glen Jickling

Assistant Professor
Department of Neurology
University of California
United States

JIANGUO ZHAO

Professor of “100 talent” at the Institute of Zoology
Chinese Academy of Sciences
China

Isik Yulug

Associate professor
Department of Molecular Biology and Genetics
Bilkent University
Turkey

Khaldon Bodoor

Associate Professor
Department of Biotechnology and Genetic Engineering
Jordan University of Science and Technology
Jordan

Alfred Sze-Lok Cheng

Associate Professor
School of Biomedical Sciences
The Chinese University of Hong Kong
Hong Kong

Huaizhen Qin

Assistant Professor
Department of Biostatistics and Bioinformatics
Tulane University School of Public Health and Tropical Medicine
United States

Hong-Wen Deng

Professor
Department of Biostatistics and Bioinformatics
Tulane University
United States
Submit Manuscript


Open Access Journals

View All Journals