Most human oocytes never get a chance to mature into eggs — a new study sheds light on why from co-lead Jun Z. Li , professor of human genetics.
“The diligent work of these passionate professionals is moving us closer to a world free of diabetes," said Charles “Chuck” Henderson, CEO of the ADA
The new genome could help researchers using rat models for the study of DNA, RNA, evolution, genes linked to disease risks.
Congratulations to Dr. Stephen Parker, Associate Professor of Computational Medicine and Bioinformatics, Human Genetics, and Biostatistics on the formation of the Epigenomic Metabolic Medicine Center (EM2C) at the U-M Medical School! The new Center aims to perform population-scale single-cell multi-omics profiling with the goal of better
The collection of close to 2,000 samples provides an unbiased view of canine genetics.
Author: Kelly Malcom
An international consortium of scientists, led by Jeff Kidd, Ph.D. , of University of Michigan, Jennifer R. S. Meadows of Uppsala University in
The U.S. Food and Drug Administration recently approved the first available therapeutic treatment for a rare, life-threatening genetic disorder. TAK-755, commercially known as Adzynma, was developed over the past two decades in the laboratory of U-M researcher David Ginsburg. This marks the seventh U-M invention that has secured FDA approval
The Kalantry Lab and Iwase Lab collaborate to publish a new manuscript in Nature Communications! Click here for more information .
Milan Kumar Samanta, Srimonta Gayen, Clair Harris, Emily
The Kalantry Lab publishes a new manuscript in Nature Communications! Click here for more information .
Marissa Cloutier, Surinder Kumar, Emily Buttigieg, Laura Keller, Brandon Lee, Aaron Williams, Sandra Mojica-
Dr. Camper's Journal of Clinical Endocrinology & Metabolism paper, Comprehensive identification of pathogenic gene variants in patients with neuroendocrine disorders, was chosen for the Endocrine Society Thematic Issue on
Often overlooked because they might not alter the amino acid production, splicing defects can play an important role in rare genetic pituitary gland diseases.
