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Your search keyword '"Sirchia, Silvia M."' showing total 21 results

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21 results on '"Sirchia, Silvia M."'

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1. Non-invasive biomarkers for sperm retrieval in non-obstructive patients: a comprehensive review.

2. Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines.

3. Primary TSC2 -/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model.

4. (Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith-Wiedemann syndrome.

5. Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients.

6. DNA Methylation in the Diagnosis of Monogenic Diseases.

7. A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins.

8. Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases.

9. Epigenetic effects of chromatin remodeling agents on organotypic cultures.

10. Germline oncopharmacogenetics, a promising field in cancer therapy.

11. ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men.

12. TSC2 epigenetic defect in primary LAM cells. Evidence of an anchorage-independent survival.

13. Role of epigenetics in human aging and longevity: genome-wide DNA methylation profile in centenarians and centenarians' offspring.

14. Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.

15. Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms.

16. DNA methylation and histone modifications modulate the β1,3 galactosyltransferase β3Gal-T5 native promoter in cancer cells.

17. Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction.

18. Misbehaviour of XIST RNA in breast cancer cells.

19. Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells.

20. Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies.

21. Endogenous reactivation of the RARbeta2 tumor suppressor gene epigenetically silenced in breast cancer.

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