16 results on '"Heathcott, Rosemary W."'
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2. Sequential WT1 and CTNNB1 mutations and alterations of (beta)-catenin localisation in intralobar nephrogenic rests and associated Wilms tumours: two case studies
3. Myogenesis in Wilms Tumors Is Associated with Mutations of the WT1 Gene and Activation of Bcl-2 and the Wnt Signaling Pathway
4. Expression of Phosphatonin-Related Genes in Sheep, Dog and Horse Kidneys Using Quantitative Reverse Transcriptase PCR
5. Sequential WT1 and CTNNB1 mutations and alterations of β-catenin localisation in intralobar nephrogenic rests and associated Wilms tumours: two case studies
6. Reply to Dr. Sredni and Colleagues
7. The novel equisetin-like compound, TA-289, causes aberrant mitochondrial morphology which is independent of the production of reactive oxygen species in Saccharomyces cerevisiae
8. Laulimalide and peloruside A inhibit mitosis of Saccharomyces cerevisiae by preventing microtubule depolymerisation-dependent steps in chromosome separation and nuclear positioning
9. Chemical genetic profiling of the microtubule-targeting agent peloruside A in budding yeast Saccharomyces cerevisiae
10. Chromosome 14q LOH in localized clear cell renal cell carcinoma
11. Pancreatoblastoma is associated with chromosome 11p loss of heterozygosity andIGF2 overexpression
12. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X
13. Myogenesis in Wilms Tumors Is Associated with Mutations of the WT1Gene and Activation of Bcl-2 and the Wnt Signaling Pathway
14. Pancreatoblastoma is associated with chromosome 11p loss of heterozygosity and IGF2 overexpression.
15. Pancreatoblastoma is associated with chromosome 11p loss of heterozygosity and <TOGGLE>IGF2</TOGGLE> overexpression
16. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X.
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