College of Medicine
Resnick Lab
Led by James L Resnick · Molecular Genetics and Microbiology
What we study
The Resnick Lab studies how genes inherited from parents cause disorders like Prader-Willi and Angelman syndromes. They use mice with engineered mutations to understand how these disorders develop.
What working here is like
- Wet lab
- Mice
- Project
- 1
- Papers
- 4
Current projects
Identifying molecular activity of PWS-IC and AS-IC
They study how DNA elements control gene expression in mice to understand these disorders.
Summaries are written by AI in plain language from public symposium abstracts and may be imperfect.
Recent papers, explained
- A novel early onset spinocerebellar ataxia 13 BAC mouse model with cerebellar atrophy, tremor, and ataxic gait
2025 · EXPERIMENTAL ANIMALS
Creates a mouse model with KCNC3 mutation to study early-onset spinocerebellar ataxia 13.
- Similar metabolic pathways are affected in both Congenital Myasthenic Syndrome-22 and Prader-Willi Syndrome
2024 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Finds similar metabolic pathways affected in Congenital Myasthenic Syndrome-22 and Prader-Willi Syndrome.
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- Health Problems in Adults with Prader–Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the Literature
2022 · Journal of Clinical Medicine
Compares physical health problems in adults with Prader-Willi Syndrome caused by different genetic subtypes.
- The Diagnostic Journey of a Patient with Prader–Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature
2021 · Genes
Describes a patient with Prader-Willi-like Syndrome and analyzes a unique genetic variant.
Plain-language summaries are AI-written and reviewed by us; check the paper for details.
How to reach out
James L Resnick hasn't set up this page yet. Their UF Scholars profile lists their publications.