Skip Header

 

1 - 25 of 65 results for author:"Rubin E.M."Drop in Literature Citations

Customize display Download...

Page of 3 | Next »

Dominant negative LRP5 decreases tumorigenicity and metastasis of osteosarcoma in an animal model.

Guo Y., Rubin E.M., Xie J., Zi X., Hoang B.H.

Clin. Orthop. Relat. Res. 466:2039-2045(2008) · Mapped (3)

Metagenomic and functional analysis of hindgut microbiota of a wood-feeding higher termite.

Warnecke F., Luginbuhl P., Ivanova N., Ghassemian M., Richardson T.H., Stege J.T., Cayouette M., McHardy A.C., Djordjevic G., Aboushadi N. et al.

Nature 450:560-565(2007) · UniProtKB (47)

New cerebellar phenotypes in YAC transgenic mouse in vivo library of human Down syndrome critical region-1.

Rachidi M., Lopes C., Vayssettes C., Smith D.J., Rubin E.M., Delabar J.M.

Biochem. Biophys. Res. Commun. 364:488-494(2007) · Mapped (4)

Runx1-mediated hematopoietic stem-cell emergence is controlled by a Gata/Ets/SCL-regulated enhancer.

Nottingham W.T., Jarratt A., Burgess M., Speck C.L., Cheng J.F., Prabhakar S., Rubin E.M., Li P.S., Sloane-Stanley J., Kong-A-San J. et al.

Blood 110:4188-4197(2007) · Mapped (17)

Deletion of ultraconserved elements yields viable mice.

Ahituv N., Zhu Y., Visel A., Holt A., Afzal V., Pennacchio L.A., Rubin E.M.

PLoS Biol. 5:e234-e234(2007) · Mapped (30)

Comparative genomics reveals functional transcriptional control sequences in the Prop1 gene.

Ward R.D., Davis S.W., Cho M., Esposito C., Lyons R.H., Cheng J.F., Rubin E.M., Rhodes S.J., Raetzman L.T., Smith T.P. et al.

Mamm. Genome 18:521-537(2007) · Mapped (1)

Symbiosis insights through metagenomic analysis of a microbial consortium.

Woyke T., Teeling H., Ivanova N.N., Huntemann M., Richter M., Gloeckner F.O., Boffelli D., Anderson I.J., Barry K.W., Shapiro H.J. et al.

Nature 443:950-955(2006) · UniProtKB (22)

A regulatory SNP causes a human genetic disease by creating a new transcriptional promoter.

De Gobbi M., Viprakasit V., Hughes J.R., Fisher C., Buckle V.J., Ayyub H., Gibbons R.J., Vernimmen D., Yoshinaga Y., de Jong P. et al.

Science 312:1215-1217(2006) · UniProtKB (7)

A distal enhancer and an ultraconserved exon are derived from a novel retroposon.

Bejerano G., Lowe C.B., Ahituv N., King B., Siepel A., Salama S.R., Rubin E.M., Kent W.J., Haussler D.

Nature 441:87-90(2006) · Mapped (4)

Apolipoprotein A-I and the molecular variant apoA-I(Milano): evaluation of the antiatherogenic effects in knock-in mouse model.

Parolini C., Chiesa G., Gong E., Caligari S., Cortese M.M., Koga T., Forte T.M., Rubin E.M.

Atherosclerosis 183:222-229(2005) · Mapped (10)

Apolipoprotein A-V deficiency results in marked hypertriglyceridemia attributable to decreased lipolysis of triglyceride-rich lipoproteins and removal of their remnants.

Grosskopf I., Baroukh N., Lee S.J., Kamari Y., Harats D., Rubin E.M., Pennacchio L.A., Cooper A.D.

Arterioscler. Thromb. Vasc. Biol. 25:2573-2579(2005) · Mapped (29)

HDLs in apoA-I transgenic Abca1 knockout mice are remodeled normally in plasma but are hypercatabolized by the kidney.

Lee J.Y., Timmins J.M., Mulya A., Smith T.L., Zhu Y., Rubin E.M., Chisholm J.W., Colvin P.L., Parks J.S.

J. Lipid Res. 46:2233-2245(2005) · Mapped (3)

Genomic deletion of a long-range bone enhancer misregulates sclerostin in Van Buchem disease.

Loots G.G., Kneissel M., Keller H., Baptist M., Chang J., Collette N.M., Ovcharenko D., Plajzer-Frick I., Rubin E.M.

Genome Res. 15:928-935(2005) · Mapped (2)

The Ter mutation in the dead end gene causes germ cell loss and testicular germ cell tumours.

Youngren K.K., Coveney D., Peng X., Bhattacharya C., Schmidt L.S., Nickerson M.L., Lamb B.T., Deng J.M., Behringer R.R., Capel B. et al.

Nature 435:360-364(2005) · UniProtKB (1) · Mapped (9)

Insulin-mediated down-regulation of apolipoprotein A5 gene expression through the phosphatidylinositol 3-kinase pathway: role of upstream stimulatory factor.

Nowak M., Helleboid-Chapman A., Jakel H., Martin G., Duran-Sandoval D., Staels B., Rubin E.M., Pennacchio L.A., Taskinen M.R., Fruchart-Najib J. et al.

Mol. Cell. Biol. 25:1537-1548(2005) · Mapped (3)

The sequence and analysis of duplication-rich human chromosome 16.

Martin J., Han C., Gordon L.A., Terry A., Prabhakar S., She X., Xie G., Hellsten U., Chan Y.M., Altherr M. et al.

Nature 432:988-994(2004) · UniProtKB (638)

Mouse strain-specific differences in vascular wall gene expression and their relationship to vascular disease.

Tabibiazar R., Wagner R.A., Spin J.M., Ashley E.A., Narasimhan B., Rubin E.M., Efron B., Tsao P.S., Tibshirani R., Quertermous T.

Arterioscler. Thromb. Vasc. Biol. 25:302-308(2005) · Mapped (9)

Intraspecies sequence comparisons for annotating genomes.

Boffelli D., Weer C.V., Weng L., Lewis K.D., Shoukry M.I., Pachter L., Keys D.N., Rubin E.M.

Genome Res. 14:2406-2411(2004) · UniProtKB (45)

Characterization of the dog Agouti gene and a nonagoutimutation in German Shepherd dogs.

Kerns J.A., Newton J., Berryere T.G., Rubin E.M., Cheng J.F., Schmutz S.M., Barsh G.S.

Mamm. Genome 15:798-808(2004) · UniProtKB (1)

Megabase deletions of gene deserts result in viable mice.

Nobrega M.A., Zhu Y., Plajzer-Frick I., Afzal V., Rubin E.M.

Nature 431:988-993(2004) · Mapped (14)

The DNA sequence and comparative analysis of human chromosome 5.

Schmutz J., Martin J., Terry A., Couronne O., Grimwood J., Lowry S., Gordon L.A., Scott D., Xie G., Huang W. et al.

Nature 431:268-274(2004) · UniProtKB (616)

Transgenic mouse in vivo library of human Down syndrome critical region 1: association between DYRK1A overexpression, brain development abnormalities, and cell cycle protein alteration.

Branchi I., Bichler Z., Minghetti L., Delabar J.M., Malchiodi-Albedi F., Gonzalez M.C., Chettouh Z., Nicolini A., Chabert C., Smith D.J. et al.

J. Neuropathol. Exp. Neurol. 63:429-440(2004) · Mapped (7)

Analysis of apolipoprotein A5, c3, and plasma triglyceride concentrations in genetically engineered mice.

Baroukh N., Bauge E., Akiyama J., Chang J., Afzal V., Fruchart J.C., Rubin E.M., Fruchart-Najib J., Pennacchio L.A.

Arterioscler. Thromb. Vasc. Biol. 24:1297-1302(2004) · Mapped (5)

The DNA sequence and biology of human chromosome 19.

Grimwood J., Gordon L.A., Olsen A.S., Terry A., Schmutz J., Lamerdin J.E., Hellsten U., Goodstein D., Couronne O., Tran-Gyamfi M. et al.

Nature 428:529-535(2004) · UniProtKB (1,180)

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.

Nature 428:493-521(2004) · UniProtKB (351) · Mapped (82)

Page of 3 | Next »