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  1. Diabetic nephropathy: Role of nitric oxide
  2. NOSH-aspirin (NBS-1120) attenuates motor defects and dopaminergic neuron degeneration in a rat model of Parkinson's disease
  3. Reprogramming inflammation: Mechanisms and therapeutic targeting of eicosanoids and pro-resolving mediators
  4. Hormetic association between sodium nitrate and liver enzymes: a study in female and male rats
  5. Inducible nitric oxide synthase (iNOS): More than an inducible enzyme? Rethinking the classification of NOS isoforms
  6. Current Approaches and Innovations in Managing Preeclampsia: Highlighting Maternal Health Disparities
  7. NOSH-aspirin (NBS-1120) inhibits estrogen receptor–negative breast cancer in vitro and in vivo by modulating redox-sensitive signaling pathways
  8. Advances in Preeclampsia Management: Addressing Racial Disparities and Improving Outcomes
  9. NO- and H2S- releasing nanomaterials: A crosstalk signaling pathway in cancer
  10. Nitric oxide-based treatments improve wound healing associated with diabetes mellitus
  11. Effect of long-term inorganic nitrate administration on myocardial ischemia-reperfusion injury in ovariectomized rats
  12. Anti-obesity and anti-diabetic effects of L-citrulline are sex-dependent
  13. Dissolving sodium hydrosulfide in drinking water is not a good source of hydrogen sulfide for animal studies
  14. Type 1 Diabetes and COVID-19: A Literature Review and Possible Management
  15. The Triple Crown: NO, CO, and H2S in cancer cell biology
  16. Long-term inorganic nitrate administration protects against myocardial ischemia-reperfusion injury in female rats
  17. Vascular nitric oxide resistance in type 2 diabetes
  18. Type1 Diabetes and COVID-19: A Systematic Review and Possible Management
  19. Protective effects of long-term nitrate administration against ovariectomy-induced kidney dysfunction in rats
  20. The evolving landscape of PCSK9 inhibition in cancer
  21. Heat shock proteins and cancer: The FoxM1 connection
  22. Altered sialin mRNA gene expression in type 2 diabetic male Wistar rats: implications for nitric oxide deficiency
  23. Why Don’t the Mutant Cells That Evade DNA Repair Cause Cancer More Frequently? Importance of the Innate Immune System in the Tumor Microenvironment
  24. Prediction of dual NF-κB/IκB inhibitors using an integrative in-silico approaches
  25. Metabolic effects of L‐citrulline in type 2 diabetes
  26. Khosrow Kashfi Bio
  27. Preface
  28. Dedication to Dr. Larry K. Keefer at the Sixth International Workshop on Nitric Oxide in Cancer and Beyond
  29. Fifty Years of Diazeniumdiolate Research: A Tribute to Dr. Larry K. Keefer
  30. Scientific Publishing in Biomedicine: A Brief History of Scientific Journals
  31. Preface
  32. The Renin–Angiotensin-Aldosterone System, Nitric Oxide, and Hydrogen Sulfide at the Crossroads of Hypertension and COVID-19: Racial Disparities and Outcomes
  33. Utility of NO and H2S donating platforms in managing COVID-19: Rationale and promise
  34. Identification of new small molecules as dual FoxM1 and Hsp70 inhibitors using computational methods
  35. Carbon monoxide in cell signaling and potential therapeutics
  36. Carbon monoxide and its role in human physiology: A brief historical perspective
  37. Chronic nitrate administration increases the expression the genes involved in the browning of white adipose tissue in female rats
  38. Behavioral and Molecular Effects of Thapsigargin-Induced Brain ER- Stress: Encompassing Inflammation, MAPK, and Insulin Signaling Pathway
  39. Scientific Publishing in Biomedicine: Information Literacy
  40. Carbon monoxide and β-cell function: Implications for type 2 diabetes mellitus
  41. Hydrogen sulfide potentiates the protective effects of nitrite against myocardial ischemia-reperfusion injury in type 2 diabetic rats
  42. Molecular targets of statins and their potential side effects: Not all the glitter is gold
  43. Association between serum hydrogen sulfide concentrations and dysglycemia: a population-based study
  44. Design and Characterization of a Recombinant Brucella abortus RB51 Vaccine That Elicits Enhanced T Cell-Mediated Immune Response
  45. Role of nitric oxide in type 1 diabetes-induced osteoporosis
  46. Lipoproteins and cancer: The role of HDL-C, LDL-C, and cholesterol-lowering drugs
  47. Long Term Sodium Nitrate Administration Positively Impacts Metabolic and Obesity Indices in Ovariectomized Rats
  48. NSAIDs and Cancer Resolution: New Paradigms beyond Cyclooxygenase
  49. Scientific Publishing in Biomedicine: Revising a Peer-reviewed Manuscript
  50. Effect of Nitrate on Gene and Protein Expression of Nitric Oxide Synthase Enzymes in Insulin-Sensitive Tissues of Type 2 Diabetic Male Rats
  51. Macrophage Reprogramming and Cancer Therapeutics: Role of iNOS-Derived NO
  52. Resolution of inflammation: An organizing principle in biology and medicine
  53. Sodium hydrosulfide has no additive effects on nitrite-inhibited renal gluconeogenesis in type 2 diabetic rats
  54. A New Perspective on Cancer Therapy: Changing the Treaded Path?
  55. Hyperuricemia-induced endothelial insulin resistance: the nitric oxide connection
  56. Scientific Publishing in Biomedicine: How to Write a Cover Letter?
  57. Lost-in-Translation of Metabolic Effects of Inorganic Nitrate in Type 2 Diabetes: Is Ascorbic Acid the Answer?
  58. Acidified Nitrite Accelerates Wound Healing in Type 2 Diabetic Male Rats: A Histological and Stereological Evaluation
  59. Effects of hydrogen sulfide on mitochondrial function and cellular bioenergetics
  60. Amino acid-based H2S donors: N-thiocarboxyanhydrides that release H2S with innocuous byproducts
  61. Long-term co-administration of sodium nitrite and sodium hydrosulfide inhibits hepatic gluconeogenesis in male type 2 diabetic rats: Role of PI3K-Akt-eNOS pathway
  62. SP1-independent inhibition of FOXM1 by modified thiazolidinediones
  63. Scientific Publishing in Biomedicine: How to Choose a Journal?
  64. Endogenous flux of nitric oxide: Citrulline is preferred to Arginine
  65. Acidified nitrite improves wound healing in type 2 diabetic rats: Role of oxidative stress and inflammation
  66. Importance of Systematic Reviews and Meta-analyses of Animal Studies: Challenges for Animal-to-Human Translation
  67. Protective effect of intermediate doses of hydrogen sulfide against myocardial ischemia-reperfusion injury in obese type 2 diabetic rats
  68. Roles and Interaction of the MAPK Signaling Cascade in Aβ25–35-Induced Neurotoxicity Using an Isolated Primary Hippocampal Cell Culture System
  69. Impaired cardiovascular function in male rats with hypo- and hyperthyroidism: Involvement of imbalanced nitric oxide synthase levels
  70. The Principles of Biomedical Scientific Writing: Citation
  71. Nitric oxide in cancer and beyond
  72. 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
  73. The evolving landscape for cellular nitric oxide and hydrogen sulfide delivery systems: A new era of customized medications
  74. Tumor associated macrophages and ‘NO’
  75. 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
  76. 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
  77. The Principles of Biomedical Scientific Writing: Abstract and Keywords
  78. Exploring the Potential of Nitric Oxide and Hydrogen Sulfide (NOSH)-Releasing Synthetic Compounds as Novel Priming Agents against Drought Stress in Medicago sativa Plants
  79. Regulation of carbohydrate metabolism by nitric oxide and hydrogen sulfide: Implications in diabetes
  80. Hydrogen sulfide potentiates the favorable metabolic effects of inorganic nitrite in type 2 diabetic rats
  81. The Principles of Biomedical Scientific Writing: Title
  82. Data Extraction from Graphs Using Adobe Photoshop: Applications for Meta-Analyses
  83. Altered gene expression of hydrogen sulfide‐producing enzymes in the liver and muscles tissues of hyperthyroid rats
  84. Effects of Hydrogen Sulfide on Carbohydrate Metabolism in Obese Type 2 Diabetic Rats
  85. Obesity, Type-2 Diabetes and Cancer: Mechanistic Insights
  86. Type 2 Diabetes and Cancer: The Nitric Oxide Connection
  87. Development of new generation of vaccines for Brucella abortus
  88. Effects of long-term oral nitrate administration on adiposity in normal adult female rats
  89. The role of hydrogen sulfide in health and disease
  90. The dichotomous role of H2S in cancer cell biology? Déjà vu all over again
  91. Regulation of vascular tone homeostasis by NO and H2S: Implications in hypertension
  92. A practical guide for induction of type-2 diabetes in rat: Incorporating a high-fat diet and streptozotocin
  93. NO-H 2 S-Releasing Chimeras as a Multifaceted Approach to Cancer Therapy
  94. Nitric Oxide Donors and Therapeutic Applications in Cancer
  95. Gastrointestinal safety, chemotherapeutic potential, and classic pharmacological profile of NOSH ‐naproxen ( AVT ‐219) a dual NO‐ and H 2 S‐releasing hybrid
  96. The dual role of iNOS in cancer
  97. 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
  98. Positional isomerism markedly affects the growth inhibition of colon cancer cells by NOSH-aspirin: COX inhibition and modeling
  99. NOSH-sulindac (AVT-18A) is a novel nitric oxide- and hydrogen sulfide-releasing hybrid that is gastrointestinal safe and has potent anti-inflammatory, analgesic, antipyretic, anti-platelet, and anti-cancer properties
  100. Synthesis and anti-cancer potential of the positional isomers of NOSH-aspirin (NBS-1120) a dual nitric oxide and hydrogen sulfide releasing hybrid
  101. HS-Naproxen
  102. Utility Of Nitric Oxide And Hydrogen Sulfide-Releasing Chimeras As Anticancer Agents
  103. NOSH-Aspirin Inhibits Colon Cancer Cell Growth: Effects Of Positional Isomerism
  104. Nitric Oxide-Releasing Aspirin Suppresses NF-κB Signaling in Estrogen Receptor Negative Breast Cancer Cells in Vitro and in Vivo
  105. NOSH-aspirin (NBS-1120), a dual nitric oxide and hydrogen sulfide-releasing hybrid, reduces inflammatory pain
  106. P77
  107. 287 Targeting NF-κB, FoxM1, and p53 in Pancreatic Cancer With NOSH-Aspirin
  108. Anti-Cancer Activity of New Designer Hydrogen Sulfide-Donating Hybrids
  109. Hydrogen sulfide-releasing aspirin inhibits the growth of leukemic Jurkat cells and modulates β-catenin expression
  110. P09 Therapeutic potential of NOSH-aspirin, a dual nitric oxide- and hydrogen sulfide-donating hybrid in colon cancer
  111. 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
  112. Flurbiprofen benzyl nitrate (NBS-242) inhibits the growth of A-431 human epidermoid carcinoma cells and targets ß-catenin
  113. Abstract 4793: NOSH-aspirin inhibits breast cancer cell growth: an effect modulated through reactive oxygen species and independent of the ER status.
  114. Dysfunctional cell signaling dynamics in oncology: Diagnostic, prognostic and treatment opportunities
  115. Biology and therapeutic potential of hydrogen sulfide and hydrogen sulfide-releasing chimeras
  116. Positional Isomers of Aspirin Are Equally Potent in Inhibiting Colon Cancer Cell Growth: Differences in Mode of Cyclooxygenase Inhibition
  117. Synthesis and biological activity of NOSH-naproxen (AVT-219) and NOSH-sulindac (AVT-18A) as potent anti-inflammatory agents with chemotherapeutic potential
  118. Abstract B34: NOSH-aspirin (NBS-1120) a dual nitric oxide and hydrogen sulfide releasing hybrid for treatment of cancer
  119. Abstract 3898: NOSH-aspirin: A novel nitric oxide- and hydrogen sulfide-releasing hybrid for treatment of colon cancer
  120. Abstract 3899: NOSH compounds: Nitric oxide- and hydrogen sulfide-releasing hybrids, a new class of anti-inflammatory pharmaceuticals
  121. Abstract 3891: NOSH-aspirin, a novel nitric oxide- and hydrogen sulfide-releasing hybrid, is a potent inhibitor of colon cancer cell growth
  122. NOSH-Aspirin: A Novel Nitric Oxide–Hydrogen Sulfide-Releasing Hybrid: A New Class of Anti-inflammatory Pharmaceuticals
  123. Hydrogen sulfide-releasing aspirin modulates xenobiotic metabolizing enzymes in vitro and in vivo
  124. 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
  125. Hydrogen sulfide-releasing aspirin suppresses NF-κB signaling in estrogen receptor negative breast cancer cells in vitro and in vivo
  126. Hydrogen sulfide-releasing NSAIDs inhibit the growth of human cancer cells: A general property and evidence of a tissue type-independent effect
  127. Nitric Oxide Release Is Not Required to Decrease the Ulcerogenic Profile of Nonsteroidal Anti-inflammatory Drugs
  128. Cell Signaling & Molecular Targets in Cancer
  129. Nitric Oxide−Releasing Hybrid Drugs Target Cellular Processes Through S-Nitrosylation
  130. Synthesis and biological activity of acetyl-protected hydroxybenzyl diethyl phosphates (EHBP) as potential chemotherapeutic agents
  131. Membrane microenvironment regulation of carnitine palmitoyltranferases I and II
  132. Abstract 807: Hydrogen sulfide-releasing aspirin modulates xenobiotic metabolizing enzymes in vitro and in vivo
  133. NO-releasing NSAIDs suppress NF-κB signaling in vitro and in vivo through S-nitrosylation
  134. JS-K; a nitric oxide-releasing prodrug, modulates β-catenin/TCF signaling in leukemic Jurkat cells: Evidence of an S-nitrosylated mechanism
  135. Comparison between 3-Nitrooxyphenyl acetylsalicylate (NO-ASA) and O2-(acetylsalicyloxymethyl)-1-(pyrrolidin-1-yl)diazen-1-ium-1,2-diolate (NONO-ASA) as Safe Anti-Inflammatory, Analgesic, Antipyretic, Antioxidant Prodrugs
  136. Modulation of stress genes expression profile by nitric oxide-releasing aspirin in Jurkat T leukemia cells
  137. Abstract 1487: Nitric oxide-releasing NSAIDs suppress NF-κB signaling and increase caspase-3 enzyme activityin vitroandin vivothrough S-nitrosylation
  138. Abstract A42: Comparison between NO-ASA and NONO-ASA as safe anti-inflammatory, analgesic, antipyretic, antioxidant chemopreventive prodrugs
  139. Abstract B86: JS‐K, a nitric oxide‐donating prodrug, modulates β‐catenin/TCF signaling in leukemic Jurkat cells through S‐nitrosylation
  140. Nitro-aspirin inhibits MCF-7 breast cancer cell growth: Effects on COX-2 expression and Wnt/β-catenin/TCF-4 signaling
  141. Anti-Inflammatory Agents as Cancer Therapeutics
  142. Abstract B109: Bioactivated chemotherapeutic agents based on ester-protected hydroxybenzyl phosphates (EHBP) for reversible alkylation of cellular nucleophiles
  143. Abstract A23: Expression profile of genes altered by ester-protected hydroxybenzyl phosphates (EHBP) in T-leukemia cells
  144. Abstract A64: Ester-protected hydroxybenzyl phosphates (EHBP) inhibit the growth of various cultured human cancer cells: Evidence of a tissue type-independent effect
  145. Abstract A35: JS-K, a nitric oxide-donating prodrug, inhibits the growth of leukemic jurkat cells and modulates β-catenin/TCF signaling
  146. The mechanism of action of nitric oxide-donating aspirin
  147. Nitric Oxide–Donating Aspirin Prevents Pancreatic Cancer in a Hamster Tumor Model
  148. NO-donating aspirin induces phase II enzymes in vitro and in vivo
  149. Non-COX-2 targets and cancer: Expanding the molecular target repertoire of chemoprevention
  150. NO-donating aspirin inhibits both the expression and catalytic activity of inducible nitric oxide synthase in HT-29 human colon cancer cells
  151. Comparison of (+)- and (-)-Hemipalmitoylcarnitinium as Inhibitors of Hepatic Mitochondrial Carnitine Palmitoyltransferases in Diabetic Rats
  152. Is COX-2 a ‘collateral’ target in cancer prevention?
  153. Molecular targets of nitric-oxide-donating aspirin in cancer
  154. Cancer Prevention: A New Era beyond Cyclooxygenase-2
  155. NO-donating aspirin inhibits the growth of leukemic Jurkat cells and modulates β-catenin expression
  156. Positional Isomerism Markedly Affects the Growth Inhibition of Colon Cancer Cells by Nitric Oxide-Donating Aspirin in Vitro and in Vivo
  157. In Vitro Metabolism of Nitric Oxide-Donating Aspirin: The Effect of Positional Isomerism
  158. Nitric-oxide-donating NSAIDs as agents for cancer prevention
  159. NO-donating nonsteroidal antiinflammatory drugs (NSAIDs) inhibit colon cancer cell growth more potently than traditional NSAIDs: a general pharmacological property?
  160. NO-donating aspirin inhibits intestinal carcinogenesis in Min (APCMin/+) mice
  161. 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
  162. No-donating NSAIDs are more potent than traditional NSAIDs in inhibiting the growth of cultured human colon cancer cells
  163. Nitric Oxide-Donating Nonsteroidal Anti-Inflammatory Drugs Inhibit the Growth of Various Cultured Human Cancer Cells: Evidence of a Tissue Type-Independent Effect
  164. Lipid Metabolism and Membrane Composition Are Altered in the Brains of Type II Diabetic Mice
  165. Inhibition of Bacterial Superantigens by Peptides and Antibodies
  166. Colon cancer prevention with NO-releasing NSAIDs
  167. The retinoid fenretinide inhibits proliferation and downregulates cyclooxygenase-2 gene expression in human colon adenocarcinoma cell lines
  168. Inhibition of Bacterial Superantigens by Peptides and Antibodies
  169. Fenretinide inhibits phorbol ester-induced cyclooxygenase-2 expression in human colon adenocarcinoma cells
  170. The effect of leukotrienes B and selected HETEs on the proliferation of colon cancer cells
  171. Comparative effects of omeprazole on xenobiotic metabolizing enzymes in the rat and human*
  172. Insulin regulates enzyme activity, malonyl-CoA sensitivity and mRNA abundance of hepatic carnitine palmitoyltransferase-I
  173. Omeprazole Coinduces Multiple Xenobiotic-metabolizing Enzymes in the Rata
  174. Phenolic Antioxidants Induce UDP-glucuronosyltransferase in Rat Livera
  175. Temperature effects on malonyl-CoA inhibition of carnitine palmitoyltransferase I
  176. Diabetes and proteolysis: Effects on carnitine palmitoyltransferase-I and malonyl-CoA binding
  177. Differential induction of glutathione S-transferase in rat aorta versus liver
  178. Hepatic carnitine palmitoyltransferase-I has two independent inhibitory binding sites for regulation of fatty acid oxidation
  179. Yonetani-Theorell analysis of hepatic carnitine palmitoyltransferase-I inhibition indicates two distinct inhibitory binding sites.
  180. Inhibition of carnitine palmitoyltransferase of the hepatic mitochondrial outer membrane (CPT-I) by 2-bromopalmitoyl-CoA
  181. Proteinase treatment of intact hepatic mitochondria has differential effects on inhibition of carnitine palmitoyltransferase by different inhibitors
  182. Malonyl-CoA inhibits proteolysis of carnitine palmitoyltransferase
  183. Effects of cholesterol loading of mouse macrophages on carnitine palmitoyltransferase activity and sensitivity to inhibition by malonyl-CoA
  184. Inhibition of mitochondrial carnitine palmitoyltransferases by adriamycin and adriamycin analogues
  185. Topology of Hepatic Mitochondrial Carnitine Palmitoyltransferase I