Molecular and Human Genetics News
Study reveals benefit of exome sequencing for infants in ICU Oct 6, 2017 A team of physicians and researchers designed a study to determine the efficacy of exome sequencing infants in intensive care units.
Study shows accurately transcribing DNA overrides DNA repair Oct 4, 2017 A groundbreaking and surprising discovery finds that in the model organism E. coli, the fidelity of transcribing DNA comes at the expense of DNA repair.
Breakdown of brain cells’ collaboration linked to Alzheimer’s Sep 28, 2017 Researchers have discovered that a critical partnership between brain cells fails, neurodegeneration follows, opening a path to a better understanding of disorders such as Alzheimer’s disease.
Test reveals possible treatments for disorders involving MeCP2 Aug 23, 2017 A team of researchers has developed a strategy that allows them to identify potential treatments that would restore altered levels of MeCP2.
Midland to host community conference for genetic conditions Aug 15, 2017 Baylor College of Medicine will hold a community conference and resource fair on Saturday, Sept. 16 in the Midland area to provide a seminar and support materials for children with special needs and their families.
Grant to compare large-scale genomic sequencing, standard clinical tests for childhood cancer patients Aug 8, 2017 Baylor’s KidsCanSeq program will compare the results of large-scale genomic testing to targeted clinical tests in childhood cancer patients.
Genome sequencing shows spiders, scorpions share ancestor Jul 31, 2017 Researchers have discovered a whole genome duplication during the evolution of spiders and scorpions that could reveal more about animal diversification.
Researchers study possible carnitine deficiency, autism link Jul 13, 2017 Dr. Arthur Beaudet's research has led him to propose that the lack of carnitine might be involved in triggering mild forms of autism.
Researchers build SEQSpark to analyze huge genetic data sets Jun 29, 2017 A led by Dr. Suzanne Leal developed software called SEQSpark to overcome obstacles processing large amounts of exome and genome data.
Patient-inspired research uncovers new link to rare disorder Jun 22, 2017 Meeting a young patient with Zellweger syndrome, a rare, life-threatening genetic disease, started a scientific investigation that culminated with an unexpected discovery.