Konstantinos (Kostas) Zarbalis - Publications

Affiliations: 
University of California, San Francisco, San Francisco, CA 

22 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 Harlan De Crescenzo A, Panoutsopoulos AA, Tat L, Schaaf Z, Racherla S, Henderson L, Leung KY, Greene NDE, Green R, Zarbalis KS. Deficient or Excess Folic Acid Supply During Pregnancy Alter Cortical Neurodevelopment in Mouse Offspring. Cerebral Cortex (New York, N.Y. : 1991). PMID 32995858 DOI: 10.1093/cercor/bhaa248  0.663
2020 Panoutsopoulos AA, De Crescenzo AH, Lee A, Lu AM, Ross AP, Borodinsky LN, Marcucio R, Trainor PA, Zarbalis KS. Pak1ip1 Loss-of-Function Leads to Cell Cycle Arrest, Loss of Neural Crest Cells, and Craniofacial Abnormalities. Frontiers in Cell and Developmental Biology. 8: 510063. PMID 32984348 DOI: 10.3389/Fcell.2020.510063  0.33
2019 Le Duc D, Giulivi C, Hiatt SM, Napoli E, Panoutsopoulos A, Harlan De Crescenzo A, Kotzaeridou U, Syrbe S, Anagnostou E, Azage M, Bend R, Begtrup A, Brown NJ, Büttner B, Cho MT, ... ... Zarbalis KS, et al. Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size. Brain : a Journal of Neurology. PMID 31327001 DOI: 10.1093/Brain/Awz198  0.671
2018 Napoli E, Song G, Panoutsopoulos A, Riyadh MA, Kaushik G, Halmai J, Levenson R, Zarbalis KS, Giulivi C. Beyond autophagy: a novel role for autism-linked Wdfy3 in brain mitophagy. Scientific Reports. 8: 11348. PMID 30054502 DOI: 10.1038/s41598-018-29421-7  0.417
2017 Napoli E, Liu S, Marsilio I, Zarbalis K, Giulivi C. Lipid-based DNA/siRNA transfection agents disrupt neuronal bioenergetics and mitophagy. The Biochemical Journal. PMID 29025974 DOI: 10.1042/BCJ20170632  0.304
2017 Gompers AL, Su-Feher L, Ellegood J, Copping NA, Riyadh MA, Stradleigh TW, Pride MC, Schaffler MD, Wade AA, Catta-Preta R, Zdilar I, Louis S, Kaushik G, Mannion BJ, Plajzer-Frick I, ... ... Zarbalis KS, et al. Germline Chd8 haploinsufficiency alters brain development in mouse. Nature Neuroscience. PMID 28671691 DOI: 10.1038/Nn.4592  0.336
2016 Kaushik G, Zarbalis KS. Prenatal Neurogenesis in Autism Spectrum Disorders. Frontiers in Chemistry. 4: 12. PMID 27014681 DOI: 10.3389/fchem.2016.00012  0.341
2015 Sohn J, Orosco L, Guo F, Chung SH, Bannerman P, Mills Ko E, Zarbalis K, Deng W, Pleasure D. The subventricular zone continues to generate corpus callosum and rostral migratory stream astroglia in normal adult mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 3756-63. PMID 25740506 DOI: 10.1523/Jneurosci.3454-14.2015  0.346
2014 Orosco LA, Ross AP, Cates SL, Scott SE, Wu D, Sohn J, Pleasure D, Pleasure SJ, Adamopoulos IE, Zarbalis KS. Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology. Nature Communications. 5: 4692. PMID 25198012 DOI: 10.1038/Ncomms5692  0.669
2014 Choe Y, Zarbalis KS, Pleasure SJ. Neural crest-derived mesenchymal cells require Wnt signaling for their development and drive invagination of the telencephalic midline. Plos One. 9: e86025. PMID 24516524 DOI: 10.1371/journal.pone.0086025  0.632
2013 Ross AP, Mansilla MA, Choe Y, Helminski S, Sturm R, Maute RL, May SR, Hozyasz KK, Wójcicki P, Mostowska A, Davidson B, Adamopoulos IE, Pleasure SJ, Murray JC, Zarbalis KS. A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting. Plos One. 8: e69333. PMID 23935987 DOI: 10.1371/journal.pone.0069333  0.677
2012 Sohn J, Selvaraj V, Wakayama K, Orosco L, Lee E, Crawford SE, Guo F, Lang J, Horiuchi M, Zarbalis K, Itoh T, Deng W, Pleasure D. PEDF is a novel oligodendrogenic morphogen acting on the adult SVZ and corpus callosum. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 12152-64. PMID 22933798 DOI: 10.1523/Jneurosci.0628-12.2012  0.333
2012 Zarbalis K, Choe Y, Siegenthaler JA, Orosco LA, Pleasure SJ. Meningeal defects alter the tangential migration of cortical interneurons in Foxc1hith/hith mice. Neural Development. 7: 2. PMID 22248045 DOI: 10.1186/1749-8104-7-2  0.765
2010 Endoh-Yamagami S, Karkar KM, May SR, Cobos I, Thwin MT, Long JE, Ashique AM, Zarbalis K, Rubenstein JL, Peterson AS. A mutation in the pericentrin gene causes abnormal interneuron migration to the olfactory bulb in mice. Developmental Biology. 340: 41-53. PMID 20096683 DOI: 10.1016/J.Ydbio.2010.01.017  0.557
2009 Siegenthaler JA, Ashique AM, Zarbalis K, Patterson KP, Hecht JH, Kane MA, Folias AE, Choe Y, May SR, Kume T, Napoli JL, Peterson AS, Pleasure SJ. Retinoic acid from the meninges regulates cortical neuron generation. Cell. 139: 597-609. PMID 19879845 DOI: 10.1016/j.cell.2009.10.004  0.75
2009 Zarbalis K, Choe Y, Maute RL, Peterson AS, Pleasure SJ. Manta ray a novel ENU mutant with brain and craniofacial defects Developmental Biology. 331: 494-495. DOI: 10.1016/j.ydbio.2009.05.407  0.669
2008 Zarbalis K, Choe Y, Siegenthaler J, Hecht J, Pleasure S. [P1.37]: Tangential migration defects in a mouse mutant for foxc1 recovered in a genetic screen International Journal of Developmental Neuroscience. 26: 853-854. DOI: 10.1016/j.ijdevneu.2008.09.087  0.676
2007 Zarbalis K, Siegenthaler JA, Choe Y, May SR, Peterson AS, Pleasure SJ. Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development. Proceedings of the National Academy of Sciences of the United States of America. 104: 14002-7. PMID 17715063 DOI: 10.1073/pnas.0702618104  0.791
2007 Dow LE, Kauffman JS, Caddy J, Zarbalis K, Peterson AS, Jane SM, Russell SM, Humbert PO. The tumour-suppressor Scribble dictates cell polarity during directed epithelial migration: regulation of Rho GTPase recruitment to the leading edge. Oncogene. 26: 2272-82. PMID 17043654 DOI: 10.1038/sj.onc.1210016  0.427
2005 May SR, Ashique AM, Karlen M, Wang B, Shen Y, Zarbalis K, Reiter J, Ericson J, Peterson AS. Loss of the retrograde motor for IFT disrupts localization of Smo to cilia and prevents the expression of both activator and repressor functions of Gli. Developmental Biology. 287: 378-89. PMID 16229832 DOI: 10.1016/J.Ydbio.2005.08.050  0.742
2004 Zarbalis K, May SR, Shen Y, Ekker M, Rubenstein JL, Peterson AS. A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development. Plos Biology. 2: E219. PMID 15314648 DOI: 10.1371/Journal.Pbio.0020219  0.768
2002 Uziel D, Mühlfriedel S, Zarbalis K, Wurst W, Levitt P, Bolz J. Miswiring of limbic thalamocortical projections in the absence of ephrin-A5. The Journal of Neuroscience. 22: 9352-9357. DOI: 10.1523/Jneurosci.22-21-09352.2002  0.331
Show low-probability matches.