142 results on '"El-Maarri, Osman"'
Search Results
2. The role of microRNAs in defining LSECs cellular identity and in regulating F8 gene expression
3. Exploring Diverse Coagulation Factor XIII Subunit Expression Datasets: A Bioinformatic Analysis
4. NLRP7 inter-domain interactions: the NACHT-associated domain is the physical mediator for oligomeric assembly
5. Stratifying Cumulus Cell Samples Based on Molecular Profiling to Help Resolve Biomarker Discrepancies and to Predict Oocyte Developmental Competence
6. Monitoring the progression of the in vitro selection of nucleic acid aptamers by denaturing high-performance liquid chromatography
7. Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in males
8. Familial molar tissues due to mutations in the inflammatory gene, NALP7, have normal postzygotic DNA methylation
9. Optimization of Quantitative MGMT Promoter Methylation Analysis Using Pyrosequencing and Combined Bisulfite Restriction Analysis
10. Molecular Analysis of Fetal and Adult Primary Human Liver Sinusoidal Endothelial Cells: A Comparison to Other Endothelial Cells
11. Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect
12. DNA methylation at promoter regions regulates the timing of gene activation in Xenopus laevis embryos
13. Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci
14. A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation
15. Methylation levels at selected CpG sites in the factor VIII and FGFR3 genes, in mature female and male germ cells: implications for male-driven evolution
16. Maternal alleles acquiring paternal methylation patterns in biparental complete hydatidiform moles
17. A rapid, quantitative, non-radioactive bisulfite-SNuPE-IP RP HPLC assay for methylation analysis at specific CpG sites
18. Multifaceted pathomolecular mechanism of a VWFlarge deletion involved in the pathogenesis of severe VWD
19. F8 Inversions at Xq28 Causing Hemophilia A Are Associated With Specific Methylation Changes: Implication for Molecular Epigenetic Diagnosis
20. Detailed methylation map of LINE‐1 5′‐promoter region reveals hypomethylated CpG hotspots associated with tumor tissue specificity
21. Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults
22. Molecular Characterization of F8 Secreting Cell
23. DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations
24. NLRP7, Involved in Hydatidiform Molar Pregnancy (HYDM1), Interacts with the Transcriptional Repressor ZBTB16
25. Inter-locus as well as intra-locus heterogeneity in LINE-1 promoter methylation in common human cancers suggests selective demethylation pressure at specific CpGs
26. 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome
27. Molecular analyses of germ lime methylation patterns and of the common intron 22 inversion mutation in the factor VIII gene
28. DNR METILINIMO POKYČIAI PERIFERINIO KRAUJO LEUKOCITUOSE PACIENTAMS, SERGANTIEMS SKRANDŽIO VĖŽIU
29. Measurements of DNA Methylation at Seven Loci in Various Tissues of CD1 Mice
30. Whole Blood DNA Aberrant Methylation in Pancreatic Adenocarcinoma Shows Association with the Course of the Disease: A Pilot Study
31. Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci
32. Methylation at Global LINE-1 Repeats in Human Blood Are Affected by Gender but Not by Age or Natural Hormone Cycles
33. Applicability of boride and nitride type ceramic coatings on surgical stainless as implant materials
34. Monitoring the progression of the in vitro selection of nucleic acid aptamers by denaturing high-performance liquid chromatography
35. Investigation of Underlying Reasons of Factor VIII Deficiency in Haemophilia A Patients with Undetectable Mutations in the Factor VIII Gene.
36. Patients with familial biparental hydatidiform moles have normal methylation at imprinted genes
37. Epigenetic reprogramming in mouse primordial germ cells
38. De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism
39. KDM2B Is Implicated in Bovine Lethal Multi-Organic Developmental Dysplasia.
40. An Integrated Genomic and Expression Analysis of 7q Deletion in Splenic Marginal Zone Lymphoma.
41. Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures.
42. Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse.
43. Optimization of Quantitative MGMTPromoter Methylation Analysis Using Pyrosequencing and Combined Bisulfite Restriction Analysis
44. Lack of F8 mRNA: a novel mechanism leading to hemophilia A
45. Lack of F8mRNA: a novel mechanism leading to hemophilia A
46. De novo factor VIIIgene intron 22 inversion in a female carrier presents as a somatic mosaicism
47. Methylation profiles of DXPas34 during the onset of X-inactivation.
48. Epigenetic control of the angiotensin-converting enzyme in endothelial cells during inflammation
49. DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins
50. Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction
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