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David B. Melville, Ph.D. - Publications

Affiliations: 
2012 Vanderbilt University, Nashville, TN 
Area:
Cell Biology, Human Development, Genetics
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19 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
2020 Melville DB, Studer S, Schekman R. Small sequence variations between two mammalian paralogs of the small GTPase SAR1 underlie functional differences in coat protein complex II assembly. The Journal of Biological Chemistry. PMID 32358066 DOI: 10.1074/Jbc.Ra120.012964  0.351
2020 Unlu G, Qi X, Gamazon ER, Melville DB, Patel N, Rushing AR, Hashem M, Al-Faifi A, Chen R, Li B, Cox NJ, Alkuraya FS, Knapik EW. Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies. Nature Medicine. 26: 98-109. PMID 31932796 DOI: 10.1038/S41591-019-0705-Y  0.662
2018 Jeong YT, Simoneschi D, Keegan S, Melville D, Adler NS, Saraf A, Florens L, Washburn MP, Cavasotto CN, Fenyö D, Cuervo AM, Rossi M, Pagano M. The ULK1-FBXW5-SEC23B nexus controls autophagy. Elife. 7. PMID 30596474 DOI: 10.7554/Elife.42253  0.363
2018 Melville D, Gorur A, Schekman R. Fatty-acid binding protein 5 modulates the SAR1 GTPase cycle and enhances budding of large COPII cargoes. Molecular Biology of the Cell. 30: 387-399. PMID 30485159 DOI: 10.1091/Mbc.E18-09-0548  0.37
2017 Raote I, Ortega Bellido M, Pirozzi M, Zhang C, Melville D, Parashuraman S, Zimmermann T, Malhotra V. TANGO1 assembles into rings around COPII coats at ER exit sites. The Journal of Cell Biology. PMID 28280121 DOI: 10.1083/Jcb.201608080  0.327
2015 Levic DS, Minkel JR, Wang WD, Rybski WM, Melville DB, Knapik EW. Animal model of Sar1b deficiency presents lipid absorption deficits similar to Anderson disease. Journal of Molecular Medicine (Berlin, Germany). 93: 165-76. PMID 25559265 DOI: 10.1007/S00109-014-1247-X  0.7
2015 Levic DS, Minkel JR, Wang WD, Rybski WM, Melville DB, Knapik EW. Animal model of Sar1b deficiency presents lipid absorption deficits similar to Anderson disease Journal of Molecular Medicine. 93: 165-176. DOI: 10.1007/s00109-014-1247-x  0.621
2014 Niu X, Hong J, Zheng X, Melville DB, Knapik EW, Meng A, Peng J. The nuclear pore complex function of sec13 protein is required for cell survival during retinal development Journal of Biological Chemistry. 289: 11971-11985. PMID 24627485 DOI: 10.1074/Jbc.M114.547190  0.678
2014 Unlu G, Levic DS, Melville DB, Knapik EW. Trafficking mechanisms of extracellular matrix macromolecules: Insights from vertebrate development and human diseases International Journal of Biochemistry and Cell Biology. 47: 57-67. PMID 24333299 DOI: 10.1016/J.Biocel.2013.11.005  0.699
2014 Venkateswaran A, Sekhar KR, Levic DS, Melville DB, Clark TA, Rybski WM, Walsh AJ, Skala MC, Crooks PA, Knapik EW, Freeman ML. The NADH oxidase ENOX1, a critical mediator of endothelial cell radiosensitization, is crucial for vascular development. Cancer Research. 74: 38-43. PMID 24247717 DOI: 10.1158/0008-5472.Can-13-1981  0.667
2013 Ge L, Melville D, Zhang M, Schekman R. The ER-Golgi intermediate compartment is a key membrane source for the LC3 lipidation step of autophagosome biogenesis. Elife. 2: e00947. PMID 23930225 DOI: 10.7554/Elife.00947  0.34
2013 Müller II, Melville DB, Tanwar V, Rybski WM, Mukherjee A, Shoemaker MB, Wang WD, Schoenhard JA, Roden DM, Darbar D, Knapik EW, Hatzopoulos AK. Functional modeling in zebrafish demonstrates that the atrial-fibrillation- associated gene GREM2 regulates cardiac laterality, cardiomyocyte differentiation and atrial rhythm Dmm Disease Models and Mechanisms. 6: 332-341. PMID 23223679 DOI: 10.1242/Dmm.010488  0.656
2013 Venkateswaran A, Levic DS, Melville DB, Sekhar KR, Walsh AJ, Skala MC, Crooks PA, Knapik EW, Freeman ML. Abstract 384: NADH oxidase, Enox1 activity, is required for vasculogenesis in Zebrafish. Cancer Research. 73: 384-384. DOI: 10.1158/1538-7445.Am2013-384  0.396
2011 Wang WD, Melville DB, Montero-Balaguer M, Hatzopoulos AK, Knapik EW. Tfap2a and Foxd3 regulate early steps in the development of the neural crest progenitor population Developmental Biology. 360: 173-185. PMID 21963426 DOI: 10.1016/J.Ydbio.2011.09.019  0.64
2011 Bradley KM, Breyer JP, Melville DB, Broman KW, Knapik EW, Smith JR. An SNP-Based Linkage Map for Zebrafish Reveals Sex Determination Loci. G3 (Bethesda, Md.). 1: 3-9. PMID 21949597 DOI: 10.1534/G3.111.000190  0.645
2011 Melville DB, Montero-Balaguer M, Levic DS, Bradley K, Smith JR, Hatzopoulos AK, Knapik EW. The feelgood mutation in zebrafish dysregulates COPII-dependent secretion of select extracellular matrix proteins in skeletal morphogenesis. Disease Models & Mechanisms. 4: 763-76. PMID 21729877 DOI: 10.1242/Dmm.007625  0.709
2011 Liu D, Wang WD, Melville DB, Cha YI, Yin Z, Issaeva N, Knapik EW, Yarbrough WG. Tumor suppressor Lzap regulates cell cycle progression, doming, and zebrafish epiboly Developmental Dynamics. 240: 1613-1625. PMID 21523853 DOI: 10.1002/Dvdy.22644  0.666
2011 Melville DB, Knapik EW. Traffic jams in fish bones: ER-to-Golgi protein transport during zebrafish development Cell Adhesion and Migration. 5: 114-118. PMID 21178403 DOI: 10.4161/Cam.5.2.14377  0.701
2010 Sarmah S, Barrallo-Gimeno A, Melville DB, Topczewski J, Solnica-Krezel L, Knapik EW. Sec24D-dependent transport of extracellular matrix proteins is required for zebrafish skeletal morphogenesis. Plos One. 5: e10367. PMID 20442775 DOI: 10.1371/Journal.Pone.0010367  0.699
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