Hemic and Lymphatic Diseases: News and Research on 22q11 Deletion Syndrome

MeSH tree: C15.604.451.249

Immunology

Recreating human thymus development in a dish using iPS cells

A team of researchers led by Professor Yoko Hamazaki and Assistant Professor Yann Pretemer (Department of Life Science Frontiers) has developed an in vitro model that faithfully recapitulates human thymic epithelial cell ...

Genetics

Genetic risk for schizophrenia linked to a malformed skull

The chromosomal disorder 22q11.2 deletion syndrome (22q) has emerged as one of the strongest risks for schizophrenia. Scientists at St. Jude Children's Research Hospital identified malformed regions of the cerebellum in laboratory ...

Genetics

Genetic screening can boost congenital heart disease detection

A recent study published in Frontiers in Genetics demonstrates that combining copy number variants sequencing (CNVs-seq) and whole exome sequencing (WES) is effective in detecting congenital heart disease (CHD). CHDs are ...

Psychology & Psychiatry

An over- or under-synchronized brain may predict psychosis

Is it possible to assess an individual's risk of psychosis? Identifying predictive markers is a key challenge in psychiatry. A team from the University of Geneva (UNIGE), part of the Synapsy Center for Neuroscience and Mental ...

Genetics

New study offers insight into genesis of spina bifida

A group of researchers at the University of California San Diego School of Medicine have led an investigation that offers new insight into the causes of spina bifida, the most common structural disorder of the human nervous ...

Psychology & Psychiatry

Two key brain systems are central to psychosis, study finds

Inside the brains of people with psychosis, two key systems are malfunctioning: a "filter" that directs attention toward important external events and internal thoughts, and a "predictor" composed of pathways that anticipate ...

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