| Year |
Citation |
Score |
| 2023 |
Sapir T, Reiner O. HNRNPU's multi-tasking is essential for proper cortical development. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. e2300039. PMID 37439444 DOI: 10.1002/bies.202300039 |
0.347 |
|
| 2023 |
Kshirsagar A, Doroshev SM, Gorelik A, Olender T, Sapir T, Tsuboi D, Rosenhek-Goldian I, Malitsky S, Itkin M, Argoetti A, Mandel-Gutfreund Y, Cohen SR, Hanna JH, Ulitsky I, Kaibuchi K, ... Reiner O, et al. LIS1 RNA-binding orchestrates the mechanosensitive properties of embryonic stem cells in AGO2-dependent and independent ways. Nature Communications. 14: 3293. PMID 37280197 DOI: 10.1038/s41467-023-38797-8 |
0.771 |
|
| 2022 |
Sapir T, Kshirsagar A, Gorelik A, Olender T, Porat Z, Scheffer IE, Goldstein DB, Devinsky O, Reiner O. Heterogeneous nuclear ribonucleoprotein U (HNRNPU) safeguards the developing mouse cortex. Nature Communications. 13: 4209. PMID 35864088 DOI: 10.1038/s41467-022-31752-z |
0.8 |
|
| 2022 |
Parichha A, Suresh V, Chatterjee M, Kshirsagar A, Ben-Reuven L, Olender T, Taketo MM, Radosevic V, Bobic-Rasonja M, Trnski S, Holtzman MJ, Jovanov-Milosevic N, Reiner O, Tole S. Constitutive activation of canonical Wnt signaling disrupts choroid plexus epithelial fate. Nature Communications. 13: 633. PMID 35110543 DOI: 10.1038/s41467-021-27602-z |
0.777 |
|
| 2020 |
Magdalon J, Mansur F, Teles E Silva AL, de Goes VA, Reiner O, Sertié AL. Complement System in Brain Architecture and Neurodevelopmental Disorders. Frontiers in Neuroscience. 14: 23. PMID 32116493 DOI: 10.3389/Fnins.2020.00023 |
0.366 |
|
| 2019 |
Ben-Reuven L, Reiner O. Dynamics of cortical progenitors and production of subcerebral neurons are altered in embryos of a maternal inflammation model for autism. Molecular Psychiatry. PMID 31740755 DOI: 10.1038/S41380-019-0594-Y |
0.384 |
|
| 2019 |
Keidar L, Gerlitz G, Kshirsagar A, Tsoory M, Olender T, Wang X, Yang Y, Chen YS, Yang YG, Voineagu I, Reiner O. Interplay of LIS1 and MeCP2: Interactions and Implications With the Neurodevelopmental Disorders Lissencephaly and Rett Syndrome. Frontiers in Cellular Neuroscience. 13: 370. PMID 31474834 DOI: 10.3389/Fncel.2019.00370 |
0.787 |
|
| 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 |
0.424 |
|
| 2019 |
Karzbrun E, Reiner O. Brain Organoids-A Bottom-Up Approach for Studying Human Neurodevelopment. Bioengineering (Basel, Switzerland). 6. PMID 30669275 DOI: 10.3390/Bioengineering6010009 |
0.32 |
|
| 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 |
0.437 |
|
| 2018 |
Karzbrun E, Kshirsagar A, Cohen SR, Hanna JH, Reiner O. Human Brain Organoids on a Chip Reveal the Physics of Folding. Nature Physics. 14: 515-522. PMID 29760764 DOI: 10.1038/S41567-018-0046-7 |
0.769 |
|
| 2018 |
Uzquiano A, Gladwyn-Ng I, Nguyen L, Reiner O, Götz M, Matsuzaki F, Francis F. Cortical progenitor biology: key features mediating proliferation versus differentiation. Journal of Neurochemistry. PMID 29570795 DOI: 10.1111/Jnc.14338 |
0.397 |
|
| 2017 |
Sapir T, Levy T, Kozer N, Shin I, Zamor V, Haffner-Krausz R, McGlade JC, Reiner O. Notch Activation by Shootin1 Opposing Activities on 2 Ubiquitin Ligases. Cerebral Cortex (New York, N.Y. : 1991). 1-14. PMID 28981589 DOI: 10.1093/Cercor/Bhx180 |
0.356 |
|
| 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 |
0.423 |
|
| 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 |
0.411 |
|
| 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 |
0.429 |
|
| 2017 |
Gorelik A, Sapir T, Reiner O. Unexpected Activities of the Complement Pathway in Migrating Neurons European Neuropsychopharmacology. 27: S509. DOI: 10.1111/Jnc.13185 |
0.41 |
|
| 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 |
0.328 |
|
| 2016 |
Ben-Reuven L, Reiner O. Modeling the autistic cell: iPSCs recapitulate developmental principles of syndromic and nonsyndromic ASD. Development, Growth & Differentiation. PMID 27111774 DOI: 10.1111/Dgd.12280 |
0.328 |
|
| 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 |
0.372 |
|
| 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 |
0.775 |
|
| 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 |
0.368 |
|
| 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 |
0.511 |
|
| 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 |
0.304 |
|
| 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 |
0.436 |
|
| 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 |
0.365 |
|
| 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 |
0.463 |
|
| 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 |
0.476 |
|
| 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 |
0.31 |
|
| 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 |
0.344 |
|
| 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 |
0.337 |
|
| 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 |
0.346 |
|
| 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 |
0.447 |
|
| 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 |
0.451 |
|
| 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 |
0.329 |
|
| 2012 |
Gorelik A, Reiner O. The role of the complement pathway in neuronal migration in the developing brain Immunobiology. 217: 1212. DOI: 10.1016/J.Imbio.2012.08.238 |
0.438 |
|
| 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 |
0.333 |
|
| 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 |
0.433 |
|
| 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 |
0.367 |
|
| 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 |
0.378 |
|
| 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 |
0.8 |
|
| 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 |
0.408 |
|
| 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 |
0.4 |
|
| 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 |
0.396 |
|
| 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 |
0.464 |
|
| 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 |
0.339 |
|
| 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 |
0.806 |
|
| 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 |
0.409 |
|
| 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 |
0.37 |
|
| 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 |
0.788 |
|
| 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 |
0.405 |
|
| 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 |
0.424 |
|
| 2006 |
Tabarés-Seisdedos R, Escámez T, MartÃnez-Giménez JA, Balanzá V, Salazar J, Selva G, Rubio C, Vieta E, Geijó-Barrientos E, MartÃnez-Arán A, Reiner O, MartÃnez 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 |
0.348 |
|
| 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 |
0.776 |
|
| 2006 |
Reiner O, Sapir T. Cdk5 checks p27kip1 in neuronal migration. Nature Cell Biology. 8: 11-3. PMID 16389288 DOI: 10.1038/Ncb0106-11 |
0.42 |
|
| 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 |
0.458 |
|
| 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 |
0.388 |
|
| 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 |
0.349 |
|
| 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 |
0.37 |
|
| 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 |
0.435 |
|
| 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 |
0.411 |
|
| 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 |
0.339 |
|
| 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 |
0.362 |
|
| 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 |
0.775 |
|
| 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 |
0.793 |
|
| 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 |
0.341 |
|
| 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 |
0.375 |
|
| 2002 |
Reiner O. Pathways of neuronal migration. Nature Genetics. 32: 341-2. PMID 12410228 DOI: 10.1038/Ng1102-341 |
0.437 |
|
| 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 |
0.373 |
|
| 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 |
0.7 |
|
| 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 |
0.382 |
|
| 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 |
0.671 |
|
| 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 |
0.807 |
|
| 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 |
0.769 |
|
| 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 |
0.72 |
|
| 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 |
0.428 |
|
| 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 |
0.685 |
|
| 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 |
0.323 |
|
| 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 |
0.758 |
|
| 1999 |
Reiner O. The unfolding story of two lissencephaly genes and brain development. Molecular Neurobiology. 20: 143-56. PMID 10966119 DOI: 10.1007/Bf02742439 |
0.467 |
|
| 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 |
0.658 |
|
| 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 |
0.7 |
|
| 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 |
0.379 |
|
| 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 |
0.393 |
|
| 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 |
0.471 |
|
| 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 |
0.76 |
|
| 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 |
0.3 |
|
| 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 |
0.455 |
|
| 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 |
0.432 |
|
| 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 |
0.433 |
|
| 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 |
0.746 |
|
| 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 |
0.454 |
|
| 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 |
0.394 |
|
| 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 |
0.314 |
|
| 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 |
0.317 |
|
| 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 |
0.322 |
|
| 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 |
0.33 |
|
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