The scientist’s investigation covers issues in Genetics, Cell biology, Cilium, Ciliopathies and Renal cell carcinoma. With her scientific publications, her incorporates both Genetics and CREB-binding protein. Her studies deal with areas such as Tumor suppressor gene and Zebrafish as well as Cell biology.
The concepts of her Cilium study are interwoven with issues in Cystic kidney and Organelle. Her Ciliopathies research is multidisciplinary, incorporating perspectives in Human genetics, Ciliopathy and Polycystic kidney disease. In her study, Sunitinib is strongly linked to Urology, which falls under the umbrella field of Renal cell carcinoma.
Her primary areas of study are Genetics, Cilium, Cell biology, Cancer research and Internal medicine. Her Genetics research integrates issues from Molecular biology and Disease. Her Cilium research also works with subjects such as
Rachel H. Giles interconnects Suppressor and Zebrafish in the investigation of issues within Cell biology. The study incorporates disciplines such as Tumor suppressor gene, Cancer, Wnt signaling pathway and Von Hippel–Lindau disease in addition to Cancer research. Her Internal medicine research is multidisciplinary, incorporating elements of Endocrinology and Oncology.
Rachel H. Giles mainly focuses on Renal cell carcinoma, Kidney cancer, Internal medicine, Cell biology and Cilium. Her study looks at the intersection of Internal medicine and topics like Oncology with Frameshift mutation. Her work carried out in the field of Cell biology brings together such families of science as Transgene and Zebrafish.
Her studies in Cilium integrate themes in fields like Phenotype, Ciliopathies, Ciliopathy and Ciliary tip. The subject of her Phenotype research is within the realm of Genetics. Her study on Genetics is mostly dedicated to connecting different topics, such as Disease.
The scientist’s investigation covers issues in Renal cell carcinoma, Genetics, Urology, Kidney cancer and Sunitinib. Genetics and Disease are frequently intertwined in her study. Rachel H. Giles combines subjects such as Cancer, Systematic review, Clear cell renal cell carcinoma and Guideline with her study of Urology.
Her work deals with themes such as Randomized controlled trial and Adjuvant therapy, which intersect with Kidney cancer. Her work investigates the relationship between Molecular genetics and topics such as Phenotype that intersect with problems in Cilium. Her research investigates the connection between Ciliary transition zone and topics such as Cell biology that intersect with problems in Intraflagellar transport.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Caught up in a Wnt storm: Wnt signaling in cancer.
Rachel H. Giles;Johan H. van Es;Hans Clevers.
Biochimica et Biophysica Acta (2003)
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
Fred Petrif;Rachel H. Giles;Hans G. Dauwerse;Jasper J. Saris.
Nature (1995)
Mutations in the APC tumour suppressor gene cause chromosomal instability
Riccardo Fodde;Jeroen Kuipers;Jeroen Kuipers;Carla Rosenberg;Ron Smits.
Nature Cell Biology (2001)
Conjunction dysfunction: CBP/p300 in human disease
Rachel H Giles;Dorien J.M Peters;Martijn H Breuning.
Trends in Genetics (1998)
Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways
Liyun Sang;Julie J. Miller;Kevin C. Corbit;Rachel H. Giles.
Cell (2011)
European Association of Urology Guidelines on Renal Cell Carcinoma: The 2019 Update.
Börje Ljungberg;Laurance Albiges;Yasmin Abu-Ghanem;Karim Bensalah.
European Urology (2019)
Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling
Moumita Chaki;Rannar Airik;Amiya K. Ghosh;Rachel H. Giles.
Cell (2012)
Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy
Edgar A Otto;Toby W Hurd;Rannar Airik;Moumita Chaki.
Nature Genetics (2010)
Genetic analysis of von Hippel-Lindau disease.
Morgan Nordstrom-O'Brien;Rob B. van der Luijt;Ellen van Rooijen;Ans M. van den Ouweland.
Human Mutation (2010)
FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair
Weibin Zhou;Edgar A Otto;Andrew Cluckey;Rannar Airik.
Nature Genetics (2012)
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