Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of
alleles, including common alleles of small effect that might be detected by genome-wide …

Schizophrenia is a complex disorder, caused by both genetic and environmental factors and
their interactions. Research on pathogenesis has traditionally focused on neurotransmitter …

Dipeptidyl peptidase IV (DPP-IV/CD26) is a multifunctional type II transmembrane serine
peptidase. This enzyme contributes to the regulation of various physiological processes, …

Deletions and reciprocal duplications of the chromosome 16p13. 1 region have recently been
reported in several cases of autism and mental retardation (MR). As genomic copy number …

Many common illnesses, for reasons that have not been identified, differentially affect men
and women. For instance, the autoimmune diseases systemic lupus erythematosus (SLE) and …

A simple and efficient method for the separation of the three phenolic diketones, curcumin 1,
demethoxycurcumin 2, and bis-demethoxycurcumin 3, isolated from the rhizomes of …

Schizophrenia is a devastating psychiatric illness with high heritability. Brain structure and
function differ, on average, between people with schizophrenia and healthy individuals. As …

We use chronologies of stable isotopes measured from elephant (Loxodonta africana) hair
to determine migration patterns and seasonal diet changes in elephants in and near …

Congenital long QT syndrome (LQTS) is a hereditary disorder that leads to sudden cardiac
death secondary to fatal cardiac arrhythmias. Although many genes for LQTS have been …

Introduction and hypothesis Epidemiological observations suggest links between
osteoporosis and risk of acute cardiovascular events and vice versa. Whether the two clinical …