Aileen Kartono

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

Heleen H. Arts, Dan Doherty, Sylvia E. C. van Beersum et al. · Nature Genetics · 2007 · 321 citations

Life Sciences, Genetics, Molecular Genetics +8

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

Anne-Marie Pulichino, I‐Ming Wang, Alexandre Caron et al. · American Journal of Respiratory Cell and Molecular Biology · 2008 · 53 citations

Life Sciences, Genetics, Molecular Biology +8

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

Erwin van Wijk, Ferry F.J. Kersten, Aileen Kartono et al. · Human Molecular Genetics · 2008 · 48 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Non‐invasive evaluation of tumour hypoxia in the Shionogi tumour model for prostate cancer with ¹⁸ F‐EF5 and positron emission tomography

Donald T. Yapp, Janet Woo, Aileen Kartono et al. · British Journal of Urology · 2007 · 27 citations

Medicine, Nuclear Medicine, Oncology +17

Adenovirus E1A regulates lung epithelial ICAM-1 expression by interacting with transcriptional regulators at its promoter

Kiyoshi Morimoto, John V. Gosselink, Aileen Kartono et al. · American Journal of Physiology-Lung Cellular and Molecular Physiology · 2008 · 14 citations

Life Sciences, Immunology, Molecular Biology +17