| Year |
Citation |
Score |
| 2020 |
Ngo J, Hashimoto M, Hamada H, Wynshaw-Boris A. Deletion of the Dishevelled family of genes disrupts anterior-posterior axis specification and selectively prevents mesoderm differentiation. Developmental Biology. PMID 32579954 DOI: 10.1016/J.Ydbio.2020.05.010 |
0.414 |
|
| 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 |
0.399 |
|
| 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 |
0.324 |
|
| 2018 |
Zhang M, Ngo J, Pirozzi F, Sun YP, Wynshaw-Boris A. Highly efficient methods to obtain homogeneous dorsal neural progenitor cells from human and mouse embryonic stem cells and induced pluripotent stem cells. Stem Cell Research & Therapy. 9: 67. PMID 29544541 DOI: 10.1186/S13287-018-0812-6 |
0.323 |
|
| 2017 |
Adegbola A, Bury LA, Fu C, Zhang M, Wynshaw-Boris A. Concise Review: Induced Pluripotent Stem Cell Models for Neuropsychiatric Diseases. Stem Cells Translational Medicine. PMID 29027744 DOI: 10.1002/Sctm.17-0150 |
0.312 |
|
| 2017 |
Bershteyn M, Nowakowski TJ, Pollen AA, Di Lullo E, Nene A, Wynshaw-Boris A, Kriegstein AR. Human iPSC-Derived Cerebral Organoids Model Cellular Features of Lissencephaly and Reveal Prolonged Mitosis of Outer Radial Glia. Cell Stem Cell. PMID 28111201 DOI: 10.1016/J.Stem.2016.12.007 |
0.367 |
|
| 2016 |
Belinson H, Savage AK, Fadrosh D, Kuo YM, Lin D, Valladares R, Nusse Y, Wynshaw-Boris A, Lynch SV, Locksley RM, Klein OD. Dual epithelial and immune cell function of Dvl1 regulates gut microbiota composition and intestinal homeostasis. Jci Insight. 1. PMID 27525310 DOI: 10.1172/Jci.Insight.85395 |
0.351 |
|
| 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 |
0.345 |
|
| 2016 |
Saito A, Taniguchi Y, Kim SH, Selvakumar B, Perez G, Ballinger MD, Zhu X, Sabra J, Jallow M, Yan P, Ito K, Rajendran S, Hirotsune S, Wynshaw-Boris A, Snyder SH, et al. Developmental Alcohol Exposure Impairs Activity-Dependent S-Nitrosylation of NDEL1 for Neuronal Maturation. Cerebral Cortex (New York, N.Y. : 1991). PMID 27371763 DOI: 10.1093/Cercor/Bhw201 |
0.336 |
|
| 2016 |
Belinson H, Nakatani J, Babineau BA, Birnbaum RY, Ellegood J, Bershteyn M, McEvilly RJ, Long JM, Willert K, Klein OD, Ahituv N, Lerch JP, Rosenfeld MG, Wynshaw-Boris A. Prenatal β-catenin/Brn2/Tbr2 transcriptional cascade regulates adult social and stereotypic behaviors. Molecular Psychiatry. PMID 26830142 DOI: 10.1038/Mp.2015.207 |
0.332 |
|
| 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 |
0.758 |
|
| 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 |
0.403 |
|
| 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 |
0.385 |
|
| 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 |
0.341 |
|
| 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 |
0.324 |
|
| 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 |
0.714 |
|
| 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 |
0.361 |
|
| 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 |
0.317 |
|
| 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 |
0.352 |
|
| 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 |
0.349 |
|
| 2012 |
Wynshaw-Boris A. Dishevelled: in vivo roles of a multifunctional gene family during development. Current Topics in Developmental Biology. 101: 213-35. PMID 23140631 DOI: 10.1016/B978-0-12-394592-1.00007-7 |
0.423 |
|
| 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 |
0.351 |
|
| 2012 |
Takitoh T, Kumamoto K, Wang CC, Sato M, Toba S, Wynshaw-Boris A, Hirotsune S. Activation of Aurora-A is essential for neuronal migration via modulation of microtubule organization. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 11050-66. PMID 22875938 DOI: 10.1523/Jneurosci.5664-11.2012 |
0.325 |
|
| 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 |
0.776 |
|
| 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 |
0.757 |
|
| 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 |
0.352 |
|
| 2012 |
Cheah PS, Ramshaw HS, Thomas PQ, Toyo-Oka K, Xu X, Martin S, Coyle P, Guthridge MA, Stomski F, van den Buuse M, Wynshaw-Boris A, Lopez AF, Schwarz QP. Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiency. Molecular Psychiatry. 17: 451-66. PMID 22124272 DOI: 10.1038/Mp.2011.158 |
0.322 |
|
| 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 |
0.45 |
|
| 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 |
0.385 |
|
| 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 |
0.362 |
|
| 2010 |
Yamada M, Hirotsune S, Wynshaw-Boris A. A novel strategy for therapeutic intervention for the genetic disease: preventing proteolytic cleavage using small chemical compound. The International Journal of Biochemistry & Cell Biology. 42: 1401-7. PMID 20541031 DOI: 10.1016/J.Biocel.2010.05.017 |
0.379 |
|
| 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 |
0.719 |
|
| 2010 |
Yamada M, Hirotsune S, Wynshaw-Boris A. The essential role of LIS1, NDEL1 and Aurora-A in polarity formation and microtubule organization during neurogensis. Cell Adhesion & Migration. 4: 180-4. PMID 20168084 DOI: 10.4161/Cam.4.2.10715 |
0.413 |
|
| 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 |
0.449 |
|
| 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 |
0.41 |
|
| 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 |
0.393 |
|
| 2009 |
Mori D, Yamada M, Mimori-Kiyosue Y, Shirai Y, Suzuki A, Ohno S, Saya H, Wynshaw-Boris A, Hirotsune S. An essential role of the aPKC-Aurora A-NDEL1 pathway in neurite elongation by modulation of microtubule dynamics. Nature Cell Biology. 11: 1057-68. PMID 19668197 DOI: 10.1038/Ncb1919 |
0.324 |
|
| 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 |
0.34 |
|
| 2009 |
Wynshaw-Boris A. Elongator bridges tubulin acetylation and neuronal migration. Cell. 136: 393-4. PMID 19203572 DOI: 10.1016/J.Cell.2009.01.024 |
0.318 |
|
| 2009 |
Hashimoto M, Ikeuchi S, Wang J, Shinohara K, Nonaka S, Wynshaw-Boris A, Hamada H. 16-P018 Cell polarity in the node for basal body positioning and nodal flow Mechanisms of Development. 126. DOI: 10.1016/J.Mod.2009.06.709 |
0.41 |
|
| 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 |
0.561 |
|
| 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 |
0.302 |
|
| 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 |
0.392 |
|
| 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 |
0.339 |
|
| 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 |
0.698 |
|
| 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 |
0.463 |
|
| 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 |
0.418 |
|
| 2007 |
Wynshaw-Boris A. Lissencephaly and LIS1: insights into the molecular mechanisms of neuronal migration and development. Clinical Genetics. 72: 296-304. PMID 17850624 DOI: 10.1111/J.1399-0004.2007.00888.X |
0.397 |
|
| 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 |
0.347 |
|
| 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 |
0.371 |
|
| 2007 |
Wynshaw-Boris A. Cell biology: lost in mitotic translation. Nature. 446: 274-5. PMID 17361171 DOI: 10.1038/446274A |
0.349 |
|
| 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 |
0.305 |
|
| 2007 |
Van De Schans VAM, Van Den Borne SWM, Strzelecka AE, Janssen BJA, Van Der Velden JLJ, Langen RCJ, Wynshaw-Boris A, Smits JFM, Blankesteijn WM. Interruption of Wnt signaling attenuates the onset of pressure overload-induced cardiac hypertrophy Hypertension. 49: 473-480. PMID 17210832 DOI: 10.1161/01.Hyp.0000255946.55091.24 |
0.358 |
|
| 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 |
0.339 |
|
| 2006 |
Wynshaw-Boris A. Inborn errors of development: disruption of pathways critical for normal development. Pediatric Clinics of North America. 53: 855-71, viii. PMID 17027614 DOI: 10.1016/J.Pcl.2006.08.008 |
0.381 |
|
| 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 |
0.394 |
|
| 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 |
0.735 |
|
| 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 |
0.671 |
|
| 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 |
0.319 |
|
| 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 |
0.402 |
|
| 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 |
0.531 |
|
| 2006 |
Dezfouli S, Bakke A, Huang J, Wynshaw-Boris A, Hurlin PJ. Inflammatory disease and lymphomagenesis caused by deletion of the Myc antagonist Mnt in T cells. Molecular and Cellular Biology. 26: 2080-92. PMID 16507988 DOI: 10.1128/Mcb.26.6.2080-2092.2006 |
0.315 |
|
| 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 |
0.348 |
|
| 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 |
0.67 |
|
| 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 |
0.378 |
|
| 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 |
0.659 |
|
| 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 |
0.479 |
|
| 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 |
0.45 |
|
| 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 |
0.678 |
|
| 2005 |
Erker L, Schubert R, Yakushiji H, Barlow C, Larson D, Mitchell JB, Wynshaw-Boris A. Cancer chemoprevention by the antioxidant tempol acts partially via the p53 tumor suppressor. Human Molecular Genetics. 14: 1699-708. PMID 15888486 DOI: 10.1093/Hmg/Ddi181 |
0.742 |
|
| 2005 |
Walker W, Zhou ZQ, Ota S, Wynshaw-Boris A, Hurlin PJ. Mnt-Max to Myc-Max complex switching regulates cell cycle entry. The Journal of Cell Biology. 169: 405-13. PMID 15866886 DOI: 10.1083/Jcb.200411013 |
0.322 |
|
| 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 |
0.365 |
|
| 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 |
0.342 |
|
| 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 |
0.35 |
|
| 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 |
0.537 |
|
| 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 |
0.381 |
|
| 2004 |
Schubert R, Erker L, Barlow C, Yakushiji H, Larson D, Russo A, Mitchell JB, Wynshaw-Boris A. Cancer chemoprevention by the antioxidant tempol in Atm-deficient mice. Human Molecular Genetics. 13: 1793-802. PMID 15213104 DOI: 10.1093/Hmg/Ddh189 |
0.739 |
|
| 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 |
0.336 |
|
| 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 |
0.334 |
|
| 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 |
0.442 |
|
| 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 DOI: 10.4161/Cc.3.2.638 |
0.325 |
|
| 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 |
0.407 |
|
| 2003 |
Furuno-Fukushi I, Masumura K, Furuse T, Noda Y, Takahagi M, Saito T, Hoki Y, Suzuki H, Wynshaw-Boris A, Nohmi T, Tatsumi K. Effect of Atm disruption on spontaneously arising and radiation-induced deletion mutations in mouse liver. Radiation Research. 160: 549-58. PMID 14565827 DOI: 10.1667/Rr3073 |
0.312 |
|
| 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 DOI: 10.1523/Jneurosci.23-25-08673.2003 |
0.373 |
|
| 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 |
0.421 |
|
| 2003 |
Cahana A, Jin XL, Reiner O, Wynshaw-Boris A, O'Neill C. A study of the nature of embryonic lethality in LIS1-/- mice. Molecular Reproduction and Development. 66: 134-42. PMID 12950100 DOI: 10.1002/Mrd.10339 |
0.37 |
|
| 2003 |
Tokuoka SM, Ishii S, Kawamura N, Satoh M, Shimada A, Sasaki S, Hirotsune S, Wynshaw-Boris A, Shimizu T. Involvement of platelet-activating factor and LIS1 in neuronal migration. The European Journal of Neuroscience. 18: 563-70. PMID 12911752 DOI: 10.1046/J.1460-9568.2003.02778.X |
0.348 |
|
| 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 |
0.683 |
|
| 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 |
0.301 |
|
| 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 |
0.407 |
|
| 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 |
0.325 |
|
| 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 |
0.344 |
|
| 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 |
0.723 |
|
| 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 |
0.321 |
|
| 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 |
0.502 |
|
| 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 |
0.533 |
|
| 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 DOI: 10.1523/Jneurosci.22-17-07548.2002 |
0.388 |
|
| 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 DOI: 10.1016/S0896-6273(02)00783-3 |
0.435 |
|
| 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 |
0.32 |
|
| 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 |
0.371 |
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| 2001 |
Wang Y, Tan J, Sutton-Smith M, Ditto D, Panico M, Campbell RM, Varki NM, Long JM, Jaeken J, Levinson SR, Wynshaw-Boris A, Morris HR, Le D, Dell A, Schachter H, et al. Modeling human congenital disorder of glycosylation type IIa in the mouse: conservation of asparagine-linked glycan-dependent functions in mammalian physiology and insights into disease pathogenesis. Glycobiology. 11: 1051-70. PMID 11805078 DOI: 10.1093/Glycob/11.12.1051 |
0.374 |
|
| 2001 |
Lechleider RJ, Ryan JL, Garrett L, Eng C, Deng Cx, Wynshaw-Boris A, Roberts AB. Targeted mutagenesis of Smad1 reveals an essential role in chorioallantoic fusion Developmental Biology. 240: 157-167. PMID 11784053 DOI: 10.1006/Dbio.2001.0469 |
0.396 |
|
| 2001 |
Wynshaw-Boris A, Gambello MJ. LIS1 and dynein motor function in neuronal migration and development Genes & Development. 15: 639-651. PMID 11274050 DOI: 10.1101/Gad.886801 |
0.395 |
|
| 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 |
0.662 |
|
| 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 |
0.37 |
|
| 2001 |
Ménisser-de Murcia J, Mark M, Wendling O, Wynshaw-Boris A, de Murcia G. Early embryonic lethality in PARP-1 Atm double-mutant mice suggests a functional synergy in cell proliferation during development. Molecular and Cellular Biology. 21: 1828-32. PMID 11238919 DOI: 10.1128/Mcb.21.5.1828-1832.2001 |
0.36 |
|
| 2001 |
Karabinis ME, Larson D, Barlow C, Wynshaw-Boris A, Moser AR. Heterozygosity for a mutation in Brca1 or Atm does not increase susceptibility to ENU-induced mammary tumors in ApcMin/+ mice Carcinogenesis. 22: 343-346. PMID 11181458 DOI: 10.1093/Carcin/22.2.343 |
0.342 |
|
| 2000 |
Sasaki S, Shionoya A, Ishida M, Gambello MJ, Yingling J, Wynshaw-Boris A, Hirotsune S. A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system Neuron. 28: 681-696. PMID 11163259 DOI: 10.1016/S0896-6273(00)00146-X |
0.696 |
|
| 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 |
0.369 |
|
| 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 |
0.351 |
|
| 2000 |
Rucker EB, Dierisseau P, Wagner KU, Garrett L, Wynshaw-Boris A, Flaws JA, Hennighausen L. Bcl-x and Bax regulate mouse primordial germ cell survival and apoptosis during embryogenesis Molecular Endocrinology. 14: 1038-1052. PMID 10894153 DOI: 10.1210/Mend.14.7.0465 |
0.342 |
|
| 2000 |
Petiniot LK, Weaver Z, Barlow C, Shen R, Eckhaus M, Steinberg SM, Ried T, Wynshaw-Boris A, Hodes RJ. Recombinase-activating gene (RAG) 2-mediated V(D)J recombination is not essential for tumorigenesis in Atm-deficient mice. Proceedings of the National Academy of Sciences of the United States of America. 97: 6664-9. PMID 10841564 DOI: 10.1073/Pnas.97.12.6664 |
0.367 |
|
| 2000 |
Barlow C, Ribaut-Barassin C, Zwingman TA, Pope AJ, Brown KD, Owens JW, Larson D, Harrington EA, Haeberle AM, Mariani J, Eckhaus M, Herrup K, Bailly Y, Wynshaw-Boris A. ATM is a cytoplasmic protein in mouse brain required to prevent lysosomal accumulation. Proceedings of the National Academy of Sciences of the United States of America. 97: 871-6. PMID 10639172 DOI: 10.1073/Pnas.97.2.871 |
0.422 |
|
| 2000 |
Fleck MW, Hirotsune S, Gambello MJ, Phillips-Tansey E, Suares G, Mervis RF, Wynshaw-Boris A, McBain CJ. Hippocampal Abnormalities and Enhanced Excitability in a Murine Model of Human Lissencephaly The Journal of Neuroscience. 20: 2439-2450. DOI: 10.1523/Jneurosci.20-07-02439.2000 |
0.342 |
|
| 2000 |
Liyanage M, Weaver Z, Barlow C, Coleman A, Pankratz DG, Anderson S, Wynshaw-Boris A, Ried T. Abnormal rearrangement within the α/δ T-cell receptor locus in lymphomas from Atm-deficient mice Blood. 96: 1940-1946. DOI: 10.1182/Blood.V96.5.1940.H8001940_1940_1946 |
0.335 |
|
| 1999 |
Kimber WL, Hsieh P, Hirotsune S, Yuva-Paylor L, Sutherland HF, Chen A, Ruiz-Lozano P, Hoogstraten-Miller SL, Chien KR, Paylor R, Scambler PJ, Wynshaw-Boris A. Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse. Human Molecular Genetics. 8: 2229-37. PMID 10545603 DOI: 10.1093/Hmg/8.12.2229 |
0.356 |
|
| 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 |
0.381 |
|
| 1999 |
Barlow C, Dennery PA, Shigenaga MK, Smith MA, Morrow JD, Roberts LJ, Wynshaw-Boris A, Levine RL. Loss of the ataxia-telangiectasia gene product causes oxidative damage in target organs. Proceedings of the National Academy of Sciences of the United States of America. 96: 9915-9. PMID 10449794 DOI: 10.1073/Pnas.96.17.9915 |
0.32 |
|
| 1999 |
Gambello MJ, Hirotsune S, Wynshaw-Boris A. Murine modelling of classical lissencephaly Neurogenetics. 2: 77-86. PMID 10369882 DOI: 10.1007/S100480050056 |
0.331 |
|
| 1999 |
Xu X, Wagner KU, Larson D, Weaver Z, Li C, Ried T, Hennighausen L, Wynshaw-Boris A, Deng CX. Conditional mutation of Brca1 in mammary epithelial cells results in blunted ductal morphogenesis and tumour formation. Nature Genetics. 22: 37-43. PMID 10319859 DOI: 10.1038/8743 |
0.379 |
|
| 1999 |
Bi L, Okabe I, Bernard DJ, Wynshaw-Boris A, Nussbaum RL. Proliferative Defect and Embryonic Lethality in Mice Homozygous for a Deletion in the p110α Subunit of Phosphoinositide 3-Kinase Journal of Biological Chemistry. 274: 10963-10968. PMID 10196176 DOI: 10.1074/Jbc.274.16.10963 |
0.362 |
|
| 1999 |
Liao MJ, Yin C, Barlow C, Wynshaw-Boris A, van Dyke T. Atm is dispensable for p53 apoptosis and tumor suppression triggered by cell cycle dysfunction. Molecular and Cellular Biology. 19: 3095-102. PMID 10082576 DOI: 10.1128/Mcb.19.4.3095 |
0.338 |
|
| 1999 |
Dantzer F, Murcia JM, Barlow C, Wynshaw-Boris A, Murcia Gd. Poly(ADP-ribose) polymerase activity is not affected in ataxia telangiectasia cells and knockout mice Carcinogenesis. 20: 177-180. PMID 9934867 DOI: 10.1093/Carcin/20.1.177 |
0.349 |
|
| 1999 |
Brown KD, Barlow C, Wynshaw-Boris A. Multiple ATM-dependent pathways: An explanation for pleiotropy American Journal of Human Genetics. 64: 46-50. PMID 9915942 DOI: 10.1086/302223 |
0.333 |
|
| 1999 |
Wynshaw-Boris A, Garrett L, Chen A, Barlow C. Chapter 3.1.2 Generation of transgenic mice by pronuclear DNA injection Techniques in the Behavioral and Neural Sciences. 13: 272-281. DOI: 10.1016/S0921-0709(99)80024-8 |
0.367 |
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| 1999 |
Wynshaw-Boris A, Garrett L, Chen A, Barlow C. Chapter 3.1.1 Embryonic stem cells and gene targeting Techniques in the Behavioral and Neural Sciences. 13: 259-271. DOI: 10.1016/S0921-0709(99)80023-6 |
0.361 |
|
| 1998 |
Yamanaka R, Lekstrom-Himes J, Barlow C, Wynshaw-Boris A, Xanthopoulos KG. CCAAT/enhancer binding proteins are critical components of the transcriptional regulation of hematopoiesis (Review). International Journal of Molecular Medicine. 1: 213-221. PMID 9852222 DOI: 10.3892/Ijmm.1.1.213 |
0.304 |
|
| 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 |
0.337 |
|
| 1998 |
Hirotsune S, Fleck MW, Gambello MJ, Bix GJ, Chen A, Clark GD, Ledbetter DH, McBain CJ, Wynshaw-Boris A. Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality. Nature Genetics. 19: 333-9. PMID 9697693 DOI: 10.1038/1221 |
0.397 |
|
| 1998 |
Jänne PA, Suchy SF, Bernard D, MacDonald M, Crawley J, Grinberg A, Wynshaw-Boris A, Westphal H, Nussbaum RL. Functional overlap between murine Inpp5b and Ocrl1 may explain why deficiency of the murine ortholog for OCRL1 does not cause Lowe syndrome in mice. The Journal of Clinical Investigation. 101: 2042-53. PMID 9593760 DOI: 10.1172/Jci2414 |
0.378 |
|
| 1997 |
Barlow C, Liyanage M, Moens PB, Deng CX, Ried T, Wynshaw-Boris A. Partial rescue of the prophase I defects of Atm-deficient mice by p53 and p21 null alleles Nature Genetics. 17: 462-466. PMID 9398851 DOI: 10.1038/Ng1297-462 |
0.381 |
|
| 1997 |
Barlow C, Brown KD, Deng CX, Tagle DA, Wynshaw-Boris A. Atm selectively regulates distinct p53-dependent cell-cycle checkpoint and apoptotic pathways Nature Genetics. 17: 453-456. PMID 9398849 DOI: 10.1038/Ng1297-453 |
0.362 |
|
| 1997 |
Yamanaka R, Barlow C, Lekstrom-Himes J, Castilla LH, Liu PP, Eckhaus M, Decker T, Wynshaw-Boris A, Xanthopoulos KG. Impaired granulopoiesis, myelodysplasia, and early lethality in CCAAT/enhancer binding protein epsilon-deficient mice. Proceedings of the National Academy of Sciences of the United States of America. 94: 13187-13192. PMID 9371821 DOI: 10.1073/Pnas.94.24.13187 |
0.371 |
|
| 1997 |
Wagner KU, Wall RJ, St-Onge L, Gruss P, Wynshaw-Boris A, Garrett L, Li M, Furth PA, Hennighausen L. Cre-mediated gene deletion in the mammary gland. Nucleic Acids Research. 25: 4323-30. PMID 9336464 DOI: 10.1093/Nar/25.21.4323 |
0.391 |
|
| 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 |
0.352 |
|
| 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 |
0.315 |
|
| 1997 |
Wynshaw-Boris A, Ryan G, Deng CX, Chan DC, Jackson-Grusby L, Larson D, Dunmore JH, Leder P. The role of a single formin isoform in the limb and renal phenotypes of limb deformity. Molecular Medicine (Cambridge, Mass.). 3: 372-84. PMID 9234242 DOI: 10.1007/Bf03401684 |
0.359 |
|
| 1997 |
Hirotsune S, Pack SD, Chong SS, Robbins CM, Pavan WJ, Ledbetter DH, Wynshaw-Boris A. Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human region. Genome Research. 7: 625-34. PMID 9199935 DOI: 10.1101/Gr.7.6.625 |
0.346 |
|
| 1997 |
Barlow C, Schroeder M, Lekstrom-Himes J, Kylefjord H, Deng CX, Wynshaw-Boris A, Spiegelman BM, Xanthopoulos KG. Targeted expression of Cre recombinase to adipose tissue of transgenic mice directs adipose-specific excision of loxP-flanked gene segments. Nucleic Acids Research. 25: 2543-5. PMID 9171115 DOI: 10.1093/Nar/25.12.2543 |
0.371 |
|
| 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 |
0.324 |
|
| 1997 |
Taylor C, Wadey R, O'Donnell H, Roberts C, Mattei MG, Kimber WL, Wynshaw-Boris A, Scambler PJ. Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein Mammalian Genome. 8: 371-375. PMID 9107688 DOI: 10.1007/S003359900445 |
0.334 |
|
| 1997 |
Liu X, Robinson GW, Wagner KU, Garrett L, Wynshaw-Boris A, Hennighausen L. Stat5a is mandatory for adult mammary gland development and lactogenesis. Genes & Development. 11: 179-86. PMID 9009201 DOI: 10.1101/Gad.11.2.179 |
0.402 |
|
| 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 |
0.327 |
|
| 1997 |
Feldman GM, Rosenthal LA, Liu X, Hayes MP, Wynshaw-Boris A, Leonard WJ, Hennighausen L, Finbloom DS. STAT5A-Deficient Mice Demonstrate a Defect in Granulocyte-Macrophage Colony-Stimulating Factor–Induced Proliferation and Gene Expression Blood. 90: 1768-1776. DOI: 10.1182/Blood.V90.5.1768 |
0.401 |
|
| 1996 |
Castilla LH, Wijmenga C, Wang Q, Stacy T, Speck NA, Eckhaus M, Marín-Padilla M, Collins FS, Wynshaw-Boris A, Liu PP. Failure of embryonic hematopoiesis and lethal hemorrhages in mouse embryos heterozygous for a knocked-in leukemia gene CBFB-MYH11. Cell. 87: 687-96. PMID 8929537 DOI: 10.1016/S0092-8674(00)81388-4 |
0.414 |
|
| 1996 |
Tsang M, Lijam N, Yang Y, Beier DR, Wynshaw-Boris A, Sussman DJ. Isolation and characterization of mouse dishevelled-3. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 207: 253-62. PMID 8922524 DOI: 10.1002/(Sici)1097-0177(199611)207:3<253::Aid-Aja2>3.0.Co;2-G |
0.374 |
|
| 1996 |
Liyanage M, Coleman A, du Manoir S, Veldman T, McCormack S, Dickson RB, Barlow C, Wynshaw-Boris A, Janz S, Wienberg J, Ferguson-Smith MA, Schröck E, Ried T. Multicolour spectral karyotyping of mouse chromosomes. Nature Genetics. 14: 312-5. PMID 8896561 DOI: 10.1038/Ng1196-312 |
0.305 |
|
| 1996 |
Barlow C, Hirotsune S, Paylor R, Liyanage M, Eckhaus M, Collins F, Shiloh Y, Crawley JN, Ried T, Tagle D, Wynshaw-Boris A. Atm-deficient mice: a paradigm of ataxia telangiectasia. Cell. 86: 159-71. PMID 8689683 DOI: 10.1016/S0092-8674(00)80086-0 |
0.393 |
|
| 1996 |
Pecker I, Avraham KB, Gilbert DJ, Savitsky K, Rotman G, Harnik R, Fukao T, Schröck E, Hirotsune S, Tagle DA, Collins FS, Wynshaw-Boris A, Ried T, Copeland NG, Jenkins NA, et al. Identification and chromosomal localization of Atm, the mouse homolog of the ataxia-telangiectasia gene. Genomics. 35: 39-45. PMID 8661102 DOI: 10.1006/Geno.1996.0320 |
0.325 |
|
| 1996 |
Schröck E, Badger P, Larson D, Erdos M, Wynshaw-Boris A, Ried T, Brody L. The murine homolog of the human breast and ovarian cancer susceptibility gene Brca1 maps to mouse chromosome 11D. Human Genetics. 97: 256-9. PMID 8566965 DOI: 10.1007/Bf02265277 |
0.326 |
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| 1995 |
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| 1994 |
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| 1994 |
Deng CX, Wynshaw-Boris A, Shen MM, Daugherty C, Ornitz DM, Leder P. Murine FGFR-1 is required for early postimplantation growth and axial organization. Genes & Development. 8: 3045-57. PMID 8001823 DOI: 10.1101/Gad.8.24.3045 |
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