Anthony Wynshaw-Boris - Publications

Affiliations: 
University of California, San Diego, La Jolla, CA 
Area:
Neuroscience Biology

100 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 Sweet DR, Vasudevan NT, Fan L, Booth CE, Keerthy KS, Liao X, Vinayachandran V, Takami Y, Tugal D, Sharma N, Chan ER, Zhang L, Qing Y, Gerson SL, Fu C, ... Wynshaw-Boris A, et al. Myeloid Krüppel-like factor 2 is a critical regulator of metabolic inflammation. Nature Communications. 11: 5872. PMID 33208733 DOI: 10.1038/s41467-020-19760-3  0.52
2020 Moon HM, Hippenmeyer S, Luo L, Wynshaw-Boris A. LIS1 determines cleavage plane positioning by regulating actomyosin-mediated cell membrane contractility. Elife. 9. PMID 32159512 DOI: 10.7554/eLife.51512  0.4
2019 Fang Z, Weng C, Li H, Tao R, Mai W, Liu X, Lu L, Lai S, Duan Q, Alvarez C, Arvan P, Wynshaw-Boris A, Li Y, Pei Y, Jin F, et al. Single-Cell Heterogeneity Analysis and CRISPR Screen Identify Key β-Cell-Specific Disease Genes. Cell Reports. 26: 3132-3144.e7. PMID 30865899 DOI: 10.1016/j.celrep.2019.02.043  0.4
2019 Sweet D, Vasudevan N, Fan L, Takami Y, Tugal D, Sharma N, Chan ER, Zhang L, Fu C, Wynshaw-Boris A, Sangwung P, Nayak L, Holvoet P, Matoba K, Lu Y, et al. SUN-LB019 Myeloid Krüppel-like Factor 2 is a Critical Regulator of Metabolic Inflammation Journal of the Endocrine Society. 3. DOI: 10.1210/js.2019-sun-lb019  0.52
2018 Liao X, Shen Y, Zhang R, Sugi K, Vasudevan NT, Alaiti MA, Sweet DR, Zhou L, Qing Y, Gerson SL, Fu C, Wynshaw-Boris A, Hu R, Schwartz MA, Fujioka H, et al. Distinct roles of resident and nonresident macrophages in nonischemic cardiomyopathy. Proceedings of the National Academy of Sciences of the United States of America. PMID 29712858 DOI: 10.1073/pnas.1720065115  0.52
2016 Marchetto MC, Belinson H, Tian Y, Freitas BC, Fu C, Vadodaria KC, Beltrao-Braga PC, Trujillo CA, Mendes AP, Padmanabhan K, Nunez Y, Ou J, Ghosh H, Wright R, Brennand KJ, ... ... Wynshaw-Boris A, et al. Altered proliferation and networks in neural cells derived from idiopathic autistic individuals. Molecular Psychiatry. PMID 27378147 DOI: 10.1038/mp.2016.95  0.32
2015 Sinha T, Lin L, Li D, Davis J, Evans S, Wynshaw-Boris A, Wang J. Mapping the dynamic expression of Wnt11 and the lineage contribution of Wnt11-expressing cells during early mouse development. Developmental Biology. 398: 177-92. PMID 25448697 DOI: 10.1016/j.ydbio.2014.11.005  1
2014 Kim T, Bershteyn M, Wynshaw-Boris A. Chromosome therapy. Correction of large chromosomal aberrations by inducing ring chromosomes in induced pluripotent stem cells (iPSCs). Nucleus (Austin, Tex.). 5: 391-5. PMID 25482192 DOI: 10.4161/nucl.36300  0.52
2014 Toyo-oka K, Wachi T, Hunt RF, Baraban SC, Taya S, Ramshaw H, Kaibuchi K, Schwarz QP, Lopez AF, Wynshaw-Boris A. 14-3-3ε and ζ regulate neurogenesis and differentiation of neuronal progenitor cells in the developing brain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 12168-81. PMID 25186760 DOI: 10.1523/JNEUROSCI.2513-13.2014  0.52
2014 Ohata S, Nakatani J, Herranz-Pérez V, Cheng J, Belinson H, Inubushi T, Snider WD, García-Verdugo JM, Wynshaw-Boris A, Alvarez-Buylla A. Loss of Dishevelleds disrupts planar polarity in ependymal motile cilia and results in hydrocephalus. Neuron. 83: 558-71. PMID 25043421 DOI: 10.1016/j.neuron.2014.06.022  0.52
2014 Stoner R, Chow ML, Boyle MP, Sunkin SM, Mouton PR, Roy S, Wynshaw-Boris A, Colamarino SA, Lein ES, Courchesne E. Patches of disorganization in the neocortex of children with autism. The New England Journal of Medicine. 370: 1209-19. PMID 24670167 DOI: 10.1056/NEJMoa1307491  0.52
2014 Ye M, Parente F, Li X, Perryman MB, Zelante L, Wynshaw-Boris A, Chen J, Grossfeld P. Gene-targeted deletion of OPCML and Neurotrimin in mice does not yield congenital heart defects. American Journal of Medical Genetics. Part A. 164: 966-74. PMID 24616287 DOI: 10.1002/ajmg.a.36441  0.32
2014 Bershteyn M, Hayashi Y, Desachy G, Hsiao EC, Sami S, Tsang KM, Weiss LA, Kriegstein AR, Yamanaka S, Wynshaw-Boris A. Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells. Nature. 507: 99-103. PMID 24413397 DOI: 10.1038/nature12923  0.52
2014 Moon HM, Youn YH, Pemble H, Yingling J, Wittmann T, Wynshaw-Boris A. LIS1 controls mitosis and mitotic spindle organization via the LIS1-NDEL1-dynein complex. Human Molecular Genetics. 23: 449-66. PMID 24030547 DOI: 10.1093/hmg/ddt436  0.52
2013 Young-Lin N, Shalev S, Glenn OA, Gardner M, Lee C, Wynshaw-Boris A, Gelfand AA. Teaching neuroimages: infant with glutaric aciduria type 1 presenting with infantile spasms and hypsarrhythmia. Neurology. 81: e182-3. PMID 24323445 DOI: 10.1212/01.wnl.0000437291.75075.53  0.52
2013 Moon HM, Wynshaw-Boris A. Cytoskeleton in action: lissencephaly, a neuronal migration disorder. Wiley Interdisciplinary Reviews. Developmental Biology. 2: 229-45. PMID 23495356 DOI: 10.1002/wdev.67  0.4
2013 Toba S, Tamura Y, Kumamoto K, Yamada M, Takao K, Hattori S, Miyakawa T, Kataoka Y, Azuma M, Hayasaka K, Amamoto M, Tominaga K, Wynshaw-Boris A, Wanibuchi H, Oka Y, et al. Post-natal treatment by a blood-brain-barrier permeable calpain inhibitor, SNJ1945 rescued defective function in lissencephaly. Scientific Reports. 3: 1224. PMID 23390575 DOI: 10.1038/srep01224  0.52
2013 Huang X, McGann JC, Liu BY, Hannoush RN, Lill JR, Pham V, Newton K, Kakunda M, Liu J, Yu C, Hymowitz SG, Hongo JA, Wynshaw-Boris A, Polakis P, Harland RM, et al. Phosphorylation of Dishevelled by protein kinase RIPK4 regulates Wnt signaling. Science (New York, N.Y.). 339: 1441-5. PMID 23371553 DOI: 10.1126/science.1232253  0.52
2013 Sebe JY, Bershteyn M, Hirotsune S, Wynshaw-Boris A, Baraban SC. ALLN rescues an in vitro excitatory synaptic transmission deficit in Lis1 mutant mice. Journal of Neurophysiology. 109: 429-36. PMID 23100132 DOI: 10.1152/jn.00431.2012  0.52
2012 Kosaka Y, Cieslik KA, Li L, Lezin G, Maguire CT, Saijoh Y, Toyo-oka K, Gambello MJ, Vatta M, Wynshaw-Boris A, Baldini A, Yost HJ, Brunelli L. 14-3-3ε plays a role in cardiac ventricular compaction by regulating the cardiomyocyte cell cycle. Molecular and Cellular Biology. 32: 5089-102. PMID 23071090 DOI: 10.1128/MCB.00829-12  0.52
2012 Sinha T, Wang B, Evans S, Wynshaw-Boris A, Wang J. Disheveled mediated planar cell polarity signaling is required in the second heart field lineage for outflow tract morphogenesis. Developmental Biology. 370: 135-44. PMID 22841628 DOI: 10.1016/j.ydbio.2012.07.023  1
2012 Wang J, Sinha T, Wynshaw-Boris A. Wnt signaling in mammalian development: lessons from mouse genetics. Cold Spring Harbor Perspectives in Biology. 4. PMID 22550229 DOI: 10.1101/cshperspect.a007963  1
2012 Chow ML, Pramparo T, Winn ME, Barnes CC, Li HR, Weiss L, Fan JB, Murray S, April C, Belinson H, Fu XD, Wynshaw-Boris A, Schork NJ, Courchesne E. Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages. Plos Genetics. 8: e1002592. PMID 22457638 DOI: 10.1371/journal.pgen.1002592  0.52
2012 Kawabata I, Kashiwagi Y, Obashi K, Ohkura M, Nakai J, Wynshaw-Boris A, Yanagawa Y, Okabe S. LIS1-dependent retrograde translocation of excitatory synapses in developing interneuron dendrites. Nature Communications. 3: 722. PMID 22395613 DOI: 10.1038/ncomms1736  0.52
2012 Chow ML, Winn ME, Li HR, April C, Wynshaw-Boris A, Fan JB, Fu XD, Courchesne E, Schork NJ. Preprocessing and Quality Control Strategies for Illumina DASL Assay-Based Brain Gene Expression Studies with Semi-Degraded Samples. Frontiers in Genetics. 3: 11. PMID 22375143 DOI: 10.3389/fgene.2012.00011  0.52
2011 Chow ML, Li HR, Winn ME, April C, Barnes CC, Wynshaw-Boris A, Fan JB, Fu XD, Courchesne E, Schork NJ. Genome-wide expression assay comparison across frozen and fixed postmortem brain tissue samples. Bmc Genomics. 12: 449. PMID 21906392 DOI: 10.1186/1471-2164-12-449  0.52
2011 Wynshaw-Boris A, Risch N, Motulsky A. Charles Joseph Epstein, M.D., 1933-2011, in memoriam American Journal of Human Genetics. 88: 684-688. PMID 21805720 DOI: 10.1016/j.ajhg.2011.05.016  0.52
2011 Pramparo T, Libiger O, Jain S, Li H, Youn YH, Hirotsune S, Schork NJ, Wynshaw-Boris A. Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects. Plos Genetics. 7: e1001331. PMID 21423666 DOI: 10.1371/journal.pgen.1001331  0.52
2010 Hippenmeyer S, Youn YH, Moon HM, Miyamichi K, Zong H, Wynshaw-Boris A, Luo L. Genetic mosaic dissection of Lis1 and Ndel1 in neuronal migration. Neuron. 68: 695-709. PMID 21092859 DOI: 10.1016/j.neuron.2010.09.027  0.52
2010 Wynshaw-Boris A, Pramparo T, Youn YH, Hirotsune S. Lissencephaly: mechanistic insights from animal models and potential therapeutic strategies. Seminars in Cell & Developmental Biology. 21: 823-30. PMID 20688183 DOI: 10.1016/j.semcdb.2010.07.008  0.4
2010 Pramparo T, Youn YH, Yingling J, Hirotsune S, Wynshaw-Boris A. Novel embryonic neuronal migration and proliferation defects in Dcx mutant mice are exacerbated by Lis1 reduction. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 3002-12. PMID 20181597 DOI: 10.1523/JNEUROSCI.4851-09.2010  0.52
2010 Hashimoto M, Shinohara K, Wang J, Ikeuchi S, Yoshiba S, Meno C, Nonaka S, Takada S, Hatta K, Wynshaw-Boris A, Hamada H. Planar polarization of node cells determines the rotational axis of node cilia. Nature Cell Biology. 12: 170-6. PMID 20098415 DOI: 10.1038/ncb2020  1
2010 Yamada M, Toba S, Takitoh T, Yoshida Y, Mori D, Nakamura T, Iwane AH, Yanagida T, Imai H, Yu-Lee LY, Schroer T, Wynshaw-Boris A, Hirotsune S. MNUDC is required for plus-end-directed transport of cytoplasmic dynein and dynactins by kinesin-1 Embo Journal. 29: 517-531. PMID 20019668 DOI: 10.1038/emboj.2009.378  0.52
2009 Youn YH, Pramparo T, Hirotsune S, Wynshaw-Boris A. Distinct dose-dependent cortical neuronal migration and neurite extension defects in Lis1 and Ndel1 mutant mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 15520-30. PMID 20007476 DOI: 10.1523/JNEUROSCI.4630-09.2009  0.4
2009 Yamada M, Yoshida Y, Mori D, Takitoh T, Kengaku M, Umeshima H, Takao K, Miyakawa T, Sato M, Sorimachi H, Wynshaw-Boris A, Hirotsune S. Inhibition of calpain increases LIS1 expression and partially rescues in vivo phenotypes in a mouse model of lissencephaly. Nature Medicine. 15: 1202-7. PMID 19734909 DOI: 10.1038/nm.2023  0.52
2009 Davies K, Wynshaw-Boris A. Human genetics: conceptual and practical advances in the post-genome era Current Opinion in Genetics and Development. 19: 193-195. PMID 19481439 DOI: 10.1016/j.gde.2009.05.002  0.52
2009 Youn YH, Wynshaw-Boris A. A new way of looking at neurogenesis at the apical surface. Embo Reports. 10: 457-8. PMID 19373250 DOI: 10.1038/embor.2009.71  0.4
2008 Etheridge SL, Ray S, Li S, Hamblet NS, Lijam N, Tsang M, Greer J, Kardos N, Wang J, Sussman DJ, Chen P, Wynshaw-Boris A. Murine dishevelled 3 functions in redundant pathways with dishevelled 1 and 2 in normal cardiac outflow tract, cochlea, and neural tube development. Plos Genetics. 4: e1000259. PMID 19008950 DOI: 10.1371/journal.pgen.1000259  0.52
2008 Ikeda M, Hikita T, Taya S, Uraguchi-Asaki J, Toyo-oka K, Wynshaw-Boris A, Ujike H, Inada T, Takao K, Miyakawa T, Ozaki N, Kaibuchi K, Iwata N. Identification of YWHAE, a gene encoding 14-3-3epsilon, as a possible susceptibility gene for schizophrenia. Human Molecular Genetics. 17: 3212-22. PMID 18658164 DOI: 10.1093/hmg/ddn217  0.52
2008 Pawlisz AS, Mutch C, Wynshaw-Boris A, Chenn A, Walsh CA, Feng Y. Lis1-Nde1-dependent neuronal fate control determines cerebral cortical size and lamination. Human Molecular Genetics. 17: 2441-55. PMID 18469343 DOI: 10.1093/hmg/ddn144  0.52
2008 Toyo-oka K, Mori D, Yano Y, Shiota M, Iwao H, Goto H, Inagaki M, Hiraiwa N, Muramatsu M, Wynshaw-Boris A, Yoshiki A, Hirotsune S. Protein phosphatase 4 catalytic subunit regulates Cdk1 activity and microtubule organization via NDEL1 dephosphorylation. The Journal of Cell Biology. 180: 1133-47. PMID 18347064 DOI: 10.1083/jcb.200705148  0.52
2008 Yingling J, Youn YH, Darling D, Toyo-Oka K, Pramparo T, Hirotsune S, Wynshaw-Boris A. Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division. Cell. 132: 474-86. PMID 18267077 DOI: 10.1016/j.cell.2008.01.026  0.52
2008 Zeng X, Huang H, Tamai K, Zhang X, Harada Y, Yokota C, Almeida K, Wang J, Doble B, Woodgett J, Wynshaw-Boris A, Hsieh JC, He X. Initiation of Wnt signaling: control of Wnt coreceptor Lrp6 phosphorylation/activation via frizzled, dishevelled and axin functions. Development (Cambridge, England). 135: 367-75. PMID 18077588 DOI: 10.1242/dev.013540  1
2008 Hebbar S, Guillotte AM, Mesngon MT, Zhou Q, Wynshaw-Boris A, Smith DS. Genetic enhancement of the Lis1+/- phenotype by a heterozygous mutation in the adenomatous polyposis coli gene. Developmental Neuroscience. 30: 157-70. PMID 18075263 DOI: 10.1159/000109860  0.52
2007 Zhou W, Lin L, Majumdar A, Li X, Zhang X, Liu W, Etheridge L, Shi Y, Martin J, Van de Ven W, Kaartinen V, Wynshaw-Boris A, McMahon AP, Rosenfeld MG, Evans SM. Modulation of morphogenesis by noncanonical Wnt signaling requires ATF/CREB family-mediated transcriptional activation of TGFbeta2. Nature Genetics. 39: 1225-34. PMID 17767158 DOI: 10.1038/ng2112  0.52
2007 Hedlund M, Tangvoranuntakul P, Takematsu H, Long JM, Housley GD, Kozutsumi Y, Suzuki A, Wynshaw-Boris A, Ryan AF, Gallo RL, Varki N, Varki A. N-glycolylneuraminic acid deficiency in mice: implications for human biology and evolution. Molecular and Cellular Biology. 27: 4340-6. PMID 17420276 DOI: 10.1128/MCB.00379-07  0.52
2007 Zhang G, Assadi AH, McNeil RS, Beffert U, Wynshaw-Boris A, Herz J, Clark GD, D'Arcangelo G. The Pafah1b complex interacts with the reelin receptor VLDLR. Plos One. 2: e252. PMID 17330141 DOI: 10.1371/journal.pone.0000252  0.52
2007 Mori D, Yano Y, Toyo-oka K, Yoshida N, Yamada M, Muramatsu M, Zhang D, Saya H, Toyoshima YY, Kinoshita K, Wynshaw-Boris A, Hirotsune S. NDEL1 phosphorylation by Aurora-A kinase is essential for centrosomal maturation, separation, and TACC3 recruitment. Molecular and Cellular Biology. 27: 352-67. PMID 17060449 DOI: 10.1128/MCB.00878-06  0.52
2006 Long JM, LaPorte P, Merscher S, Funke B, Saint-Jore B, Puech A, Kucherlapati R, Morrow BE, Skoultchi AI, Wynshaw-Boris A. Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome. Neurogenetics. 7: 247-57. PMID 16900388 DOI: 10.1007/s10048-006-0054-0  0.52
2006 Erker L, Schubert R, Elchuri S, Huang TT, Tarin D, Mueller K, Zielen S, Epstein CJ, Wynshaw-Boris A. Effect of the reduction of superoxide dismutase 1 and 2 or treatment with alpha-tocopherol on tumorigenesis in Atm-deficient mice. Free Radical Biology & Medicine. 41: 590-600. PMID 16863992 DOI: 10.1016/j.freeradbiomed.2006.04.032  0.52
2006 Toyo-oka K, Bowen TJ, Hirotsune S, Li Z, Jain S, Ota S, Escoubet-Lozach L, Lozach LE, Garcia-Bassets I, Bassett IG, Lozach J, Rosenfeld MG, Glass CK, Eisenman R, Ren B, ... ... Wynshaw-Boris A, et al. Mnt-deficient mammary glands exhibit impaired involution and tumors with characteristics of myc overexpression. Cancer Research. 66: 5565-73. PMID 16740691 DOI: 10.1158/0008-5472.CAN-05-2683  0.52
2006 Greer JM, Wynshaw-Boris A. Pten and the brain: sizing up social interaction. Neuron. 50: 343-5. PMID 16675386 DOI: 10.1016/j.neuron.2006.04.021  0.52
2006 Nasrallah IM, McManus MF, Pancoast MM, Wynshaw-Boris A, Golden JA. Analysis of non-radial interneuron migration dynamics and its disruption in Lis1+/- mice. The Journal of Comparative Neurology. 496: 847-58. PMID 16628622 DOI: 10.1002/cne.20966  0.52
2006 Wang J, Hamblet NS, Mark S, Dickinson ME, Brinkman BC, Segil N, Fraser SE, Chen P, Wallingford JB, Wynshaw-Boris A. Dishevelled genes mediate a conserved mammalian PCP pathway to regulate convergent extension during neurulation. Development (Cambridge, England). 133: 1767-78. PMID 16571627 DOI: 10.1242/dev.02347  0.44
2006 Kholmanskikh SS, Koeller HB, Wynshaw-Boris A, Gomez T, Letourneau PC, Ross ME. Calcium-dependent interaction of Lis1 with IQGAP1 and Cdc42 promotes neuronal motility. Nature Neuroscience. 9: 50-7. PMID 16369480 DOI: 10.1038/nn1619  0.52
2005 Bowen TJ, Yakushiji H, Montagna C, Jain S, Ried T, Wynshaw-Boris A. Atm heterozygosity cooperates with loss of Brca1 to increase the severity of mammary gland cancer and reduce ductal branching. Cancer Research. 65: 8736-46. PMID 16204043 DOI: 10.1158/0008-5472.CAN-05-1598  0.52
2005 Toyo-Oka K, Sasaki S, Yano Y, Mori D, Kobayashi T, Toyoshima YY, Tokuoka SM, Ishii S, Shimizu T, Muramatsu M, Hiraiwa N, Yoshiki A, Wynshaw-Boris A, Hirotsune S. Recruitment of katanin p60 by phosphorylated NDEL1, an LIS1 interacting protein, is essential for mitotic cell division and neuronal migration. Human Molecular Genetics. 14: 3113-28. PMID 16203747 DOI: 10.1093/hmg/ddi339  0.52
2005 Darling DL, Yingling J, Wynshaw-Boris A. Role of 14-3-3 proteins in eukaryotic signaling and development. Current Topics in Developmental Biology. 68: 281-315. PMID 16125003 DOI: 10.1016/S0070-2153(05)68010-6  0.52
2005 Wang J, Mark S, Zhang X, Qian D, Yoo SJ, Radde-Gallwitz K, Zhang Y, Lin X, Collazo A, Wynshaw-Boris A, Chen P. Regulation of polarized extension and planar cell polarity in the cochlea by the vertebrate PCP pathway. Nature Genetics. 37: 980-5. PMID 16116426 DOI: 10.1038/ng1622  1
2005 Sasaki S, Mori D, Toyo-oka K, Chen A, Garrett-Beal L, Muramatsu M, Miyagawa S, Hiraiwa N, Yoshiki A, Wynshaw-Boris A, Hirotsune S. Complete loss of Ndel1 results in neuronal migration defects and early embryonic lethality. Molecular and Cellular Biology. 25: 7812-27. PMID 16107726 DOI: 10.1128/MCB.25.17.7812-7827.2005  0.52
2005 Winrow CJ, Pankratz DG, Vibat CR, Bowen TJ, Callahan MA, Warren AJ, Hilbush BS, Wynshaw-Boris A, Hasel KW, Weaver Z, Lockhart DJ, Barlow C. Aberrant recombination involving the granzyme locus occurs in Atm-/- T-cell lymphomas. Human Molecular Genetics. 14: 2671-84. PMID 16087685 DOI: 10.1093/hmg/ddi301  0.52
2005 Arkan MC, Hevener AL, Greten FR, Maeda S, Li ZW, Long JM, Wynshaw-Boris A, Poli G, Olefsky J, Karin M. IKK-beta links inflammation to obesity-induced insulin resistance. Nature Medicine. 11: 191-8. PMID 15685170 DOI: 10.1038/nm1185  0.52
2005 Rosso SB, Sussman D, Wynshaw-Boris A, Salinas PC. Wnt signaling through Dishevelled, Rac and JNK regulates dendritic development. Nature Neuroscience. 8: 34-42. PMID 15608632 DOI: 10.1038/nn1374  0.52
2005 Zhou X, Long JM, Geyer MA, Masliah E, Kelsoe JR, Wynshaw-Boris A, Chien KR. Reduced expression of the Sp4 gene in mice causes deficits in sensorimotor gating and memory associated with hippocampal vacuolization. Molecular Psychiatry. 10: 393-406. PMID 15558077 DOI: 10.1038/sj.mp.4001621  0.52
2004 Lumsden JM, McCarty T, Petiniot LK, Shen R, Barlow C, Wynn TA, Morse HC, Gearhart PJ, Wynshaw-Boris A, Max EE, Hodes RJ. Immunoglobulin class switch recombination is impaired in Atm-deficient mice. The Journal of Experimental Medicine. 200: 1111-21. PMID 15504820 DOI: 10.1084/jem.20041074  0.52
2004 Wang J, Wynshaw-Boris A. The canonical Wnt pathway in early mammalian embryogenesis and stem cell maintenance/differentiation. Current Opinion in Genetics & Development. 14: 533-9. PMID 15380245 DOI: 10.1016/j.gde.2004.07.013  1
2004 McManus MF, Nasrallah IM, Pancoast MM, Wynshaw-Boris A, Golden JA. Lis1 is necessary for normal non-radial migration of inhibitory interneurons. The American Journal of Pathology. 165: 775-84. PMID 15331402 DOI: 10.1016/S0002-9440(10)63340-8  0.52
2004 Tanaka T, Serneo FF, Higgins C, Gambello MJ, Wynshaw-Boris A, Gleeson JG. Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration. The Journal of Cell Biology. 165: 709-21. PMID 15173193 DOI: 10.1083/jcb.200309025  0.52
2004 Angata K, Long JM, Bukalo O, Lee W, Dityatev A, Wynshaw-Boris A, Schachner M, Fukuda M, Marth JD. Sialyltransferase ST8Sia-II assembles a subset of polysialic acid that directs hippocampal axonal targeting and promotes fear behavior. The Journal of Biological Chemistry. 279: 32603-13. PMID 15140899 DOI: 10.1074/jbc.M403429200  0.52
2004 Toyo-oka K, Hirotsune S, Gambello MJ, Zhou ZQ, Olson L, Rosenfeld MG, Eisenman R, Hurlin P, Wynshaw-Boris A. Loss of the Max-interacting protein Mnt in mice results in decreased viability, defective embryonic growth and craniofacial defects: relevance to Miller-Dieker syndrome. Human Molecular Genetics. 13: 1057-67. PMID 15028671 DOI: 10.1093/hmg/ddh116  0.52
2004 Hurlin PJ, Zhou ZQ, Toyo-Oka K, Ota S, Walker WL, Hirotsune S, Wynshaw-Boris A. Evidence of mnt-myc antagonism revealed by mnt gene deletion. Cell Cycle (Georgetown, Tex.). 3: 97-9. PMID 14712062  0.52
2003 Assadi AH, Zhang G, Beffert U, McNeil RS, Renfro AL, Niu S, Quattrocchi CC, Antalffy BA, Sheldon M, Armstrong DD, Wynshaw-Boris A, Herz J, D'Arcangelo G, Clark GD. Interaction of reelin signaling and Lis1 in brain development. Nature Genetics. 35: 270-6. PMID 14578885 DOI: 10.1038/ng1257  0.52
2003 Kholmanskikh SS, Dobrin JS, Wynshaw-Boris A, Letourneau PC, Ross ME. Disregulated RhoGTPases and actin cytoskeleton contribute to the migration defect in Lis1-deficient neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 8673-81. PMID 14507966  0.52
2003 Hurlin PJ, Zhou ZQ, Toyo-oka K, Ota S, Walker WL, Hirotsune S, Wynshaw-Boris A. Deletion of Mnt leads to disrupted cell cycle control and tumorigenesis. The Embo Journal. 22: 4584-96. PMID 12970171 DOI: 10.1093/emboj/cdg442  0.52
2003 Yingling J, Toyo-Oka K, Wynshaw-Boris A. Miller-Dieker syndrome: analysis of a human contiguous gene syndrome in the mouse. American Journal of Human Genetics. 73: 475-88. PMID 12905154 DOI: 10.1086/378096  0.52
2003 Schriml LM, Hill DP, Blake JA, Bono H, Wynshaw-Boris A, Pavan WJ, Ring BZ, Beisel K, Setou M, Okazaki Y. Human disease genes and their cloned mouse orthologs: exploration of the FANTOM2 cDNA sequence data set. Genome Research. 13: 1496-500. PMID 12819148 DOI: 10.1101/gr.979503  0.52
2003 Toyo-oka K, Shionoya A, Gambello MJ, Cardoso C, Leventer R, Ward HL, Ayala R, Tsai LH, Dobyns W, Ledbetter D, Hirotsune S, Wynshaw-Boris A. 14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome. Nature Genetics. 34: 274-85. PMID 12796778 DOI: 10.1038/ng1169  0.52
2003 Scheel JR, Garrett LJ, Allen DM, Carter TA, Randolph-Moore L, Gambello MJ, Gage FH, Wynshaw-Boris A, Barlow C. An inbred 129SvEv GFPCre transgenic mouse that deletes loxP-flanked genes in all tissues. Nucleic Acids Research. 31: e57. PMID 12736323 DOI: 10.1093/NAR/GNG057  0.52
2003 Hirotsune S, Yoshida N, Chen A, Garrett L, Sugiyama F, Takahashi S, Yagami K, Wynshaw-Boris A, Yoshiki A. An expressed pseudogene regulates the messenger-RNA stability of its homologous coding gene. Nature. 423: 91-6. PMID 12721631 DOI: 10.1038/nature01535  0.44
2003 Baek SH, Kioussi C, Briata P, Wang D, Nguyen HD, Ohgi KA, Glass CK, Wynshaw-Boris A, Rose DW, Rosenfeld MG. Regulated subset of G1 growth-control genes in response to derepression by the Wnt pathway. Proceedings of the National Academy of Sciences of the United States of America. 100: 3245-50. PMID 12629224 DOI: 10.1073/pnas.0330217100  0.52
2003 Gambello MJ, Darling DL, Yingling J, Tanaka T, Gleeson JG, Wynshaw-Boris A. Multiple dose-dependent effects of Lis1 on cerebral cortical development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 1719-29. PMID 12629176 DOI: 10.1523/JNEUROSCI.23-05-01719.2003  0.52
2003 Cardoso C, Leventer RJ, Ward HL, Toyo-oka K, Chung J, Gross A, Martin CL, Allanson J, Pilz DT, Olney AH, Mutchinick OM, Hirotsune S, Wynshaw-Boris A, Dobyns WB, Ledbetter DH. Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3 American Journal of Human Genetics. 72: 918-930. PMID 12621583 DOI: 10.1086/374320  0.52
2002 Kioussi C, Briata P, Baek SH, Rose DW, Hamblet NS, Herman T, Ohgi KA, Lin C, Gleiberman A, Wang J, Brault V, Ruiz-Lozano P, Nguyen HD, Kemler R, Glass CK, ... Wynshaw-Boris A, et al. Identification of a Wnt/Dvl/beta-Catenin --> Pitx2 pathway mediating cell-type-specific proliferation during development. Cell. 111: 673-85. PMID 12464179 DOI: 10.1016/S0092-8674(02)01084-X  0.52
2002 Hamblet NS, Lijam N, Ruiz-Lozano P, Wang J, Yang Y, Luo Z, Mei L, Chien KR, Sussman DJ, Wynshaw-Boris A. Dishevelled 2 is essential for cardiac outflow tract development, somite segmentation and neural tube closure. Development (Cambridge, England). 129: 5827-38. PMID 12421720 DOI: 10.1242/dev.00164  1
2002 Corbo JC, Deuel TA, Long JM, LaPorte P, Tsai E, Wynshaw-Boris A, Walsh CA. Doublecortin is required in mice for lamination of the hippocampus but not the neocortex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 7548-57. PMID 12196578  0.52
2002 Luo ZG, Wang Q, Zhou JZ, Wang J, Luo Z, Liu M, He X, Wynshaw-Boris A, Xiong WC, Lu B, Mei L. Regulation of AChR clustering by Dishevelled interacting with MuSK and PAK1. Neuron. 35: 489-505. PMID 12165471  1
2002 Gupta A, Tsai LH, Wynshaw-Boris A. Life is a journey: a genetic look at neocortical development. Nature Reviews. Genetics. 3: 342-55. PMID 11988760 DOI: 10.1038/nrg799  0.4
2002 Roberts C, Sutherland HF, Farmer H, Kimber W, Halford S, Carey A, Brickman JM, Wynshaw-Boris A, Scambler PJ. Targeted mutagenesis of the Hira gene results in gastrulation defects and patterning abnormalities of mesoendodermal derivatives prior to early embryonic lethality. Molecular and Cellular Biology. 22: 2318-28. PMID 11884616 DOI: 10.1128/MCB.22.7.2318-2328.2002  0.52
2001 Resor L, Bowen TJ, Wynshaw-Boris A. Unraveling human cancer in the mouse: recent refinements to modeling and analysis. Human Molecular Genetics. 10: 669-75. PMID 11257098 DOI: 10.1093/hmg/10.7.669  0.72
2001 Merscher S, Funke B, Epstein JA, Heyer J, Puech A, Lu MM, Xavier RJ, Demay MB, Russell RG, Factor S, Tokooya K, Jore BS, Lopez M, Pandita RK, Lia M, ... ... Wynshaw-Boris A, et al. TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome. Cell. 104: 619-29. PMID 11239417 DOI: 10.1016/S0092-8674(01)00247-1  0.52
2000 Kaneshige M, Kaneshige K, Zhu X, Dace A, Garrett L, Carter TA, Kazlauskaite R, Pankratz DG, Wynshaw-Boris A, Refetoff S, Weintraub B, Willingham MC, Barlow C, Cheng S. Mice with a targeted mutation in the thyroid hormone beta receptor gene exhibit impaired growth and resistance to thyroid hormone. Proceedings of the National Academy of Sciences of the United States of America. 97: 13209-14. PMID 11069286 DOI: 10.1073/pnas.230285997  0.52
2000 Smith DS, Niethammer M, Ayala R, Zhou Y, Gambello MJ, Wynshaw-Boris A, Tsai LH. Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1. Nature Cell Biology. 2: 767-75. PMID 11056530 DOI: 10.1038/35041000  0.52
1999 Paylor R, Hirotsune S, Gambello MJ, Yuva-Paylor L, Crawley JN, Wynshaw-Boris A. Impaired learning and motor behavior in heterozygous Pafah1b1 (Lis1) mutant mice. Learning & Memory (Cold Spring Harbor, N.Y.). 6: 521-37. PMID 10541472 DOI: 10.1101/lm.6.5.521  0.4
1998 Ding J, Yang L, Yan YT, Chen A, Desai N, Wynshaw-Boris A, Shen MM. Cripto is required for correct orientation of the anterior-posterior axis in the mouse embryo. Nature. 395: 702-7. PMID 9790191 DOI: 10.1038/27215  0.52
1997 Lijam N, Paylor R, McDonald MP, Crawley JN, Deng CX, Herrup K, Stevens KE, Maccaferri G, McBain CJ, Sussman DJ, Wynshaw-Boris A. Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1. Cell. 90: 895-905. PMID 9298901 DOI: 10.1016/S0092-8674(00)80354-2  0.52
1997 Crawley JN, Belknap JK, Collins A, Crabbe JC, Frankel W, Henderson N, Hitzemann RJ, Maxson SC, Miner LL, Silva AJ, Wehner JM, Wynshaw-Boris A, Paylor R. Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies. Psychopharmacology. 132: 107-24. PMID 9266608 DOI: 10.1007/s002130050327  0.52
1997 Baskaran R, Wood LD, Whitaker LL, Canman CE, Morgan SE, Xu Y, Barlow C, Baltimore D, Wynshaw-Boris A, Kastan MB, Wang JY. Ataxia telangiectasia mutant protein activates c-Abl tyrosine kinase in response to ionizing radiation. Nature. 387: 516-9. PMID 9168116 DOI: 10.1038/387516a0  0.52
1997 Wang Q, Stacy T, Miller JD, Lewis AF, Gu TL, Huang X, Bushweller JH, Bories JC, Alt FW, Ryan G, Liu PP, Wynshaw-Boris A, Binder M, Marín-Padilla M, Sharpe AH, et al. The CBFbeta subunit is essential for CBFalpha2 (AML1) function in vivo. Cell. 87: 697-708. PMID 8929538 DOI: 10.1016/S0092-8674(00)81389-6  0.44
1994 Oettgen HC, Martin TR, Wynshaw-Boris A, Deng C, Drazen JM, Leder P. Active anaphylaxis in IgE-deficient mice. Nature. 370: 367-70. PMID 8047141 DOI: 10.1038/370367a0  0.52
1992 Vogt TF, Jackson-Grusby L, Wynshaw-Boris AJ, Chan DC, Leder P. The same genomic region is disrupted in two transgene-induced limb deformity alleles. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 3: 431-7. PMID 1643305 DOI: 10.1007/BF00356152  0.52
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