23 results on '"Sher, Gulab"'
Search Results
2. In vitro evaluation of Neosetophomone B inducing apoptosis in cutaneous T cell lymphoma by targeting the FOXM1 signaling pathway
3. Dysregulated FOXM1 signaling in the regulation of cancer stem cells
4. Outcome associated with EPCAM founder mutation c.499dup in Qatar
5. Beyond Viral Infections: The Multifaceted Roles of Human Papillomavirus and Epstein-Barr Virus in Shaping the Tumor Microenvironment
6. The effect of protein mutations on drug binding suggests ensuing personalised drug selection
7. Molecular characteristics of Neisseria meningitidis in Qatar
8. Embelin inhibits viability of cutaneous T cell lymphoma cell lines HuT78 and H9 by targeting inhibitors of apoptosis
9. The cross-talk between miRNAs and JAK/STAT pathway in cutaneous T cell lymphoma: Emphasis on therapeutic opportunities
10. Epigenetic and breast cancer therapy: Promising diagnostic and therapeutic applications
11. Role of non-coding RNAs in the progression and resistance of cutaneous malignancies and autoimmune diseases
12. Bioinformatics Analysis Reveals FOXM1/BUB1B Signaling Pathway as a Key Target of Neosetophomone B in Human Leukemic Cells: A Gene Network-Based Microarray Analysis
13. Treatment and molecular profiling of acrodermatitis continua of Hallopeau during pregnancy using targeted therapy
14. Epigenetic and breast cancer therapy : promising diagnostic and therapeutic applications
15. Prevalence and Type Distribution of High-Risk Human Papillomavirus (HPV) in Breast Cancer: A Qatar Based Study
16. Discovery of Novel Gene Variants in a Cohort of Qatari Breast Cancer Patients and Ensuing Personalised Drug Selection
17. Molecular Diagnosis of Rare Autosomal Recessive Escobar Syndrome in a Consanguineous Pakistani Family
18. Genetic Testing of a Large Consanguineous Pakistani Family Affected with Mucolipidosis III Gamma Through Next-Generation Sequencing
19. A novel CHSY1 gene mutation underlies Temtamy preaxial brachydactyly syndrome in a Pakistani family
20. Nitazoxanide and probiotics for the treatment of recurrent Clostridium difficile infection in a peritoneal dialysis patient
21. UGT1A1Gene Mutations in Pakistani Children Suffering from Inherited Nonhemolytic Unconjugated Hyperbilirubinemias
22. Nitazoxanide for the Treatment of Recurrent Clostridium difficile Infection (Cdi) in a Peritoneal Dialysis Patient
23. UGT1A1 Gene Mutations in Pakistani Children Suffering from Inherited Nonhemolytic Unconjugated Hyperbilirubinemias.
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