| Year |
Citation |
Score |
| 2023 |
Zhang R, Yang M, Schreiber J, O'Day DR, Turner JMA, Shendure J, Disteche CM, Deng X, Noble WS. Cross-species imputation and comparison of single-cell transcriptomic profiles. Biorxiv : the Preprint Server For Biology. PMID 37905060 DOI: 10.1101/2023.10.19.563173 |
0.33 |
|
| 2023 |
Lin J, Zhang J, Ma L, Fang H, Ma R, Groneck C, Filippova GN, Deng X, Ma W, Disteche CM, Berletch JB. KDM6A facilitates Xist upregulation at the onset of X inactivation. Biorxiv : the Preprint Server For Biology. PMID 37645756 DOI: 10.1101/2023.08.16.553617 |
0.56 |
|
| 2023 |
Fang H, Tronco AR, Bonora G, Nguyen T, Thakur J, Berletch JB, Filippova GN, Henikoff S, Shendure J, Noble WS, Disteche CM, Deng X. CTCF-mediated insulation and chromatin environment modulate escape from X inactivation. Biorxiv : the Preprint Server For Biology. PMID 37205597 DOI: 10.1101/2023.05.04.539469 |
0.57 |
|
| 2023 |
Liu S, Akula N, Reardon PK, Russ J, Torres E, Clasen LS, Blumenthal J, Lalonde F, McMahon FJ, Szele F, Disteche CM, Cader MZ, Raznahan A. Aneuploidy effects on human gene expression across three cell types. Proceedings of the National Academy of Sciences of the United States of America. 120: e2218478120. PMID 37192167 DOI: 10.1073/pnas.2218478120 |
0.519 |
|
| 2022 |
Ma W, Fang H, Pease N, Filippova GN, Disteche CM, Berletch JB. Sex-biased and parental allele-specific gene regulation by KDM6A. Biology of Sex Differences. 13: 40. PMID 35871105 DOI: 10.1186/s13293-022-00452-0 |
0.385 |
|
| 2021 |
Bonora G, Ramani V, Singh R, Fang H, Jackson DL, Srivatsan S, Qiu R, Lee C, Trapnell C, Shendure J, Duan Z, Deng X, Noble WS, Disteche CM. Single-cell landscape of nuclear configuration and gene expression during stem cell differentiation and X inactivation. Genome Biology. 22: 279. PMID 34579774 DOI: 10.1186/s13059-021-02432-w |
0.345 |
|
| 2021 |
Fang H, Deng X, Disteche CM. X-factors in human disease: Impact of gene content and dosage regulation. Human Molecular Genetics. PMID 34387327 DOI: 10.1093/hmg/ddab221 |
0.573 |
|
| 2020 |
Fang H, Bonora G, Lewandowski JP, Thakur J, Filippova GN, Henikoff S, Shendure J, Duan Z, Rinn JL, Deng X, Noble WS, Disteche CM. Trans- and cis-acting effects of Firre on epigenetic features of the inactive X chromosome. Nature Communications. 11: 6053. PMID 33247132 DOI: 10.1038/s41467-020-19879-3 |
0.426 |
|
| 2020 |
Raznahan A, Disteche CM. X-Chromosome Regulation and Sex Differences in Brain Anatomy. Neuroscience and Biobehavioral Reviews. PMID 33171144 DOI: 10.1016/j.neubiorev.2020.10.024 |
0.431 |
|
| 2020 |
Gravholt CH, Tartaglia N, Disteche C. Sex chromosome aneuploidies in 2020-The state of care and research in the world. American Journal of Medical Genetics Part C-Seminars in Medical Genetics. 184: 197-201. PMID 32496026 DOI: 10.1002/Ajmg.C.31808 |
0.398 |
|
| 2019 |
Fang H, Disteche CM, Berletch JB. X Inactivation and Escape: Epigenetic and Structural Features. Frontiers in Cell and Developmental Biology. 7: 219. PMID 31632970 DOI: 10.3389/Fcell.2019.00219 |
0.638 |
|
| 2019 |
Deng X, Disteche CM. Rapid transcriptional bursts upregulate the X chromosome. Nature Structural & Molecular Biology. 26: 851-853. PMID 31582850 DOI: 10.1038/S41594-019-0314-Y |
0.63 |
|
| 2019 |
Ramani V, Deng X, Qiu R, Lee C, Disteche CM, Noble WS, Shendure J, Duan Z. Sci-Hi-C: a single-cell Hi-C method for mapping 3D genome organization in large number of single cells. Methods (San Diego, Calif.). PMID 31536770 DOI: 10.1016/J.Ymeth.2019.09.012 |
0.355 |
|
| 2019 |
Yin Y, Jiang Y, Lam KG, Berletch JB, Disteche CM, Noble WS, Steemers FJ, Camerini-Otero RD, Adey AC, Shendure J. High-Throughput Single-Cell Sequencing with Linear Amplification. Molecular Cell. PMID 31495564 DOI: 10.1016/J.Molcel.2019.08.002 |
0.312 |
|
| 2018 |
Arnold AP, Disteche CM. Sexual Inequality in the Cancer Cell. Cancer Research. 78: 5504-5505. PMID 30275051 DOI: 10.1158/0008-5472.Can-18-2219 |
0.32 |
|
| 2018 |
Ma W, Bonora G, Berletch JB, Deng X, Noble WS, Disteche CM. X-Chromosome Inactivation and Escape from X Inactivation in Mouse. Methods in Molecular Biology (Clifton, N.J.). 1861: 205-219. PMID 30218369 DOI: 10.1007/978-1-4939-8766-5_15 |
0.665 |
|
| 2018 |
Cusanovich DA, Hill AJ, Aghamirzaie D, Daza RM, Pliner HA, Berletch JB, Filippova GN, Huang X, Christiansen L, DeWitt WS, Lee C, Regalado SG, Read DF, Steemers FJ, Disteche CM, et al. A Single-Cell Atlas of In Vivo Mammalian Chromatin Accessibility. Cell. PMID 30078704 DOI: 10.1016/J.Cell.2018.06.052 |
0.366 |
|
| 2018 |
Bonora G, Deng X, Fang H, Ramani V, Qiu R, Berletch JB, Filippova GN, Duan Z, Shendure J, Noble WS, Disteche CM. Orientation-dependent Dxz4 contacts shape the 3D structure of the inactive X chromosome. Nature Communications. 9: 1445. PMID 29654302 DOI: 10.1038/S41467-018-03694-Y |
0.503 |
|
| 2018 |
Ma W, Ay F, Lee C, Gulsoy G, Deng X, Cook S, Hesson J, Cavanaugh C, Ware CB, Krumm A, Shendure J, Blau CA, Disteche CM, Noble WS, Duan Z. Using DNase Hi-C techniques to map global and local three-dimensional genome architecture at high resolution. Methods (San Diego, Calif.). PMID 29382556 DOI: 10.1016/J.Ymeth.2018.01.014 |
0.326 |
|
| 2018 |
Catteruccia F, Disteche CM. Decision letter: Guy1, a Y-linked embryonic signal, regulates dosage compensation in Anopheles stephensi by increasing X gene expression Elife. DOI: 10.7554/Elife.43570.022 |
0.483 |
|
| 2017 |
Bonora G, Disteche CM. Structural aspects of the inactive X chromosome. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 372. PMID 28947656 DOI: 10.1098/Rstb.2016.0357 |
0.579 |
|
| 2017 |
Keown CL, Berletch JB, Castanon R, Nery JR, Disteche CM, Ecker JR, Mukamel EA. Allele-specific non-CG DNA methylation marks domains of active chromatin in female mouse brain. Proceedings of the National Academy of Sciences of the United States of America. PMID 28320934 DOI: 10.1073/Pnas.1611905114 |
0.578 |
|
| 2017 |
Ramani V, Deng X, Qiu R, Gunderson KL, Steemers FJ, Disteche CM, Noble WS, Duan Z, Shendure J. Massively multiplex single-cell Hi-C. Nature Methods. PMID 28135255 DOI: 10.1038/Nmeth.4155 |
0.34 |
|
| 2016 |
Ramani V, Cusanovich DA, Hause RJ, Ma W, Qiu R, Deng X, Blau CA, Disteche CM, Noble WS, Shendure J, Duan Z. Mapping 3D genome architecture through in situ DNase Hi-C. Nature Protocols. 11: 2104-2121. PMID 27685100 DOI: 10.1038/Nprot.2016.126 |
0.399 |
|
| 2016 |
Wei G, Deng X, Agarwal S, Iwase S, Disteche C, Xu J. Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells. Journal of Molecular Neuroscience : Mn. PMID 27421841 DOI: 10.1007/S12031-016-0770-3 |
0.356 |
|
| 2016 |
Disteche CM. Dosage compensation of the sex chromosomes and autosomes. Seminars in Cell & Developmental Biology. PMID 27112542 DOI: 10.1016/J.Semcdb.2016.04.013 |
0.531 |
|
| 2015 |
Berletch JB, Ma W, Yang F, Shendure J, Noble WS, Disteche CM, Deng X. Identification of genes escaping X inactivation by allelic expression analysis in a novel hybrid mouse model. Data in Brief. 5: 761-9. PMID 26693509 DOI: 10.1016/J.Dib.2015.10.033 |
0.62 |
|
| 2015 |
Disteche CM, Berletch JB. X-chromosome inactivation and escape. Journal of Genetics. 94: 591-9. PMID 26690513 DOI: 10.1007/S12041-015-0574-1 |
0.603 |
|
| 2015 |
Deng X, Ma W, Ramani V, Hill A, Yang F, Ay F, Berletch JB, Blau CA, Shendure J, Duan Z, Noble WS, Disteche CM. Bipartite structure of the inactive mouse X chromosome. Genome Biology. 16: 152. PMID 26248554 DOI: 10.1186/S13059-015-0728-8 |
0.645 |
|
| 2015 |
Yang F, Deng X, Ma W, Berletch JB, Rabaia N, Wei G, Moore JM, Filippova GN, Xu J, Liu Y, Noble WS, Shendure J, Disteche CM. The lncRNA Firre anchors the inactive X chromosome to the nucleolus by binding CTCF and maintains H3K27me3 methylation. Genome Biology. 16: 52. PMID 25887447 DOI: 10.1186/S13059-015-0618-0 |
0.654 |
|
| 2015 |
Berletch JB, Ma W, Yang F, Shendure J, Noble WS, Disteche CM, Deng X. Escape from X inactivation varies in mouse tissues. Plos Genetics. 11: e1005079. PMID 25785854 DOI: 10.1371/Journal.Pgen.1005079 |
0.606 |
|
| 2015 |
Ma W, Ay F, Lee C, Gulsoy G, Deng X, Cook S, Hesson J, Cavanaugh C, Ware CB, Krumm A, Shendure J, Blau CA, Disteche CM, Noble WS, Duan Z. Fine-scale chromatin interaction maps reveal the cis-regulatory landscape of human lincRNA genes. Nature Methods. 12: 71-8. PMID 25437436 DOI: 10.1038/Nmeth.3205 |
0.389 |
|
| 2015 |
Deng X, Ma W, Ramani V, Hill A, Yang F, Ay F, Berletch JB, Blau CA, Shendure J, Duan Z, Noble WS, Disteche CM. Bipartite structure of the inactive mouse X chromosome Genome Biology. 16. DOI: 10.1186/s13059-015-0728-8 |
0.512 |
|
| 2015 |
Berletch JB, Ma W, Yang F, Shendure J, Noble WS, Disteche CM, Deng X. Identification of genes escaping X inactivation by allelic expression analysis in a novel hybrid mouse model Data in Brief. 5: 761-769. DOI: 10.1016/j.dib.2015.10.033 |
0.472 |
|
| 2014 |
Yue F, Cheng Y, Breschi A, Vierstra J, Wu W, Ryba T, Sandstrom R, Ma Z, Davis C, Pope BD, Shen Y, Pervouchine DD, Djebali S, Thurman RE, Kaul R, ... ... Disteche C, et al. A comparative encyclopedia of DNA elements in the mouse genome. Nature. 515: 355-64. PMID 25409824 DOI: 10.1038/Nature13992 |
0.412 |
|
| 2014 |
Deng X, Berletch JB, Nguyen DK, Disteche CM. X chromosome regulation: diverse patterns in development, tissues and disease. Nature Reviews. Genetics. 15: 367-78. PMID 24733023 DOI: 10.1038/Nrg3687 |
0.851 |
|
| 2013 |
Disteche CM. How to correct chromosomal trisomy. Cell Research. 23: 1345-6. PMID 24080727 DOI: 10.1038/Cr.2013.135 |
0.563 |
|
| 2013 |
Berletch JB, Deng X, Nguyen DK, Disteche CM. Female bias in Rhox6 and 9 regulation by the histone demethylase KDM6A. Plos Genetics. 9: e1003489. PMID 23658530 DOI: 10.1371/Journal.Pgen.1003489 |
0.827 |
|
| 2013 |
Deng X, Berletch JB, Ma W, Nguyen DK, Hiatt JB, Noble WS, Shendure J, Disteche CM. Mammalian X upregulation is associated with enhanced transcription initiation, RNA half-life, and MOF-mediated H4K16 acetylation. Developmental Cell. 25: 55-68. PMID 23523075 DOI: 10.1016/J.Devcel.2013.01.028 |
0.82 |
|
| 2012 |
Disteche CM. Dosage compensation of the sex chromosomes. Annual Review of Genetics. 46: 537-60. PMID 22974302 DOI: 10.1146/Annurev-Genet-110711-155454 |
0.605 |
|
| 2012 |
Moore JM, Rabaia NA, Smith LE, Fagerlie S, Gurley K, Loukinov D, Disteche CM, Collins SJ, Kemp CJ, Lobanenkov VV, Filippova GN. Loss of maternal CTCF is associated with peri-implantation lethality of Ctcf null embryos. Plos One. 7: e34915. PMID 22532833 DOI: 10.1371/Journal.Pone.0034915 |
0.358 |
|
| 2011 |
Deng X, Hiatt JB, Nguyen DK, Ercan S, Sturgill D, Hillier LW, Schlesinger F, Davis CA, Reinke VJ, Gingeras TR, Shendure J, Waterston RH, Oliver B, Lieb JD, Disteche CM. Evidence for compensatory upregulation of expressed X-linked genes in mammals, Caenorhabditis elegans and Drosophila melanogaster. Nature Genetics. 43: 1179-85. PMID 22019781 DOI: 10.1038/Ng.948 |
0.843 |
|
| 2011 |
Berletch JB, Yang F, Xu J, Carrel L, Disteche CM. Genes that escape from X inactivation. Human Genetics. 130: 237-45. PMID 21614513 DOI: 10.1007/S00439-011-1011-Z |
0.617 |
|
| 2011 |
Nguyen DK, Yang F, Kaul R, Alkan C, Antonellis A, Friery KF, Zhu B, de Jong PJ, Disteche CM. Clcn4-2 genomic structure differs between the X locus in Mus spretus and the autosomal locus in Mus musculus: AT motif enrichment on the X. Genome Research. 21: 402-9. PMID 21282478 DOI: 10.1101/Gr.108563.110 |
0.84 |
|
| 2010 |
Changolkar LN, Singh G, Cui K, Berletch JB, Zhao K, Disteche CM, Pehrson JR. Genome-wide distribution of macroH2A1 histone variants in mouse liver chromatin. Molecular and Cellular Biology. 30: 5473-83. PMID 20937776 DOI: 10.1128/Mcb.00518-10 |
0.504 |
|
| 2010 |
Berletch JB, Yang F, Disteche CM. Escape from X inactivation in mice and humans. Genome Biology. 11: 213. PMID 20573260 DOI: 10.1186/Gb-2010-11-6-213 |
0.642 |
|
| 2010 |
Yang F, Babak T, Shendure J, Disteche CM. Global survey of escape from X inactivation by RNA-sequencing in mouse. Genome Research. 20: 614-22. PMID 20363980 DOI: 10.1101/Gr.103200.109 |
0.604 |
|
| 2010 |
Deng X, Disteche CM. Genomic responses to abnormal gene dosage: the X chromosome improved on a common strategy. Plos Biology. 8: e1000318. PMID 20186268 DOI: 10.1371/Journal.Pbio.1000318 |
0.617 |
|
| 2009 |
Deng X, Nguyen DK, Hansen RS, Van Dyke DL, Gartler SM, Disteche CM. Dosage regulation of the active X chromosome in human triploid cells. Plos Genetics. 5: e1000751. PMID 19997486 DOI: 10.1371/Journal.Pgen.1000751 |
0.84 |
|
| 2009 |
Disteche CM, Nguyen DK. Dosage compensation of the active X chromosome Access Science. DOI: 10.1036/1097-8542.Yb090112 |
0.577 |
|
| 2008 |
Xu J, Deng X, Disteche CM. Sex-specific expression of the X-linked histone demethylase gene Jarid1c in brain. Plos One. 3: e2553. PMID 18596936 DOI: 10.1371/Journal.Pone.0002553 |
0.479 |
|
| 2008 |
Rubio ED, Reiss DJ, Welcsh PL, Disteche CM, Filippova GN, Baliga NS, Aebersold R, Ranish JA, Krumm A. CTCF physically links cohesin to chromatin. Proceedings of the National Academy of Sciences of the United States of America. 105: 8309-14. PMID 18550811 DOI: 10.1073/Pnas.0801273105 |
0.482 |
|
| 2008 |
Disteche CM. The not-so-silent X. Nature Genetics. 40: 689-90. PMID 18509310 DOI: 10.1038/Ng0608-689 |
0.619 |
|
| 2008 |
Xu J, Deng X, Watkins R, Disteche CM. Sex-specific differences in expression of histone demethylases Utx and Uty in mouse brain and neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 4521-7. PMID 18434530 DOI: 10.1523/Jneurosci.5382-07.2008 |
0.545 |
|
| 2007 |
Graves JA, Disteche CM. Does gene dosage really matter? Journal of Biology. 6: 1. PMID 17381829 DOI: 10.1186/Jbiol55 |
0.485 |
|
| 2007 |
Deng X, Disteche CM. Decoding dosage compensation. Genome Biology. 8: 204. PMID 17328790 DOI: 10.1186/Gb-2007-8-2-204 |
0.385 |
|
| 2006 |
Nguyen DK, Disteche CM. High expression of the mammalian X chromosome in brain. Brain Research. 1126: 46-9. PMID 16978591 DOI: 10.1016/J.Brainres.2006.08.053 |
0.858 |
|
| 2006 |
Xu J, Disteche CM. Sex differences in brain expression of X- and Y-linked genes. Brain Research. 1126: 50-5. PMID 16962077 DOI: 10.1016/J.Brainres.2006.08.049 |
0.526 |
|
| 2006 |
Heard E, Disteche CM. Dosage compensation in mammals: fine-tuning the expression of the X chromosome. Genes & Development. 20: 1848-67. PMID 16847345 DOI: 10.1101/Gad.1422906 |
0.666 |
|
| 2006 |
Cheng MK, Disteche CM. A balancing act between the X chromosome and the autosomes. Journal of Biology. 5: 2. PMID 16515717 DOI: 10.1186/Jbiol32 |
0.623 |
|
| 2006 |
Nguyen DK, Disteche CM. Dosage compensation of the active X chromosome in mammals. Nature Genetics. 38: 47-53. PMID 16341221 DOI: 10.1038/Ng1705 |
0.851 |
|
| 2006 |
Cheng MK, Nguyen DK, Disteche CM. Dosage compensation of the X chromosome and Turner syndrome International Congress Series. 1298: 3-8. DOI: 10.1016/j.ics.2006.06.012 |
0.473 |
|
| 2005 |
Koina E, Wakefield MJ, Walcher C, Disteche CM, Whitehead S, Ross M, Marshall Graves JA. Isolation, X location and activity of the marsupial homologue of SLC16A2, an XIST-flanking gene in eutherian mammals. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 13: 687-98. PMID 16235118 DOI: 10.1007/S10577-005-1006-5 |
0.659 |
|
| 2005 |
Okamoto I, Arnaud D, Le Baccon P, Otte AP, Disteche CM, Avner P, Heard E. Evidence for de novo imprinted X-chromosome inactivation independent of meiotic inactivation in mice. Nature. 438: 369-73. PMID 16227973 DOI: 10.1038/Nature04155 |
0.659 |
|
| 2005 |
Battaglia A, Chen Z, Brothman AR, Morelli S, Palumbos JC, Carey JC, Hudgins L, Disteche C. Karyotype/phenotype correlations in duplication 4q: evidence for a critical region within 4q27-28 for preaxial defects. American Journal of Medical Genetics Part A. 134: 334-337. PMID 15759263 DOI: 10.1002/Ajmg.A.30644 |
0.36 |
|
| 2005 |
Filippova GN, Cheng MK, Moore JM, Truong JP, Hu YJ, Nguyen DK, Tsuchiya KD, Disteche CM. Boundaries between chromosomal domains of X inactivation and escape bind CTCF and lack CpG methylation during early development. Developmental Cell. 8: 31-42. PMID 15669143 DOI: 10.1016/J.Devcel.2004.10.018 |
0.814 |
|
| 2004 |
Cheng MK, Disteche CM. Silence of the fathers: early X inactivation. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 26: 821-4. PMID 15273983 DOI: 10.1002/Bies.20082 |
0.605 |
|
| 2004 |
Delbridge ML, Longepied G, Depetris D, Mattei MG, Disteche CM, Marshall Graves JA, Mitchell MJ. TSPY, the candidate gonadoblastoma gene on the human Y chromosome, has a widely expressed homologue on the X - implications for Y chromosome evolution. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 12: 345-56. PMID 15241014 DOI: 10.1023/B:Chro.0000034134.91243.1C |
0.662 |
|
| 2004 |
Leppig KA, Sybert VP, Ross JL, Cunniff C, Trejo T, Raskind WH, Disteche CM. Phenotype and X inactivation in 45,X/46,X,r(X) cases. American Journal of Medical Genetics. Part A. 128: 276-84. PMID 15216549 DOI: 10.1002/Ajmg.A.30002 |
0.449 |
|
| 2004 |
Tsuchiya KD, Greally JM, Yi Y, Noel KP, Truong JP, Disteche CM. Comparative sequence and x-inactivation analyses of a domain of escape in human xp11.2 and the conserved segment in mouse. Genome Research. 14: 1275-84. PMID 15197169 DOI: 10.1101/Gr.2575904 |
0.582 |
|
| 2004 |
Disteche CM, Filippova GN, Tsuchiya KD. Escape from X inactivation. Cytogenetic and Genome Research. 99: 36-43. PMID 12900543 DOI: 10.1159/000071572 |
0.662 |
|
| 2003 |
Souter VL, Glass IA, Chapman DB, Raff ML, Parisi MA, Opheim KE, Disteche CM. Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangements. Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology. 21: 609-15. PMID 12808681 DOI: 10.1002/uog.112 |
0.365 |
|
| 2003 |
Ferrante MI, Barra A, Truong JP, Banfi S, Disteche CM, Franco B. Characterization of the OFD1/Ofd1 genes on the human and mouse sex chromosomes and exclusion of Ofd1 for the Xpl mouse mutant. Genomics. 81: 560-9. PMID 12782125 DOI: 10.1016/S0888-7543(03)00091-0 |
0.614 |
|
| 2002 |
James RD, Schmiesing JA, Peters AH, Yokomori K, Disteche CM. Differential association of SMC1alpha and SMC3 proteins with meiotic chromosomes in wild-type and SPO11-deficient male mice. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 10: 549-60. PMID 12498344 DOI: 10.1023/A:1020910601858 |
0.785 |
|
| 2002 |
Doty RT, Vanasse GJ, Disteche CM, Willerford DM. The leukemia-associated gene Mllt1/ENL: characterization of a murine homolog and demonstration of an essential role in embryonic development. Blood Cells, Molecules & Diseases. 28: 407-17. PMID 12367585 DOI: 10.1006/Bcmd.2002.0525 |
0.528 |
|
| 2002 |
Sultana R, Yu CE, Yu J, Munson J, Chen D, Hua W, Estes A, Cortes F, de la Barra F, Yu D, Haider ST, Trask BJ, Green ED, Raskind WH, Disteche CM, et al. Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins. Genomics. 80: 129-34. PMID 12160723 DOI: 10.1006/Geno.2002.6810 |
0.45 |
|
| 2001 |
Schreck RR, Distèche CM. Chromosome banding techniques Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. PMID 18428280 DOI: 10.1002/0471142905.Hg0402S00 |
0.455 |
|
| 2001 |
Schreck RR, Distèche CM, Adler D. ISCN standard idiograms Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. PMID 18428229 DOI: 10.1002/0471142905.Hga04Bs18 |
0.506 |
|
| 2001 |
Schreck RR, Distèche C. Karyotyping Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. PMID 18428228 DOI: 10.1002/0471142905.Hga04As18 |
0.391 |
|
| 2001 |
Brannan CI, Disteche CM, Park LS, Copeland NG, Jenkins NA. Autosomal telomere exchange results in the rapid amplification and dispersion of Csf2ra genes in wild-derived mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 882-6. PMID 11707773 DOI: 10.1007/S00335-001-2084-0 |
0.486 |
|
| 2001 |
Leppig KA, Disteche CM. Ring X and other structural X chromosome abnormalities: X inactivation and phenotype. Seminars in Reproductive Medicine. 19: 147-57. PMID 11480912 DOI: 10.1055/S-2001-15395 |
0.599 |
|
| 2001 |
Lingenfelter PA, Delbridge ML, Thomas S, Hoekstra HE, Mitchell MJ, Graves JA, Disteche CM. Expression and conservation of processed copies of the RBMX gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 538-45. PMID 11420617 DOI: 10.1007/S00335001-0003-Z |
0.635 |
|
| 2001 |
Kalantry S, Manning S, Haub O, Tomihara-Newberger C, Lee HG, Fangman J, Disteche CM, Manova K, Lacy E. The amnionless gene, essential for mouse gastrulation, encodes a visceral-endoderm-specific protein with an extracellular cysteine-rich domain. Nature Genetics. 27: 412-6. PMID 11279523 DOI: 10.1038/86912 |
0.384 |
|
| 2001 |
Miano JM, Thomas S, Disteche CM. Expression and chromosomal mapping of the mouse smooth muscle calponin gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 12: 187-91. PMID 11252166 DOI: 10.1007/S003350010266 |
0.405 |
|
| 2000 |
Cheng EY, Chen YJ, Disteche CM, Gartler SM. Analysis of a paracentric inversion in human oocytes: nonhomologous pairing in pachytene. Human Genetics. 105: 191-6. PMID 10987644 DOI: 10.1007/s004399900120 |
0.387 |
|
| 2000 |
Marshall AJ, Niiro H, Lerner CG, Yun TJ, Thomas S, Disteche CM, Clark EA. A novel B lymphocyte-associated adaptor protein, Bam32, regulates antigen receptor signaling downstream of phosphatidylinositol 3-kinase. The Journal of Experimental Medicine. 191: 1319-32. PMID 10770799 DOI: 10.1084/Jem.191.8.1319 |
0.342 |
|
| 2000 |
Warren EH, Gavin MA, Simpson E, Chandler P, Page DC, Disteche C, Stankey KA, Greenberg PD, Riddell SR. The human UTY gene encodes a novel HLA-B8-restricted H-Y antigen. Journal of Immunology (Baltimore, Md. : 1950). 164: 2807-14. PMID 10679124 DOI: 10.4049/Jimmunol.164.5.2807 |
0.402 |
|
| 2000 |
Disteche CM. Escapees on the X chromosome. Proceedings of the National Academy of Sciences of the United States of America. 96: 14180-2. PMID 10588671 DOI: 10.1073/Pnas.96.25.14180 |
0.647 |
|
| 1999 |
Li CM, Park JH, He X, Levy B, Chen F, Arai K, Adler DA, Disteche CM, Koch J, Sandhoff K, Schuchman EH. The human acid ceramidase gene (ASAH): Structure, chromosomal location, mutation analysis, and expression Genomics. 62: 223-231. PMID 10610716 DOI: 10.1006/Geno.1999.5940 |
0.483 |
|
| 1999 |
Delbridge ML, Lingenfelter PA, Disteche CM, Graves JA. The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome. Nature Genetics. 22: 223-4. PMID 10391206 DOI: 10.1038/10279 |
0.644 |
|
| 1999 |
Vanasse GJ, Halbrook J, Thomas S, Burgess A, Hoekstra MF, Disteche CM, Willerford DM. Genetic pathway to recurrent chromosome translocations in murine lymphoma involves V(D)J recombinase. The Journal of Clinical Investigation. 103: 1669-75. PMID 10377173 DOI: 10.1172/Jci6658 |
0.443 |
|
| 1999 |
Buaas FW, Lee K, Edelhoff S, Disteche C, Braun RE. Cloning and characterization of the mouse Interleukin Enhancer Binding Factor 3 (Ilf3) homolog in a screen for RNA binding proteins Mammalian Genome. 10: 451-456. PMID 10337617 DOI: 10.1007/S003359901022 |
0.372 |
|
| 1999 |
Meagher MJ, Schumacher JM, Lee K, Holdcraft RW, Edelhoff S, Disteche C, Braun RE. Identification of ZFR, an ancient and highly conserved murine chromosome-associated zinc finger protein. Gene. 228: 197-211. PMID 10072773 DOI: 10.1016/S0378-1119(98)00615-5 |
0.42 |
|
| 1999 |
Goldman MA, Reeves PS, Wirth CM, Zupko WJ, Wong MA, Edelhoff S, Disteche CM. Comparative methylation analysis of murine transgenes that undergo or escape X-chromosome inactivation. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 6: 397-404. PMID 9872669 DOI: 10.1023/A:1009229423535 |
0.63 |
|
| 1998 |
Disteche CM, Dinulos MB, Bassi MT, Elliott RW, Rugarli EI. Mapping of the murine tbl1 gene reveals a new rearrangement between mouse and human X Chromosomes. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 1062-4. PMID 9880679 DOI: 10.1007/S003359900926 |
0.605 |
|
| 1998 |
Twist CJ, Beier DR, Disteche CM, Edelhoff S, Tedder TF. The mouse Cd83 gene: structure, domain organization, and chromosome localization. Immunogenetics. 48: 383-93. PMID 9799334 DOI: 10.1007/S002510050449 |
0.412 |
|
| 1998 |
Wright MB, Hugo C, Seifert R, Disteche CM, Bowen-Pope DF. Proliferating and migrating mesangial cells responding to injury express a novel receptor protein-tyrosine phosphatase in experimental mesangial proliferative glomerulonephritis. The Journal of Biological Chemistry. 273: 23929-37. PMID 9727007 DOI: 10.1074/Jbc.273.37.23929 |
0.39 |
|
| 1998 |
Graves JA, Disteche CM, Toder R. Gene dosage in the evolution and function of mammalian sex chromosomes. Cytogenetics and Cell Genetics. 80: 94-103. PMID 9678341 DOI: 10.1159/000014963 |
0.649 |
|
| 1998 |
Nasir J, Duan K, Nichol K, Engelender S, Ashworth R, Colomer V, Thomas S, Disteche CM, Hayden MR, Ross CA. Gene structure and map location of the murine homolog of the Huntington-associated protein, Hap1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 565-70. PMID 9657855 DOI: 10.1007/S003359900819 |
0.499 |
|
| 1998 |
Hacker BM, Tomlinson JE, Wayman GA, Sultana R, Chan G, Villacres E, Disteche C, Storm DR. Cloning, chromosomal mapping, and regulatory properties of the human type 9 adenylyl cyclase (ADCY9). Genomics. 50: 97-104. PMID 9628827 DOI: 10.1006/Geno.1998.5293 |
0.422 |
|
| 1998 |
Zhong J, Edelhoff S, Disteche C, Braun RE. The gene encoding PRBP, the mouse homolog of human TRBP, maps to distal chromosome 15 Mammalian Genome. 9: 413-414. PMID 9545508 DOI: 10.1007/S003359900786 |
0.532 |
|
| 1998 |
Lingenfelter PA, Adler DA, Poslinski D, Thomas S, Elliott RW, Chapman VM, Disteche CM. Escape from X inactivation of Smcx is preceded by silencing during mouse development. Nature Genetics. 18: 212-3. PMID 9500539 DOI: 10.1038/Ng0398-212 |
0.504 |
|
| 1998 |
Dal Zotto L, Quaderi NA, Elliott R, Lingerfelter PA, Carrel L, Valsecchi V, Montini E, Yen CH, Chapman V, Kalcheva I, Arrigo G, Zuffardi O, Thomas S, Willard HF, Ballabio A, ... Disteche CM, et al. The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. Human Molecular Genetics. 7: 489-99. PMID 9467009 DOI: 10.1093/Hmg/7.3.489 |
0.581 |
|
| 1998 |
Schwartz A, Chan DC, Brown LG, Alagappan R, Pettay D, Disteche C, McGillivray B, De La Chapelle A, Page DC. Reconstructing hominid Y evolution: X-homologous block, created by X-Y transposition, was disrupted by Yp inversion through LINE-LINE recombination Human Molecular Genetics. 7: 1-11. PMID 9384598 DOI: 10.1093/Hmg/7.1.1 |
0.588 |
|
| 1997 |
Eubanks J, Srinivasan J, Dinulos MB, Disteche CM, Catterall WA. Structure and chromosomal localization of the beta2 subunit of the human brain sodium channel. Neuroreport. 8: 2775-9. PMID 9295116 DOI: 10.1097/00001756-199708180-00025 |
0.423 |
|
| 1997 |
Adler DA, Rugarli EI, Lingenfelter PA, Tsuchiya K, Poslinski D, Liggitt HD, Chapman VM, Elliott RW, Ballabio A, Disteche CM. Evidence of evolutionary up-regulation of the single active X chromosome in mammals based on Clc4 expression levels in Mus spretus and Mus musculus. Proceedings of the National Academy of Sciences of the United States of America. 94: 9244-8. PMID 9256467 DOI: 10.1073/Pnas.94.17.9244 |
0.635 |
|
| 1997 |
Reeves RH, Patch D, Sharpe AH, Borriello F, Freeman GJ, Edelhoff S, Disteche C. The costimulatory genes Cd80 and Cd86 are linked on mouse chromosome 16 and human chromosome 3 Mammalian Genome. 8: 581-582. PMID 9250865 DOI: 10.1007/S003359900508 |
0.452 |
|
| 1997 |
Boyd Y, Herman GE, Avner P, Disteche CM, Adler D, Reed V, Blair HJ. Mouse X chromosome. Mammalian Genome : Official Journal of the International Mammalian Genome Society. S313-26. PMID 9233403 DOI: 10.1007/S003359900332 |
0.558 |
|
| 1997 |
Li WF, Matthews C, Disteche CM, Costa LG, Furlong CE. Paraoxonase (PON1) gene in mice: sequencing, chromosomal localization and developmental expression. Pharmacogenetics. 7: 137-44. PMID 9170151 DOI: 10.1097/00008571-199704000-00007 |
0.493 |
|
| 1997 |
Liu X, Wu H, Loring J, Hormuzdi S, Disteche CM, Bornstein P, Jaenisch R. Trisomy eight in ES cells is a common potential problem in gene targeting and interferes with germ line transmission. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 209: 85-91. PMID 9142498 DOI: 10.1002/(Sici)1097-0177(199705)209:1<85::Aid-Aja8>3.0.Co;2-T |
0.375 |
|
| 1997 |
Hsu LY, Yu MT, Neu RL, Van Dyke DL, Benn PA, Bradshaw CL, Shaffer LG, Higgins RR, Khodr GS, Morton CC, Wang H, Brothman AR, Chadwick D, Disteche CM, Jenkins LS, et al. Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations. Prenatal Diagnosis. 17: 201-42. PMID 9110367 DOI: 10.1002/(Sici)1097-0223(199703)17:3<201::Aid-Pd56>3.0.Co;2-H |
0.361 |
|
| 1997 |
Luo C, Copeland NG, Jenkins NA, Edelhoff S, Disteche C, Hogan PG, Rao A. Normal function of the transcription factor NFAT1 in wasted mice. Chromosome localization of NFAT1 gene. Gene. 180: 29-36. PMID 8973343 DOI: 10.1016/S0378-1119(96)00396-4 |
0.456 |
|
| 1997 |
Jobling MA, Samara V, Pandya A, Fretwell N, Bernasconi B, Mitchell RJ, Gerelsaikhan T, Dashnyam B, Sajantila A, Salo PJ, Nakahori Y, Disteche CM, Thangaraj K, Singh L, Crawford MH, et al. Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal males. Human Molecular Genetics. 5: 1767-75. PMID 8923005 DOI: 10.1093/Hmg/5.11.1767 |
0.497 |
|
| 1997 |
Huq AH, Lovell RS, Sampson MJ, Decker WK, Dinulos MB, Disteche CM, Craigen WJ. Isolation, mapping, and functional expression of the mouse X chromosome glycerol kinase gene. Genomics. 36: 530-4. PMID 8884278 DOI: 10.1006/Geno.1996.0500 |
0.529 |
|
| 1997 |
Korth MJ, Edelhoff S, Disteche CM, Katze MG. Chromosomal assignment of the gene encoding the human 58-kDa inhibitor (PRKRI) of the interferon-induced dsRNA-activated protein kinase to chromosome 13q32. Genomics. 31: 238-9. PMID 8824808 DOI: 10.1006/Geno.1996.0038 |
0.497 |
|
| 1997 |
Gotlib RW, Bishop DF, Wang AM, Zeidner KM, Ioannou YA, Adler DA, Disteche CM, Desnick RJ. The entire genomic sequence and cDNA expression of mouse alpha-galactosidase A. Biochemical and Molecular Medicine. 57: 139-48. PMID 8733892 DOI: 10.1006/Bmme.1996.0020 |
0.356 |
|
| 1997 |
Watrin F, Roëckel N, Lacroix L, Mignon C, Mattei MG, Disteche C, Muscatelli F. The Mouse Necdin Gene Is Expressed from the Paternal Allele Only and Lies in the 7C Region of the Mouse Chromosome 7, a Region of Conserved Synteny to the Human Prader-Willi Syndrome Region European Journal of Human Genetics. 5: 324-332. DOI: 10.1007/Bf03405936 |
0.534 |
|
| 1996 |
Saxena R, Brown LG, Hawkins T, Alagappan RK, Skaletsky H, Reeve MP, Reijo R, Rozen S, Dinulos MB, Disteche CM, Page DC. The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned Nature Genetics. 14: 292-299. PMID 8896558 DOI: 10.1038/Ng1196-292 |
0.61 |
|
| 1996 |
Bressler SL, Gray MD, Sopher BL, Hu Q, Hearn MG, Pham DG, Dinulos MB, Fukuchi K, Sisodia SS, Miller MA, Disteche CM, Martin GM. cDNA cloning and chromosome mapping of the human Fe65 gene: interaction of the conserved cytoplasmic domains of the human beta-amyloid precursor protein and its homologues with the mouse Fe65 protein. Human Molecular Genetics. 5: 1589-98. PMID 8894693 DOI: 10.1093/Hmg/5.10.1589 |
0.339 |
|
| 1996 |
Borrow J, Stanton VP, Andresen JM, Becher R, Behm FG, Chaganti RS, Civin CI, Disteche C, Dubé I, Frischauf AM, Horsman D, Mitelman F, Volinia S, Watmore AE, Housman DE. The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein. Nature Genetics. 14: 33-41. PMID 8782817 DOI: 10.1038/Ng0996-33 |
0.422 |
|
| 1996 |
Borges LG, Seifert RA, Grant FJ, Hart CE, Disteche CM, Edelhoff S, Solca FF, Lieberman MA, Lindner V, Fischer EH, Lok S, Bowen-Pope DF. Cloning and characterization of rat density-enhanced phosphatase-1, a protein tyrosine phosphatase expressed by vascular cells. Circulation Research. 79: 570-80. PMID 8781490 DOI: 10.1161/01.Res.79.3.570 |
0.399 |
|
| 1996 |
Reijo R, Seligman J, Dinulos MB, Jaffe T, Brown LG, Disteche CM, Page DC. Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty Genomics. 35: 346-352. PMID 8661148 DOI: 10.1006/Geno.1996.0366 |
0.532 |
|
| 1996 |
Dinulos MB, Bassi MT, Rugarli EI, Chapman V, Ballabio A, Disteche CM. A new region of conservation is defined between human and mouse X chromosomes. Genomics. 35: 244-7. PMID 8661129 DOI: 10.1006/Geno.1996.0347 |
0.569 |
|
| 1996 |
Wang X, Bornslaeger EA, Haub O, Tomihara-Newberger C, Lonberg N, Dinulos MB, Disteche CM, Copeland N, Gilbert DJ, Jenkins NA, Lacy E. A candidate gene for the amnionless gastrulation stage mouse mutation encodes a TRAF-related protein. Developmental Biology. 177: 274-90. PMID 8660894 DOI: 10.1006/Dbio.1996.0162 |
0.48 |
|
| 1996 |
Yagi M, Edelhoff S, Disteche CM, Roth GJ. Human platelet glycoproteins V and IX: mapping of two leucine-rich glycoprotein genes to chromosome 3 and analysis of structures. Biochemistry. 34: 16132-7. PMID 8519770 DOI: 10.1021/Bi00049A028 |
0.466 |
|
| 1995 |
Tsuchiya K, Mulcahy RT, Reid LL, Disteche CM, Kavanagh TJ. Mapping of the Glutamate-Cysteine Ligase Catalytic Subunit Gene (GLCLC) to Human Chromosome 6p12 and Mouse Chromosome 9D-E and of the Regulatory Subunit Gene (GLCLR) to Human Chromosome 1p21-p22 and Mouse Chromosome 3H1-3 Genomics. 30: 630-632. PMID 8825659 DOI: 10.1006/geno.1995.1293 |
0.438 |
|
| 1995 |
Adler DA, Quaderi NA, Brown SD, Chapman VM, Moore J, Tate P, Disteche CM. The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouse. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 491-2. PMID 8589515 DOI: 10.1007/Bf00356163 |
0.544 |
|
| 1995 |
Disteche CM. Escape from X inactivation in human and mouse. Trends in Genetics : Tig. 11: 17-22. PMID 7900190 DOI: 10.1016/S0168-9525(00)88981-7 |
0.657 |
|
| 1995 |
Edelhoff S, Lai C, Disteche CM. Mapping of the receptor protein-tyrosine kinase 10 to human chromosome 1q21-q23 and mouse chromosome 1H1-5 by fluorescence in situ hybridization. Genomics. 25: 337-9. PMID 7774952 DOI: 10.1016/0888-7543(95)80158-I |
0.382 |
|
| 1995 |
Edelhoff S, Sweetser DA, Disteche CM. Mapping of the NEP receptor tyrosine kinase gene to human chromosome 6p21.3 and mouse chromosome 17C. Genomics. 25: 309-11. PMID 7774938 DOI: 10.1016/0888-7543(95)80144-B |
0.526 |
|
| 1995 |
Edelhoff S, Villacres EC, Storm DR, Disteche CM. Mapping of adenylyl cyclase genes type I, II, III, IV, V, and VI in mouse. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 111-3. PMID 7766992 DOI: 10.1007/Bf00303253 |
0.505 |
|
| 1995 |
Sultana R, Adler DA, Edelhoff S, Carrel L, Lee KH, Chapman VC, Willard HF, Disteche CM. The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation. Human Molecular Genetics. 4: 257-63. PMID 7757076 DOI: 10.1093/Hmg/4.2.257 |
0.641 |
|
| 1995 |
Rugarli EI, Adler DA, Borsani G, Tsuchiya K, Franco B, Hauge X, Disteche C, Chapman V, Ballabio A. Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J mice. Nature Genetics. 10: 466-71. PMID 7670496 DOI: 10.1038/Ng0895-466 |
0.578 |
|
| 1995 |
Sultana R, Myerson D, Disteche CM. In situ hybridization analysis of the Y chromosome in gonadoblastoma Genes Chromosomes and Cancer. 13: 257-262. PMID 7547633 DOI: 10.1002/Gcc.2870130405 |
0.543 |
|
| 1994 |
Korenberg JR, Chen XN, Schipper R, Sun Z, Gonsky R, Gerwehr S, Carpenter N, Daumer C, Dignan P, Disteche C. Down syndrome phenotypes: the consequences of chromosomal imbalance. Proceedings of the National Academy of Sciences of the United States of America. 91: 4997-5001. PMID 8197171 DOI: 10.1073/Pnas.91.11.4997 |
0.51 |
|
| 1994 |
Chang M, Burmer GC, Sweasy J, Loeb LA, Edelhoff S, Disteche CM, Yu CE, Anderson L, Oshima J, Nakura J. Evidence against DNA polymerase beta as a candidate gene for Werner syndrome. Human Genetics. 93: 507-12. PMID 8168825 DOI: 10.1007/Bf00202813 |
0.399 |
|
| 1994 |
Skonier J, Bennett K, Rothwell V, Kosowski S, Plowman G, Wallace P, Edelhoff S, Disteche C, Neubauer M, Marquardt H. beta ig-h3: a transforming growth factor-beta-responsive gene encoding a secreted protein that inhibits cell attachment in vitro and suppresses the growth of CHO cells in nude mice. Dna and Cell Biology. 13: 571-84. PMID 8024701 DOI: 10.1089/Dna.1994.13.571 |
0.344 |
|
| 1994 |
Grant DF, Spearow JL, Storms DH, Edelhoff S, Adler DA, Disteche CM, Taylor BA, Hammock BD. Chromosomal mapping and expression levels of a mouse soluble epoxide hydrolase gene. Pharmacogenetics. 4: 64-72. PMID 7915936 DOI: 10.1097/00008571-199404000-00003 |
0.548 |
|
| 1994 |
Cummings DE, Edelhoff S, Disteche CM, McKnight GS. Cloning of a mouse protein kinase A catalytic subunit pseudogene and chromosomal mapping of C subunit isoforms. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5: 701-6. PMID 7873880 DOI: 10.1007/Bf00426076 |
0.396 |
|
| 1994 |
Oshima J, Yu CE, Boehnke M, Weber JL, Edelhoff S, Wagner MJ, Wells DE, Wood S, Disteche CM, Martin GM, Schellenberg GD. Integrated Mapping Analysis of the Werner Syndrome Region of Chromosome 8 Genomics. 23: 100-113. PMID 7829057 DOI: 10.1006/Geno.1994.1464 |
0.415 |
|
| 1994 |
Ord DC, Edelhoff S, Dushkin H, Zhou LJ, Beier DR, Disteche C, Tedder TF. CD19 maps to a region of conservation between human chromosome 16 and mouse chromosome 7. Immunogenetics. 39: 322-8. PMID 7513297 DOI: 10.1007/Bf00189228 |
0.535 |
|
| 1993 |
Bornstein P, Devarayalu S, Edelhoff S, Disteche CM. Isolation and characterization of the mouse thrombospondin 3 (Thbs3) gene. Genomics. 15: 607-13. PMID 8468055 DOI: 10.1006/Geno.1993.1114 |
0.46 |
|
| 1993 |
Chance PF, Alderson MK, Leppig KA, Lensch MW, Matsunami N, Smith B, Swanson PD, Odelberg SJ, Disteche CM, Bird TD. DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell. 72: 143-51. PMID 8422677 DOI: 10.1016/0092-8674(93)90058-X |
0.379 |
|
| 1993 |
Edelhoff S, Grubin CE, Karlsen AE, Alder DA, Foster D, Disteche CM, Lernmark A. Mapping of glutamic acid decarboxylase (GAD) genes. Genomics. 17: 93-7. PMID 8406475 DOI: 10.1006/Geno.1993.1288 |
0.528 |
|
| 1993 |
Leppig KA, Brown CJ, Bressler SL, Gustashaw K, Pagon RA, Willard HF, Disteche CM. Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST. Human Molecular Genetics. 2: 883-7. PMID 8364571 DOI: 10.1093/Hmg/2.7.883 |
0.621 |
|
| 1993 |
Villacres EC, Xia Z, Bookbinder LH, Edelhoff S, Disteche CM, Storm DR. Cloning, chromosomal mapping, and expression of human fetal brain type I adenylyl cyclase. Genomics. 16: 473-8. PMID 8314585 DOI: 10.1006/Geno.1993.1213 |
0.432 |
|
| 1993 |
Humbert R, Adler DA, Disteche CM, Hassett C, Omiecinski CJ, Furlong CE. The molecular basis of the human serum paraoxonase activity polymorphism. Nature Genetics. 3: 73-6. PMID 8098250 DOI: 10.1038/Ng0193-73 |
0.379 |
|
| 1993 |
Barber GN, Edelhoff S, Katze MG, Disteche CM. Chromosomal Assignment of the Interferon-Inducible Double-Stranded RNA-Dependent Protein Kinase (PRKR) to Human Chromosome 2p21-p22 and Mouse Chromosome 17 E2 Genomics. 16: 765-767. PMID 7686883 DOI: 10.1006/Geno.1993.1262 |
0.502 |
|
| 1993 |
Bressler SL, Lee KH, Adler DA, Chapman VM, Disteche CM. Maintenance of X inactivation of the Rps4, Zfx, and Ube1 genes in a mouse in vitro system. Somatic Cell and Molecular Genetics. 19: 29-37. PMID 7681608 DOI: 10.1007/Bf01233952 |
0.659 |
|
| 1993 |
Allen RC, Armitage RJ, Conley ME, Rosenblatt H, Jenkins NA, Copeland NG, Bedell MA, Edelhoff S, Disteche CM, Simoneaux DK. CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome. Science (New York, N.Y.). 259: 990-3. PMID 7679801 DOI: 10.1126/Science.7679801 |
0.367 |
|
| 1993 |
Disteche CM, Brannan CI, Larsen A, Adler DA, Schorderet DF, Gearing D, Copeland NG, Jenkins NA, Park LS. The human pseudoautosomal GM-CSF receptor alpha subunit gene is autosomal in mouse. Nature Genetics. 1: 333-6. PMID 1363815 DOI: 10.1038/Ng0892-333 |
0.528 |
|
| 1992 |
Uhrich S, FitzSimmons J, Easterling TR, Mack L, Disteche CM. Duplication (6q) syndrome diagnosed in utero. American Journal of Medical Genetics. 41: 282-3. PMID 1789280 DOI: 10.1002/Ajmg.1320410304 |
0.317 |
|
| 1992 |
Tait JF, Frankenberry DA, Shiang R, Murray JC, Adler DA, Disteche CM. Chromosomal localization of the human gene for annexin V (placental anticoagulant protein I) to 4q26----q28. Cytogenetics and Cell Genetics. 57: 187-92. PMID 1683830 DOI: 10.1159/000133143 |
0.443 |
|
| 1992 |
Disteche CM, Zacksenhaus E, Adler DA, Bressler SL, Keitz BT, Chapman VM. Mapping and expression of the ubiquitin-activating enzyme E1 (Ube1) gene in the mouse. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 3: 156-61. PMID 1617221 DOI: 10.1007/Bf00352460 |
0.625 |
|
| 1992 |
LaBell TL, Milewicz DJ, Disteche CM, Byers PH. Thrombospondin II: partial cDNA sequence, chromosome location, and expression of a second member of the thrombospondin gene family in humans. Genomics. 12: 421-9. PMID 1559694 DOI: 10.1016/0888-7543(92)90430-Z |
0.46 |
|
| 1992 |
Tait JF, Smith C, Frankenberry DA, Miao CH, Adler DA, Disteche CM. Chromosomal mapping of the human annexin IV (ANX4) gene. Genomics. 12: 313-8. PMID 1346776 DOI: 10.1016/0888-7543(92)90379-7 |
0.511 |
|
| 1992 |
Freeman G, Disteche C, Gribben J, Adler D, Freedman A, Dougery J, Nadler L. The gene for B7, a costimulatory signal for T-cell activation, maps to chromosomal region 3q13.3-3q21 Blood. 79: 489-494. DOI: 10.1182/BLOOD.V79.2.489.BLOODJOURNAL792489 |
0.39 |
|
| 1992 |
Zinn AR, Bressler SL, Beer-Romero P, Adler DA, Chapman VM, Page DC, Disteche CM. Erratum: Inactivation of the Rps4 gene on the mouse X chromosome (Genomics (1991) 11 (1097-1101)) Genomics. 13. DOI: 10.1016/0888-7543(92)90192-U |
0.623 |
|
| 1991 |
Adler DA, Bressler SL, Chapman VM, Page DC, Disteche CM. Inactivation of the Zfx gene on the mouse X chromosome. Proceedings of the National Academy of Sciences of the United States of America. 88: 4592-5. PMID 2052543 DOI: 10.1073/Pnas.88.11.4592 |
0.644 |
|
| 1991 |
Adler DA, Tseng BY, Wang TS, Disteche CM. Physical mapping of the genes for three components of the mouse DNA replication complex: polymerase alpha to the X chromosome, primase p49 subunit to chromosome 10, and primase p58 subunit to chromosome 1. Genomics. 9: 642-6. PMID 2037291 DOI: 10.1016/0888-7543(91)90357-K |
0.591 |
|
| 1991 |
Chapman VM, Stephenson DA, Mullins LJ, Keitz BT, Disteche C, Orkin SH. Linkage of the erythroid transcription factor gene (Gf-1) to the proximal region of the X chromosome of mice. Genomics. 9: 309-13. PMID 2004781 DOI: 10.1016/0888-7543(91)90258-G |
0.661 |
|
| 1991 |
da Veiga Pereira L, Desnick RJ, Adler DA, Disteche CM, Schuchman EH. Regional assignment of the human acid sphingomyelinase gene (SMPD1) by PCR analysis of somatic cell hybrids and in situ hybridization to 11p15.1→p15.4 Genomics. 9: 229-234. PMID 2004772 DOI: 10.1016/0888-7543(91)90246-B |
0.523 |
|
| 1991 |
Bornstein P, Devarayalu S, Li P, Disteche CM, Framson P. A second thrombospondin gene in the mouse is similar in organization to thrombospondin 1 but does not respond to serum. Proceedings of the National Academy of Sciences of the United States of America. 88: 8636-40. PMID 1924325 DOI: 10.1073/Pnas.88.19.8636 |
0.464 |
|
| 1991 |
Karlsen AE, Hagopian WA, Grubin CE, Dube S, Disteche CM, Adler DA, Bärmeier H, Mathewes S, Grant FJ, Foster D, Lernmark A. Cloning and primary structure of a human islet isoform of glutamic acid decarboxylase from chromosome 10 Proceedings of the National Academy of Sciences of the United States of America. 88: 8337-8341. PMID 1924293 DOI: 10.1073/Pnas.88.19.8337 |
0.364 |
|
| 1991 |
Tait JF, Frankenberry DA, Miao CH, Killary AM, Adler DA, Disteche CM. Chromosomal localization of the human annexin III (ANX3) gene. Genomics. 10: 441-8. PMID 1830024 DOI: 10.1016/0888-7543(91)90330-H |
0.482 |
|
| 1991 |
Zinn AR, Bressler SL, Beer-Romero P, Adler DA, Chapman VM, Page DC, Disteche CM. Inactivation of the Rps4 gene on the mouse X chromosome. Genomics. 11: 1097-101. PMID 1783379 DOI: 10.1016/0888-7543(91)90037-F |
0.66 |
|
| 1991 |
Chapman VM, Keitz BT, Disteche CM, Lau EC, Snead ML. Linkage of amelogenin (Amel) to the distal portion of the mouse X chromosome. Genomics. 10: 23-8. PMID 1675194 DOI: 10.1016/0888-7543(91)90479-X |
0.648 |
|
| 1990 |
Jaffe E, Bornstein P, Disteche CM. Mapping of the thrombospondin gene to human chromosome 15 and mouse chromosome 2 by in situ hybridization. Genomics. 7: 123-6. PMID 2335352 DOI: 10.1016/0888-7543(90)90528-3 |
0.558 |
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| 1990 |
Plowman GD, Green JM, McDonald VL, Neubauer MG, Disteche CM, Todaro GJ, Shoyab M. The amphiregulin gene encodes a novel epidermal growth factor-related protein with tumor-inhibitory activity. Molecular and Cellular Biology. 10: 1969-81. PMID 2325643 DOI: 10.1128/Mcb.10.5.1969 |
0.346 |
|
| 1990 |
Disteche CM, Adler DA. Localization of a mouse centromeric DNA repeat in interphase nuclei. Cytometry. 11: 119-25. PMID 2307052 DOI: 10.1002/Cyto.990110114 |
0.479 |
|
| 1990 |
Nasir J, Fisher EM, Brockdorff N, Disteche CM, Lyon MF, Brown SD. Unusual molecular characteristics of a repeat sequence island within a Giemsa-positive band on the mouse X chromosome. Proceedings of the National Academy of Sciences of the United States of America. 87: 399-403. PMID 2296595 DOI: 10.1073/Pnas.87.1.399 |
0.413 |
|
| 1990 |
Page DC, Disteche CM, Simpson EM, de la Chapelle A, Andersson M, Alitalo T, Brown LG, Green P, Akots G. Chromosomal localization of ZFX--a human gene that escapes X inactivation--and its murine homologs. Genomics. 7: 37-46. PMID 1970799 DOI: 10.1016/0888-7543(90)90516-W |
0.657 |
|
| 1990 |
Swisshelm K, Disteche CM, Thorvaldsen J, Nelson A, Salk D. Age-related increase in methylation of ribosomal genes and inactivation of chromosome-specific rRNA gene clusters in mouse. Mutation Research. 237: 131-46. PMID 1700292 DOI: 10.1016/0921-8734(90)90019-N |
0.49 |
|
| 1990 |
Gronwald RG, Adler DA, Kelly JD, Disteche CM, Bowen-Pope DF. The human PDGF receptor alpha-subunit gene maps to chromosome 4 in close proximity to c-kit. Human Genetics. 85: 383-5. PMID 1697560 DOI: 10.1007/Bf00206767 |
0.522 |
|
| 1990 |
Windle JJ, Albert DM, O'Brien JM, Marcus DM, Disteche CM, Bernards R, Mellon PL. Retinoblastoma in transgenic mice Nature. 343: 665-669. PMID 1689463 DOI: 10.1038/343665A0 |
0.321 |
|
| 1989 |
Disteche CM, McConnell GK, Grant SG, Stephenson DA, Chapman VM, Gandy S, Adler DA. Comparison of the physical and recombination maps of the mouse X chromosome. Genomics. 5: 177-84. PMID 2571569 DOI: 10.1016/0888-7543(89)90044-X |
0.598 |
|
| 1989 |
Cantrell MA, Bicknell JN, Pagon RA, Page DC, Walker DC, Saal HM, Zinn AB, Disteche CM. Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe. Human Genetics. 83: 88-92. PMID 2570023 DOI: 10.1007/Bf00274156 |
0.538 |
|
| 1989 |
Mardon G, Mosher R, Disteche CM, Nishioka Y, McLaren A, Page DC. Duplication, deletion, and polymorphism in the sex-determining region of the mouse Y chromosome. Science (New York, N.Y.). 243: 78-80. PMID 2563173 DOI: 10.1126/Science.2563173 |
0.582 |
|
| 1988 |
SIMPSON E, CHANDLER P, GOULMY E, DISTECHE CM, FERGUSON-SMITH MA, PAGE DC. Separation of the Genetic Loci for the H-Y Antigen and for Testis Determination on Human Y Chromosome Obstetrical & Gynecological Survey. 43: 52-54. DOI: 10.1097/00006254-198801000-00016 |
0.357 |
|
| 1987 |
Disteche CM, Brown L, Saal H, Friedman C, Thuline HC, Hoar DI, Pagon RA, Page DC. Molecular detection of a translocation (Y;15) in a 45,X male. Human Genetics. 74: 372-7. PMID 3793100 DOI: 10.1007/Bf00280488 |
0.568 |
|
| 1987 |
Disteche CM, Gandy SL, Adler DA. Translocation and amplification of an X-chromosome DNA repeat in inbred strains of mice. Nucleic Acids Research. 15: 4393-401. PMID 3588301 DOI: 10.1093/Nar/15.11.4393 |
0.506 |
|
| 1987 |
Simpson E, Chandler P, Goulmy E, Disteche CM, Ferguson-Smith MA, Page DC. Separation of the genetic loci for the H-Y antigen and for testis determination on human Y chromosome. Nature. 326: 876-8. PMID 3494951 DOI: 10.1097/00006254-198801000-00016 |
0.57 |
|
| 1987 |
Aleixandre C, Miller DA, Mitchell AR, Warburton DA, Gersen SL, Disteche C, Miller OJ. p82H identifies sequences at every human centromere. Human Genetics. 77: 46-50. PMID 3476456 DOI: 10.1007/Bf00284712 |
0.451 |
|
| 1987 |
Raskind WH, Disteche CM, Keating A, Singer JW. Correlation between cytogenetic and molecular findings in human chronic myelogenous leukemia lines EM-2 and EM-3 Cancer Genetics and Cytogenetics. 25: 271-284. PMID 3030532 DOI: 10.1016/0165-4608(87)90188-9 |
0.408 |
|
| 1986 |
Seboun E, Leroy P, Casanova M, Magenis E, Boucekkine C, Disteche C, Bishop C, Fellous M. A molecular approach to the study of the human Y chromosome and anomalies of sex determination in man. Cold Spring Harbor Symposia On Quantitative Biology. 51: 237-48. PMID 3472720 DOI: 10.1101/Sqb.1986.051.01.029 |
0.486 |
|
| 1986 |
Disteche CM, Casanova M, Saal H, Friedman C, Sybert V, Graham J, Thuline H, Page DC, Fellous M. Small deletions of the short arm of the Y chromosome in 46,XY females. Proceedings of the National Academy of Sciences of the United States of America. 83: 7841-4. PMID 3464001 DOI: 10.1073/Pnas.83.20.7841 |
0.58 |
|
| 1986 |
Marth JD, Disteche C, Pravtcheva D, Ruddle F, Krebs EG, Perlmutter RM. Localization of a lymphocyte-specific protein tyrosine kinase gene (lck) at a site of frequent chromosomal abnormalities in human lymphomas. Proceedings of the National Academy of Sciences of the United States of America. 83: 7400-4. PMID 3463975 DOI: 10.1073/Pnas.83.19.7400 |
0.534 |
|
| 1986 |
Starr J, Sela S, Disteche CM, Rabinovitch PS, Ogburn CE, Smith AC, Martin GM. Resistance to paraquat in a mammalian cell line. Somatic Cell and Molecular Genetics. 12: 141-52. PMID 3457475 DOI: 10.1007/Bf01560661 |
0.482 |
|
| 1986 |
Deeb SS, Disteche C, Motulsky AG, Lebo RV, Kan YW. Chromosomal localization of the human apolipoprotein B gene and detection of homologous RNA in monkey intestine. Proceedings of the National Academy of Sciences of the United States of America. 83: 419-22. PMID 3455779 DOI: 10.1073/Pnas.83.2.419 |
0.458 |
|
| 1986 |
Müller U, Lalande M, Disteche CM, Latt SA. Construction, analysis, and application to 46,XY gonadal dysgenesis of a recombinant phage DNA library from flow-sorted human Y chromosomes. Cytometry. 7: 418-24. PMID 3019620 DOI: 10.1002/Cyto.990070505 |
0.495 |
|
| 1985 |
Sparkes RS, Sparkes MC, Kalina RE, Pagon RA, Salk DJ, Disteche CM. Separation of retinoblastoma and esterase D loci in a patient with sporadic retinoblastoma and del(13)(q14.1q22.3). Human Genetics. 68: 258-9. PMID 6500578 DOI: 10.1007/Bf00418397 |
0.39 |
|
| 1985 |
Loughran TP, Kadin ME, Starkebaum G, Abkowitz JL, Clark EA, Disteche C, Lum LG, Slichter SJ. Leukemia of Large Granular Lymphocytes: Association with Clonal Chromosomal Abnormalities and Autoimmune Neutropenia, Thrombocytopenia, and Hemolytic Anemia Annals of Internal Medicine. 102: 169-175. PMID 3966754 DOI: 10.7326/0003-4819-102-2-169 |
0.434 |
|
| 1985 |
Kranz DM, Saito H, Disteche CM, Swisshelm K, Pravtcheva D, Ruddle FH, Eisen HN, Tonegawa S. Chromosomal locations of the murine T-cell receptor alpha-chain gene and the T-cell gamma gene. Science (New York, N.Y.). 227: 941-5. PMID 3918347 DOI: 10.1126/Science.3918347 |
0.503 |
|
| 1985 |
Disteche CM, Tantravahi U, Gandy S, Eisenhard M, Adler D, Kunkel LM. Isolation and characterization of two repetitive DNA fragments located near the centromere of the mouse X chromosome. Cytogenetics and Cell Genetics. 39: 262-8. PMID 2932308 DOI: 10.1159/000132155 |
0.595 |
|
| 1984 |
Disteche C, Luthy D, Haslam DB, Hoar D. Prenatal identification of a deleted Y chromosome by cytogenetics and a Y-specific repetitive DNA probe. Human Genetics. 67: 222-4. PMID 6745944 DOI: 10.1007/Bf00273007 |
0.536 |
|
| 1984 |
Disteche CM, Swisshelm K, Forbes S, Pagon RA. X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes. Human Genetics. 66: 71-6. PMID 6698557 DOI: 10.1007/Bf00275190 |
0.521 |
|
| 1984 |
Disteche CM, Adler D. Localization of cloned mouse chromosome 7-specific DNA to lethal albino deletions. Somatic Cell and Molecular Genetics. 10: 211-5. PMID 6585968 DOI: 10.1007/Bf01535243 |
0.573 |
|
| 1984 |
Horn PL, Turker MS, Ogburn CE, Disteche CM, Martin GM. A cloning assay for 6-thioguanine resistance provides evidence against certain somatic mutational theories of aging. Journal of Cellular Physiology. 121: 309-15. PMID 6490730 DOI: 10.1002/Jcp.1041210207 |
0.418 |
|
| 1982 |
Disteche CM, Kunkel LM, Lojewski A, Orkin SH, Eisenhard M, Sahar E, Travis B, Latt SA. Isolation of mouse x-chromosome specific DNA from an x-enriched lambda phage library derived from flow sorted chromosomes. Cytometry. 2: 282-6. PMID 6210515 DOI: 10.1002/Cyto.990020503 |
0.595 |
|
| 1981 |
Breslau EJ, Disteche C, Hall JG, Thuline H, Cooper P, Opitz JM. Prometaphase chromosomes in five patients with the Brachmann-de Lange syndrome. American Journal of Medical Genetics. 10: 179-186. PMID 7315874 DOI: 10.1002/Ajmg.1320100211 |
0.478 |
|
| 1981 |
Disteche CM, Eicher EM, Latt SA. Late replication patterns in adult and embryonic mice carrying Searle's X-autosome translocation Experimental Cell Research. 133: 357-362. PMID 7238606 DOI: 10.1016/0014-4827(81)90328-1 |
0.53 |
|
| 1981 |
Disteche CM, Carrano AV, Ashworth LK, Burkhart-Schultz K, Latt SA. Flow sorting of the mouse Cattanach X chromosome, T (X; 7) 1 Ct, in an active or inactive state. Cytogenetics and Cell Genetics. 29: 189-97. PMID 7016465 DOI: 10.1159/000131569 |
0.534 |
|
| 1979 |
Disteche CM, Eicher EM, Latt SA. Late replication in an X-autosome translocation in the mouse: Correlation with genetic inactivation and evidence for selective effects during embryogenesis Proceedings of the National Academy of Sciences of the United States of America. 76: 5234-5238. PMID 291940 DOI: 10.1073/Pnas.76.10.5234 |
0.427 |
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