Genetic series provides updates on neurofibromatosis type 1 May 31, 2016 Neurofibromatosis type 1, a disorder characterized by the growth of noncancerous tumors, will be the focus of discussion in the June 7 Evenings with Genetics
Largest genomic study on kidney cancer brings hope for more effective treatments Mar 4, 2016 Baylor's Dr. Chad Creighton led a study that distinguished nine major subtypes of kidney cancer.
Evenings With Genetics focuses on neurofibromatosis type 1 Mar 3, 2016 Neurofibromatosis type 1, a disorder characterized by the growth of noncancerous tumors, will be the focus of the next Evenings with Genetics on March 8.
Whole genome sequencing advances pancreatic tumor classification Feb 26, 2016 Researchers from the Human Genome Sequencing Center and the Elkins Pancreas Center at Baylor College of Medicine have collaborated with researchers in a breakthrough reclassification of pancreatic cancer.
Blood sucking fated in bed bug’s genome Feb 2, 2016 International consortium sequence the genome of the common bed bug, findings could lead to pesticide resistance.
Zoghbi to receive the prestigious Jessie Stevenson Kovalenko Medal Feb 1, 2016 The National Academy of Science announced Dr. Huda Zoghbi will be the recipient of this year’s prestigious Jessie Stevenson Kovalenko Medal.
Exome sequencing helps identify cataract gene in members of religious sect Jan 14, 2016 Link between a type of cataract and sudden cardiac death may have been found thanks to exome sequencing.
A new, multidisciplinary approach to classify cell types in the brain Dec 21, 2015 New test leads team to vital clues for understanding neuropsychiatric disorders such as autism and schizophrenia.
Normalizing the levels of MeCP2 in a mouse model of MECP2 duplication syndrome restores neurological function Nov 25, 2015 Using genetic techniques and a small molecule that can target specific genetic material, Baylor researchers find it is possible to reverse the effects of neurological disorders in mice.
Researchers discover genetic cause of second-most common kidney cancer in children Nov 19, 2015 Researchers have uncovered a genetic mutation associated with clear cell sarcoma of the kidney that has opened a new path of research and could point the way toward a new diagnostic test for the disease.