211 results on '"El-Maarri, Osman"'
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2. The role of microRNAs in defining LSECs cellular identity and in regulating F8 gene expression
3. In Contrast to Full-Length Factor VIII, the Calnexin (ER Chaperone) and LMAN1 (ERGIC transporter) Knockouts Have Minimal Effect on the Secretion of B-Domain-Deleted Factor VIII: Implication for Gene Therapy
4. Exploring Diverse Coagulation Factor XIII Subunit Expression Datasets: A Bioinformatic Analysis
5. Methods: DNA Methylation
6. DNA Methylation and Human Diseases
7. Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association
8. NLRP7 inter-domain interactions: the NACHT-associated domain is the physical mediator for oligomeric assembly
9. Stratifying Cumulus Cell Samples Based on Molecular Profiling to Help Resolve Biomarker Discrepancies and to Predict Oocyte Developmental Competence
10. Epigenetic alteration of the dopamine transporter gene in alcohol-dependent patients is associated with age
11. Monitoring the progression of the in vitro selection of nucleic acid aptamers by denaturing high-performance liquid chromatography
12. Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in males
13. Familial molar tissues due to mutations in the inflammatory gene, NALP7, have normal postzygotic DNA methylation
14. New Insight into the Molecular Basis of Hemophilia A
15. Optimization of Quantitative MGMT Promoter Methylation Analysis Using Pyrosequencing and Combined Bisulfite Restriction Analysis
16. Molecular Profiling of Fetal and Adult Liver Sinusoidal Endothelial Cells: A F8 Secreting Cell
17. Molecular Profiling of Liver Sinusoidal Endothelial Cells in Comparison to Hepatocytes: Reflection on Which Cell Type Should Be the Target for Gene Therapy
18. Analyzing intracellular F8 mRNA and Protein of a Methionine Missense Mutation (c.[2T>G];[0]) in a Patient-Specific IPS Cell Model
19. Inversions at Xq28 Causing Hemophilia A Are Associated with Specific
20. Over Expression of Specific Transcription Factors to Boost FVIII Expression
21. Analysis of Single-Cell Expression Data of Liver Sinusoidal Endothelial Cells Reveals Strong Variability of F8 Expression Associated with Specific Expression Profile
22. Molecular Analysis of Fetal and Adult Primary Human Liver Sinusoidal Endothelial Cells: A Comparison to Other Endothelial Cells
23. DNA Methylation at the 11p15 Locus in 20 Monozygotic Twin Pairs after Severe Feto-Fetal Transfusion Syndrome
24. SIRPH: An HPLC-Based SNuPE for Quantitative Methylation Measurement at Specific CpG Sites
25. Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect
26. DNA methylation at promoter regions regulates the timing of gene activation in Xenopus laevis embryos
27. 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
28. A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation
29. 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
30. Bisulfite-Based Methylation Analysis of Imprinted Genes
31. Maternal alleles acquiring paternal methylation patterns in biparental complete hydatidiform moles
32. A rapid, quantitative, non-radioactive bisulfite-SNuPE-IP RP HPLC assay for methylation analysis at specific CpG sites
33. Multifaceted pathomolecular mechanism of a VWFlarge deletion involved in the pathogenesis of severe VWD
34. Intron 22-specific long PCR for the Xba I polymorphism in the factor VIII gene
35. F8 Inversions at Xq28 Causing Hemophilia A Are Associated With Specific Methylation Changes: Implication for Molecular Epigenetic Diagnosis
36. Detailed methylation map of LINE‐1 5′‐promoter region reveals hypomethylated CpG hotspots associated with tumor tissue specificity
37. Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults
38. Analysis of the two microsatellite repeat polymorphisms of the factor VIII gene in the Turkish population
39. Skewed X-chromosome inactivation and XIST locus methylation levels do not contribute to the lower prevalence of Parkinson's disease in females
40. Molecular Characterization of F8 Secreting Cell
41. Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies ImplicateZIC3andFOXF1in Human VATER/VACTERL Association
42. DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations
43. NLRP7, Involved in Hydatidiform Molar Pregnancy (HYDM1), Interacts with the Transcriptional Repressor ZBTB16
44. Inter-locus as well as intra-locus heterogeneity in LINE-1 promoter methylation in common human cancers suggests selective demethylation pressure at specific CpGs
45. DNA-Methylation Analysis by the Bisulfite-Assisted Genomic Sequencing Method
46. 11p15 DNA-methylation analysis in monozygotic twins with discordant intrauterine development due to severe twin-to-twin transfusion syndrome
47. Molecular analyses of germ lime methylation patterns and of the common intron 22 inversion mutation in the factor VIII gene
48. DNR METILINIMO POKYČIAI PERIFERINIO KRAUJO LEUKOCITUOSE PACIENTAMS, SERGANTIEMS SKRANDŽIO VĖŽIU
49. Measurements of DNA Methylation at Seven Loci in Various Tissues of CD1 Mice
50. Whole Blood DNA Aberrant Methylation in Pancreatic Adenocarcinoma Shows Association with the Course of the Disease: A Pilot Study
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