Debdeep Dutta, Ph.D.
Affiliations: | Molecular and Human Genetics | Baylor College of Medicine, Houston, TX |
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"Debdeep Dutta"
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| Moulton MJ, Atala K, Zheng Y, et al. (2024) Dominant Missense Variants in SREBF2 are Associated with Complex Dermatological, Neurological, and Skeletal Abnormalities. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101174 |
| Liao JZ, Chung HL, Shih C, et al. (2024) Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in Drosophila. Nature Communications. 15: 3326 |
| Dutta D, Kanca O, Shridharan RV, et al. (2024) Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability. Proceedings of the National Academy of Sciences of the United States of America. 121: e2322582121 |
| Ma M, Zheng Y, Lu S, et al. (2024) variants in are associated with hearing impairment, ocular pathology, and cardiac defects. Medrxiv : the Preprint Server For Health Sciences |
| Dutta D, Kanca O, Byeon SK, et al. (2023) A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levels. Nature Metabolism |
| Pan X, Dutta D, Lu S, et al. (2023) Sphingolipids in neurodegenerative diseases. Frontiers in Neuroscience. 17: 1137893 |
| Sinha Ray S, Dutta D, Dennys C, et al. (2022) Mechanisms of IRF2BPL-related disorders and identification of a potential therapeutic strategy. Cell Reports. 41: 111751 |
| Kanca O, Zirin J, Hu Y, et al. (2022) An expanded toolkit for Drosophila gene tagging using synthesized homology donor constructs for CRISPR mediated homologous recombination. Elife. 11 |
| Marcogliese PC, Dutta D, Ray SS, et al. (2022) Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling. Science Advances. 8: eabl5613 |
| Goodman LD, Cope H, Nil Z, et al. (2021) TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila. American Journal of Human Genetics |