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Salma Omer - Publications

Affiliations: 
Neuroscience Vanderbilt University, Nashville, TN 
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6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Omer S, Jin SC, Koumangoye R, Robert SM, Duran D, Nelson-Williams C, Huttner A, DiLuna M, Kahle KT, Delpire E. Protein kinase D1 variant associated with human epilepsy and peripheral nerve hypermyelination. Clinical Genetics. PMID 33904160 DOI: 10.1111/cge.13973  0.473
2020 Omer S, Koumangoye R, Delpire E. A mutation in the Na-K-2Cl cotransporter-1 leads to changes in cellular metabolism. Journal of Cellular Physiology. PMID 32039487 DOI: 10.1002/Jcp.29623  0.604
2019 Koumangoye R, Omer S, Kabeer MH, Delpire E. Novel human NKCC1 mutations cause defects in goblet cells mucus secretion and chronic inflammation. Cellular and Molecular Gastroenterology and Hepatology. PMID 31655271 DOI: 10.1016/J.Jcmgh.2019.10.006  0.581
2019 Koumangoye R, Omer S, Delpire E. A Dileucine Motif in the C-Terminal Domain of NKCC1 targets the cotransporter to the plasma membrane. American Journal of Physiology. Cell Physiology. PMID 30865516 DOI: 10.1152/Ajpcell.00023.2019  0.609
2018 Koumangoye R, Omer S, Delpire E. Mistargeting of a truncated Na-K-2Cl cotransporter in epithelial cells. American Journal of Physiology. Cell Physiology. PMID 29719172 DOI: 10.1152/Ajpcell.00130.2018  0.645
2016 Delpire E, Wolfe L, Flores B, Koumangoye R, Schornak CC, Omer S, Pusey B, Lau C, Markello T, Adams DR. A patient with multisystem dysfunction carries a truncation mutation in human SLC12A2, the gene encoding the Na-K-2Cl cotransporter, NKCC1. Cold Spring Harbor Molecular Case Studies. 2: a001289. PMID 27900370 DOI: 10.1101/mcs.a001289  0.553
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