Janine LaSalle - Publications

University of California, Davis, Davis, CA 

99 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
2019 Zhu Y, Mordaunt CE, Yasui DH, Marathe R, Coulson RL, Dunaway KW, Jianu JM, Walker CK, Ozonoff S, Hertz-Picciotto I, Schmidt RJ, LaSalle JM. Placental DNA methylation levels at CYP2E1 and IRS2 are associated with child outcome in a prospective autism study. Human Molecular Genetics. PMID 31009952 DOI: 10.1093/hmg/ddz084  0.64
2018 Ciernia AV, Yasui DH, Pride MC, Durbin-Johnson B, Noronha A, Chang A, Knotts T, Rutkowsky J, Ramsey JJ, Crawley JN, LaSalle JM. MeCP2 isoform e1 mutant mice recapitulate motor and metabolic phenotypes of Rett syndrome. Human Molecular Genetics. PMID 30137367 DOI: 10.1093/hmg/ddy301  0.64
2018 Coulson RL, Powell WT, Yasui DH, Dileep G, Resnick J, LaSalle JM. Prader-Willi locus Snord116 RNA processing requires an active endogenous allele and neuron-specific splicing by Rbfox3/NeuN. Human Molecular Genetics. PMID 30124848 DOI: 10.1093/hmg/ddy296  0.64
2018 Adhikari A, Copping NA, Onaga B, Pride MC, Coulson RL, Yang M, Yasui DH, LaSalle JM, Silverman JL. Cognitive Deficits in the Snord116 Deletion Mouse Model for Prader-Willi Syndrome. Neurobiology of Learning and Memory. PMID 29800646 DOI: 10.1016/j.nlm.2018.05.011  0.64
2018 Coulson RL, Yasui DH, Dunaway KW, Laufer BI, Vogel Ciernia A, Zhu Y, Mordaunt CE, Totah TS, LaSalle JM. Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex. Nature Communications. 9: 1616. PMID 29691382 DOI: 10.1038/s41467-018-03676-0  0.64
2018 Vogel Ciernia A, Laufer BI, Dunaway KW, Mordaunt CE, Coulson RL, Totah TS, Stolzenberg DS, Frahm J, Singh-Taylor A, Baram TZ, LaSalle JM, Yasui DH. Experience-dependent neuroplasticity of the developing hypothalamus: integrative epigenomic approaches. Epigenetics. 1-37. PMID 29613827 DOI: 10.1080/15592294.2018.1451720  0.64
2017 Vogel Ciernia A, Pride M, Durbin-Johnson B, Noronha A, Chang A, Yasui DH, Crawley JN, LaSalle JM. Early motor phenotype detection in a female mouse model of Rett syndrome is improved by cross-fostering. Human Molecular Genetics. PMID 28334953 DOI: 10.1093/hmg/ddx087  0.64
2016 Schmidt RJ, Schroeder DI, Crary-Dooley FK, Barkoski JM, Tancredi DJ, Walker CK, Ozonoff S, Hertz-Picciotto I, LaSalle JM. Self-reported pregnancy exposures and placental DNA methylation in the MARBLES prospective autism sibling study. Environmental Epigenetics. 2. PMID 28781890 DOI: 10.1093/eep/dvw024  0.36
2016 Schroeder DI, Schmidt RJ, Crary-Dooley FK, Walker CK, Ozonoff S, Tancredi DJ, Hertz-Picciotto I, LaSalle JM. Placental methylome analysis from a prospective autism study. Molecular Autism. 7: 51. PMID 28018572 DOI: 10.1186/s13229-016-0114-8  0.36
2016 Dunaway KW, Islam MS, Coulson RL, Lopez SJ, Vogel Ciernia A, Chu RG, Yasui DH, Pessah IN, Lott P, Mordaunt C, Meguro-Horike M, Horike SI, Korf I, LaSalle JM. Cumulative Impact of Polychlorinated Biphenyl and Large Chromosomal Duplications on DNA Methylation, Chromatin, and Expression of Autism Candidate Genes. Cell Reports. 17: 3035-3048. PMID 27974215 DOI: 10.1016/j.celrep.2016.11.058  0.64
2016 Medici V, Kieffer DA, Shibata NM, Chima H, Kim K, Canovas A, Medrano JF, Islas-Trejo AD, Kharbanda KK, Olson K, Su RJ, Islam MS, Syed R, Keen CL, Miller AY, ... ... LaSalle JM, et al. Wilson Disease: epigenetic effects of choline supplementation on phenotype and clinical course in a mouse model. Epigenetics. 0. PMID 27611852 DOI: 10.1080/15592294.2016.1231289  1
2016 Veeraragavan S, Wan YW, Connolly DR, Hamilton SM, Ward CS, Soriano S, Pitcher MR, McGraw CM, Huang SG, Green JR, Yuva LA, Liang AJ, Neul JL, Yasui DH, LaSalle JM, et al. Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome. Human Molecular Genetics. PMID 27365498 DOI: 10.1093/hmg/ddw178  0.96
2016 Rube HT, Lee W, Hejna M, Chen H, Yasui DH, Hess JF, LaSalle JM, Song JS, Gong Q. Sequence features accurately predict genome-wide MeCP2 binding in vivo. Nature Communications. 7: 11025. PMID 27008915 DOI: 10.1038/ncomms11025  1
2015 LaSalle JM, Reiter LT, Chamberlain SJ. Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders. Epigenomics. PMID 26585570 DOI: 10.2217/epi.15.70  1
2015 Schroeder DI, Jayashankar K, Douglas KC, Thirkill TL, York D, Dickinson PJ, Williams LE, Samollow PB, Ross PJ, Bannasch DL, Douglas GC, LaSalle JM. Early Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas. Plos Genetics. 11: e1005442. PMID 26241857 DOI: 10.1371/journal.pgen.1005442  1
2015 Powell WT, LaSalle JM. Epigenetic mechanisms in diurnal cycles of metabolism and neurodevelopment. Human Molecular Genetics. 24: R1-9. PMID 26105183 DOI: 10.1093/hmg/ddv234  1
2015 Li MM, Addepalli B, Tu MJ, Chen QX, Wang WP, Limbach PA, LaSalle JM, Zeng S, Huang M, Yu AM. Chimeric MicroRNA-1291 Biosynthesized Efficiently in Escherichia coli Is Effective to Reduce Target Gene Expression in Human Carcinoma Cells and Improve Chemosensitivity. Drug Metabolism and Disposition: the Biological Fate of Chemicals. 43: 1129-36. PMID 25934574 DOI: 10.1124/dmd.115.064493  1
2014 Lee W, Yun JM, Woods R, Dunaway K, Yasui DH, Lasalle JM, Gong Q. MeCP2 regulates activity-dependent transcriptional responses in olfactory sensory neurons. Human Molecular Genetics. 23: 6366-74. PMID 25008110 DOI: 10.1093/hmg/ddu358  1
2014 Le A, Shibata NM, French SW, Kim K, Kharbanda KK, Islam MS, LaSalle JM, Halsted CH, Keen CL, Medici V. Characterization of timed changes in hepatic copper concentrations, methionine metabolism, gene expression, and global DNA methylation in the Jackson toxic milk mouse model of Wilson disease. International Journal of Molecular Sciences. 15: 8004-23. PMID 24810691 DOI: 10.3390/ijms15058004  1
2014 Selmi C, Cavaciocchi F, Lleo A, Cheroni C, De Francesco R, Lombardi SA, De Santis M, Meda F, Raimondo MG, Crotti C, Folci M, Zammataro L, Mayo MJ, Bach N, Shimoda S, ... ... Lasalle JM, et al. Genome-wide analysis of DNA methylation, copy number variation, and gene expression in monozygotic twins discordant for primary biliary cirrhosis. Frontiers in Immunology. 5: 128. PMID 24734033 DOI: 10.3389/fimmu.2014.00128  1
2014 Medici V, Schroeder DI, Woods R, LaSalle JM, Geng Y, Shibata NM, Peerson J, Hodzic E, Dayal S, Tsukamoto H, Kharbanda KK, Tillman B, French SW, Halsted CH. Methylation and gene expression responses to ethanol feeding and betaine supplementation in the cystathionine beta synthase-deficient mouse. Alcoholism, Clinical and Experimental Research. 38: 1540-9. PMID 24730561 DOI: 10.1111/acer.12405  1
2014 Conant KD, Finucane B, Cleary N, Martin A, Muss C, Delany M, Murphy EK, Rabe O, Luchsinger K, Spence SJ, Schanen C, Devinsky O, Cook EH, LaSalle J, Reiter LT, et al. A survey of seizures and current treatments in 15q duplication syndrome. Epilepsia. 55: 396-402. PMID 24502430 DOI: 10.1111/epi.12530  1
2014 Yasui DH, Gonzales ML, Aflatooni JO, Crary FK, Hu DJ, Gavino BJ, Golub MS, Vincent JB, Carolyn Schanen N, Olson CO, Rastegar M, Lasalle JM. Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome. Human Molecular Genetics. 23: 2447-58. PMID 24352790 DOI: 10.1093/hmg/ddt640  1
2014 Medici V, Shibata NM, Kharbanda KK, Islam MS, Keen CL, Kim K, Tillman B, French SW, Halsted CH, LaSalle JM. Maternal choline modifies fetal liver copper, gene expression, DNA methylation, and neonatal growth in the tx-j mouse model of Wilson disease. Epigenetics : Official Journal of the Dna Methylation Society. 9: 286-96. PMID 24220304 DOI: 10.4161/epi.27110  1
2014 Selmi C, Cavaciocchi F, Lleo A, Cheroni C, de Francesco R, Lombardi SA, de Santis M, Meda F, Raimondo MG, Crotti C, Folci M, Zammataro L, Mayo MJ, Bach N, Shimoda S, ... ... LaSalle JM, et al. Corrigendum: Genome-wide analysis of DNA methylation, copy number variation, and gene expression in monozygotic twins discordant for primary biliary cirrhosis Frontiers in Immunology. 5. DOI: 10.3389/fimmu.2014.00371  1
2014 Woods R, Lasalle JM. Epigenetic epidemiology of autism and other neurodevelopmental disorders Epigenetic Epidemiology. 2147483647: 321-342. DOI: 10.1007/978-94-007-2495-2_17  1
2013 Schroeder DI, LaSalle JM. How has the study of the human placenta aided our understanding of partially methylated genes? Epigenomics. 5: 645-54. PMID 24283879 DOI: 10.2217/epi.13.62  1
2013 Powell WT, Coulson RL, Gonzales ML, Crary FK, Wong SS, Adams S, Ach RA, Tsang P, Yamada NA, Yasui DH, Chédin F, LaSalle JM. R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensation. Proceedings of the National Academy of Sciences of the United States of America. 110: 13938-43. PMID 23918391 DOI: 10.1073/pnas.1305426110  1
2013 Powell WT, Coulson RL, Crary FK, Wong SS, Ach RA, Tsang P, Alice Yamada N, Yasui DH, Lasalle JM. A Prader-Willi locus lncRNA cloud modulates diurnal genes and energy expenditure. Human Molecular Genetics. 22: 4318-28. PMID 23771028 DOI: 10.1093/hmg/ddt281  1
2013 LaSalle JM, Powell WT, Yasui DH. Epigenetic layers and players underlying neurodevelopment. Trends in Neurosciences. 36: 460-70. PMID 23731492 DOI: 10.1016/j.tins.2013.05.001  1
2013 LaSalle JM. Epigenomic strategies at the interface of genetic and environmental risk factors for autism. Journal of Human Genetics. 58: 396-401. PMID 23677056 DOI: 10.1038/jhg.2013.49  1
2013 Schroeder DI, Blair JD, Lott P, Yu HO, Hong D, Crary F, Ashwood P, Walker C, Korf I, Robinson WP, LaSalle JM. The human placenta methylome. Proceedings of the National Academy of Sciences of the United States of America. 110: 6037-42. PMID 23530188 DOI: 10.1073/pnas.1215145110  1
2013 Yasui DH, Xu H, Dunaway KW, Lasalle JM, Jin LW, Maezawa I. MeCP2 modulates gene expression pathways in astrocytes. Molecular Autism. 4: 3. PMID 23351786 DOI: 10.1186/2040-2392-4-3  0.64
2013 Medici V, Shibata NM, Kharbanda KK, LaSalle JM, Woods R, Liu S, Engelberg JA, Devaraj S, Török NJ, Jiang JX, Havel PJ, Lönnerdal B, Kim K, Halsted CH. Wilson's disease: changes in methionine metabolism and inflammation affect global DNA methylation in early liver disease. Hepatology (Baltimore, Md.). 57: 555-65. PMID 22945834 DOI: 10.1002/hep.26047  1
2013 Adams S, LaSalle JM. MeCP2 and Autism Spectrum Disorders The Neuroscience of Autism Spectrum Disorders. 421-436. DOI: 10.1016/B978-0-12-391924-3.00031-4  1
2013 Powell WT, LaSalle JM. Imprinting in the CNS and Neurodevelopmental Disorders Epigenetic Regulation in the Nervous System. 267-279. DOI: 10.1016/B978-0-12-391494-1.00010-0  1
2013 Lasalle JM, Islam MS. Recurrent CNVs in the etiology of epigenetic neurodevelopmental disorders Epigenetics and Complex Traits. 2147483647: 147-178. DOI: 10.1007/978-1-4614-8078-5_7  1
2012 Mitchell MM, Woods R, Chi LH, Schmidt RJ, Pessah IN, Kostyniak PJ, LaSalle JM. Levels of select PCB and PBDE congeners in human postmortem brain reveal possible environmental involvement in 15q11-q13 duplication autism spectrum disorder. Environmental and Molecular Mutagenesis. 53: 589-98. PMID 22930557 DOI: 10.1002/em.21722  1
2012 Selmi C, Feghali-Bostwick CA, Lleo A, Lombardi SA, De Santis M, Cavaciocchi F, Zammataro L, Mitchell MM, Lasalle JM, Medsger T, Gershwin ME. X chromosome gene methylation in peripheral lymphocytes from monozygotic twins discordant for scleroderma. Clinical and Experimental Immunology. 169: 253-62. PMID 22861365 DOI: 10.1111/j.1365-2249.2012.04621.x  1
2012 Gonzales ML, Adams S, Dunaway KW, LaSalle JM. Phosphorylation of distinct sites in MeCP2 modifies cofactor associations and the dynamics of transcriptional regulation. Molecular and Cellular Biology. 32: 2894-903. PMID 22615490 DOI: 10.1128/MCB.06728-11  1
2012 Woods R, Vallero RO, Golub MS, Suarez JK, Ta TA, Yasui DH, Chi LH, Kostyniak PJ, Pessah IN, Berman RF, LaSalle JM. Long-lived epigenetic interactions between perinatal PBDE exposure and Mecp2308 mutation. Human Molecular Genetics. 21: 2399-411. PMID 22343140 DOI: 10.1093/hmg/dds046  1
2012 Martins-Taylor K, Schroeder DI, LaSalle JM, Lalande M, Xu RH. Role of DNMT3B in the regulation of early neural and neural crest specifiers. Epigenetics : Official Journal of the Dna Methylation Society. 7: 71-82. PMID 22207353 DOI: 10.4161/epi.7.1.18750  1
2011 Scoles HA, Urraca N, Chadwick SW, Reiter LT, Lasalle JM. Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples. Molecular Autism. 2: 19. PMID 22152151 DOI: 10.1186/2040-2392-2-19  1
2011 Yasui DH, Scoles HA, Horike S, Meguro-Horike M, Dunaway KW, Schroeder DI, Lasalle JM. 15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain. Human Molecular Genetics. 20: 4311-23. PMID 21840925 DOI: 10.1093/hmg/ddr357  1
2011 Schroeder DI, Lott P, Korf I, LaSalle JM. Large-scale methylation domains mark a functional subset of neuronally expressed genes. Genome Research. 21: 1583-91. PMID 21784875 DOI: 10.1101/gr.119131.110  1
2011 Meguro-Horike M, Yasui DH, Powell W, Schroeder DI, Oshimura M, Lasalle JM, Horike S. Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome. Human Molecular Genetics. 20: 3798-810. PMID 21725066 DOI: 10.1093/hmg/ddr298  1
2011 LaSalle JM. A genomic point-of-view on environmental factors influencing the human brain methylome. Epigenetics : Official Journal of the Dna Methylation Society. 6: 862-9. PMID 21617367 DOI: 10.4161/epi.6.7.16353  1
2011 Artuso R, Papa FT, Grillo E, Mucciolo M, Yasui DH, Dunaway KW, Disciglio V, Mencarelli MA, Pollazzon M, Zappella M, Hayek G, Mari F, Renieri A, Lasalle JM, Ariani F. Investigation of modifier genes within copy number variations in Rett syndrome. Journal of Human Genetics. 56: 508-15. PMID 21593744 DOI: 10.1038/jhg.2011.50  1
2011 Singleton MK, Gonzales ML, Leung KN, Yasui DH, Schroeder DI, Dunaway K, LaSalle JM. MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation. Neurobiology of Disease. 43: 190-200. PMID 21420494 DOI: 10.1016/j.nbd.2011.03.011  1
2011 Leung KN, Chamberlain SJ, Lalande M, LaSalle JM. Neuronal chromatin dynamics of imprinting in development and disease. Journal of Cellular Biochemistry. 112: 365-73. PMID 21268055 DOI: 10.1002/jcb.22958  1
2011 Mitchell MM, Lleo A, Zammataro L, Mayo MJ, Invernizzi P, Bach N, Shimoda S, Gordon S, Podda M, Gershwin ME, Selmi C, LaSalle JM. Epigenetic investigation of variably X chromosome inactivated genes in monozygotic female twins discordant for primary biliary cirrhosis. Epigenetics : Official Journal of the Dna Methylation Society. 6: 95-102. PMID 20864813 DOI: 10.4161/epi.6.1.13405  1
2010 Gonzales ML, LaSalle JM. The role of MeCP2 in brain development and neurodevelopmental disorders. Current Psychiatry Reports. 12: 127-34. PMID 20425298 DOI: 10.1007/s11920-010-0097-7  1
2010 Hogart A, Wu D, LaSalle JM, Schanen NC. The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13. Neurobiology of Disease. 38: 181-91. PMID 18840528 DOI: 10.1016/j.nbd.2008.08.011  1
2010 Berman RF, Koenig CM, Hunsaker MR, Pessah IN, Lasalle JM. Neurodevelopmental Toxicology and Autism Spectrum Disorders Developmental Neurotoxicology Research: Principles, Models, Techniques, Strategies, and Mechanisms. 439-476. DOI: 10.1002/9780470917060.ch21  1
2009 LaSalle JM, Yasui DH. Evolving role of MeCP2 in Rett syndrome and autism. Epigenomics. 1: 119-30. PMID 20473347 DOI: 10.2217/epi.09.13  1
2009 Leung KN, Vallero RO, DuBose AJ, Resnick JL, LaSalle JM. Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size. Human Molecular Genetics. 18: 4227-38. PMID 19656775 DOI: 10.1093/hmg/ddp373  1
2009 Maezawa I, Swanberg S, Harvey D, LaSalle JM, Jin LW. Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 5051-61. PMID 19386901 DOI: 10.1523/JNEUROSCI.0324-09.2009  1
2009 Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM. Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism. Human Molecular Genetics. 18: 525-34. PMID 19000991 DOI: 10.1093/hmg/ddn380  1
2009 Adegbola AA, Gonzales ML, Chess A, LaSalle JM, Cox GF. A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype. Human Genetics. 124: 615-23. PMID 18989701 DOI: 10.1007/s00439-008-0585-6  1
2009 Hogart A, Leung KN, Wang NJ, Wu DJ, Driscoll J, Vallero RO, Schanen NC, LaSalle JM. Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number. Journal of Medical Genetics. 46: 86-93. PMID 18835857 DOI: 10.1136/jmg.2008.061580  1
2008 Nagarajan RP, Patzel KA, Martin M, Yasui DH, Swanberg SE, Hertz-Picciotto I, Hansen RL, Van de Water J, Pessah IN, Jiang R, Robinson WP, LaSalle JM. MECP2 promoter methylation and X chromosome inactivation in autism. Autism Research : Official Journal of the International Society For Autism Research. 1: 169-78. PMID 19132145 DOI: 10.1002/aur.24  1
2008 Hogart A, Patzel KA, LaSalle JM. Gender influences monoallelic expression of ATP10A in human brain. Human Genetics. 124: 235-42. PMID 18726118 DOI: 10.1007/s00439-008-0546-0  1
2008 Pessah IN, Seegal RF, Lein PJ, LaSalle J, Yee BK, Van De Water J, Berman RF. Immunologic and neurodevelopmental susceptibilities of autism. Neurotoxicology. 29: 532-45. PMID 18394707 DOI: 10.1016/j.neuro.2008.02.006  1
2008 Kumar A, Kamboj S, Malone BM, Kudo S, Twiss JL, Czymmek KJ, LaSalle JM, Schanen NC. Analysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivo. Journal of Cell Science. 121: 1128-37. PMID 18334558 DOI: 10.1242/jcs.016865  1
2008 Wang NJ, Parokonny AS, Thatcher KN, Driscoll J, Malone BM, Dorrani N, Sigman M, LaSalle JM, Schanen NC. Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15. Bmc Genetics. 9: 2. PMID 18177502 DOI: 10.1186/1471-2156-9-2  1
2007 Yasui DH, Peddada S, Bieda MC, Vallero RO, Hogart A, Nagarajan RP, Thatcher KN, Farnham PJ, Lasalle JM. Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes. Proceedings of the National Academy of Sciences of the United States of America. 104: 19416-21. PMID 18042715 DOI: 10.1073/pnas.0707442104  1
2007 LaSalle JM. The odyssey of MeCP2 and parental imprinting. Epigenetics : Official Journal of the Dna Methylation Society. 2: 5-10. PMID 17486180  1
2007 Hogart A, Nagarajan RP, Patzel KA, Yasui DH, Lasalle JM. 15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders. Human Molecular Genetics. 16: 691-703. PMID 17339270 DOI: 10.1093/hmg/ddm014  1
2006 Nagarajan RP, Hogart AR, Gwye Y, Martin MR, LaSalle JM. Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation. Epigenetics : Official Journal of the Dna Methylation Society. 1: e1-11. PMID 17486179 DOI: 10.4161/epi.1.4.3514  1
2006 Thatcher KN, LaSalle JM. Dynamic changes in Histone H3 lysine 9 acetylation localization patterns during neuronal maturation require MeCP2. Epigenetics : Official Journal of the Dna Methylation Society. 1: 24-31. PMID 17464364 DOI: 10.4161/epi.1.1.2339  1
2006 Delgado IJ, Kim DS, Thatcher KN, LaSalle JM, Van den Veyver IB. Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients. Bmc Medical Genetics. 7: 61. PMID 16859563 DOI: 10.1186/1471-2350-7-61  1
2006 Peddada S, Yasui DH, LaSalle JM. Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome. Human Molecular Genetics. 15: 2003-14. PMID 16682435 DOI: 10.1093/hmg/ddl124  1
2005 LaSalle JM, Hogart A, Thatcher KN. Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism. International Review of Neurobiology. 71: 131-65. PMID 16512349 DOI: 10.1016/S0074-7742(05)71006-0  1
2005 Thatcher KN, Peddada S, Yasui DH, Lasalle JM. Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples. Human Molecular Genetics. 14: 785-97. PMID 15689352 DOI: 10.1093/hmg/ddi073  1
2005 Samaco RC, Hogart A, LaSalle JM. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Human Molecular Genetics. 14: 483-92. PMID 15615769 DOI: 10.1093/hmg/ddi045  1
2004 Braunschweig D, Simcox T, Samaco RC, LaSalle JM. X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain. Human Molecular Genetics. 13: 1275-86. PMID 15115765 DOI: 10.1093/hmg/ddh142  1
2004 LaSalle JM. Paradoxical role of methyl-CpG-binding protein 2 in Rett syndrome. Current Topics in Developmental Biology. 59: 61-86. PMID 14975247 DOI: 10.1016/S0070-2153(04)59003-8  1
2004 Samaco RC, Nagarajan RP, Braunschweig D, LaSalle JM. Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders. Human Molecular Genetics. 13: 629-39. PMID 14734626 DOI: 10.1093/hmg/ddh063  1
2003 Balmer D, Goldstine J, Rao YM, LaSalle JM. Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation. Journal of Molecular Medicine (Berlin, Germany). 81: 61-8. PMID 12545250 DOI: 10.1007/s00109-002-0396-5  1
2002 Gandour-Edwards R, Lara PN, Folkins AK, LaSalle JM, Beckett L, Li Y, Meyers FJ, DeVere-White R. Does HER2/neu expression provide prognostic information in patients with advanced urothelial carcinoma? Cancer. 95: 1009-15. PMID 12209684 DOI: 10.1002/cncr.10808  1
2002 Balmer D, Arredondo J, Samaco RC, LaSalle JM. MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain. Human Genetics. 110: 545-52. PMID 12107440 DOI: 10.1007/s00439-002-0724-4  1
2002 Gandour-Edwards R, LaSalle J. 18 Combined detection of low level her-2/neu expression and gene amplification in prostate cancer by immunofluorescence and fluorescence in situ hybridization Handbook of Immunohistochemistry and in Situ Hybridization of Human Carcinomas. 2: 457-461. DOI: 10.1016/S1874-5784(02)80050-2  1
2001 LaSalle J, Lalande M. Flow cytometry and FISH to investigate allele-specific replication timing and homologous association of imprinted chromosomes. Methods in Molecular Biology (Clifton, N.J.). 181: 181-92. PMID 12843450 DOI: 10.1385/1-59259-211-2:181  1
2001 Liu HL, Gandour-Edwards R, Lara PN, de Vere White R, LaSalle JM. Detection of low level HER-2/neu gene amplification in prostate cancer by fluorescence in situ hybridization. Cancer Journal (Sudbury, Mass.). 7: 395-403. PMID 11693898  1
2001 LaSalle JM, Goldstine J, Balmer D, Greco CM. Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry. Human Molecular Genetics. 10: 1729-40. PMID 11532982  1
2001 Douglas GC, Thirkill TL, LaSalle J. Automated quantitation of cell-mediated HIV type 1 infection of human syncytiotrophoblast cells by fluorescence in situ hybridization and laser scanning cytometry. Aids Research and Human Retroviruses. 17: 507-16. PMID 11350664 DOI: 10.1089/08892220151126562  1
2001 Balmer D, LaSalle JM. Clonal maintenance of imprinted expression of SNRPN and IPW in normal lymphocytes: correlation with allele-specific methylation of SNRPN intron 1 but not intron 7. Human Genetics. 108: 116-22. PMID 11281449 DOI: 10.1007/s004390000455  1
1998 LaSalle JM, Ritchie RJ, Glatt H, Lalande M. Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes. Proceedings of the National Academy of Sciences of the United States of America. 95: 1675-80. PMID 9465075 DOI: 10.1073/pnas.95.4.1675  1
1997 Strehl S, LaSalle JM, Lalande M. High-resolution analysis of DNA replication domain organization across an R/G-band boundary. Molecular and Cellular Biology. 17: 6157-66. PMID 9315676  1
1997 Mizuta R, LaSalle JM, Cheng HL, Shinohara A, Ogawa H, Copeland N, Jenkins NA, Lalande M, Alt FW. RAB22 and RAB163/mouse BRCA2: proteins that specifically interact with the RAD51 protein. Proceedings of the National Academy of Sciences of the United States of America. 94: 6927-32. PMID 9192668 DOI: 10.1073/pnas.94.13.6927  1
1996 LaSalle JM, Lalande M. Homologous association of oppositely imprinted chromosomal domains. Science (New York, N.Y.). 272: 725-8. PMID 8614834  1
1995 LaSalle JM, Lalande M. Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution. Nature Genetics. 9: 386-94. PMID 7795644 DOI: 10.1038/ng0495-386  1
1994 LaSalle JM, Hafler DA. T cell anergy. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 8: 601-8. PMID 8005388  1
1993 LaSalle JM, Toneguzzo F, Saadeh M, Golan DE, Taber R, Hafler DA. T-cell presentation of antigen requires cell-to-cell contact for proliferation and anergy induction. Differential MHC requirements for superantigen and autoantigen. Journal of Immunology (Baltimore, Md. : 1950). 151: 649-57. PMID 7687620  1
1993 Hafler DA, Zhang JW, LaSalle J, Donnelly C, Weiner HL, Wucherpfeffnig K. The development of antigen specific therapies for autoimmune diseases; investigations in multiple sclerosis as a paradigm for rheumatoid arthritis. Clinical and Experimental Rheumatology. 11: S39-40. PMID 7686832  1
1993 Oettinger HF, al-Sabbagh A, Jingwu Z, LaSalle JM, Weiner HL, Hafler DA. Biological activity of recombinant human myelin basic protein. Journal of Neuroimmunology. 44: 157-62. PMID 7685037 DOI: 10.1016/0165-5728(93)90037-Y  1
1992 LaSalle JM, Tolentino PJ, Freeman GJ, Nadler LM, Hafler DA. Early signaling defects in human T cells anergized by T cell presentation of autoantigen. The Journal of Experimental Medicine. 176: 177-86. PMID 1535366  1
1991 LaSalle JM, Hafler DA. The coexpression of CD45RA and CD45RO isoforms on T cells during the S/G2/M stages of cell cycle. Cellular Immunology. 138: 197-206. PMID 1833074 DOI: 10.1016/0008-8749(91)90144-Z  1
1991 LaSalle JM, Ota K, Hafler DA. Presentation of autoantigen by human T cells. Journal of Immunology (Baltimore, Md. : 1950). 147: 774-80. PMID 1713605  1
Show low-probability matches.