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Non-invasive evaluation of tumour hypoxia in the Shionogi tumour model for prostate cancer with <sup>18</sup>F-EF5 and positron emission tomography.
Published in:
BJU International, 2007, v. 99, n. 5, p. 1154, doi. 10.1111/j.1464-410X.2007.06761.x
By:
- Yapp, Donald T. T.;
- Woo, Janet;
- Kartono, Aileen;
- Sy, Jonathan;
- Oliver, Thomas;
- Skov, Kirsten A.;
- Koch, Cameron J.;
- Adomat, Hans;
- Dragowska, Wieslawa H.;
- Fadzli, Ladan;
- Ruth, Thomas;
- Adam, Michael J.;
- Green, David;
- Gleave, Martin
Publication type:
Article
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
Published in:
Nature Genetics, 2007, v. 39, n. 7, p. 882, doi. 10.1038/ng2069
By:
- Arts, Heleen H.;
- Doherty, Dan;
- van Beersum, Sylvia E. C.;
- Parisi, Melissa A.;
- Letteboer, Stef J. F.;
- Gorden, Nicholas T.;
- Peters, Theo A.;
- Märker, Tina;
- Voesenek, Krysta;
- Kartono, Aileen;
- Ozyurek, Hamit;
- Farin, Federico M.;
- Kroes, Hester Y.;
- Wolfrum, Uwe;
- Brunner, Han G.;
- Cremers, Frans P. M.;
- Glass, Ian A.;
- Knoers, Nine V. A. M.;
- Roepman, Ronald
Publication type:
Article
Identification of Transforming Growth Factor β1--Driven Genetic Programs of Acute Lung Fibrosis.
Published in:
American Journal of Respiratory Cell & Molecular Biology, 2008, v. 39, n. 3, p. 324, doi. 10.1165/rcmb.2007-0186OC
By:
- Pulichino, Anne-Marie;
- I.-Ming Wang;
- Caron, Alexandre;
- Mortimer, James;
- Auger, Anick;
- Boie, Yves;
- Elias, Jack A.;
- Kartono, Aileen;
- Lijing Xu;
- Menetski, Joseph;
- Sayegh, Camil E.
Publication type:
Article
Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein.
Published in:
Human Molecular Genetics, 2009, v. 18, n. 1, p. 51, doi. 10.1093/hmg/ddn312
By:
- van Wijk, Erwin;
- Kersten, Ferry F.J.;
- Kartono, Aileen;
- Mans, Dorus A.;
- Brandwijk, Kim;
- Letteboer, Stef J.F.;
- Peters, Theo A.;
- Märker, Tina;
- Yan, Xiumin;
- Cremers, Cor W.R.J.;
- Cremers, Frans P.M.;
- Wolfrum, Uwe;
- Roepman, Ronald;
- Kremer, Hannie
Publication type:
Article

Found: 4

Non-invasive evaluation of tumour hypoxia in the Shionogi tumour model for prostate cancer with <sup>18</sup>F-EF5 and positron emission tomography.

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.

Identification of Transforming Growth Factor β1--Driven Genetic Programs of Acute Lung Fibrosis.

Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein.