134 results on '"Launonen V"'
Search Results
2. No evidence for dual role of loss of heterozygosity in hereditary non-polyposis colorectal cancer
3. Frequent loss of SMAD4/DPC4 protein in colorectal cancers. (Colorectal Cancer)
4. Increased risk of cancer in patients with fumarate hydratase germline mutation
5. LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome
6. Mutation and LOH analysis of ACO2 in colorectal cancer: no evidence of biallelic genetic inactivation
7. Frequent loss of SMAD4/DPC4 protein in colorectal cancers
8. Screening for microsatellite instability target genes in colorectal cancers
9. ATM mutations in Finnish breast cancer patients
10. Aberrant succination of proteins in fumarate hydratase-deficient mice and HLRCC patients is a robust biomarker of mutation status
11. The analysis of LOH target genes in 11q21-q24
12. The role of aryl hydrocarbon receptor interacting protein in endocrine neoplasia with a particular focus on papillary thyroid cancer
13. EXCO1 variants occur commonly in normal population: vidence against a role in hereditary nonpolyposis colorectal cancer
14. Mutation analysis of BRCA1 and BRCA2 in Turkish cancer families: a novel mutation BRCA2 3414de14 found in male breast cancer
15. Genetic aberrations and their clinical significance in breast and ovarian cancer
16. Mutation screening of fumarate hydratase by multiplex ligation-dependent probe amplification: Detection of exonic deletion in a patient with leiomyomatosis and renal cell cancer
17. Germ line insertions of moloney murine leukemia virus in the TLL mouse causes site-specific differences in lymphoma/leukemia frequency and tumor immunophenotype
18. Frequent loss of SMAD4/DPC4 protein in colorectal cancers
19. No evidence of somatic aryl hydrocarbon receptor interacting protein mutations in sporadic endocrine neoplasia
20. Mutation analysis of aryl hydrocarbon receptor interacting protein (AIP) gene in colorectal, breast, and prostate cancers
21. No evidence for dual role of loss of heterozygosity in hereditary non-polyposis colorectal cancer
22. Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome
23. Mutation analysis of the CHK2gene in families with hereditary breast cancer
24. E-cadherinis not frequently mutated in hereditary gastric cancer
25. No SMAD4 hypermethylation in colorectal cancer
26. Mutation analysis of BRCA1 and BRCA2 in Turkish cancer families: a novel mutation BRCA2 3414del4 found in male breast cancer
27. Mutation analysis of theCHK2gene in families with hereditary breast cancer.
28. European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables.
29. Loss of heterozygosity at chromosomes 3, 6, 8, 11, 16, and 17 in ovarian cancer
30. Mutation analysis of BRCA1 and BRCA2 in Turkish cancer families: a novel mutation BRCA2 3414del4 found in male breast cancer
31. Germ-Line TP53 Mutations in Finnish Cancer Families Exhibiting Features of the Li-Fraumeni Syndrome and Negative for BRCA1 and BRCA2 - characterization and development of standards
32. Mutation screening of fumarate hydratase by multiplex ligation-dependent probe amplification: detection of exonic deletion in a patient with leiomyomatosis and renal cell cancer
33. Few FH mutations in sporadic counterparts of tumor types observed in hereditary Leiomyomatosis and renal cell cancer families
34. EXO1 variants occur commonly in normal population: Evidence against a role in hereditary nonpolyposis colorectal cancer
35. Low-level microsatellite instability in most colorectal carcinomas
36. Few FH mutations in sporadic counterparts of tumor types observed in hereditary leiomyomatosis and renal cell cancer families
37. EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer
38. The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency
39. Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer
40. Presence of Stromal Cells Enhances Epithelial-to-Mesenchymal Transition (EMT) Induction in Lung Bronchial Epithelium after Protracted Exposure to Oxidative Stress of Gamma Radiation.
41. Assessment of targeted and non-targeted responses in cells deficient in ATM function following exposure to low and high dose X-rays.
42. A laboratory inter-comparison of the importance of serum serotonin levels in the measurement of a range of radiation-induced bystander effects: overview of study and results presentation.
43. Analysis of a Finnish family confirms RHBDF2 mutations as the underlying factor in tylosis with esophageal cancer.
44. MED12, the mediator complex subunit 12 gene, is mutated at high frequency in uterine leiomyomas.
45. Aberrant succination of proteins in fumarate hydratase-deficient mice and HLRCC patients is a robust biomarker of mutation status.
46. Analysis of KLHDC8B in familial nodular lymphocyte predominant Hodgkin lymphoma.
47. Exome sequencing reveals germline NPAT mutation as a candidate risk factor for Hodgkin lymphoma.
48. Expression profiling in progressive stages of fumarate-hydratase deficiency: the contribution of metabolic changes to tumorigenesis.
49. Mutations in the circadian gene CLOCK in colorectal cancer.
50. No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome.
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