Louis Kunkel, PhD
Affiliations: | Genetics | Childrens Hospital, St. Louis, MO, United States |
Area:
Human genetics, muscular dystrophyGoogle:
"Louis Kunkel"Mean distance: 106866
Children
Sign in to add trainee| Anthony P. Monaco | grad student | ||
| Alan H. Beggs | post-doc | (GenetiTree) | |
| Kathryn N. North | post-doc | (GenetiTree) | |
| Eric Hoffman | post-doc | 1986-1990 | Childrens National Medical Center |
| Elizabeth Carson Engle | post-doc | 1992-1994 | Harvard Medical School - Boston Children's Hospital |
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Publications
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| Widrick JJ, Lambert MR, Kunkel LM, et al. (2023) Optimizing assays of zebrafish larvae swimming performance for drug discovery. Expert Opinion On Drug Discovery. 1-13 |
| Estrella E, Rockowitz S, Thorne M, et al. (2022) Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome Cohort. Advanced Genetics (Hoboken, N.J.). 4: 2200013 |
| Shelton GD, Minor KM, Vieira NM, et al. (2022) Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype. Neuromuscular Disorders : Nmd |
| Alexander MS, Hightower RM, Reid AL, et al. (2021) hnRNP L is essential for myogenic differentiation and modulates myotonic dystrophy pathologies. Muscle & Nerve |
| Lambert MR, Spinazzola JM, Widrick JJ, et al. (2020) PDE10A inhibition reduces the manifestation of pathology in DMD zebrafish and represses the genetic modifier PITPNA. Molecular Therapy : the Journal of the American Society of Gene Therapy |
| Lek A, Zhang Y, Woodman KG, et al. (2020) Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy. Science Translational Medicine. 12 |
| Widrick JJ, Kawahara G, Alexander MS, et al. (2019) Discovery of Novel Therapeutics for Muscular Dystrophies using Zebrafish Phenotypic Screens. Journal of Neuromuscular Diseases |
| Saha M, Reddy HM, Salih MA, et al. (2018) Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan. Physiological Genomics. 50: 929-939 |
| Pakula A, Lek A, Widrick J, et al. (2018) Transgenic zebrafish model of DUX4 misexpression reveals a developmental role in FSHD pathogenesis. Human Molecular Genetics |
| Serafini PR, Feyder MJ, Hightower RM, et al. (2018) A limb-girdle muscular dystrophy 2I model of muscular dystrophy identifies corrective drug compounds for dystroglycanopathies. Jci Insight. 3 |