47 results on '"Prinsen, Clemens"'
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2. Mismatch repair deficiency as a predictive marker for response to adjuvant radiotherapy in endometrial cancer
3. Lessons from 10 years' experience running the Fiom KID-DNA database, a voluntary DNA-linking register for donor-conceived people and donors in The Netherlands.
4. Whole-exome sequencing of a meningeal melanocytic tumour reveals activating CYSLTR2 and EIF1AX hotspot mutations and similarities to uveal melanoma
5. Data from Cytoglobin, the Newest Member of the Globin Family, Functions as a Tumor Suppressor Gene
6. Supplementary Figure 1 from Cytoglobin, the Newest Member of the Globin Family, Functions as a Tumor Suppressor Gene
7. Supplementary Figure Legends 1-2 from Cytoglobin, the Newest Member of the Globin Family, Functions as a Tumor Suppressor Gene
8. Supplementary Figure 2 from Cytoglobin, the Newest Member of the Globin Family, Functions as a Tumor Suppressor Gene
9. Lessons from 10 years’ experience running the Fiom KID-DNA database, a voluntary DNA-linking register for donor-conceived people and donors in The Netherlands
10. A Rapid Cycle Real-Time Quantitative β-globin PCR for Quantification of Human DNA in Feces
11. The Retinal Rod and Cone Na+/Ca2+-K+Exchangers
12. DNA hypermethylation analysis in sputum of asymptomatic subjects at risk for lung cancer participating in the NELSON trial: argument for maximum screening interval of 2 years
13. Diagnosing Peripheral Lung Cancer: The Additional Value of the Ras-Association Domain Family 1A Gene Methylation and Kirsten Rat Sarcoma 2 Viral Oncogene Homolog Mutation Analyses in Washings in Nondiagnostic Bronchoscopy
14. Structural and Functional Studies on the Heart Fatty Acid-Binding Protein
15. Circulating DNA is a non-invasive prognostic factor for survival in non-small cell lung cancer
16. Application of a methylation gene panel by quantitative PCR for lung cancers
17. Stoichiometry of the retinal cone Na/Ca-K exchanger heterologously expressed in insect cells: comparison with the bovine heart Na/Ca exchanger
18. EGFR and KRAS quality assurance schemes in pathology: generating normative data for molecular predictive marker analysis in targeted therapy
19. Mismatch repair deficiency as a predictor of adjuvant radiotherapy response in endometrioid endometrial carcinoma.
20. Whole-exome sequencing of a meningeal melanocytic tumour reveals activating CYSLTR2 and EIF1AX hotspot mutations and similarities to uveal melanoma
21. A T cell receptor beta-chain variable region polymorphism associated with radiographic progression in rheumatoid arthritis
22. SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas
23. SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas
24. DNA hypermethylation analysis in sputum of asymptomatic subjects at risk for lung cancer participating in the NELSON trial: argument for maximum screening interval of 2 years
25. SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas
26. Whole-exome sequencing of a meningeal melanocytic tumour reveals activating <italic>CYSLTR2</italic> and <italic>EIF1AX</italic> hotspot mutations and similarities to uveal melanoma.
27. EUELC project: a multi-centre, multipurpose study to investigate early stage NSCLC, and to establish a biobank for ongoing collaboration
28. Methylation analysis in spontaneous sputum for lung cancer diagnosis
29. Cytoglobin, the Newest Member of the Globin Family, Functions as a Tumor Suppressor Gene
30. Differential Methylation of a Short CpG-Rich Sequence within Exon 1 of TCF21 Gene: A Promising Cancer Biomarker Assay
31. B4-07: Sputum Methylation Analysis Detects Patients With Lung Cancer
32. The Na/Ca-K Exchanger Gene Family
33. DNA Microarray Format for Detection and Subtyping of Human Papillomavirus
34. P-496 Naked DNA in sputum
35. Quantification of Human DNA in Feces as a Diagnostic Test for the Presence of Colorectal Cancer
36. Microarray as a Model for Quantitative Visualization Chemistry
37. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
38. Molecular Cloning and Functional Expression of the Potassium-Dependent Sodium–Calcium Exchanger from Human and Chicken Retinal Cone Photoreceptors
39. Identification of a human heart FABP pseudogene located on chromosome 13
40. Assignment of the Human Adipocyte Fatty Acid-Binding Protein Gene (FABP4) to Chromosome 8q21 Using Somatic Cell Hybrid and Fluorescencein SituHybridization Techniques
41. Fatty acid binding and conformational stability of mutants of human muscle fatty acid-binding protein
42. No significant tyrosine phosphorylation of muscle fatty acid-binding protein
43. Fatty acid-binding proteins: Structural and functional diversity
44. The Na/Ca-K Exchanger Gene Family.
45. Sputum Methylation Analysis Detects Patients With Lung Cancer.
46. Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases.
47. The retinal rod and cone Na+/Ca2+-K+ exchangers.
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