Orly Reiner, Ph.D. - Publications

Affiliations: 
Molecular Genetics Weizmann Institute of Science, Rehovot, Israel 

104 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 Reiner O, Sapir T, Parichha A. Using multi-organ culture systems to study Parkinson's disease. Molecular Psychiatry. PMID 33154567 DOI: 10.1038/s41380-020-00936-8  0.56
2020 Reiner O, Parichha A, Sapir T. Modeling human neuronal migration deficits in 3D. Current Opinion in Neurobiology. 66: 30-36. PMID 33069990 DOI: 10.1016/j.conb.2020.09.005  0.56
2019 Sapir T, Barakat TS, Paredes MF, Lerman-Sagie T, Aronica E, Klonowski W, Nguyen L, Ben Zeev B, Bahi-Buisson N, Leventer R, Rachmian N, Reiner O. Building Bridges Between the Clinic and the Laboratory: A Meeting Review - Brain Malformations: A Roadmap for Future Research. Frontiers in Cellular Neuroscience. 13: 434. PMID 31611776 DOI: 10.3389/fncel.2019.00434  0.56
2019 Sapir T, Segal M, Grigoryan G, Hansson KM, James P, Segal M, Reiner O. The Interactome of Palmitoyl-Protein Thioesterase 1 (PPT1) Affects Neuronal Morphology and Function. Frontiers in Cellular Neuroscience. 13: 92. PMID 30918483 DOI: 10.3389/fncel.2019.00092  0.56
2019 Chan SM, Sapir T, Park SS, Rual JF, Contreras-Galindo R, Reiner O, Markovitz DM. The HERV-K accessory protein Np9 controls viability and migration of teratocarcinoma cells. Plos One. 14: e0212970. PMID 30818388 DOI: 10.1371/journal.pone.0212970  0.56
2018 Gorelik A, Sapir T, Ben-Reuven L, Reiner O. Complement C3 Affects Rac1 Activity in the Developing Brain. Frontiers in Molecular Neuroscience. 11: 150. PMID 29867343 DOI: 10.3389/fnmol.2018.00150  0.56
2018 Reiner O, Sapir T. A Coated Sponge: Toward Neonatal Brain Repair. Cell Stem Cell. 22: 3-4. PMID 29304341 DOI: 10.1016/j.stem.2017.12.007  0.56
2017 Gorelik A, Sapir T, Woodruff TM, Reiner O. Serping1/C1 Inhibitor Affects Cortical Development in a Cell Autonomous and Non-cell Autonomous Manner. Frontiers in Cellular Neuroscience. 11: 169. PMID 28670268 DOI: 10.3389/fncel.2017.00169  0.56
2017 Gorelik A, Sapir T, Haffner-Krausz R, Olender T, Woodruff TM, Reiner O. Developmental activities of the complement pathway in migrating neurons. Nature Communications. 8: 15096. PMID 28462915 DOI: 10.1038/ncomms15096  0.56
2017 Segal-Salto M, Hansson K, Sapir T, Kaplan A, Levy T, Schwizer M, Frotscher M, James P, Reiner O. Proteomics insights into Infantile Neuronal Ceroid Lipofuscinosis (CLN1) point to the involvement of cilia pathology in the disease. Human Molecular Genetics. PMID 28334871 DOI: 10.1093/hmg/ddx074  0.56
2017 Gorelik A, Sapir T, Reiner O. Unexpected Activities of the Complement Pathway in Migrating Neurons European Neuropsychopharmacology. 27: S509. DOI: 10.1016/j.euroneuro.2016.09.617  0.56
2017 Reiner O, Johnstone M, Sapir T. Novel Insights, Modeling and Translational Approaches in Autism-Schizophrenia Spectrum Diseases European Neuropsychopharmacology. 27: S509. DOI: 10.1016/j.euroneuro.2016.09.616  0.56
2016 Segal-Salto M, Sapir T, Reiner O. Reversible Cysteine Acylation Regulates the Activity of Human Palmitoyl-Protein Thioesterase 1 (PPT1). Plos One. 11: e0146466. PMID 26731412 DOI: 10.1371/journal.pone.0146466  1
2015 Reiner O, Karzburn E, Kshirsagar A, Kaibuchi K. Regulation of Neuronal Migration, an Emerging Topic in Autism Spectrum Disorders (ASD). Journal of Neurochemistry. PMID 26485324 DOI: 10.1111/jnc.13403  1
2015 Greenman R, Gorelik A, Sapir T, Baumgart J, Zamor V, Segal-Salto M, Levin-Zaidman S, Aidinis V, Aoki J, Nitsch R, Vogt J, Reiner O. Non-cell autonomous and non-catalytic activities of ATX in the developing brain. Frontiers in Neuroscience. 9: 53. PMID 25788872 DOI: 10.3389/fnins.2015.00053  1
2015 Vinograd-Byk H, Sapir T, Cantarero L, Lazo PA, Zeligson S, Lev D, Lerman-Sagie T, Renbaum P, Reiner O, Levy-Lahad E. The spinal muscular atrophy with pontocerebellar hypoplasia gene VRK1 regulates neuronal migration through an amyloid-β precursor protein-dependent mechanism. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 936-42. PMID 25609612 DOI: 10.1523/JNEUROSCI.1998-14.2015  1
2014 Liu P, Kaplan A, Yuan B, Hanna JH, Lupski JR, Reiner O. Passage number is a major contributor to genomic structural variations in mouse iPSCs. Stem Cells (Dayton, Ohio). 32: 2657-67. PMID 24965231 DOI: 10.1002/stem.1779  1
2014 Reiner O, Sapir T. Mark/Par-1 marking the polarity of migrating neurons. Advances in Experimental Medicine and Biology. 800: 97-111. PMID 24243102 DOI: 10.1007/978-94-007-7687-6_6  1
2013 Vomund S, Sapir T, Reiner O, Silva MA, Korth C. Generation of topically transgenic rats by in utero electroporation and in vivo bioluminescence screening. Journal of Visualized Experiments : Jove. e50146. PMID 24084570 DOI: 10.3791/50146  1
2013 Reiner O, Sapir T. LIS1 functions in normal development and disease. Current Opinion in Neurobiology. 23: 951-6. PMID 23973156 DOI: 10.1016/j.conb.2013.08.001  1
2013 Sapir T, Levy T, Sakakibara A, Rabinkov A, Miyata T, Reiner O. Shootin1 acts in concert with KIF20B to promote polarization of migrating neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 11932-48. PMID 23864681 DOI: 10.1523/JNEUROSCI.5425-12.2013  1
2013 Gerlitz G, Reiner O, Bustin M. Microtubule dynamics alter the interphase nucleus. Cellular and Molecular Life Sciences : Cmls. 70: 1255-68. PMID 23117601 DOI: 10.1007/s00018-012-1200-5  1
2013 Reiner O, Gerlitz G. Nucleokinesis Cellular Migration and Formation of Neuronal Connections. 261-279. DOI: 10.1016/B978-0-12-397266-8.00026-0  1
2012 Reiner O, Gorelik A, Greenman R. Use of RNA interference by in utero electroporation to study cortical development: the example of the doublecortin superfamily. Genes. 3: 759-78. PMID 24705084 DOI: 10.3390/genes3040759  1
2012 Page RM, Münch A, Horn T, Kuhn PH, Colombo A, Reiner O, Boutros M, Steiner H, Lichtenthaler SF, Haass C. Loss of PAFAH1B2 reduces amyloid-β generation by promoting the degradation of amyloid precursor protein C-terminal fragments. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 18204-14. PMID 23238734 DOI: 10.1523/JNEUROSCI.2681-12.2012  1
2012 Segal M, Soifer I, Petzold H, Howard J, Elbaum M, Reiner O. Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon. Biology Open. 1: 220-31. PMID 23213412 DOI: 10.1242/bio.2012307  1
2012 Babaev AV, Gogolev DE, Reiner OV, Korochkin IM, Fandeev AV, Pivovarov VY, Fedulaev YN, Drachan KM. Effect of intravenous low-intensity laser irradiation of the blood on clinical and laboratory parameters of hepatocellular insufficiency. Bulletin of Experimental Biology and Medicine. 153: 754-7. PMID 23113277 DOI: 10.1007/s10517-012-1818-1  1
2012 Sapir T, Frotscher M, Levy T, Mandelkow EM, Reiner O. Tau's role in the developing brain: implications for intellectual disability. Human Molecular Genetics. 21: 1681-92. PMID 22194194 DOI: 10.1093/hmg/ddr603  1
2012 Mejia-Gervacio S, Murray K, Sapir T, Belvindrah R, Reiner O, Lledo PM. MARK2/Par-1 guides the directionality of neuroblasts migrating to the olfactory bulb. Molecular and Cellular Neurosciences. 49: 97-103. PMID 22061967 DOI: 10.1016/j.mcn.2011.10.006  1
2012 Reiner O, Sapir T, Gerlitz G. Interkinetic nuclear movement in the ventricular zone of the cortex. Journal of Molecular Neuroscience : Mn. 46: 516-26. PMID 21881827 DOI: 10.1007/s12031-011-9633-0  1
2011 Kaplan A, Reiner O. Linking cytoplasmic dynein and transport of Rab8 vesicles to the midbody during cytokinesis by the doublecortin domain-containing 5 protein. Journal of Cell Science. 124: 3989-4000. PMID 22159412 DOI: 10.1242/jcs.085407  1
2011 Yamasaki T, Kawasaki H, Arakawa S, Shimizu K, Shimizu S, Reiner O, Okano H, Nishina S, Azuma N, Penninger JM, Katada T, Nishina H. Stress-activated protein kinase MKK7 regulates axon elongation in the developing cerebral cortex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 16872-83. PMID 22090513 DOI: 10.1523/JNEUROSCI.1111-11.2011  1
2010 Bilimoria PM, de la Torre-Ubieta L, Ikeuchi Y, Becker EB, Reiner O, Bonni A. A JIP3-regulated GSK3β/DCX signaling pathway restricts axon branching. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 16766-76. PMID 21159948 DOI: 10.1523/JNEUROSCI.1362-10.2010  1
2010 Livnat I, Finkelshtein D, Ghosh I, Arai H, Reiner O. PAF-AH Catalytic Subunits Modulate the Wnt Pathway in Developing GABAergic Neurons. Frontiers in Cellular Neuroscience. 4. PMID 20725507 DOI: 10.3389/fncel.2010.00019  1
2010 Shmueli A, Segal M, Sapir T, Tsutsumi R, Noritake J, Bar A, Sapoznik S, Fukata Y, Orr I, Fukata M, Reiner O. Ndel1 palmitoylation: a new mean to regulate cytoplasmic dynein activity. The Embo Journal. 29: 107-19. PMID 19927128 DOI: 10.1038/emboj.2009.325  1
2009 Reiner O, Shmueli A, Sapir T. Neuronal migration and neurodegeneration: 2 sides of the same coin. Cerebral Cortex (New York, N.Y. : 1991). 19: i42-8. PMID 19346270 DOI: 10.1093/cercor/bhp039  1
2009 Reiner O, Sapir T. Polarity regulation in migrating neurons in the cortex. Molecular Neurobiology. 40: 1-14. PMID 19330467 DOI: 10.1007/s12035-009-8065-0  1
2009 Bi W, Sapir T, Shchelochkov OA, Zhang F, Withers MA, Hunter JV, Levy T, Shinder V, Peiffer DA, Gunderson KL, Nezarati MM, Shotts VA, Amato SS, Savage SK, Harris DJ, ... ... Reiner O, et al. Increased LIS1 expression affects human and mouse brain development. Nature Genetics. 41: 168-77. PMID 19136950 DOI: 10.1038/ng.302  1
2008 Sapir T, Shmueli A, Levy T, Timm T, Elbaum M, Mandelkow EM, Reiner O. Antagonistic effects of doublecortin and MARK2/Par-1 in the developing cerebral cortex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 13008-13. PMID 19036994 DOI: 10.1523/JNEUROSCI.2363-08.2008  1
2008 Gorelik A, Sapir T, Reiner O. Gene trapping: an antibody-dependent approach for verifying integration in your favorite gene. Cellular & Molecular Biology Letters. 13: 614-20. PMID 18618084 DOI: 10.2478/s11658-008-0028-3  1
2008 Sapir T, Sapoznik S, Levy T, Finkelshtein D, Shmueli A, Timm T, Mandelkow EM, Reiner O. Accurate balance of the polarity kinase MARK2/Par-1 is required for proper cortical neuronal migration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 5710-20. PMID 18509032 DOI: 10.1523/JNEUROSCI.0911-08.2008  1
2008 Cohen D, Segal M, Reiner O. Doublecortin supports the development of dendritic arbors in primary hippocampal neurons. Developmental Neuroscience. 30: 187-99. PMID 18075265 DOI: 10.1159/000109862  1
2007 Gerlitz G, Livnat I, Ziv C, Yarden O, Bustin M, Reiner O. Migration cues induce chromatin alterations. Traffic (Copenhagen, Denmark). 8: 1521-9. PMID 17822403 DOI: 10.1111/j.1600-0854.2007.00638.x  1
2007 Valdés-Sánchez L, Escámez T, Echevarria D, Ballesta JJ, Tabarés-Seisdedos R, Reiner O, Martinez S, Geijo-Barrientos E. Postnatal alterations of the inhibitory synaptic responses recorded from cortical pyramidal neurons in the Lis1/sLis1 mutant mouse. Molecular and Cellular Neurosciences. 35: 220-9. PMID 17433713 DOI: 10.1016/j.mcn.2007.02.017  1
2006 Reiner O, Sapoznik S, Sapir T. Lissencephaly 1 linking to multiple diseases: mental retardation, neurodegeneration, schizophrenia, male sterility, and more. Neuromolecular Medicine. 8: 547-65. PMID 17028375 DOI: 10.1385/NMM:8:4:547  1
2006 Reiner O, Coquelle FM, Peter B, Levy T, Kaplan A, Sapir T, Orr I, Barkai N, Eichele G, Bergmann S. The evolving doublecortin (DCX) superfamily. Bmc Genomics. 7: 188. PMID 16869982 DOI: 10.1186/1471-2164-7-188  1
2006 Coquelle FM, Levy T, Bergmann S, Wolf SG, Bar-El D, Sapir T, Brody Y, Orr I, Barkai N, Eichele G, Reiner O. Common and divergent roles for members of the mouse DCX superfamily. Cell Cycle (Georgetown, Tex.). 5: 976-83. PMID 16628014 DOI: 10.4161/cc.5.9.2715  1
2006 Tabarés-Seisdedos R, Escámez T, Martínez-Giménez JA, Balanzá V, Salazar J, Selva G, Rubio C, Vieta E, Geijó-Barrientos E, Martínez-Arán A, Reiner O, Martínez S. Variations in genes regulating neuronal migration predict reduced prefrontal cognition in schizophrenia and bipolar subjects from mediterranean Spain: a preliminary study. Neuroscience. 139: 1289-300. PMID 16549273 DOI: 10.1016/j.neuroscience.2006.01.054  1
2006 Shmueli A, Gdalyahu A, Sapoznik S, Sapir T, Tsukada M, Reiner O. Site-specific dephosphorylation of doublecortin (DCX) by protein phosphatase 1 (PP1). Molecular and Cellular Neurosciences. 32: 15-26. PMID 16530423 DOI: 10.1016/j.mcn.2006.01.014  1
2006 Reiner O, Sapir T. Cdk5 checks p27kip1 in neuronal migration. Nature Cell Biology. 8: 11-3. PMID 16389288 DOI: 10.1038/ncb0106-11  1
2006 Shu T, Tseng HC, Sapir T, Stern P, Zhou Y, Sanada K, Fischer A, Coquelle FM, Reiner O, Tsai LH. Doublecortin-like kinase controls neurogenesis by regulating mitotic spindles and M phase progression. Neuron. 49: 25-39. PMID 16387637 DOI: 10.1016/j.neuron.2005.10.039  1
2006 Tabares-Seisdedos R, Escamez T, Martinez-Gimenez J, Balanza V, Salazar J, Selva G, Rubio C, Vieta E, Geijo-Barrientos E, Martinez-Aran A, Reiner O, Martinez S. Mutations in genes regulating neuronal migration predict reduced prefrontal cognition in schizophrenia and bipolar disorder: a preliminary study Annals of General Psychiatry. 5. DOI: 10.1186/1744-859X-5-S1-S157  0.32
2005 Gerlitz G, Darhin E, Giorgio G, Franco B, Reiner O. Novel functional features of the Lis-H domain: role in protein dimerization, half-life and cellular localization. Cell Cycle (Georgetown, Tex.). 4: 1632-40. PMID 16258276 DOI: 10.4161/cc.4.11.2151  1
2005 Reiner O, Sapir T. Similarities and differences between the Wnt and reelin pathways in the forming brain. Molecular Neurobiology. 31: 117-34. PMID 15953816 DOI: 10.1385/MN:31:1-3:117  1
2005 Jiménez-Mateos EM, Wandosell F, Reiner O, Avila J, González-Billault C. Binding of microtubule-associated protein 1B to LIS1 affects the interaction between dynein and LIS1. The Biochemical Journal. 389: 333-41. PMID 15762842 DOI: 10.1042/BJ20050244  1
2005 Reiner O, Coquelle FM. Missense mutations resulting in type 1 lissencephaly. Cellular and Molecular Life Sciences : Cmls. 62: 425-34. PMID 15719169 DOI: 10.1007/s00018-004-4344-0  1
2005 Epie N, Ammosova T, Sapir T, Voloshin Y, Lane WS, Turner W, Reiner O, Nekhai S. HIV-1 Tat interacts with LIS1 protein. Retrovirology. 2: 6. PMID 15698475 DOI: 10.1186/1742-4690-2-6  1
2004 Kim MH, Cooper DR, Oleksy A, Devedjiev Y, Derewenda U, Reiner O, Otlewski J, Derewenda ZS. The structure of the N-terminal domain of the product of the lissencephaly gene Lis1 and its functional implications. Structure (London, England : 1993). 12: 987-98. PMID 15274919 DOI: 10.1016/j.str.2004.03.024  1
2004 Reiner O, Gdalyahu A, Ghosh I, Levy T, Sapoznik S, Nir R, Sapir T. DCX's phosphorylation by not just another kinase (JNK). Cell Cycle (Georgetown, Tex.). 3: 747-51. PMID 15118415 DOI: 10.4161/cc.3.6.909  1
2004 Gdalyahu A, Ghosh I, Levy T, Sapir T, Sapoznik S, Fishler Y, Azoulai D, Reiner O. DCX, a new mediator of the JNK pathway. The Embo Journal. 23: 823-32. PMID 14765123 DOI: 10.1038/sj.emboj.7600079  1
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  1
2003 Caspi M, Coquelle FM, Koifman C, Levy T, Arai H, Aoki J, De Mey JR, Reiner O. LIS1 missense mutations: variable phenotypes result from unpredictable alterations in biochemical and cellular properties. The Journal of Biological Chemistry. 278: 38740-8. PMID 12885786 DOI: 10.1074/jbc.M301147200  1
2002 Reiner O. Pathways of neuronal migration. Nature Genetics. 32: 341-2. PMID 12410228 DOI: 10.1038/ng1102-341  1
2002 Coquelle FM, Caspi M, Cordelières FP, Dompierre JP, Dujardin DL, Koifman C, Martin P, Hoogenraad CC, Akhmanova A, Galjart N, De Mey JR, Reiner O. LIS1, CLIP-170's key to the dynein/dynactin pathway. Molecular and Cellular Biology. 22: 3089-102. PMID 11940666 DOI: 10.1128/MCB.22.9.3089-3102.2002  1
2002 Burgess HA, Reiner O. Alternative splice variants of doublecortin-like kinase are differentially expressed and have different kinase activities. The Journal of Biological Chemistry. 277: 17696-705. PMID 11884394 DOI: 10.1074/jbc.M111981200  1
2002 Reiner O, Cahana A, Escamez T, Martinez S. LIS1-no more no less. Molecular Psychiatry. 7: 12-6. PMID 11803439 DOI: 10.1038/sj/mp/4000975  1
2001 Burgess HA, Reiner O. Cleavage of doublecortin-like kinase by calpain releases an active kinase fragment from a microtubule anchorage domain. The Journal of Biological Chemistry. 276: 36397-403. PMID 11473121 DOI: 10.1074/jbc.M105153200  1
2001 Cahana A, Escamez T, Nowakowski RS, Hayes NL, Giacobini M, von Holst A, Shmueli O, Sapir T, McConnell SK, Wurst W, Martinez S, Reiner O. Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization. Proceedings of the National Academy of Sciences of the United States of America. 98: 6429-34. PMID 11344260 DOI: 10.1073/pnas.101122598  1
2001 Shmueli O, Gdalyahu A, Sorokina K, Nevo E, Avivi A, Reiner O. DCX in PC12 cells: CREB-mediated transcription and neurite outgrowth. Human Molecular Genetics. 10: 1061-70. PMID 11331616 DOI: 10.1093/hmg/10.10.1061  1
2000 Reiner O. LIS1. let's interact sometimes... (part 1). Neuron. 28: 633-6. PMID 11163254 DOI: 10.1016/S0896-6273(00)00142-2  1
2000 Burgess HA, Reiner O. Doublecortin-like kinase is associated with microtubules in neuronal growth cones. Molecular and Cellular Neurosciences. 16: 529-41. PMID 11083916 DOI: 10.1006/mcne.2000.0891  1
2000 Caspi M, Atlas R, Kantor A, Sapir T, Reiner O. Interaction between LIS1 and doublecortin, two lissencephaly gene products. Human Molecular Genetics. 9: 2205-13. PMID 11001923 DOI: 10.1093/oxfordjournals.hmg.a018911  1
2000 Gothelf D, Soreni N, Nachman RP, Tyano S, Hiss Y, Reiner O, Weizman A. Evidence for the involvement of the hippocampus in the pathophysiology of schizophrenia. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 10: 389-95. PMID 10974611  1
2000 Sapir T, Horesh D, Caspi M, Atlas R, Burgess HA, Wolf SG, Francis F, Chelly J, Elbaum M, Pietrokovski S, Reiner O. Doublecortin mutations cluster in evolutionarily conserved functional domains. Human Molecular Genetics. 9: 703-12. PMID 10749977 DOI: 10.1093/hmg/9.5.703  1
2000 Sheffield PJ, Garrard S, Caspi M, Aoki J, Arai H, Derewenda U, Inoue K, Suter B, Reiner O, Derewenda ZS. Homologs of the alpha- and beta-subunits of mammalian brain platelet-activating factor acetylhydrolase Ib in the Drosophila melanogaster genome. Proteins. 39: 1-8. PMID 10737922 DOI: 10.1002/(SICI)1097-0134(20000401)39:1<1::AID-PROT1>3.0.CO;2-N  1
2000 Shmueli O, Reiner O. Expression of chLIS1, a chicken homolog of LIS1. Development Genes and Evolution. 210: 51-4. PMID 10603088 DOI: 10.1007/s004270050010  1
1999 Reiner O. The unfolding story of two lissencephaly genes and brain development. Molecular Neurobiology. 20: 143-56. PMID 10966119 DOI: 10.1007/BF02742439  1
1999 Sapir T, Eisenstein M, Burgess HA, Horesh D, Cahana A, Aoki J, Hattori M, Arai H, Inoue K, Reiner O. Analysis of lissencephaly-causing LIS1 mutations. European Journal of Biochemistry / Febs. 266: 1011-20. PMID 10583396 DOI: 10.1046/j.1432-1327.1999.00942.x  1
1999 Burgess HA, Martinez S, Reiner O. KIAA0369, doublecortin-like kinase, is expressed during brain development. Journal of Neuroscience Research. 58: 567-75. PMID 10533048 DOI: 10.1002/(SICI)1097-4547(19991115)58:4<567::AID-JNR9>3.0.CO;2-T  1
1999 Sapir T, Cahana A, Seger R, Nekhai S, Reiner O. LIS1 is a microtubule-associated phosphoprotein. European Journal of Biochemistry / Febs. 265: 181-8. PMID 10491172 DOI: 10.1046/j.1432-1327.1999.00711.x  1
1999 Horesh D, Sapir T, Francis F, Wolf SG, Caspi M, Elbaum M, Chelly J, Reiner O. Doublecortin, a stabilizer of microtubules. Human Molecular Genetics. 8: 1599-610. PMID 10441322 DOI: 10.1093/hmg/8.9.1599  1
1999 Francis F, Koulakoff A, Boucher D, Chafey P, Schaar B, Vinet MC, Friocourt G, McDonnell N, Reiner O, Kahn A, McConnell SK, Berwald-Netter Y, Denoulet P, Chelly J. Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons. Neuron. 23: 247-56. PMID 10399932 DOI: 10.1016/S0896-6273(00)80777-1  1
1999 Shmueli O, Cahana A, Reiner O. Platelet-activating factor (PAF) acetylhydrolase activity, LIS1 expression, and seizures. Journal of Neuroscience Research. 57: 176-84. PMID 10398295 DOI: 10.1002/(SICI)1097-4547(19990715)57:2<176::AID-JNR3>3.0.CO;2-U  1
1999 Cahana A, Reiner O. LIS1 and platelet-activating factor acetylhydrolase (Ib) catalytic subunits, expression in the mouse oocyte and zygote. Febs Letters. 451: 99-102. PMID 10371146 DOI: 10.1016/S0014-5793(99)00548-7  1
1998 Reiner O, Sapir T. Abnormal cortical development; towards elucidation of the LIS1 gene product function (review). International Journal of Molecular Medicine. 1: 849-53. PMID 9852306 DOI: 10.3892/ijmm.1.5.849  1
1998 Morris SM, Albrecht U, Reiner O, Eichele G, Yu-Lee LY. The lissencephaly gene product Lis1, a protein involved in neuronal migration, interacts with a nuclear movement protein, NudC. Current Biology : Cb. 8: 603-6. PMID 9601647 DOI: 10.1016/S0960-9822(98)70232-5  1
1998 Reiner O, Lombroso PJ. Development of the cerebral cortex: II. Lissencephaly. Journal of the American Academy of Child and Adolescent Psychiatry. 37: 231-2. PMID 9473922 DOI: 10.1097/00004583-199802000-00018  1
1997 Sapir T, Elbaum M, Reiner O. Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit. The Embo Journal. 16: 6977-84. PMID 9384577 DOI: 10.1093/emboj/16.23.6977  1
1996 Garcia-Higuera I, Fenoglio J, Li Y, Lewis C, Panchenko MP, Reiner O, Smith TF, Neer EJ. Folding of proteins with WD-repeats: comparison of six members of the WD-repeat superfamily to the G protein beta subunit. Biochemistry. 35: 13985-94. PMID 8909296 DOI: 10.1021/bi9612879  1
1996 Hildebrandt F, Cybulla M, Strahm B, Nothwang HG, Singh-Sawhney I, Berz K, Nicklin M, Reiner O, Brandis M. Physical mapping of the gene for juvenile nephronophthisis (NPH1) by construction of a complete YAC contig of 7 Mb on chromosome 2q13. Cytogenetics and Cell Genetics. 73: 235-9. PMID 8697815 DOI: 10.1159/000134346  1
1996 Jin DY, Myung Soo Lyu, Kozak CA, Jeang KT, Reiner O, Caskey CT. Function of 14-3-3 proteins Nature. 382: 308. PMID 8684458 DOI: 10.1038/382308b0  1
1995 Reiner O, Bar-Am I, Sapir T, Shmueli O, Carrozzo R, Lindsay EA, Baldini A, Ledbetter DH, Cahana A. LIS2, gene and pseudogene, homologous to LIS1 (lissencephaly 1), located on the short and long arms of chromosome 2. Genomics. 30: 251-6. PMID 8586424 DOI: 10.1006/geno.1995.9880  1
1995 Reiner O, Albrecht U, Gordon M, Chianese KA, Wong C, Gal-Gerber O, Sapir T, Siracusa LD, Buchberg AM, Caskey CT. Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 15: 3730-8. PMID 7751941 DOI: 10.1523/JNEUROSCI.15-05-03730.1995  1
1994 Spurr NK, Barton H, Bashir R, Bryson GM, Bushby K, Cox S, Gringrich JC, Hentati A, Hildebrandt F, Kao FT, Kruse T, Lai E, Liu J, Menke M, Naylor S, ... ... Reiner O, et al. Report of the Third International Workshop on Human Chromosome 2 Mapping 1994 Cytogenetics and Cell Genetics. 67: 215-237. PMID 7924452  1
1993 Reiner O, Carrozzo R, Shen Y, Wehnert M, Faustinella F, Dobyns WB, Caskey CT, Ledbetter DH. Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats. Nature. 364: 717-21. PMID 8355785 DOI: 10.1038/364717a0  1
1993 Wehnert M, Reiner O, Caskey CT. Four STR polymorphisms map to a 500 kb region between DXS15 and DXS134. Human Molecular Genetics. 2: 1503. PMID 8242082 DOI: 10.1093/hmg/2.9.1503  1
1993 Dobyns WB, Reiner O, Carrozzo R, Ledbetter DH. Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13. Jama. 270: 2838-42. PMID 7907669 DOI: 10.1001/jama.1993.03510230076039  1
1991 Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang FP. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell. 65: 905-14. PMID 1710175 DOI: 10.1016/0092-8674(91)90397-H  1
1989 Horowitz M, Wilder S, Horowitz Z, Reiner O, Gelbart T, Beutler E. The human glucocerebrosidase gene and pseudogene: structure and evolution. Genomics. 4: 87-96. PMID 2914709 DOI: 10.1016/0888-7543(89)90319-4  1
1989 Reiner O, Dagan O, Horowitz M. Human sphingolipid activator protein-1 and sphingolipid activator protein-2 are encoded by the same gene. Journal of Molecular Neuroscience : Mn. 1: 225-33. PMID 2484333  1
1989 Wigderson M, Firon N, Horowitz Z, Wilder S, Frishberg Y, Reiner O, Horowitz M. Characterization of mutations in Gaucher patients by cDNA cloning. American Journal of Human Genetics. 44: 365-77. PMID 2464926  1
1988 Reiner O, Wigderson M, Horowitz M. Structural analysis of the human glucocerebrosidase genes. Dna (Mary Ann Liebert, Inc.). 7: 107-16. PMID 3359914 DOI: 10.1089/dna.1988.7.107  1
1988 Reiner O, Horowitz M. Differential expression of the human glucocerebrosidase-coding gene. Gene. 73: 469-78. PMID 2468581 DOI: 10.1016/0378-1119(88)90511-2  1
1987 Reiner O, Wilder S, Givol D, Horowitz M. Efficient in vitro and in vivo expression of human glucocerebrosidase cDNA. Dna (Mary Ann Liebert, Inc.). 6: 101-8. PMID 2438102 DOI: 10.1089/dna.1987.6.101  1
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