Displaying items by tag: department of genetics

The O’Neal Invests program funds UAB investigators starting new cancer-related projects to initiate key, preliminary work needed to enable competitive R01 applications from the NIH.

Fecal-dominant donor microbes in the recipient patients after fecal microbe transplantation did not correlate with response to anti-PD-1 therapy.

Record $95 million Heersink lead gift to advance strategic growth and biomedical innovation.
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The higher infectivity correlates with mutations that increase viral binding to a cell surface glucosaminoglycan, heparan sulfate.

Six graduate students in the Academic Medical Center of the 21st Century scholarship program will network with medical professionals, train with top research doctors and receive research funding from the UAB School of Medicine. 
The genetic counseling field has become an important component of medicine in the past decade. Alabama law now mandates all genetic counselors practicing in the state be licensed by fall of 2021.
This digital solution will help doctors offer patients timely genetic testing for hereditary cancer, greater clinical support and counseling, coupled with shorter wait times and more counselors to expand into other clinical areas when needed.
Gift from the Altec / Styslinger Foundation acted as catalyst for the Altec / Styslinger Genomic Medicine and Data Sciences Building, which is set to have worldwide impact.
PAGER-CoV offers a data-driven, precision medicine approach to help researchers around the world better understand COVID-19.
AGHI published data on 176 rare-disease participants and 5,369 participants, showcasing how genetic analysis can help provide important medical information.
This potential preventive treatment for Crohn’s disease was tested on a mouse model and on immune-reactive T cells from patients with Crohn’s disease.
Anindya Dutta, Ph.D., MBBS, will begin his role as chair at UAB on March 15, 2021.
The Altec Styslinger Genomic Medicine and Data Sciences Building will help cement UAB’s place as a leading research institution in genomic and precision medicine.
This study used powerful genomic tools and supercomputers to analyze massive amounts of genetic data and identify individual strains within single species of the gut microbiome present during an infant’s first 6 years of life.
This year’s symposium will focus on the application of informatics in rare disease research.
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