82 results on '"Susca, F."'
Search Results
2. The Italian External Quality Assessment Scheme in Classical Cytogenetics : Four Years of Activity
3. Effects of Rumen-protected Choline Supplementation in Periparturient Dairy Goats
4. Determination of Malonaldehyde in Bovine Plasma During the Receiving Period and Effects of Phytoderivative Diet Supplementation
5. Effects of Rumen-protected Choline Supplementation in Periparturient Dairy Goats
6. L'asse HSF1-FOXO3 regola la risposta cellulare allo stress mediante l'allele G dello SNP rs2802292 associato alla longevità
7. The familial adenomatous polyposis region exhibits many different haplotypes
8. La vacca in transizione: un possibile ruolo per la colina
9. De novo balanced chromosome rearrangements in prenatal diagnosis
10. Congenital hepatic fibrosis associated with other malformations in two brothers
11. Leptin Genotype Is Associated with Lactation Performance and Health of Holstein Cows
12. Infertility in carriers of two bisatellited marker chromosomes
13. Effect of Feeding Yeast Culture on Performance, Health, and Immunocompetence of Dairy Calves
14. Rumen-protected choline and vitamin E supplementation in periparturient dairy goats: effects on milk production and folate, vitamin B12 and vitamin E status
15. Folate, vitamin B12, alpha-tocopherol and selected liver components in periparturient dairy goats supplemented with choline and vitamin E
16. A novel cell type-specific role of p38α in the control of autophagy and cell death in colorectal cancer cells
17. Nine novel APC mutations in Italian FAP patients
18. Lack of effect by prostaglandin F2alpha on the proliferation of the HCT-8 and HT-29 human adenocarcinoma cell lines.
19. O-244. Cytogenetics and molecular studies in infertile males
20. P-191. Xq deletion and premature ovarian failure
21. Bradykinin stimulation does not induce intracellular Ca2+ elevation in cells from desmoid tumors
22. Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients
23. The Italian External Quality Assessment Scheme in Classical Cytogenetics: Four Years of Activity.
24. A novel cell type-specific role of p38α in the control of autophagy and cell death in colorectal cancer cells.
25. Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family.
26. Infertility in carriers of two bisatellited marker chromosomes.
27. Effect of prostaglandin E2 on the proliferation, Ca2+ mobilization and cAMP in HT-29 human colon adenocarcinoma cells
28. Two B~1 and B~2 bradykinin receptor antagonists fail to inhibit the Ca^2^+ response elicited by bradykinin in human skin fibroblasts
29. Uso dei marcatori polimorfi del cromosoma 5 per l'identificazione preclinica dei soggetti con poliposi familiare adenomatosa (FAP)
30. Molecular characterization of novel melanoma cell lines
31. STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer
32. COACH syndrome: Report of two brothers with congenital hepatic fibrosis, cerebellar vermis hypoplasia, oligophrenia, ataxia, and mental retardation
33. Holt-Oram syndrome: cardiological, radiological and genetic evaluation
34. Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family
35. Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients
36. Depressed level of natural killer cells in cancer family syndrome
37. Molecular characterization of novel melanoma cell lines.
38. Effects of rumen-protected choline supplementation in periparturient dairy goats.
39. Duplication of 9 p11.2-p13.1: a benign cytogenetic variant.
40. Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients.
41. Sex chromosome loss, micronuclei, sister chromatid exchange and aging: a study including 16 centenarians.
42. 17-alpha-ethinylestradiol and norgestrel in combination induce micronucleus increases and aneuploidy in human lymphocyte and fibroblast cultures.
43. Increment of sister chromatid exchange frequencies (SCE) due to epichlorohydrin (ECH) in vitro treatment in human lymphocytes.
44. STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer.
45. The familial adenomatous polyposis region exhibits many different haplotypes.
46. COACH syndrome: report of two brothers with congenital hepatic fibrosis, cerebellar vermis hypoplasia, oligophrenia, ataxia, and mental retardation.
47. An unusual dicentric Y chromosome with a functional centromere with no detectable alpha-satellite.
48. [Holt-Oram syndrome: cardiological, radiological and genetic evaluation].
49. Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP)
50. Linkage studies in Italian families with familial adenomatous polyposis.
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