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1. Innovative Delivery Systems for Curcumin: Exploring Nanosized and Conventional Formulations

2. Effect of Essential Oil Components on the Activity of Steroidogenic Cytochrome P450

3. Exploring Novel Variants of the Cytochrome P450 Reductase Gene (POR) from the Genome Aggregation Database by Integrating Bioinformatic Tools and Functional Assays

4. Loss of LGR4/GPR48 causes severe neonatal salt wasting due to disrupted WNT signaling altering adrenal zonation

5. Variant predictions in congenital adrenal hyperplasia caused by mutations in CYP21A2

6. Exploring the Potential of Sulfur Moieties in Compounds Inhibiting Steroidogenesis

7. Recognition of fold- and function-specific sites in the ligand-binding domain of the thyroid hormone receptor-like family

8. Biased cytochrome P450-mediated metabolism via small-molecule ligands binding P450 oxidoreductase

9. Synthesis and Structure–Activity Relationships of Novel Non-Steroidal CYP17A1 Inhibitors as Potential Prostate Cancer Agents

10. Variability in Loss of Multiple Enzyme Activities Due to the Human Genetic Variation P284T Located in the Flexible Hinge Region of NADPH Cytochrome P450 Oxidoreductase

11. GATA4 Variants in Individuals With a 46,XY Disorder of Sex Development (DSD) May or May Not Be Associated With Cardiac Defects Depending on Second Hits in Other DSD Genes

13. Altered CYP19A1 and CYP3A4 Activities Due to Mutations A115V, T142A, Q153R and P284L in the Human P450 Oxidoreductase

14. Mechanism of the Dual Activities of Human CYP17A1 and Binding to Anti-Prostate Cancer Drug Abiraterone Revealed by a Novel V366M Mutation Causing 17,20 Lyase Deficiency

15. Expanding the p.(Arg85Trp) Variant-Specific Phenotype of HNF4A: Features of Glycogen Storage Disease, Liver Cirrhosis, Impaired Mitochondrial Function, and Glomerular Changes

16. Characterization of Mutations Causing CYP21A2 Deficiency in Brazilian and Portuguese Populations

17. Loss of Protein Stability and Function Caused by P228L Variation in NADPH-Cytochrome P450 Reductase Linked to Lower Testosterone Levels

18. Loss Of Protein Stability And Function Caused By POR-Rs17853284 Linked To Lower Testosterone Levels

19. Reducing FASN expression sensitizes acute myeloid leukemia cells to differentiation therapy

20. PMON52 Use of PDE5 Inhibitors as Potential Treatment for Isolated Growth Hormone Deficiency Caused by Alternate Splicing of GH1 Gene

23. Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD Phenotype

24. Loss of LGR4/GPR48 causes severe neonatal salt-wasting due to disrupted WNT signaling altering adrenal zonation

25. Characterization of mutations causing steroid 21-hydroxylase deficiency in Brazilian and Portuguese populations

26. P450 Oxidoreductase Deficiency: Loss of Activity Caused by Protein Instability From a Novel L374H Mutation

27. Unstable argininosuccinate lyase in variant forms of the urea cycle disorder argininosuccinic aciduria

28. In silico and functional studies reveal novel loss-of-function variants of SRD5A2, but no variants explaining excess 5α-reductase activity

29. Biased cytochrome P450-mediated metabolism via small-molecule ligands binding P450 oxidoreductase

30. Finding New Molecular Targets of Familiar Natural Products Using In Silico Target Prediction

31. Across kingdom biased CYP-mediated metabolism via small-molecule ligands docking on P450 oxidoreductase

32. Across kingdom biased CYP-mediated metabolism via small-molecule ligands docking on P450 oxidoreductase

33. Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia

34. MON-LB014 Autosomal Dominant Growth Hormone Deficiency Due to a Novel c.178g>A Mutation in the GH1 Gene Is Caused by Alternative Splicing to Produce a Small GH Isoform

35. Molecular Basis of CYP19A1 Deficiency in a 46, XX Patient with R550W Mutation in POR: Expanding the PORD Phenotype

38. Bioactivity of Curcumin on the Cytochrome P450 Enzymes of the Steroidogenic Pathway

39. Molecular Basis of Aromatase Deficiency in a 46, XX Patient with Mutation of Arginine 550 to Tryptophan in POR: Expanding the Endocrine Phenotype in PORD

40. Differential effects of variations in human P450 oxidoreductase on the aromatase activity of CYP19A1 polymorphisms R264C and R264H

41. Loss of multiple enzyme activities due to the human genetic variation P284T in NADPH cytochrome P450 oxidoreductase

42. Variability in human drug metabolizing cytochrome P450 CYP2C9, CYP2C19 and CYP3A5 activities caused by genetic variations in cytochrome P450 oxidoreductase

43. In silico and in vitro analysis of genetic variants of the equine CYP3A94, CYP3A95 and CYP3A97 isoenzymes

48. MON-219 In Silico and in Vitro Studies of Human 5α-Reductase Type II Variants in Search for Activating Variants Explaining Androgen Excess Reveal New Loss-Of-Function Variants

49. Human P450 Oxidoreductase Deficiency

50. Endoplasmic Reticulum Stress Enhances Mitochondrial Metabolic Activity in Mammalian Adrenals and Gonads

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