Displaying items by tag: department of genetics
A genomics tool can determine whether twins maintained identical gut strains, even after living apart for years.
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UAB is continuing its world-class patient care with the establishment of a new Division of Breast and Endocrine Surgery.
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Antibiotic treatment can disrupt the gut microbiome at the strain level, with changes lasting as long as six months.
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UAB researchers have found a previously unknown gene variant that appears to contribute to movement disorders.
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These kidney macrophages reprogram to a developmental state after kidney injury, similar to those in newborn mice.
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The hygiene hypothesis says increased sanitation in industrialized countries has led to increases in asthma.
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A novel informatics technique allows researchers to identify different strains of the same bacterial species.
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The Gilbert Family Foundation’s Gene Therapy Initiative funds researchers at UAB exploring developmental and curative therapies for NF1.
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UAB investigators are on the track of new technologies to better guide brain tumor therapy decisions.
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Examination of a larger group of patients extends the clinical manifestations first described 11 years ago.
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This discovery may lead to personalized care for congestive heart failure, also known as ischemic cardiomyopathy.
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A gene mutation causes wrinkled skin and hair loss; turning off that mutation restores the mouse to normal appearance.
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UAB’s PREP Scholars proves successful by furthering student dreams as it receives a grant to continue preparing minority baccalaureate students for graduate programs.
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- release
- graduate school
- college of arts and sciences
- department of biochemistry and molecular genetics
- department of biology
- department of cell developmental and integrative biology
- neuroscience
- department of genetics
- division of clinical immunology and rheumatology
- department of biomedical engineering
- school of engineering
- department of neurology
- school of medicine
Researchers have detailed, for the first time, the normal human transcriptome of the blood-nerve barrier.
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Patients with such mutations potentially need increased disease surveillance and show a high predisposition to develop malignancies.