Tag Archives:gene
G protein signaling: a major culprit of essential hypertension
Blood pressure (BP) is the driving force that distributes the blood to the organs of the body according to their instantanous needs. It may be increased by pressor agents acting on the heart, vessels, and blood volume,
Genome sequence of the natural antagonist Pseudomonas fluorescens 2-79 against fungal plant diseases
In agriculture we have to deal with a huge variety of diseases caused by phytopathogenic bacteria, fungi or insects for instance. Many of these plant pathogens live in the soil and attack the respective cultivar at the
Why do people undergo genetic testing – for personal benefits, for family, or for science and society?
Prader-Willi syndrome: most common genetic cause of life-threatening obesity
Association of polymorphism gene with clinical variability in cystic fibrosis patients
Whole-cell computational models can predict how genes influence behavior
Genes are read backwards to restructure our DNA
How to know transcription factors by the company they keep
A resource for studying the role of RNA-binding proteins in human disease
Escherichia coli K-12 as a model to understand gene regulation
Controlling gene expression in bacteria
From milliseconds to lifetimes: dynamic behavior of transcription factors in gene networks
Public attitudes to GM food
Public concern can often be a stumbling block to successful innovation, particularly when the underlying science breaks new ground. This does not just affect peoples’ readiness to consume new products, but may also affect the regulatory environment.
Differentiation of pathogenic races of the lentil anthracnose pathogen C.lentis using effectors
属炭疽菌一直在修正for the last decade. It contains species of high economic importance as pathogens of major crops, but also includes species that are model organisms to study host-pathogen interactions. The hemibiotroph
Mutations in the gene DLL4 cause Adams-Oliver syndrome
Adams-Oliver syndrome (AOS) is a rare hereditary disorder that occurs in 1 in 225.000 individuals and is characterized by the presence of both scalp and limb defects. Congenital anomalies of the heart and blood vessels are also