21 results on '"Jamil, Muhammad Ahmer"'
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2. Multifaceted pathomolecular mechanism of a VWF large deletion involved in the pathogenesis of severe VWD
3. The role of microRNAs in defining LSECs cellular identity and in regulating F8 gene expression
4. Heterozygosity in FXIII genes and the manifestation of mild inherited FXIII Deficiency
5. Revealing Pathogenic Molecular Mechanism in a Type 3 von Willebrand Disease Patient by Inspecting VWF Gene Whole Intronic Region and Study of The Patient-Derived Endothelial Cells
6. Exploring Diverse Coagulation Factor XIII Subunit Expression Datasets: A Bioinformatic Analysis
7. A Homozygous Deep Intronic Variant Causes Von Willebrand Factor Deficiency and Lack of Endothelial-Specific Secretory Organelles, Weibel–Palade Bodies
8. Stratifying Cumulus Cell Samples Based on Molecular Profiling to Help Resolve Biomarker Discrepancies and to Predict Oocyte Developmental Competence
9. Molecular Profiling of Fetal and Adult Liver Sinusoidal Endothelial Cells: A F8 Secreting Cell
10. Molecular Profiling of Liver Sinusoidal Endothelial Cells in Comparison to Hepatocytes: Reflection on Which Cell Type Should Be the Target for Gene Therapy
11. Analyzing intracellular F8 mRNA and Protein of a Methionine Missense Mutation (c.[2T>G];[0]) in a Patient-Specific IPS Cell Model
12. Inversions at Xq28 Causing Hemophilia A Are Associated with Specific
13. Over Expression of Specific Transcription Factors to Boost FVIII Expression
14. Analysis of Single-Cell Expression Data of Liver Sinusoidal Endothelial Cells Reveals Strong Variability of F8 Expression Associated with Specific Expression Profile
15. Molecular Analysis of Fetal and Adult Primary Human Liver Sinusoidal Endothelial Cells: A Comparison to Other Endothelial Cells
16. Multifaceted pathomolecular mechanism of a VWFlarge deletion involved in the pathogenesis of severe VWD
17. F8 Inversions at Xq28 Causing Hemophilia A Are Associated With Specific Methylation Changes: Implication for Molecular Epigenetic Diagnosis
18. DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations
19. Molecular Characterization of F8 Secreting Cell
20. DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations
21. Inter-locus as well as intra-locus heterogeneity in LINE-1 promoter methylation in common human cancers suggests selective demethylation pressure at specific CpGs
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