Year |
Citation |
Score |
2024 |
Singh N, Richtsmeier JT, Reeves RH. Comparative analysis of craniofacial shape in two mouse models of Down syndrome: Ts65Dn and TcMAC21. Journal of Anatomy. PMID 38264931 DOI: 10.1111/joa.14012 |
0.493 |
|
2023 |
Shao LR, Gao F, Chinnasamy V, Kazuki Y, Oshimura M, Reeves RH, Stafstrom CE. Increased propensity for infantile spasms and altered neocortical excitation-inhibition balance in a mouse model of down syndrome carrying human chromosome 21. Neurobiology of Disease. 184: 106198. PMID 37315904 DOI: 10.1016/j.nbd.2023.106198 |
0.375 |
|
2023 |
Moyer AJ, Fernandez FX, Li Y, Klinedinst DK, Florea LD, Kazuki Y, Oshimura M, Reeves RH. Overexpression screen of chromosome 21 genes reveals modulators of Sonic hedgehog signaling relevant to Down syndrome. Disease Models & Mechanisms. PMID 36995257 DOI: 10.1242/dmm.049712 |
0.81 |
|
2022 |
Sarver DC, Xu C, Velez LM, Aja S, Jaffe AE, Seldin MM, Reeves RH, Wong GW. Dysregulated systemic metabolism in a Down syndrome mouse model. Molecular Metabolism. 68: 101666. PMID 36587842 DOI: 10.1016/j.molmet.2022.101666 |
0.335 |
|
2022 |
Kazuki Y, Gao FJ, Yamakawa M, Hirabayashi M, Kazuki K, Kajitani N, Miyagawa-Tomita S, Abe S, Sanbo M, Hara H, Kuniishi H, Ichisaka S, Hata Y, Koshima M, Takayama H, ... ... Reeves RH, et al. A transchromosomic rat model with human chromosome 21 shows robust Down syndrome features. American Journal of Human Genetics. PMID 35077668 DOI: 10.1016/j.ajhg.2021.12.015 |
0.791 |
|
2021 |
Gao FJ, Klinedinst D, Fernandez FX, Cheng B, Savonenko A, Devenney B, Li Y, Wu D, Pomper MG, Reeves RH. Forebrain Shh overexpression improves cognitive function and locomotor hyperactivity in an aneuploid mouse model of Down syndrome and its euploid littermates. Acta Neuropathologica Communications. 9: 137. PMID 34399854 DOI: 10.1186/s40478-021-01237-z |
0.337 |
|
2020 |
Moyer AJ, Gardiner K, Reeves RH. All Creatures Great and Small: New Approaches for Understanding Down Syndrome Genetics. Trends in Genetics : Tig. PMID 33097276 DOI: 10.1016/j.tig.2020.09.017 |
0.789 |
|
2020 |
Kazuki Y, Gao FJ, Li Y, Moyer AJ, Devenney B, Hiramatsu K, Miyagawa-Tomita S, Abe S, Kazuki K, Kajitani N, Uno N, Takehara S, Takiguchi M, Yamakawa M, Hasegawa A, ... ... Reeves RH, et al. A non-mosaic transchromosomic mouse model of Down syndrome carrying the long arm of human chromosome 21. Elife. 9. PMID 32597754 DOI: 10.7554/Elife.56223 |
0.813 |
|
2020 |
Kazuki Y, Gao FJ, Li Y, Moyer AJ, Devenney B, Hiramatsu K, Miyagawa-Tomita S, Abe S, Kazuki K, Kajitani N, Uno N, Takehara S, Takiguchi M, Yamakawa M, Hasegawa A, ... ... Reeves RH, et al. A non-mosaic transchromosomic mouse model of Down syndrome carrying the long arm of human chromosome 21. Elife. 9. PMID 32597754 DOI: 10.7554/Elife.56223 |
0.813 |
|
2020 |
Antonarakis SE, Skotko BG, Rafii MS, Strydom A, Pape SE, Bianchi DW, Sherman SL, Reeves RH. Down syndrome. Nature Reviews. Disease Primers. 6: 9. PMID 32029743 DOI: 10.1038/s41572-019-0143-7 |
0.411 |
|
2020 |
Antonarakis SE, Skotko BG, Rafii MS, Strydom A, Pape SE, Bianchi DW, Sherman SL, Reeves RH. Down syndrome. Nature Reviews. Disease Primers. 6: 9. PMID 32029743 DOI: 10.1038/s41572-019-0143-7 |
0.411 |
|
2020 |
Kazuki Y, Gao FJ, Li Y, Moyer AJ, Devenney B, Hiramatsu K, Miyagawa-Tomita S, Abe S, Kazuki K, Kajitani N, Uno N, Takehara S, Takiguchi M, Yamakawa M, Hasegawa A, ... ... Reeves RH, et al. Author response: A non-mosaic transchromosomic mouse model of Down syndrome carrying the long arm of human chromosome 21 Elife. DOI: 10.7554/Elife.56223.Sa2 |
0.353 |
|
2018 |
Edie S, Zaghloul NA, Leitch CC, Klinedinst DK, Lebron J, Thole JF, McCallion AS, Katsanis N, Reeves RH. Survey of Human Chromosome 21 Gene Expression Effects on Early Development in . G3 (Bethesda, Md.). PMID 29760202 DOI: 10.1534/G3.118.200144 |
0.818 |
|
2018 |
Edie S, Zaghloul NA, Leitch CC, Klinedinst DK, Lebron J, Thole JF, McCallion AS, Katsanis N, Reeves RH. Survey of Human Chromosome 21 Gene Expression Effects on Early Development in . G3 (Bethesda, Md.). PMID 29760202 DOI: 10.1534/G3.118.200144 |
0.818 |
|
2017 |
Rambo-Martin BL, Mulle JG, Cutler DJ, Bean LJH, Rosser TC, Dooley KJ, Cua C, Capone G, Maslen CL, Reeves RH, Sherman SL, Zwick ME. Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. G3 (Bethesda, Md.). PMID 29141989 DOI: 10.1534/G3.117.300366 |
0.358 |
|
2017 |
Rambo-Martin BL, Mulle JG, Cutler DJ, Bean LJH, Rosser TC, Dooley KJ, Cua C, Capone G, Maslen CL, Reeves RH, Sherman SL, Zwick ME. Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. G3 (Bethesda, Md.). PMID 29141989 DOI: 10.1534/G3.117.300366 |
0.358 |
|
2016 |
Burnicka-Turek O, Steimle JD, Huang W, Felker L, Kamp A, Kweon J, Peterson M, Reeves RH, Maslen CL, Gruber PJ, Yang XH, Shendure J, Moskowitz IP. Cilia Gene Mutations Cause Atrioventricular Septal Defects by Multiple Mechanisms. Human Molecular Genetics. PMID 27340223 DOI: 10.1093/Hmg/Ddw155 |
0.339 |
|
2016 |
Burnicka-Turek O, Steimle JD, Huang W, Felker L, Kamp A, Kweon J, Peterson M, Reeves RH, Maslen CL, Gruber PJ, Yang XH, Shendure J, Moskowitz IP. Cilia Gene Mutations Cause Atrioventricular Septal Defects by Multiple Mechanisms. Human Molecular Genetics. PMID 27340223 DOI: 10.1093/Hmg/Ddw155 |
0.339 |
|
2016 |
Li H, Edie S, Klinedinst D, Jeong JS, Blackshaw S, Maslen CL, Reeves RH. Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic Modifier. Genetics. PMID 27029737 DOI: 10.1534/Genetics.116.188045 |
0.819 |
|
2016 |
Li H, Edie S, Klinedinst D, Jeong JS, Blackshaw S, Maslen CL, Reeves RH. Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic Modifier. Genetics. PMID 27029737 DOI: 10.1534/Genetics.116.188045 |
0.819 |
|
2016 |
Yang A, Currier D, Poitras JL, Reeves RH. Increased Skin Tumor Incidence and Keratinocyte Hyper-Proliferation in a Mouse Model of Down Syndrome. Plos One. 11: e0146570. PMID 26752700 DOI: 10.1371/journal.pone.0146570 |
0.849 |
|
2016 |
Yang A, Currier D, Poitras JL, Reeves RH. Increased Skin Tumor Incidence and Keratinocyte Hyper-Proliferation in a Mouse Model of Down Syndrome. Plos One. 11: e0146570. PMID 26752700 DOI: 10.1371/journal.pone.0146570 |
0.46 |
|
2016 |
Yang A, Currier D, Poitras JL, Reeves RH. Increased skin tumor incidence and keratinocyte hyper-proliferation in a mouse model of down syndrome Plos One. 11. DOI: 10.1371/journal.pone.0146570 |
0.783 |
|
2015 |
Singh N, Dutka T, Reeves RH, Richtsmeier JT. Chronic up-regulation of sonic hedgehog has little effect on postnatal craniofacial morphology of euploid and trisomic mice. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 26509735 DOI: 10.1002/Dvdy.24361 |
0.832 |
|
2015 |
Singh N, Dutka T, Reeves RH, Richtsmeier JT. Chronic up-regulation of sonic hedgehog has little effect on postnatal craniofacial morphology of euploid and trisomic mice. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 26509735 DOI: 10.1002/Dvdy.24361 |
0.832 |
|
2015 |
Polk RC, Gergics P, Steimle JD, Li H, Moskowitz IP, Camper SA, Reeves RH. The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model. Bmc Developmental Biology. 15: 30. PMID 26208718 DOI: 10.1186/s12861-015-0080-y |
0.643 |
|
2015 |
Polk RC, Gergics P, Steimle JD, Li H, Moskowitz IP, Camper SA, Reeves RH. The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model. Bmc Developmental Biology. 15: 30. PMID 26208718 DOI: 10.1186/s12861-015-0080-y |
0.643 |
|
2015 |
Singh N, Dutka T, Devenney BM, Kawasaki K, Reeves RH, Richtsmeier JT. Acute upregulation of hedgehog signaling in mice causes differential effects on cranial morphology. Disease Models & Mechanisms. 8: 271-9. PMID 25540129 DOI: 10.1242/Dmm.017889 |
0.81 |
|
2015 |
Singh N, Dutka T, Devenney BM, Kawasaki K, Reeves RH, Richtsmeier JT. Acute upregulation of hedgehog signaling in mice causes differential effects on cranial morphology. Disease Models & Mechanisms. 8: 271-9. PMID 25540129 DOI: 10.1242/Dmm.017889 |
0.81 |
|
2015 |
Dutka T, Hallberg D, Reeves RH. Chronic up-regulation of the SHH pathway normalizes some developmental effects of trisomy in Ts65Dn mice. Mechanisms of Development. 135: 68-80. PMID 25511459 DOI: 10.1016/j.mod.2014.11.004 |
0.838 |
|
2015 |
Dutka T, Hallberg D, Reeves RH. Chronic up-regulation of the SHH pathway normalizes some developmental effects of trisomy in Ts65Dn mice. Mechanisms of Development. 135: 68-80. PMID 25511459 DOI: 10.1016/j.mod.2014.11.004 |
0.838 |
|
2014 |
Starbuck JM, Dutka T, Ratliff TS, Reeves RH, Richtsmeier JT. Overlapping trisomies for human chromosome 21 orthologs produce similar effects on skull and brain morphology of Dp(16)1Yey and Ts65Dn mice. American Journal of Medical Genetics. Part A. 164: 1981-90. PMID 24788405 DOI: 10.1002/Ajmg.A.36594 |
0.839 |
|
2014 |
Starbuck JM, Dutka T, Ratliff TS, Reeves RH, Richtsmeier JT. Overlapping trisomies for human chromosome 21 orthologs produce similar effects on skull and brain morphology of Dp(16)1Yey and Ts65Dn mice. American Journal of Medical Genetics. Part A. 164: 1981-90. PMID 24788405 DOI: 10.1002/Ajmg.A.36594 |
0.839 |
|
2013 |
Das I, Park JM, Shin JH, Jeon SK, Lorenzi H, Linden DJ, Worley PF, Reeves RH. Hedgehog agonist therapy corrects structural and cognitive deficits in a Down syndrome mouse model. Science Translational Medicine. 5: 201ra120. PMID 24005160 DOI: 10.1126/scitranslmed.3005983 |
0.714 |
|
2013 |
Starbuck JM, Cole TM, Reeves RH, Richtsmeier JT. Trisomy 21 and facial developmental instability. American Journal of Physical Anthropology. 151: 49-57. PMID 23505010 DOI: 10.1002/Ajpa.22255 |
0.314 |
|
2013 |
Starbuck JM, Cole TM, Reeves RH, Richtsmeier JT. Trisomy 21 and facial developmental instability. American Journal of Physical Anthropology. 151: 49-57. PMID 23505010 DOI: 10.1002/Ajpa.22255 |
0.314 |
|
2012 |
Currier DG, Polk RC, Reeves RH. A Sonic hedgehog (Shh) response deficit in trisomic cells may be a common denominator for multiple features of Down syndrome Progress in Brain Research. 197: 223-236. PMID 22541295 DOI: 10.1016/B978-0-444-54299-1.00011-X |
0.802 |
|
2012 |
Currier DG, Polk RC, Reeves RH. A Sonic hedgehog (Shh) response deficit in trisomic cells may be a common denominator for multiple features of Down syndrome Progress in Brain Research. 197: 223-236. PMID 22541295 DOI: 10.1016/B978-0-444-54299-1.00011-X |
0.802 |
|
2012 |
Haydar TF, Reeves RH. Trisomy 21 and early brain development. Trends in Neurosciences. 35: 81-91. PMID 22169531 DOI: 10.1016/J.Tins.2011.11.001 |
0.41 |
|
2012 |
Haydar TF, Reeves RH. Trisomy 21 and early brain development. Trends in Neurosciences. 35: 81-91. PMID 22169531 DOI: 10.1016/J.Tins.2011.11.001 |
0.41 |
|
2011 |
Das I, Reeves RH. The use of mouse models to understand and improve cognitive deficits in down syndrome Dmm Disease Models and Mechanisms. 4: 596-606. PMID 21816951 DOI: 10.1242/dmm.007716 |
0.692 |
|
2011 |
Yang A, Reeves RH. Increased survival following tumorigenesis in Ts65Dn mice that model down syndrome Cancer Research. 71: 3573-3581. PMID 21467166 DOI: 10.1158/0008-5472.CAN-10-4489 |
0.738 |
|
2010 |
Moore CS, Hawkins C, Franca A, Lawler A, Devenney B, Das I, Reeves RH. Increased male reproductive success in Ts65Dn "Down syndrome" mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 543-9. PMID 21110029 DOI: 10.1007/s00335-010-9300-8 |
0.741 |
|
2010 |
Moore CS, Hawkins C, Franca A, Lawler A, Devenney B, Das I, Reeves RH. Increased male reproductive success in Ts65Dn "Down syndrome" mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 543-9. PMID 21110029 DOI: 10.1007/s00335-010-9300-8 |
0.741 |
|
2010 |
Lorenzi H, Duvall N, Cherry SM, Reeves RH, Roper RJ. PCR prescreen for genotyping the Ts65Dn mouse model of Down syndrome. Biotechniques. 48: 35-8. PMID 20095097 DOI: 10.2144/000113342 |
0.483 |
|
2010 |
Lorenzi H, Duvall N, Cherry SM, Reeves RH, Roper RJ. PCR prescreen for genotyping the Ts65Dn mouse model of Down syndrome. Biotechniques. 48: 35-8. PMID 20095097 DOI: 10.2144/000113342 |
0.483 |
|
2009 |
Hill CA, Sussan TE, Reeves RH, Richtsmeier JT. Complex contributions of Ets2 to craniofacial and thymus phenotypes of trisomic "Down syndrome" mice. American Journal of Medical Genetics. Part A. 149: 2158-65. PMID 19764029 DOI: 10.1002/Ajmg.A.33012 |
0.775 |
|
2009 |
Hill CA, Sussan TE, Reeves RH, Richtsmeier JT. Complex contributions of Ets2 to craniofacial and thymus phenotypes of trisomic "Down syndrome" mice. American Journal of Medical Genetics. Part A. 149: 2158-65. PMID 19764029 DOI: 10.1002/Ajmg.A.33012 |
0.775 |
|
2009 |
Belichenko NP, Belichenko PV, Kleschevnikov AM, Salehi A, Reeves RH, Mobley WC. The "Down syndrome critical region" is sufficient in the mouse model to confer behavioral, neurophysiological, and synaptic phenotypes characteristic of Down syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 5938-48. PMID 19420260 DOI: 10.1523/Jneurosci.1547-09.2009 |
0.452 |
|
2009 |
Belichenko NP, Belichenko PV, Kleschevnikov AM, Salehi A, Reeves RH, Mobley WC. The "Down syndrome critical region" is sufficient in the mouse model to confer behavioral, neurophysiological, and synaptic phenotypes characteristic of Down syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 5938-48. PMID 19420260 DOI: 10.1523/Jneurosci.1547-09.2009 |
0.452 |
|
2009 |
Roper RJ, VanHorn JF, Cain CC, Reeves RH. A neural crest deficit in Down syndrome mice is associated with deficient mitotic response to Sonic hedgehog. Mechanisms of Development. 126: 212-9. PMID 19056491 DOI: 10.1016/J.Mod.2008.11.002 |
0.446 |
|
2009 |
Roper RJ, VanHorn JF, Cain CC, Reeves RH. A neural crest deficit in Down syndrome mice is associated with deficient mitotic response to Sonic hedgehog. Mechanisms of Development. 126: 212-9. PMID 19056491 DOI: 10.1016/J.Mod.2008.11.002 |
0.446 |
|
2008 |
Pritchard M, Reeves RH, Dierssen M, Patterson D, Gardiner KJ. Down syndrome and the genes of human chromosome 21: Current knowledge and future potentials. Report on the Expert workshop on the biology of chromosome 21 genes: Towards gene-phenotype correlations in Down syndrome. Washington D.C., September 28-October 1, 2007 Cytogenetic and Genome Research. 121: 67-77. PMID 18544929 DOI: 10.1159/000124384 |
0.43 |
|
2008 |
Sussan TE, Yang A, Li F, Ostrowski MC, Reeves RH. Trisomy represses Apc(Min)-mediated tumours in mouse models of Down's syndrome. Nature. 451: 73-5. PMID 18172498 DOI: 10.1038/Nature06446 |
0.842 |
|
2008 |
Sussan TE, Yang A, Li F, Ostrowski MC, Reeves RH. Trisomy represses Apc(Min)-mediated tumours in mouse models of Down's syndrome. Nature. 451: 73-5. PMID 18172498 DOI: 10.1038/Nature06446 |
0.842 |
|
2007 |
Sultan M, Piccini I, Balzereit D, Herwig R, Saran NG, Lehrach H, Reeves RH, Yaspo ML. Gene expression variation in Down's syndrome mice allows prioritization of candidate genes. Genome Biology. 8: R91. PMID 17531092 DOI: 10.1186/Gb-2007-8-5-R91 |
0.85 |
|
2007 |
Sultan M, Piccini I, Balzereit D, Herwig R, Saran NG, Lehrach H, Reeves RH, Yaspo ML. Gene expression variation in Down's syndrome mice allows prioritization of candidate genes. Genome Biology. 8: R91. PMID 17531092 DOI: 10.1186/Gb-2007-8-5-R91 |
0.85 |
|
2007 |
Aldridge K, Reeves RH, Olson LE, Richtsmeier JT. Differential effects of trisomy on brain shape and volume in related aneuploid mouse models. American Journal of Medical Genetics. Part A. 143: 1060-70. PMID 17431903 DOI: 10.1002/Ajmg.A.31721 |
0.777 |
|
2007 |
Aldridge K, Reeves RH, Olson LE, Richtsmeier JT. Differential effects of trisomy on brain shape and volume in related aneuploid mouse models. American Journal of Medical Genetics. Part A. 143: 1060-70. PMID 17431903 DOI: 10.1002/Ajmg.A.31721 |
0.777 |
|
2007 |
Olson LE, Roper RJ, Sengstaken CL, Peterson EA, Aquino V, Galdzicki Z, Siarey R, Pletnikov M, Moran TH, Reeves RH. Trisomy for the Down syndrome 'critical region' is necessary but not sufficient for brain phenotypes of trisomic mice. Human Molecular Genetics. 16: 774-82. PMID 17339268 DOI: 10.1093/Hmg/Ddm022 |
0.769 |
|
2007 |
Olson LE, Roper RJ, Sengstaken CL, Peterson EA, Aquino V, Galdzicki Z, Siarey R, Pletnikov M, Moran TH, Reeves RH. Trisomy for the Down syndrome 'critical region' is necessary but not sufficient for brain phenotypes of trisomic mice. Human Molecular Genetics. 16: 774-82. PMID 17339268 DOI: 10.1093/Hmg/Ddm022 |
0.769 |
|
2006 |
Lorenzi HA, Reeves RH. Hippocampal hypocellularity in the Ts65Dn mouse originates early in development Brain Research. 1104: 153-159. PMID 16828061 DOI: 10.1016/j.brainres.2006.05.022 |
0.333 |
|
2006 |
Reeves RH. Down syndrome mouse models are looking up Trends in Molecular Medicine. 12: 237-240. PMID 16677859 DOI: 10.1016/j.molmed.2006.04.005 |
0.468 |
|
2006 |
Reeves RH. Down syndrome mouse models are looking up Trends in Molecular Medicine. 12: 237-240. PMID 16677859 DOI: 10.1016/j.molmed.2006.04.005 |
0.468 |
|
2006 |
Roper RJ, Reeves RH. Understanding the basis for Down syndrome phenotypes. Plos Genetics. 2: e50. PMID 16596169 DOI: 10.1371/Journal.Pgen.0020050 |
0.409 |
|
2006 |
Roper RJ, Reeves RH. Understanding the basis for Down syndrome phenotypes. Plos Genetics. 2: e50. PMID 16596169 DOI: 10.1371/Journal.Pgen.0020050 |
0.409 |
|
2006 |
Fulton WB, Reeves RH, Takeya M, De Maio A. A quantitative trait loci analysis to map genes involved in lipopolysaccharide-induced inflammatory response: Identification of macrophage scavenger receptor 1 as a candidate gene Journal of Immunology. 176: 3767-3773. PMID 16517746 |
0.32 |
|
2006 |
Fulton WB, Reeves RH, Takeya M, De Maio A. A quantitative trait loci analysis to map genes involved in lipopolysaccharide-induced inflammatory response: Identification of macrophage scavenger receptor 1 as a candidate gene Journal of Immunology. 176: 3767-3773. PMID 16517746 |
0.32 |
|
2006 |
Roper RJ, Baxter LL, Saran NG, Klinedinst DK, Beachy PA, Reeves RH. Defective cerebellar response to mitogenic Hedgehog signaling in Down [corrected] syndrome mice. Proceedings of the National Academy of Sciences of the United States of America. 103: 1452-6. PMID 16432181 DOI: 10.1073/Pnas.0510750103 |
0.839 |
|
2006 |
Roper RJ, St John HK, Philip J, Lawler A, Reeves RH. Perinatal loss of Ts65Dn Down syndrome mice. Genetics. 172: 437-43. PMID 16172497 DOI: 10.1534/Genetics.105.050898 |
0.404 |
|
2006 |
Roper RJ, St John HK, Philip J, Lawler A, Reeves RH. Perinatal loss of Ts65Dn Down syndrome mice. Genetics. 172: 437-43. PMID 16172497 DOI: 10.1534/Genetics.105.050898 |
0.404 |
|
2006 |
Roper RJ, Baxter LL, Saran NG, Klinedinst DK, Beachy PA, Reeves RH. Erratum: Defective cerebellar response to mitogenic Hedgehog signaling in Down's syndrome mice (Proceedings of the National Academy of Sciences of the United States of America (January 31, 2006) 103, 5 (1452-1456) 10.1073/pnas.0510750103)) Proceedings of the National Academy of Sciences of the United States of America. 103. DOI: 10.1073/Pnas.0601630103 |
0.795 |
|
2005 |
Torres MB, Trentzsch H, Stewart D, Mooney ML, Fuentes JM, Saad DF, Reeves RH, De Maio A. Protection from lethal endotoxic shock after testosterone depletion is linked to chromosome X Shock. 24: 318-323. PMID 16205315 DOI: 10.1097/01.shk.0000177639.22863.99 |
0.302 |
|
2005 |
Torres MB, Trentzsch H, Stewart D, Mooney ML, Fuentes JM, Saad DF, Reeves RH, De Maio A. Protection from lethal endotoxic shock after testosterone depletion is linked to chromosome X Shock. 24: 318-323. PMID 16205315 DOI: 10.1097/01.shk.0000177639.22863.99 |
0.302 |
|
2005 |
Olson LE, Tien J, South S, Reeves RH. Long-range chromosomal engineering is more efficient in vitro than in vivo. Transgenic Research. 14: 325-32. PMID 16145840 DOI: 10.1007/s11248-005-0389-6 |
0.745 |
|
2005 |
Olson LE, Tien J, South S, Reeves RH. Long-range chromosomal engineering is more efficient in vitro than in vivo. Transgenic Research. 14: 325-32. PMID 16145840 DOI: 10.1007/s11248-005-0389-6 |
0.745 |
|
2005 |
Sussan TE, Pletcher MT, Murakami Y, Reeves RH. Tumor suppressor in lung cancer 1 (TSLC1) alters tumorigenic growth properties and gene expression Molecular Cancer. 4. PMID 16083501 DOI: 10.1186/1476-4598-4-28 |
0.799 |
|
2005 |
Sultan M, Balzereit D, Saran NG, Guenther S, Guegler K, Lehrach H, Reeves RH, Yaspo M. Gene expression variation in three brain tissues of a mouse model of down syndrome Gbm Annual Fall Meeting Berlin/Potsdam 2005. 2005. DOI: 10.1240/SAV_GBM_2005_H_001289 |
0.817 |
|
2004 |
Olson LE, Richtsmeier JT, Leszl J, Reeves RH. A chromosome 21 critical region does not cause specific Down syndrome phenotypes. Science (New York, N.Y.). 306: 687-90. PMID 15499018 DOI: 10.1126/Science.1098992 |
0.78 |
|
2004 |
Kahlem P, Sultan M, Herwig R, Steinfath M, Balzereit D, Eppens B, Saran NG, Pletcher MT, South ST, Stetten G, Lehrach H, Reeves RH, Yaspo ML. Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome. Genome Research. 14: 1258-67. PMID 15231742 DOI: 10.1101/Gr.1951304 |
0.841 |
|
2004 |
Olson LE, Roper RJ, Baxter LL, Carlson EJ, Epstein CJ, Reeves RH. Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 230: 581-9. PMID 15188443 DOI: 10.1002/Dvdy.20079 |
0.85 |
|
2003 |
Olson LE, Bedja D, Alvey SJ, Cardounel AJ, Gabrielson KL, Reeves RH. Protection from doxorubicin-induced cardiac toxicity in mice with a null allele of carbonyl reductase 1. Cancer Research. 63: 6602-6. PMID 14583452 |
0.717 |
|
2003 |
Olson LE, Bedja D, Alvey SJ, Cardounel AJ, Gabrielson KL, Reeves RH. Protection from doxorubicin-induced cardiac toxicity in mice with a null allele of carbonyl reductase 1. Cancer Research. 63: 6602-6. PMID 14583452 |
0.717 |
|
2003 |
Saran NG, Pletcher MT, Natale JE, Cheng Y, Reeves RH. Global disruption of the cerebellar transcriptome in a Down syndrome mouse model. Human Molecular Genetics. 12: 2013-9. PMID 12913072 DOI: 10.1093/Hmg/Ddg217 |
0.841 |
|
2003 |
Saran NG, Pletcher MT, Natale JE, Cheng Y, Reeves RH. Global disruption of the cerebellar transcriptome in a Down syndrome mouse model. Human Molecular Genetics. 12: 2013-9. PMID 12913072 DOI: 10.1093/Hmg/Ddg217 |
0.841 |
|
2002 |
Villanueva MP, Aiyer AR, Muller S, Pletcher MT, Liu X, Emanuel B, Srivastava D, Reeves RH. Genetic and comparative mapping of genes dysregulated in mouse hearts lacking the Hand2 transcription factor gene Genomics. 80: 593-600. PMID 12504851 DOI: 10.1006/Geno.2002.7009 |
0.741 |
|
2002 |
Villanueva MP, Aiyer AR, Muller S, Pletcher MT, Liu X, Emanuel B, Srivastava D, Reeves RH. Genetic and comparative mapping of genes dysregulated in mouse hearts lacking the Hand2 transcription factor gene Genomics. 80: 593-600. PMID 12504851 DOI: 10.1006/Geno.2002.7009 |
0.741 |
|
2002 |
Reeves RH. Functional genomics: A time and place for every gene Nature. 420: 518-519. PMID 12466849 DOI: 10.1038/420518a |
0.399 |
|
2002 |
Moran TH, Capone GT, Knipp S, Davisson MT, Reeves RH, Gearhart JD. The effects of piracetam on cognitive performance in a mouse model of Down's syndrome. Physiology & Behavior. 77: 403-9. PMID 12419416 DOI: 10.1016/S0031-9384(02)00873-9 |
0.31 |
|
2002 |
Toyoda A, Noguchi H, Taylor TD, Ito T, Pletcher MT, Sakaki Y, Reeves RH, Hattori M. Comparative genomic sequence analysis of the human chromosome 21 down syndrome critical region Genome Research. 12: 1323-1332. PMID 12213769 DOI: 10.1101/gr.153702 |
0.752 |
|
2002 |
Toyoda A, Noguchi H, Taylor TD, Ito T, Pletcher MT, Sakaki Y, Reeves RH, Hattori M. Comparative genomic sequence analysis of the human chromosome 21 down syndrome critical region Genome Research. 12: 1323-1332. PMID 12213769 DOI: 10.1101/gr.153702 |
0.752 |
|
2002 |
Cabin DE, Olson LE, Reeves RH. Meeting Report: 15th International Mouse Genome Conference. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 229-33. PMID 12016509 DOI: 10.1007/s0033502-4001-2 |
0.769 |
|
2002 |
Richtsmeier JT, Zumwalt A, Carlson EJ, Epstein CJ, Reeves RH. Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome. American Journal of Medical Genetics. 107: 317-24. PMID 11840489 DOI: 10.1002/Ajmg.10175 |
0.507 |
|
2002 |
Richtsmeier JT, Zumwalt A, Carlson EJ, Epstein CJ, Reeves RH. Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome. American Journal of Medical Genetics. 107: 317-24. PMID 11840489 DOI: 10.1002/Ajmg.10175 |
0.507 |
|
2001 |
Reeves RH, Cabin DE, Lamb B. Introduction of large insert DNA into mammalian cells and embryos Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. PMID 18428286 DOI: 10.1002/0471142905.hg0512s30 |
0.694 |
|
2001 |
Pletcher MT, Nobukuni T, Fukuhara H, Kuramochi M, Maruyama T, Sekiya T, Sussan T, Isomura M, Murakami Y, Reeves RH. Identification of tumor suppressor candidate genes by physical and sequence mapping of the TSLC1 region of human chromosome 11q23 Gene. 273: 181-189. PMID 11595164 DOI: 10.1016/S0378-1119(01)00592-3 |
0.821 |
|
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 |
0.829 |
|
2001 |
Shinohara T, Tomizuka K, Miyabara S, Takehara S, Kazuki Y, Inoue J, Katoh M, Nakane H, Iino A, Ohguma A, Ikegami S, Inokuchi K, Ishida I, Reeves RH, Oshimura M. Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome. Human Molecular Genetics. 10: 1163-75. PMID 11371509 DOI: 10.1093/Hmg/10.11.1163 |
0.501 |
|
2001 |
Kuramochi M, Fukuhara H, Nobukuni T, Kanbe T, Maruyama T, Ghosh HP, Pletcher M, Isomura M, Onizuka M, Kitamura T, Sekiya T, Reeves RH, Murakami Y. TSLC1 is a tumor-suppressor gene in human non-small-cell lung cancer. Nature Genetics. 27: 427-30. PMID 11279526 DOI: 10.1038/86934 |
0.682 |
|
2001 |
Reeves RH, Baxter LL, Richtsmeier JT. Too much of a good thing: Mechanisms of gene action in Down syndrome Trends in Genetics. 17: 83-88. PMID 11173117 DOI: 10.1016/S0168-9525(00)02172-7 |
0.693 |
|
2000 |
Matesic LE, Niemitz EL, De Maio A, Reeves RH. Quantitative trait loci modulate neutrophil infiltration in the liver during LPS-induced inflammation Faseb Journal. 14: 2247-2254. PMID 11053246 DOI: 10.1096/Fj.99-1051Com |
0.729 |
|
2000 |
Pletcher MT, Roe BA, Chen F, Do T, Do A, Malaj E, Reeves RH. Chromosome evolution: the junction of mammalian chromosomes in the formation of mouse chromosome 10. Genome Research. 10: 1463-7. PMID 11042146 DOI: 10.1101/gr.146600 |
0.713 |
|
2000 |
Reeves RH. Recounting a genetic story Nature. 405: 283-284. PMID 10830941 DOI: 10.1038/35012790 |
0.353 |
|
2000 |
Richtsmeier JT, Baxter LL, Reeves RH. Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice Developmental Dynamics. 217: 137-145. PMID 10706138 DOI: 10.1002/(Sici)1097-0177(200002)217:2<137::Aid-Dvdy1>3.0.Co;2-N |
0.774 |
|
2000 |
Lund J, Chen F, Hua A, Roe B, Budarf M, Emanuel BS, Reeves RH. Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2. Genomics. 63: 374-83. PMID 10704284 DOI: 10.1006/Geno.1999.6044 |
0.362 |
|
2000 |
Baxter LL, Moran TH, Richtsmeier JT, Troncoso J, Reeves RH. Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse. Human Molecular Genetics. 9: 195-202. PMID 10607830 DOI: 10.1093/Hmg/9.2.195 |
0.746 |
|
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 |
0.713 |
|
1999 |
Matesic LE, De Maio A, Reeves RH. Mapping lipopolysaccharide response loci in mice using recombinant inbred and congenic strains Genomics. 62: 34-41. PMID 10585765 DOI: 10.1006/geno.1999.5986 |
0.677 |
|
1999 |
Reeves RH, Cabin DE. Mouse Chromosome 16 Mammalian Genome. 10: 957. PMID 10501958 DOI: 10.1007/s003359901135 |
0.757 |
|
1999 |
Migeon BR, Kazi E, Haisley-Royster C, Hu J, Reeves R, Call L, Lawler A, Moore CS, Morrison H, Jeppesen P. Human X inactivation center induces random X chromosome inactivation in male transgenic mice. Genomics. 59: 113-21. PMID 10409422 DOI: 10.1006/GENO.1999.5861 |
0.313 |
|
1999 |
Moore CS, Lee JS, Birren B, Stetten G, Baxter LL, Reeves RH. Integration of cytogenetic with recombinational and physical maps of mouse chromosome 16 Genomics. 59: 1-5. PMID 10395793 DOI: 10.1006/geno.1999.5812 |
0.662 |
|
1999 |
Lund J, Roe B, Chen F, Budarf M, Galili N, Riblet R, Miller RD, Emanuel BS, Reeves RH. Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 438-43. PMID 10337614 DOI: 10.1007/S003359901019 |
0.344 |
|
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 |
0.331 |
|
1999 |
Matesic LE, Niemitz EL, Maio AD, Reeves RH. MAPPING OF GENES THAT MODULATE THE INFLAMMATORY RESPONSE INDUCED BY ENDOTOXIN Shock. 11: 47. DOI: 10.1097/00024382-199906001-00165 |
0.696 |
|
1998 |
Cole SE, Reeves RH. A cluster of keratin-associated proteins on mouse chromosome 10 in the region of conserved linkage with human chromosome 21. Genomics. 54: 437-42. PMID 9878246 DOI: 10.1006/geno.1998.5590 |
0.344 |
|
1998 |
O'Malley J, Matesic LE, Zink MC, Strandberg JD, Mooney ML, De Maio A, Reeves RH. Comparison of acute endotoxin-induced lesions in A/J and C57BL/6J mice. The Journal of Heredity. 89: 525-30. PMID 9864862 DOI: 10.1093/JHERED/89.6.525 |
0.738 |
|
1998 |
De Maio A, Mooney ML, Matesic LE, Paidas CN, Reeves RH. Genetic component in the inflammatory response induced by bacterial lipopolysaccharide. Shock (Augusta, Ga.). 10: 319-23. PMID 9840645 DOI: 10.1097/00024382-199811000-00002 |
0.717 |
|
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 DOI: 10.1101/Gr.8.9.940 |
0.818 |
|
1998 |
Cabin DE, Reeves RH. Encyclopedia of the mouse genome VII. Mouse chromosome 16 Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8. PMID 9662633 DOI: 10.1007/s003359900661 |
0.754 |
|
1998 |
Murakami Y, Nobukuni T, Tamura K, Maruyama T, Sekiya T, Arai Y, Gomyou H, Tanigami A, Ohki M, Cabin D, Frischmeyer P, Hunt P, Reeves RH. Localization of tumor suppressor activity important in nonsmall cell lung carcinoma on chromosome 11q Proceedings of the National Academy of Sciences of the United States of America. 95: 8153-8158. PMID 9653156 DOI: 10.1073/Pnas.95.14.8153 |
0.74 |
|
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 |
0.352 |
|
1998 |
Reeves RH, Rue E, Yu J, Kao FT. STCH maps to mouse chromosome 16, extending the conserved synteny with human chromosome 21 Genomics. 49: 156-157. PMID 9570963 DOI: 10.1006/geno.1998.5215 |
0.303 |
|
1998 |
Cancilla MR, Graves J, Matesic LE, Reeves RH, Tainton KM, Choo KHA, Resnick MA, Larionov VL, Kouprina NY. Rapid cloning of mouse DNA as yeast artificial chromosomes by transformation-associated recombination (TAR) Mammalian Genome. 9: 157-159. PMID 9457679 DOI: 10.1007/S003359900708 |
0.68 |
|
1998 |
De Maio A, Mooney ML, Matesic L, Reeves RH, Paidas CN. GENETIC CONTRIBUTION TO THE INFLAMMATORY RESPONSE. Shock. 9: 27-28. DOI: 10.1097/00024382-199806001-00092 |
0.661 |
|
1997 |
Korenberg JR, Aaltonen J, Brahe C, Cabin D, Creau N, Delabar JM, Doering J, Gardiner K, Hubert RS, Ives J, Kessling A, Kudoh J, Lafrenière R, Murakami Y, Ohira M, ... ... Reeves RH, et al. Report and abstracts of the Sixth International Workshop on Human Chromosome 21 Mapping 1996. Cold Spring Harbor, New York, USA. May 6-8,1996. Cytogenetics and Cell Genetics. 79: 21-52. PMID 9533011 |
0.732 |
|
1997 |
Reeves RH, Rue EE, Citron MP, Cabin DE. High-resolution recombinational map of mouse chromosome 16. Genomics. 43: 202-8. PMID 9244437 DOI: 10.1006/geno.1997.4807 |
0.738 |
|
1997 |
Reeves RH, Cabin DE. Mouse chromosome 16. Mammalian Genome : Official Journal of the International Mammalian Genome Society. S264-73. PMID 9233399 DOI: 10.1007/s003359900328 |
0.757 |
|
1997 |
Galili N, Baldwin HS, Lund J, Reeves R, Gong W, Wang Z, Roe BA, Emanuel BS, Nayak S, Mickanin C, Budarf MI, Buck CA. A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region. Genome Research. 7: 399. PMID 9110179 |
0.314 |
|
1996 |
Cabin DE, Gardiner K, Reeves RH. Molecular genetic characterization and comparative mapping of the human PCP4 gene Somatic Cell and Molecular Genetics. 22: 167-175. PMID 8914602 DOI: 10.1007/Bf02369907 |
0.803 |
|
1995 |
Mjaatvedt AE, Cabin DE, Cole SE, Long LJ, Breitwieser GE, Reeves RH. Assessment of a mutation in the H5 domain of Girk2 as a candidate for the weaver mutation. Genome Research. 5: 453-63. PMID 8808466 DOI: 10.1101/GR.5.5.453 |
0.737 |
|
1995 |
Reeves RH, Irving NG, Moran TH, Wohn A, Kitt C, Sisodia SS, Schmidt C, Bronson RT, Davisson MT. A mouse model for Down syndrome exhibits learning and behaviour deficits. Nature Genetics. 11: 177-84. PMID 7550346 DOI: 10.1038/ng1095-177 |
0.465 |
|
1994 |
Irving NG, Cabin DE, Swanson DA, Reeves RH. Gene Order Is Conserved within the Human Chromosome 21 Linkage Group on Mouse Chromosome 10 Genomics. 21: 144-149. PMID 7916323 DOI: 10.1006/geno.1994.1236 |
0.777 |
|
1993 |
Gregor P, Reeves RH, Jabs EW, Yang X, Dackowski W, Rochelle JM, Brown RH, Haines JL, O'Hara BF, Uhl GR. Chromosomal localization of glutamate receptor genes: relationship to familial amyotrophic lateral sclerosis and other neurological disorders of mice and humans. Proceedings of the National Academy of Sciences of the United States of America. 90: 3053-7. PMID 8464923 DOI: 10.1073/Pnas.90.7.3053 |
0.343 |
|
1993 |
Mjaatvedt AE, Citron MP, Reeves RH. High-resolution mapping of D16led-1, Gart, Gas-4, Cbr, Pcp-4, and Erg on distal mouse chromosome 16. Genomics. 17: 382-6. PMID 8406490 DOI: 10.1006/geno.1993.1336 |
0.374 |
|
1992 |
Reeves RH, Miller RD, Riblet R. Mouse chromosome 16. Mammalian Genome : Official Journal of the International Mammalian Genome Society. S269-79. PMID 1799804 DOI: 10.1007/BF00656497 |
0.314 |
|
1992 |
Reeves RH, Miller RD. Mouse chromosome 16. Mammalian Genome : Official Journal of the International Mammalian Genome Society. S233-40. PMID 1498436 DOI: 10.1007/BF00648434 |
0.314 |
|
1992 |
Taylor BA, Frankel WN, Reeves RH. Mouse chromosome 10. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 3: S153-61. PMID 1498429 DOI: 10.1007/BF00648428 |
0.314 |
|
1992 |
Reeves RH, Pavan WJ, Hieter P. [49] Yeast artificial chromosome modification and manipulation Methods in Enzymology. 216: 584-603. PMID 1336105 DOI: 10.1016/0076-6879(92)16051-K |
0.559 |
|
1991 |
Pavan WJ, Hieter P, Sears D, Burkhoff A, Reeves RH. High-efficiency yeast artificial chromosome fragmentation vectors Gene. 106: 125-127. PMID 1937033 DOI: 10.1016/0378-1119(91)90576-W |
0.531 |
|
1991 |
Pavan WJ, Reeves RH. Integrative selection of human chromosome-specific yeast artificial chromosomes Proceedings of the National Academy of Sciences of the United States of America. 88: 7788-7791. PMID 1881915 DOI: 10.1073/PNAS.88.17.7788 |
0.56 |
|
1991 |
Taylor BA, Justice MJ, Reeves R. Mouse chromosome 10. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 1: S146-57. PMID 1799797 DOI: 10.1007/Bf00656491 |
0.366 |
|
1990 |
Pavan WJ, Hieter P, Reeves RH. Generation of deletion derivatives by targeted transformation of human-derived yeast artificial chromosomes Proceedings of the National Academy of Sciences of the United States of America. 87: 1300-1304. PMID 2406718 DOI: 10.1073/Pnas.87.4.1300 |
0.54 |
|
1990 |
Pavan WJ, Hieter P, Reeves RH. Modification and transfer into an embryonal carcinoma cell line of a 360-kilobase human-derived yeast artificial chromosome Molecular and Cellular Biology. 10: 4163-4169. PMID 2196449 DOI: 10.1128/mcb.10.8.4163-4169.1990 |
0.547 |
|
1990 |
Reeves RH, Pavan WJ, Hieter P. Modification and manipulation of mammalian DNA cloned as YACs Gene Analysis Techniques. 7: 107-113. PMID 2091692 DOI: 10.1016/0735-0651(90)90015-8 |
0.425 |
|
1990 |
Camper SA, Saunders TL, Katz RW, Reeves RH. The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation Genomics. 8: 586-590. PMID 1981057 DOI: 10.1016/0888-7543(90)90050-5 |
0.378 |
|
1989 |
Reeves RH, Gearhart JD, Hecht NB, Yelick P, Johnson P, O'brien SJ. Mapping of PRM 1 to human chromosome 16 and tight linkage of Prm-1 and Prm-2 on mouse chromosome 16 Journal of Heredity. 80: 442-446. PMID 2614060 DOI: 10.1093/Oxfordjournals.Jhered.A110895 |
0.534 |
|
1989 |
Reeves RH, Crowley MR, Lorenzon N, Pavan WJ, Smeyne RJ, Goldowitz D. The mouse neurological mutant weaver maps within the region of chromosome 16 that is homologous to human chromosome 21. Genomics. 5: 522-6. PMID 2575584 DOI: 10.1016/0888-7543(89)90018-9 |
0.615 |
|
1988 |
O'Hara BF, Bendotti C, Reeves RH, Oster-Granite ML, Coyle JT, Gearhart JD. Genetic mapping and analysis of somatostatin expression in Snell dwarf mice. Brain Research. 464: 283-92. PMID 2906811 DOI: 10.1016/0169-328X(88)90037-X |
0.421 |
|
1988 |
Reeves RH, O'Hara BF, Pavan WJ, Gearhart JD, Haller O. Genetic mapping of the Mx influenza virus resistance gene within the region of mouse chromosome 16 that is homologous to human chromosome 21. Journal of Virology. 62: 4372-5. PMID 2902234 DOI: 10.1128/Jvi.62.11.4372-4375.1988 |
0.621 |
|
1988 |
Coyle JT, Oster-Granite ML, Reeves RH, Gearhart JD. Down syndrome, Alzheimer's disease and the trisomy 16 mouse. Trends in Neurosciences. 11: 390-4. PMID 2469204 DOI: 10.1016/0166-2236(88)90075-6 |
0.39 |
|
1987 |
Gearhart JD, Oster-Granite ML, Reeves RH, Coyle JT. Developmental consequences of autosomal aneuploidy in mammals. Developmental Genetics. 8: 249-65. PMID 2971493 DOI: 10.1002/Dvg.1020080408 |
0.435 |
|
1987 |
Reeves RH, Robakis NK, Oster-Granite ML, Wisniewski HM, Coyle JT, Gearhart JD. Genetic linkage in the mouse of genes involved in Down syndrome and Alzheimer's disease in man. Brain Research. 388: 215-21. PMID 2960420 DOI: 10.1016/0169-328X(87)90028-3 |
0.452 |
|
1987 |
Reeves RH, Gallahan D, O'Hara BF, Callahan R, Gearhart JD. Genetic mapping of Prm-1, Igl-1, Smst, Mtv-6, Sod-1, and Ets-2 and localization of the Down syndrome region on mouse chromosome 16. Cytogenetics and Cell Genetics. 44: 76-81. PMID 2882955 DOI: 10.1159/000132347 |
0.362 |
|
1986 |
Watson DK, McWilliams-Smith MJ, Kozak C, Reeves R, Gearhart J, Nunn MF, Nash W, Fowle JR, Duesberg P, Papas TS. Conserved chromosomal positions of dual domains of the ets protooncogene in cats, mice, and humans. Proceedings of the National Academy of Sciences of the United States of America. 83: 1792-6. PMID 3513188 DOI: 10.1073/Pnas.83.6.1792 |
0.3 |
|
1986 |
Reeves RH, Gearhart JD, Littlefield JW. Genetic basis for a mouse model of down syndrome Brain Research Bulletin. 16: 803-814. PMID 2944567 DOI: 10.1016/0361-9230(86)90076-6 |
0.434 |
|
1985 |
Reeves RH, Nash WG, O'Brien SJ. Genetic mapping of endogenous RD-114 retroviral sequences of domestic cats Journal of Virology. 56: 303-306. PMID 4032538 DOI: 10.1128/Jvi.56.1.303-306.1985 |
0.467 |
|
1985 |
Reeves R, Fedako C, O'Hara B, Gearhart J, Little-Field JW. 850 GENETIC LOCALIZATION OF THE DOWN SYNDROME REGION IN THE MOUSE Pediatric Research. 19: 252A-252A. DOI: 10.1203/00006450-198504000-00880 |
0.391 |
|
1984 |
Reeves RH, O'Brien SJ. Molecular genetic characterization of the RD-114 gene family of endogenous feline retroviral sequences Journal of Virology. 52: 164-171. PMID 6090693 DOI: 10.1128/Jvi.52.1.164-171.1984 |
0.406 |
|
1983 |
O'Brien SJ, Reeves RH, Simonson JM, Eichelberger MA, Nash WG. Parallels of genomic organization and of endogenous retrovirus organization in cat and man Developmental Genetics. 4: 341-354. DOI: 10.1002/Dvg.1020040410 |
0.497 |
|
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