Tim Wiltshire - Publications

Affiliations: 
Genetics & Molecular Biology University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Molecular Biology, Genetics

70 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
2016 Frick A, Benton CS, Scolaro KL, McLaughlin JE, Bradley CL, Suzuki OT, Wang N, Wiltshire T. Transitioning Pharmacogenomics into the Clinical Setting: Training Future Pharmacists. Frontiers in Pharmacology. 7: 241. PMID 27551265 DOI: 10.3389/fphar.2016.00241  0.8
2016 Song G, Suzuki OT, Santos CM, Lucas AT, Wiltshire T, Zamboni WC. Gulp1 Is Associated with the Pharmacokinetics of PEGylated Liposomal Doxorubicin (PLD) in Inbred Mouse Strains. Nanomedicine : Nanotechnology, Biology, and Medicine. PMID 27288666 DOI: 10.1016/j.nano.2016.05.019  0.8
2015 Segall SK, Shabalina SA, Meloto CB, Wen X, Cunningham D, Tarantino LM, Wiltshire T, Gauthier J, Tohyama S, Martin LJ, Mogil JS, Diatchenko L. Molecular genetic mechanisms of allelic specific regulation of murine Comt expression. Pain. PMID 26067582 DOI: 10.1097/j.pain.0000000000000258  0.8
2015 Frick A, Suzuki OT, Benton C, Parks B, Fedoriw Y, Richards KL, Thomas RS, Wiltshire T. Identifying genes that mediate anthracyline toxicity in immune cells. Frontiers in Pharmacology. 6: 62. PMID 25926793 DOI: 10.3389/fphar.2015.00062  0.8
2015 Frick A, Fedoriw Y, Richards K, Damania B, Parks B, Suzuki O, Benton CS, Chan E, Thomas RS, Wiltshire T. Immune cell-based screening assay for response to anticancer agents: applications in pharmacogenomics. Pharmacogenomics and Personalized Medicine. 8: 81-98. PMID 25897258 DOI: 10.2147/PGPM.S73312  0.8
2015 Zhuang GZ, Keeler B, Grant J, Bianchi L, Fu ES, Zhang YP, Erasso DM, Cui JG, Wiltshire T, Li Q, Hao S, Sarantopoulos KD, Candiotti K, Wishnek SM, Smith SB, et al. Carbonic anhydrase-8 regulates inflammatory pain by inhibiting the ITPR1-cytosolic free calcium pathway. Plos One. 10: e0118273. PMID 25734498 DOI: 10.1371/journal.pone.0118273  0.8
2015 Wiltshire T, Ervin RB, Duan H, Bogue MA, Zamboni WC, Cook S, Chung W, Zou F, Tarantino LM. Initial locomotor sensitivity to cocaine varies widely among inbred mouse strains. Genes, Brain, and Behavior. 14: 271-80. PMID 25727211 DOI: 10.1111/gbb.12209  0.8
2015 Benton CS, Wiltshire T. Pharmacogenomics of antidepressant drugs: Focus on key findings and future directions Current Pharmacogenomics and Personalized Medicine. 12: 141-147.  0.8
2014 Suzuki OT, Frick A, Parks BB, Trask OJ, Butz N, Steffy B, Chan E, Scoville DK, Healy E, Benton C, McQuaid PE, Thomas RS, Wiltshire T. A cellular genetics approach identifies gene-drug interactions and pinpoints drug toxicity pathway nodes. Frontiers in Genetics. 5: 272. PMID 25221565 DOI: 10.3389/fgene.2014.00272  0.8
2014 Xu X, Jaeger ER, Wang X, Lagler-Ferrez E, Batalov S, Mathis NL, Wiltshire T, Walker JR, Cooke MP, Sauer K, Huang YH. Mst1 directs Myosin IIa partitioning of low and higher affinity integrins during T cell migration. Plos One. 9: e105561. PMID 25133611 DOI: 10.1371/journal.pone.0105561  0.8
2014 Nichols JL, Gladwell W, Verhein KC, Cho HY, Wess J, Suzuki O, Wiltshire T, Kleeberger SR. Genome-wide association mapping of acute lung injury in neonatal inbred mice. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 28: 2538-50. PMID 24571919 DOI: 10.1096/fj.13-247221  0.8
2013 Frick A, Suzuki O, Butz N, Chan E, Wiltshire T. In vitro and in vivo mouse models for pharmacogenetic studies. Methods in Molecular Biology (Clifton, N.J.). 1015: 263-78. PMID 23824862 DOI: 10.1007/978-1-62703-435-7_17  0.8
2013 Shimomura K, Kumar V, Koike N, Kim TK, Chong J, Buhr ED, Whiteley AR, Low SS, Omura C, Fenner D, Owens JR, Richards M, Yoo SH, Hong HK, Vitaterna MH, ... ... Wiltshire T, et al. Usf1, a suppressor of the circadian Clock mutant, reveals the nature of the DNA-binding of the CLOCK:BMAL1 complex in mice. Elife. 2: e00426. PMID 23580255 DOI: 10.7554/eLife.00426  0.8
2013 Beisner DR, Langerak P, Parker AE, Dahlberg C, Otero FJ, Sutton SE, Poirot L, Barnes W, Young MA, Niessen S, Wiltshire T, Bodendorf U, Martoglio B, Cravatt B, Cooke MP. The intramembrane protease Sppl2a is required for B cell and DC development and survival via cleavage of the invariant chain. The Journal of Experimental Medicine. 210: 23-30. PMID 23267013 DOI: 10.1084/jem.20121072  0.8
2013 Eisener-Dorman AF, Bailey JS, Grabowski-Boase L, Huitron-Resendiz S, Roberts AJ, Wiltshire T, Tarantino LM. Characterization of Highper, an ENU-induced mouse mutant with abnormal psychostimulant and stress responses. Psychopharmacology. 225: 407-19. PMID 22948668 DOI: 10.1007/s00213-012-2827-5  0.8
2012 Segall SK, Maixner W, Belfer I, Wiltshire T, Seltzer Z, Diatchenko L. Janus molecule I: dichotomous effects of COMT in neuropathic vs nociceptive pain modalities. Cns & Neurological Disorders Drug Targets. 11: 222-35. PMID 22483297  0.8
2012 Wang S, Zhang H, Wiltshire T, Sealock R, Faber JE. Genetic dissection of the Canq1 locus governing variation in extent of the collateral circulation. Plos One. 7: e31910. PMID 22412848 DOI: 10.1371/journal.pone.0031910  0.8
2012 Iraqi FA, Mahajne M, Salaymah Y, Sandovski H, Tayem H, Vered K, Balmer L, Hall M, Manship G, Morahan G, Pettit K, Scholten J, Tweedie K, Wallace A, Weerasekera L, ... ... Wiltshire T, et al. The genome architecture of the collaborative cross mouse genetic reference population Genetics. 190: 389-401. PMID 22345608 DOI: 10.1534/genetics.111.132639  0.8
2012 Benton CS, Miller BH, Skwerer S, Suzuki O, Schultz LE, Cameron MD, Marron JS, Pletcher MT, Wiltshire T. Evaluating genetic markers and neurobiochemical analytes for fluoxetine response using a panel of mouse inbred strains. Psychopharmacology. 221: 297-315. PMID 22113448 DOI: 10.1007/s00213-011-2574-z  0.8
2011 Wiltshire T, Maixner W, Diatchenko L. Relax, you won't feel the pain. Nature Neuroscience. 14: 1496-7. PMID 22119947 DOI: 10.1038/nn.2987  0.8
2011 White MA, Steffy B, Wiltshire T, Payseur BA. Genetic dissection of a key reproductive barrier between nascent species of house mice. Genetics. 189: 289-304. PMID 21750261 DOI: 10.1534/genetics.111.129171  0.8
2011 Dumont BL, White MA, Steffy B, Wiltshire T, Payseur BA. Extensive recombination rate variation in the house mouse species complex inferred from genetic linkage maps. Genome Research. 21: 114-25. PMID 20978138 DOI: 10.1101/gr.111252.110  0.8
2010 Segall SK, Nackley AG, Diatchenko L, Lariviere WR, Lu X, Marron JS, Grabowski-Boase L, Walker JR, Slade G, Gauthier J, Bailey JS, Steffy BM, Maynard TM, Tarantino LM, Wiltshire T. Comt1 genotype and expression predicts anxiety and nociceptive sensitivity in inbred strains of mice. Genes, Brain, and Behavior. 9: 933-46. PMID 20659173 DOI: 10.1111/j.1601-183X.2010.00633.x  0.8
2010 Bopp SE, Ramachandran V, Henson K, Luzader A, Lindstrom M, Spooner M, Steffy BM, Suzuki O, Janse C, Waters AP, Zhou Y, Wiltshire T, Winzeler EA. Genome wide analysis of inbred mouse lines identifies a locus containing Ppar-gamma as contributing to enhanced malaria survival. Plos One. 5: e10903. PMID 20531941 DOI: 10.1371/journal.pone.0010903  0.8
2010 Eisener-Dorman AF, Grabowski-Boase L, Steffy BM, Wiltshire T, Tarantino LM. Quantitative trait locus and haplotype mapping in closely related inbred strains identifies a locus for open field behavior. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 231-46. PMID 20473506 DOI: 10.1007/s00335-010-9260-z  0.8
2010 Kelly SA, Nehrenberg DL, Peirce JL, Hua K, Steffy BM, Wiltshire T, Pardo-Manuel de Villena F, Garland T, Pomp D. Genetic architecture of voluntary exercise in an advanced intercross line of mice. Physiological Genomics. 42: 190-200. PMID 20388837 DOI: 10.1152/physiolgenomics.00028.2010  0.8
2010 Rakhra-Burris TK, Auman JT, Deverka P, Dressler LG, Evans JP, Goldberg RM, Havener TM, Hoskins JM, Jonas DE, Long KM, Motsinger-Reif AA, Irvin WJ, Richards KL, Roederer MW, Valgus JM, ... ... Wiltshire T, et al. Institutional profile. UNC Institute for Pharmacogenomics and Individualized Therapy: interdisciplinary research for individual care. Pharmacogenomics. 11: 13-21. PMID 20017668 DOI: 10.2217/pgs.09.167  0.8
2009 Schwander M, Lopes V, Sczaniecka A, Gibbs D, Lillo C, Delano D, Tarantino LM, Wiltshire T, Williams DS, Müller U. A novel allele of myosin VIIa reveals a critical function for the C-terminal FERM domain for melanosome transport in retinal pigment epithelial cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 15810-8. PMID 20016096 DOI: 10.1523/JNEUROSCI.4876-09.2009  0.8
2009 Grillet N, Schwander M, Hildebrand MS, Sczaniecka A, Kolatkar A, Velasco J, Webster JA, Kahrizi K, Najmabadi H, Kimberling WJ, Stephan D, Bahlo M, Wiltshire T, Tarantino LM, Kuhn P, et al. Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans. American Journal of Human Genetics. 85: 328-37. PMID 19732867 DOI: 10.1016/j.ajhg.2009.07.017  0.8
2009 Bryant CD, Chang HP, Zhang J, Wiltshire T, Tarantino LM, Palmer AA. A major QTL on chromosome 11 influences psychostimulant and opioid sensitivity in mice. Genes, Brain, and Behavior. 8: 795-805. PMID 19694818 DOI: 10.1111/j.1601-183X.2009.00525.x  0.8
2009 Harrill AH, Watkins PB, Su S, Ross PK, Harbourt DE, Stylianou IM, Boorman GA, Russo MW, Sackler RS, Harris SC, Smith PC, Tennant R, Bogue M, Paigen K, Harris C, ... ... Wiltshire T, et al. Mouse population-guided resequencing reveals that variants in CD44 contribute to acetaminophen-induced liver injury in humans. Genome Research. 19: 1507-15. PMID 19416960 DOI: 10.1101/gr.090241.108  0.8
2009 Schwander M, Xiong W, Tokita J, Lelli A, Elledge HM, Kazmierczak P, Sczaniecka A, Kolatkar A, Wiltshire T, Kuhn P, Holt JR, Kachar B, Tarantino L, Müller U. A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells. Proceedings of the National Academy of Sciences of the United States of America. 106: 5252-7. PMID 19270079 DOI: 10.1073/pnas.0900691106  0.8
2009 Barouch-Bentov R, Che J, Lee CC, Yang Y, Herman A, Jia Y, Velentza A, Watson J, Sternberg L, Kim S, Ziaee N, Miller A, Jackson C, Fujimoto M, Young M, ... ... Wiltshire T, et al. A conserved salt bridge in the G loop of multiple protein kinases is important for catalysis and for in vivo Lyn function. Molecular Cell. 33: 43-52. PMID 19150426 DOI: 10.1016/j.molcel.2008.12.024  0.8
2008 Bailey JS, Grabowski-Boase L, Steffy BM, Wiltshire T, Churchill GA, Tarantino LM. Identification of quantitative trait loci for locomotor activation and anxiety using closely related inbred strains. Genes, Brain, and Behavior. 7: 761-9. PMID 19130624 DOI: 10.1111/j.1601-183X.2008.00415.x  0.8
2008 Howden R, Liu E, Miller-DeGraff L, Keener HL, Walker C, Clark JA, Myers PH, Rouse DC, Wiltshire T, Kleeberger SR. The genetic contribution to heart rate and heart rate variability in quiescent mice. American Journal of Physiology. Heart and Circulatory Physiology. 295: H59-68. PMID 18456734 DOI: 10.1152/ajpheart.00941.2007  0.8
2008 Cheli Y, Jensen D, Marchese P, Habart D, Wiltshire T, Cooke M, Fernandez JA, Ware J, Ruggeri ZM, Kunicki TJ. The Modifier of hemostasis (Mh) locus on chromosome 4 controls in vivo hemostasis of Gp6-/- mice. Blood. 111: 1266-73. PMID 17991808 DOI: 10.1182/blood-2007-09-111369  0.8
2008 Labialle S, Yang L, Ruan X, Villemain A, Schmidt JV, Hernandez A, Wiltshire T, Cermakian N, Naumova AK. Coordinated diurnal regulation of genes from the Dlk1-Dio3 imprinted domain: implications for regulation of clusters of non-paralogous genes. Human Molecular Genetics. 17: 15-26. PMID 17901046 DOI: 10.1093/hmg/ddm281  0.8
2007 Schwander M, Sczaniecka A, Grillet N, Bailey JS, Avenarius M, Najmabadi H, Steffy BM, Federe GC, Lagler EA, Banan R, Hice R, Grabowski-Boase L, Keithley EM, Ryan AF, Housley GD, ... Wiltshire T, et al. A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 2163-75. PMID 17329413 DOI: 10.1523/JNEUROSCI.4975-06.2007  0.8
2007 Wiltshire T, Senft J, Wang Y, Konat GW, Wenger SL, Reed E, Wang W. BRCA1 contributes to cell cycle arrest and chemoresistance in response to the anticancer agent irofulven. Molecular Pharmacology. 71: 1051-60. PMID 17229870 DOI: 10.1124/mol.106.029504  0.8
2007 Wang Y, Wiltshire T, Senft J, Reed E, Wang W. Irofulven induces replication-dependent CHK2 activation related to p53 status. Biochemical Pharmacology. 73: 469-80. PMID 17118344 DOI: 10.1016/j.bcp.2006.10.023  0.8
2006 Wang Y, Wiltshire T, Senft J, Wenger SL, Reed E, Wang W. Fanconi anemia D2 protein confers chemoresistance in response to the anticancer agent, irofulven. Molecular Cancer Therapeutics. 5: 3153-61. PMID 17172419 DOI: 10.1158/1535-7163.MCT-06-0427  0.8
2006 Walker JR, Wiltshire T. Databases of free expression. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 1141-6. PMID 17143588 DOI: 10.1007/s00335-006-0043-5  0.8
2006 Reijmers LG, Coats JK, Pletcher MT, Wiltshire T, Tarantino LM, Mayford M. A mutant mouse with a highly specific contextual fear-conditioning deficit found in an N-ethyl-N-nitrosourea (ENU) mutagenesis screen. Learning & Memory (Cold Spring Harbor, N.Y.). 13: 143-9. PMID 16585790 DOI: 10.1101/lm.98606  0.8
2006 Moran JL, Bolton AD, Tran PV, Brown A, Dwyer ND, Manning DK, Bjork BC, Li C, Montgomery K, Siepka SM, Vitaterna MH, Takahashi JS, Wiltshire T, Kwiatkowski DJ, Kucherlapati R, et al. Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse. Genome Research. 16: 436-40. PMID 16461637 DOI: 10.1101/gr.4563306  0.8
2006 Tabeta K, Hoebe K, Janssen EM, Du X, Georgel P, Crozat K, Mudd S, Mann N, Sovath S, Goode J, Shamel L, Herskovits AA, Portnoy DA, Cooke M, Tarantino LM, ... Wiltshire T, et al. The Unc93b1 mutation 3d disrupts exogenous antigen presentation and signaling via Toll-like receptors 3, 7 and 9. Nature Immunology. 7: 156-64. PMID 16415873 DOI: 10.1038/ni1297  0.8
2006 Fries S, Grosser T, Price TS, Lawson JA, Kapoor S, DeMarco S, Pletcher MT, Wiltshire T, FitzGerald GA. Marked interindividual variability in the response to selective inhibitors of cyclooxygenase-2. Gastroenterology. 130: 55-64. PMID 16401468 DOI: 10.1053/j.gastro.2005.10.002  0.8
2006 Ishimori N, Li R, Walsh KA, Korstanje R, Rollins JA, Petkov P, Pletcher MT, Wiltshire T, Donahue LR, Rosen CJ, Beamer WG, Churchill GA, Paigen B. Quantitative trait loci that determine BMD in C57BL/6J and 129S1/SvImJ inbred mice. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 21: 105-12. PMID 16355279 DOI: 10.1359/JBMR.050902  0.8
2005 Delano DL, Montesinos MC, D'Eustachio P, Wiltshire T, Cronstein BN. An interaction between genetic factors and gender determines the magnitude of the inflammatory response in the mouse air pouch model of acute inflammation. Inflammation. 29: 1-7. PMID 16502340 DOI: 10.1007/s10753-006-8962-6  0.8
2005 Delano DL, Montesinos MC, Desai A, Wilder T, Fernandez P, D'Eustachio P, Wiltshire T, Cronstein BN. Genetically based resistance to the antiinflammatory effects of methotrexate in the air-pouch model of acute inflammation. Arthritis and Rheumatism. 52: 2567-75. PMID 16059892 DOI: 10.1002/art.21208  0.8
2005 Owens SE, Broman KW, Wiltshire T, Elmore JB, Bradley KM, Smith JR, Southard-Smith EM. Genome-wide linkage identifies novel modifier loci of aganglionosis in the Sox10Dom model of Hirschsprung disease. Human Molecular Genetics. 14: 1549-58. PMID 15843399 DOI: 10.1093/hmg/ddi163  0.8
2005 Sandberg ML, Sutton SE, Pletcher MT, Wiltshire T, Tarantino LM, Hogenesch JB, Cooke MP. c-Myb and p300 regulate hematopoietic stem cell proliferation and differentiation. Developmental Cell. 8: 153-66. PMID 15691758 DOI: 10.1016/j.devcel.2004.12.015  0.8
2004 Pletcher M, Wiltshire T. Can we find the genes involved in complex traits? Genome Biology. 5: 347. PMID 15461809 DOI: 10.1186/gb-2004-5-10-347  0.8
2004 Wang J, Wiltshire T, Wang Y, Mikell C, Burks J, Cunningham C, Van Laar ES, Waters SJ, Reed E, Wang W. ATM-dependent CHK2 activation induced by anticancer agent, irofulven. The Journal of Biological Chemistry. 279: 39584-92. PMID 15269203 DOI: 10.1074/jbc.M400015200  0.8
2004 Wen BG, Pletcher MT, Warashina M, Choe SH, Ziaee N, Wiltshire T, Sauer K, Cooke MP. Inositol (1,4,5) trisphosphate 3 kinase B controls positive selection of T cells and modulates Erk activity. Proceedings of the National Academy of Sciences of the United States of America. 101: 5604-9. PMID 15064401 DOI: 10.1073/pnas.0306907101  0.8
2003 Wiltshire T, Pletcher MT, Batalov S, Barnes SW, Tarantino LM, Cooke MP, Wu H, Smylie K, Santrosyan A, Copeland NG, Jenkins NA, Kalush F, Mural RJ, Glynne RJ, Kay SA, et al. Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse. Proceedings of the National Academy of Sciences of the United States of America. 100: 3380-5. PMID 12612341 DOI: 10.1073/pnas.0130101100  0.8
2001 Crabtree J, Wiltshire T, Brunk B, Zhao S, Schug J, Stoeckert CJ, Bucan M. High-resolution BAC-based map of the central portion of mouse chromosome 5 Genome Research. 11: 1746-1757. PMID 11591652 DOI: 10.1101/gr.195101  0.8
2001 Pletcher MT, Wiltshire T, Cabin DE, Villanueva M, Reeves RH. Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21 Genomics. 74: 45-54. PMID 11374901 DOI: 10.1006/geno.2001.6533  0.8
2000 Tarantino LM, Feiner L, Alavizadeh A, Wiltshire T, Hurle B, Ornitz DM, Webber AL, Raper J, Lengeling A, Rowe LB, Bucan M. A high-resolution radiation hybrid map of the proximal portion of mouse chromosome 5. Genomics. 66: 55-64. PMID 10843805 DOI: 10.1006/geno.2000.6183  0.8
2000 Moreira ES, Wiltshire TJ, Faulkner G, Nilforoushan A, Vainzof M, Suzuki OT, Valle G, Reeves R, Zatz M, Passos-Bueno MR, Jenne DE. Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin. Nature Genetics. 24: 163-6. PMID 10655062 DOI: 10.1038/72822  0.8
1999 Wiltshire T, Pletcher M, Cole SE, Villanueva M, Birren B, Lehoczky J, Dewar K, Reeves RH. Perfect conserved linkage across the entire mouse chromosome 10 region homologous to human chromosome 21. Genome Research. 9: 1214-22. PMID 10613844 DOI: 10.1101/gr.9.12.1214  0.8
1999 Lengeling A, Wiltshire T, Otmani C, Bucan M. A sequence-ready BAC contig of the GABA(A) receptor gene cluster Gabrg1-Gabra2-Gabrb1 on mouse chromosome 5 Genome Research. 9: 732-738. PMID 10447508  0.8
1999 Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly Nature Genetics. 22: 196-198. PMID 10369266 DOI: 10.1038/9718  0.8
1999 Cole SE, Wiltshire T, Rue EE, Morrow D, Hieter P, Brahe C, Fisher EM, Katsanis N, Reeves RH. High-resolution comparative physical mapping of mouse chromosome 10 in the region of homology with human chromosome 21. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 229-34. PMID 10051316 DOI: 10.1007/s003359900978  0.8
1998 Cabin DE, McKee-Johnson JW, Matesic LE, Wiltshire T, Rue EE, Mjaatvedt AE, Huo YK, Korenberg JR, Reeves RH. Physical and comparative mapping of distal mouse chromosome 16. 5 p5. Genome Research. 8: 940-50. PMID 9750193  0.8
1998 Cole SE, Wiltshire T, Reeves RH. Physical mapping of the evolutionary boundary between human chromosomes 21 and 22 on mouse chromosome 10. Genomics. 50: 109-11. PMID 9628829 DOI: 10.1006/geno.1998.5312  0.8
1998 Fang Y, Spisz TS, Wiltshire T, D'Costa NP, Bankman IN, Reeves RH, Hoh JH. Solid-State DNA Sizing by Atomic Force Microscopy Analytical Chemistry. 70: 2123-2129. PMID 9608850  0.8
1998 Wiltshire T, Park C, Handel MA. Chromatin configuration during meiosis I prophase of spermatogenesis Molecular Reproduction and Development. 49: 70-80. PMID 9406197 DOI: 10.1002/(SICI)1098-2795(199801)49:1<70::AID-MRD8>3.0.CO;2-L  0.8
1996 Caldwell KA, Wiltshire T, Handel MA. A genetic strategy for differential screening of meiotic germ-cell cDNA libraries Molecular Reproduction and Development. 43: 403-413. PMID 9052930 DOI: 10.1002/(SICI)1098-2795(199604)43:4<403::AID-MRD1>3.0.CO;2-T  0.8
1995 Wiltshire T, Park C, Caldwell KA, Handel MA. Induced Premature G2/M-Phase Transition in Pachytene Spermatocytes Includes Events Unique to Meiosis Developmental Biology. 169: 557-567. PMID 7781899 DOI: 10.1006/dbio.1995.1169  0.8
1995 Handel MA, Caldwell KA, Wiltshire T. Culture of pachytene spermatocytes for analysis of meiosis Developmental Genetics. 16: 128-139. PMID 7736663 DOI: 10.1002/dvg.1020160206  0.8
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