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39
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for author:"de Jong P.J."
in Literature Citations
| Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Kwiatkowski T.J. Jr., Bosco D.A., Leclerc A.L., Tamrazian E., Vanderburg C.R., Russ C., Davis A., Gilchrist J., Kasarskis E.J., Munsat T. et al. |
| Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy. Zhang Z., Alpert D., Francis R., Chatterjee B., Yu Q., Tansey T., Sabol S.L., Cui C., Bai Y., Koriabine M. et al. Proc. Natl. Acad. Sci. U.S.A. 106:3219-3224(2009) · Mapped (1) |
| Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event. Rudd M.K., Endicott R.M., Friedman C., Walker M., Young J.M., Osoegawa K., de Jong P.J., Green E.D., Trask B.J. Genome Res. 19:33-41(2009) · UniProtKB (1) |
| The amphioxus genome and the evolution of the chordate karyotype. Putnam N.H., Butts T., Ferrier D.E.K., Furlong R.F., Hellsten U., Kawashima T., Robinson-Rechavi M., Shoguchi E., Terry A., Yu J.-K. et al. Nature 453:1064-1071(2008) · UniProtKB (28,535) |
| Downregulation of death-associated protein kinase 1 (DAPK1) in chronic lymphocytic leukemia. Raval A., Tanner S.M., Byrd J.C., Angerman E.B., Perko J.D., Chen S.S., Hackanson B., Grever M.R., Lucas D.M., Matkovic J.J. et al. Cell 129:879-890(2007) · Mapped (8) |
| Draft genome sequence of the sexually transmitted pathogen Trichomonas vaginalis. Carlton J.M., Hirt R.P., Silva J.C., Delcher A.L., Schatz M., Zhao Q., Wortman J.R., Bidwell S.L., Alsmark U.C.M., Besteiro S. et al. Science 315:207-212(2007) · UniProtKB (50,189) |
| BAC clones generated from sheared DNA. Osoegawa K., Vessere G.M., Li Shu C., Hoskins R.A., Abad J.P., de Pablos B., Villasante A., de Jong P.J. Genomics 89:291-299(2007) · Mapped (3) |
| DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage. Zody M.C., Garber M., Adams D.J., Sharpe T., Harrow J., Lupski J.R., Nicholson C., Searle S.M., Wilming L., Young S.K. et al. Nature 440:1045-1049(2006) · UniProtKB (913) |
| The DNA sequence of the human X chromosome. Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P. et al. Nature 434:325-337(2005) · UniProtKB (1,199) |
| The genomic sequence of the accidental pathogen Legionella pneumophila. Chien M., Morozova I., Shi S., Sheng H., Chen J., Gomez S.M., Asamani G., Hill K., Nuara J., Feder M. et al. Science 305:1966-1968(2004) · UniProtKB (2,930) |
| Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. Vissers L.E.L.M., van Ravenswaaij C.M.A., Admiraal R., Hurst J.A., de Vries B.B.A., Janssen I.M., van der Vliet W.A., Huys E.H.L.P.G., de Jong P.J., Hamel B.C.J. et al. |
| TAHRE, a novel telomeric retrotransposon from Drosophila melanogaster, reveals the origin of Drosophila telomeres. Abad J.P., De Pablos B., Osoegawa K., De Jong P.J., Martin-Gallardo A., Villasante A. Mol. Biol. Evol. 21:1620-1624(2004) · UniProtKB (7) |
| Genomic analysis of Drosophila melanogaster telomeres: full-length copies of HeT-A and TART elements at telomeres. Abad J.P., De Pablos B., Osoegawa K., De Jong P.J., Martin-Gallardo A., Villasante A. Mol. Biol. Evol. 21:1613-1619(2004) · UniProtKB (13) |
| Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Gibbs R.A., Weinstock G.M., Metzker M.L., Muzny D.M., Sodergren E.J., Scherer S., Scott G., Steffen D., Worley K.C., Burch P.E. et al. |
| Comparative analyses of multi-species sequences from targeted genomic regions. Thomas J.W., Touchman J.W., Blakesley R.W., Bouffard G.G., Beckstrom-Sternberg S.M., Margulies E.H., Blanchette M., Siepel A.C., Thomas P.J., McDowell J.C. et al. Nature 424:788-793(2003) · UniProtKB (95) |
| Assessing the impact of comparative genomic sequence data on the functional annotation of the Drosophila genome. Bergman C.M., Pfeiffer B.D., Rincon-Limas D.E., Hoskins R.A., Gnirke A., Mungall C.J., Wang A.M., Kronmiller B., Pacleb J.M., Park S. et al. Genome Biol. 3:RESEARCH0086.1-RESEARCH0086.20(2002) · UniProtKB (31) · Mapped (194) |
| Genomic analysis of human chromosome 10q and 4q telomeres suggests a common origin. van Geel M., Dickson M.C., Beck A.F., Bolland D.J., Frants R.R., van der Maarel S.M., de Jong P.J., Hewitt J.E. Genomics 79:210-217(2002) · UniProtKB (2) |
| Genetic, physical, and comparative map of the subtelomeric region of mouse chromosome 4. Li X., Bachmanov A.A., Li S., Chen Z., Tordoff M.G., Beauchamp G.K., de Jong P.J., Wu C., Chen L., West D.B. et al. Mamm. Genome 13:5-19(2002) · UniProtKB (1) |
| A cascade of complex subtelomeric duplications during the evolution of the hominoid and Old World monkey genomes. van Geel M., Eichler E.E., Beck A.F., Shan Z., Haaf T., van der Maarel S.M., Frants R.R., de Jong P.J. Am. J. Hum. Genet. 70:269-278(2002) · UniProtKB (4) · Mapped (1) |
| Positional cloning of the mouse saccharin preference (Sac) locus. Bachmanov A.A., Li X., Reed D.R., Ohmen J.D., Li S., Chen Z., Tordoff M.G., de Jong P.J., Wu C., West D.B. et al. |
| Source and component genes of a 6-200 Mb gene cluster in the house mouse. Weichenhan D., Kunze B., Winking H., Van Geel M., Osoegawa K., De Jong P.J., Traut W. |
| Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35. van Geel M., van Deutekom J.C.T., van Staalduinen A.A., Lemmers R.J.L.F., Dickson M.C., Hofker M.H., Padberg G.W., Hewitt J.E., De Jong P.J., Frants R.R. Cytogenet. Cell Genet. 88:316-321(2000) · UniProtKB (1) |
| The t(14;21)(q11.2;q22) chromosomal translocation associated with T-cell acute lymphoblastic leukemia activates the BHLHB1 gene. Wang J., Jani-Sait S.N., Escalon E.A., Carroll A.J., de Jong P.J., Kirsch I.R., Aplan P.D. Proc. Natl. Acad. Sci. U.S.A. 97:3497-3502(2000) · UniProtKB (1) |
| Bacterial artificial chromosome libraries for mouse sequencing and functional analysis. Osoegawa K., Tateno M., Woon P.Y., Frengen E., Mammoser A.G., Catanese J.J., Hayashizaki Y., de Jong P.J. Genome Res. 10:116-128(2000) · Mapped (13) |
| The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements. van Geel M., Heather L.J., Lyle R., Hewitt J.E., Frants R.R., de Jong P.J. Genomics 61:55-65(1999) · UniProtKB (1) |
