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  1. Khosrow Kashfi Bio
  2. Preface
  3. Preface
  4. Carbon monoxide in cell signaling and potential therapeutics
  5. Acidified nitrite improves wound healing in type 2 diabetic rats: Role of oxidative stress and inflammation
  6. Impaired cardiovascular function in male rats with hypo- and hyperthyroidism: Involvement of imbalanced nitric oxide synthase levels
  7. The Principles of Biomedical Scientific Writing: Citation
  8. Nitric oxide in cancer and beyond
  9. Chemical stimulation of the lateral hypothalamus induces antiallodynic and anti-thermal hyperalgesic effects in animal model of neuropathic pain: Involvement of orexin receptors in the spinal cord
  10. The evolving landscape for cellular nitric oxide and hydrogen sulfide delivery systems: A new era of customized medications
  11. Tumor associated macrophages and ‘NO’
  12. Dose-Dependent Effects of Long-Term Administration of Hydrogen Sulfide on Myocardial Ischemia–Reperfusion Injury in Male Wistar Rats: Modulation of RKIP, NF-κB, and Oxidative Stress
  13. NOSH-aspirin (NBS-1120) inhibits pancreatic cancer cell growth in a xenograft mouse model: Modulation of FoxM1, p53, NF-κB, iNOS, caspase-3 and ROS
  14. The Principles of Biomedical Scientific Writing: Abstract and Keywords
  15. Exploring the Potential of Nitric Oxide and Hydrogen Sulfide (NOSH)-Releasing Synthetic Compounds as Novel Priming Agents against Drought Stress in Medicago sativa Plants
  16. Regulation of carbohydrate metabolism by nitric oxide and hydrogen sulfide: Implications in diabetes
  17. Hydrogen sulfide potentiates the favorable metabolic effects of inorganic nitrite in type 2 diabetic rats
  18. The Principles of Biomedical Scientific Writing: Title
  19. Data Extraction from Graphs Using Adobe Photoshop: Applications for Meta-Analyses
  20. Altered gene expression of hydrogen sulfide‐producing enzymes in the liver and muscles tissues of hyperthyroid rats
  21. Effects of Hydrogen Sulfide on Carbohydrate Metabolism in Obese Type 2 Diabetic Rats
  22. Obesity, Type-2 Diabetes and Cancer: Mechanistic Insights
  23. Type 2 Diabetes and Cancer: The Nitric Oxide Connection
  24. Development of new generation of vaccines for Brucella abortus
  25. Effects of long-term oral nitrate administration on adiposity in normal adult female rats
  26. The role of hydrogen sulfide in health and disease
  27. The dichotomous role of H2S in cancer cell biology? Déjà vu all over again
  28. Regulation of vascular tone homeostasis by NO and H2S: Implications in hypertension
  29. A practical guide for induction of type-2 diabetes in rat: Incorporating a high-fat diet and streptozotocin
  30. NO-H 2 S-Releasing Chimeras as a Multifaceted Approach to Cancer Therapy
  31. Nitric Oxide Donors and Therapeutic Applications in Cancer
  32. Gastrointestinal safety, chemotherapeutic potential, and classic pharmacological profile of NOSH ‐naproxen ( AVT ‐219) a dual NO‐ and H 2 S‐releasing hybrid
  33. The dual role of iNOS in cancer
  34. NOSH-aspirin (NBS-1120), a novel nitric oxide- and hydrogen sulfide-releasing hybrid has enhanced chemo-preventive properties compared to aspirin, is gastrointestinal safe with all the classic therapeutic indications
  35. Positional isomerism markedly affects the growth inhibition of colon cancer cells by NOSH-aspirin: COX inhibition and modeling
  36. Synthesis and anti-cancer potential of the positional isomers of NOSH-aspirin (NBS-1120) a dual nitric oxide and hydrogen sulfide releasing hybrid
  37. HS-Naproxen
  38. Utility Of Nitric Oxide And Hydrogen Sulfide-Releasing Chimeras As Anticancer Agents
  39. NOSH-Aspirin Inhibits Colon Cancer Cell Growth: Effects Of Positional Isomerism
  40. NOSH-aspirin (NBS-1120), a dual nitric oxide and hydrogen sulfide-releasing hybrid, reduces inflammatory pain
  41. P77
  42. 287 Targeting NF-κB, FoxM1, and p53 in Pancreatic Cancer With NOSH-Aspirin
  43. Anti-Cancer Activity of New Designer Hydrogen Sulfide-Donating Hybrids
  44. Hydrogen sulfide-releasing aspirin inhibits the growth of leukemic Jurkat cells and modulates β-catenin expression
  45. P09 Therapeutic potential of NOSH-aspirin, a dual nitric oxide- and hydrogen sulfide-donating hybrid in colon cancer
  46. NOSH-aspirin (NBS-1120), a novel nitric oxide and hydrogen sulfide releasing hybrid, attenuates neuroinflammation induced by microglial and astrocytic activation: A new candidate for treatment of neurodegenerative disorders
  47. Flurbiprofen benzyl nitrate (NBS-242) inhibits the growth of A-431 human epidermoid carcinoma cells and targets ß-catenin
  48. Abstract 4793: NOSH-aspirin inhibits breast cancer cell growth: an effect modulated through reactive oxygen species and independent of the ER status.
  49. Dysfunctional cell signaling dynamics in oncology: Diagnostic, prognostic and treatment opportunities
  50. Biology and therapeutic potential of hydrogen sulfide and hydrogen sulfide-releasing chimeras
  51. Positional Isomers of Aspirin Are Equally Potent in Inhibiting Colon Cancer Cell Growth: Differences in Mode of Cyclooxygenase Inhibition
  52. Synthesis and biological activity of NOSH-naproxen (AVT-219) and NOSH-sulindac (AVT-18A) as potent anti-inflammatory agents with chemotherapeutic potential
  53. Abstract B34: NOSH-aspirin (NBS-1120) a dual nitric oxide and hydrogen sulfide releasing hybrid for treatment of cancer
  54. Abstract 3898: NOSH-aspirin: A novel nitric oxide- and hydrogen sulfide-releasing hybrid for treatment of colon cancer
  55. Abstract 3899: NOSH compounds: Nitric oxide- and hydrogen sulfide-releasing hybrids, a new class of anti-inflammatory pharmaceuticals
  56. Abstract 3891: NOSH-aspirin, a novel nitric oxide- and hydrogen sulfide-releasing hybrid, is a potent inhibitor of colon cancer cell growth
  57. NOSH-Aspirin: A Novel Nitric Oxide–Hydrogen Sulfide-Releasing Hybrid: A New Class of Anti-inflammatory Pharmaceuticals
  58. Hydrogen sulfide-releasing aspirin modulates xenobiotic metabolizing enzymes in vitro and in vivo
  59. NOSH–aspirin (NBS-1120), a novel nitric oxide- and hydrogen sulfide-releasing hybrid is a potent inhibitor of colon cancer cell growth in vitro and in a xenograft mouse model
  60. Hydrogen sulfide-releasing aspirin suppresses NF-κB signaling in estrogen receptor negative breast cancer cells in vitro and in vivo
  61. Hydrogen sulfide-releasing NSAIDs inhibit the growth of human cancer cells: A general property and evidence of a tissue type-independent effect
  62. Nitric Oxide Release Is Not Required to Decrease the Ulcerogenic Profile of Nonsteroidal Anti-inflammatory Drugs
  63. Cell Signaling & Molecular Targets in Cancer
  64. Nitric Oxide−Releasing Hybrid Drugs Target Cellular Processes Through S-Nitrosylation
  65. Synthesis and biological activity of acetyl-protected hydroxybenzyl diethyl phosphates (EHBP) as potential chemotherapeutic agents
  66. Abstract 807: Hydrogen sulfide-releasing aspirin modulates xenobiotic metabolizing enzymes in vitro and in vivo
  67. NO-releasing NSAIDs suppress NF-κB signaling in vitro and in vivo through S-nitrosylation
  68. JS-K; a nitric oxide-releasing prodrug, modulates β-catenin/TCF signaling in leukemic Jurkat cells: Evidence of an S-nitrosylated mechanism
  69. Modulation of stress genes expression profile by nitric oxide-releasing aspirin in Jurkat T leukemia cells
  70. Abstract 1487: Nitric oxide-releasing NSAIDs suppress NF-κB signaling and increase caspase-3 enzyme activityin vitroandin vivothrough S-nitrosylation
  71. Abstract A42: Comparison between NO-ASA and NONO-ASA as safe anti-inflammatory, analgesic, antipyretic, antioxidant chemopreventive prodrugs
  72. Abstract B86: JS‐K, a nitric oxide‐donating prodrug, modulates β‐catenin/TCF signaling in leukemic Jurkat cells through S‐nitrosylation
  73. Nitro-aspirin inhibits MCF-7 breast cancer cell growth: Effects on COX-2 expression and Wnt/β-catenin/TCF-4 signaling
  74. Anti-Inflammatory Agents as Cancer Therapeutics
  75. Abstract B109: Bioactivated chemotherapeutic agents based on ester-protected hydroxybenzyl phosphates (EHBP) for reversible alkylation of cellular nucleophiles
  76. Abstract A23: Expression profile of genes altered by ester-protected hydroxybenzyl phosphates (EHBP) in T-leukemia cells
  77. Abstract A64: Ester-protected hydroxybenzyl phosphates (EHBP) inhibit the growth of various cultured human cancer cells: Evidence of a tissue type-independent effect
  78. Abstract A35: JS-K, a nitric oxide-donating prodrug, inhibits the growth of leukemic jurkat cells and modulates β-catenin/TCF signaling
  79. The mechanism of action of nitric oxide-donating aspirin
  80. NO-donating aspirin induces phase II enzymes in vitro and in vivo
  81. Non-COX-2 targets and cancer: Expanding the molecular target repertoire of chemoprevention
  82. NO-donating aspirin inhibits both the expression and catalytic activity of inducible nitric oxide synthase in HT-29 human colon cancer cells
  83. Is COX-2 a ‘collateral’ target in cancer prevention?
  84. NO-donating aspirin inhibits the growth of leukemic Jurkat cells and modulates β-catenin expression
  85. Positional Isomerism Markedly Affects the Growth Inhibition of Colon Cancer Cells by Nitric Oxide-Donating Aspirin in Vitro and in Vivo
  86. Nitric-oxide-donating NSAIDs as agents for cancer prevention
  87. NO-donating nonsteroidal antiinflammatory drugs (NSAIDs) inhibit colon cancer cell growth more potently than traditional NSAIDs: a general pharmacological property?
  88. NO-donating aspirin inhibits intestinal carcinogenesis in Min (APCMin/+) mice
  89. Nitric oxide-donating aspirin inhibits β-catenin/T cell factor (TCF) signaling in SW480 colon cancer cells by disrupting the nuclear β-catenin–TCF association
  90. No-donating NSAIDs are more potent than traditional NSAIDs in inhibiting the growth of cultured human colon cancer cells
  91. Lipid Metabolism and Membrane Composition Are Altered in the Brains of Type II Diabetic Mice
  92. Inhibition of Bacterial Superantigens by Peptides and Antibodies
  93. Colon cancer prevention with NO-releasing NSAIDs
  94. The retinoid fenretinide inhibits proliferation and downregulates cyclooxygenase-2 gene expression in human colon adenocarcinoma cell lines
  95. The effect of leukotrienes B and selected HETEs on the proliferation of colon cancer cells
  96. Comparative effects of omeprazole on xenobiotic metabolizing enzymes in the rat and human*
  97. Omeprazole Coinduces Multiple Xenobiotic-metabolizing Enzymes in the Rata
  98. Phenolic Antioxidants Induce UDP-glucuronosyltransferase in Rat Livera
  99. Temperature effects on malonyl-CoA inhibition of carnitine palmitoyltransferase I
  100. Diabetes and proteolysis: Effects on carnitine palmitoyltransferase-I and malonyl-CoA binding
  101. Differential induction of glutathione S-transferase in rat aorta versus liver
  102. Hepatic carnitine palmitoyltransferase-I has two independent inhibitory binding sites for regulation of fatty acid oxidation
  103. Malonyl-CoA inhibits proteolysis of carnitine palmitoyltransferase
  104. Effects of cholesterol loading of mouse macrophages on carnitine palmitoyltransferase activity and sensitivity to inhibition by malonyl-CoA
  105. Inhibition of mitochondrial carnitine palmitoyltransferases by adriamycin and adriamycin analogues
  106. Topology of Hepatic Mitochondrial Carnitine Palmitoyltransferase I