All Stories

  1. Platelet aging and desialylation increase apoptotic priming and BCL-XL dependence
  2. Data from Radiotherapy-Induced Neurocognitive Impairment Is Driven by Heightened Apoptotic Priming in Early Life and Prevented by Blocking BAX
  3. Supplementary Figure S1 from Radiotherapy-Induced Neurocognitive Impairment Is Driven by Heightened Apoptotic Priming in Early Life and Prevented by Blocking BAX
  4. Supplementary Figure S2 from Radiotherapy-Induced Neurocognitive Impairment Is Driven by Heightened Apoptotic Priming in Early Life and Prevented by Blocking BAX
  5. Supplementary Figure S3 from Radiotherapy-Induced Neurocognitive Impairment Is Driven by Heightened Apoptotic Priming in Early Life and Prevented by Blocking BAX
  6. Supplementary Figure S4 from Radiotherapy-Induced Neurocognitive Impairment Is Driven by Heightened Apoptotic Priming in Early Life and Prevented by Blocking BAX
  7. Supplementary Figure S5 from Radiotherapy-Induced Neurocognitive Impairment Is Driven by Heightened Apoptotic Priming in Early Life and Prevented by Blocking BAX
  8. Supplementary Figure S6 from Radiotherapy-Induced Neurocognitive Impairment Is Driven by Heightened Apoptotic Priming in Early Life and Prevented by Blocking BAX
  9. Late apoptotic effects after treatment with 177 Lu-octreotate in small-intestine neuroendocrine GOT1 tumor model
  10. Data from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  11. Supplementary Figure S1 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  12. Supplementary Figure S1 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  13. Supplementary Figure S2 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  14. Supplementary Figure S2 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  15. Supplementary Figure S3 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  16. Supplementary Figure S3 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  17. Supplementary Figure S4 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  18. Supplementary Figure S4 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  19. Supplementary Figure S5 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  20. Supplementary Figure S5 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  21. Supplementary Figure S6 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  22. Supplementary Figure S6 from Radiation therapy-induced neurocognitive impairment is driven by heightened apoptotic priming in early life and prevented by blocking BAX
  23. Synergistic Antitumor Effects of 177Lu-Octreotide Combined with an ALK Inhibitor in a High-Risk Neuroblastoma Xenograft Model
  24. Late Age- and Dose-Related Effects on the Proteome of Thyroid Tissue in Rats after 131I Exposure
  25. Comparison of 177Lu-octreotate and 177Lu-octreotide for treatment in human neuroblastoma-bearing mice
  26. Late Age- and Dose-Related Effects on the Proteome of Thyroid Tissue in Rats after <sup>131</sup>I Exposure
  27. Synergistic Antitumor Effects of 177Lu-Octreotide Combined with an ALK Inhibitor in a High-Risk Neuroblastoma Xenograft Model
  28. Data from Radiotherapy-Induced Neurocognitive Impairment Is Driven by Heightened Apoptotic Priming in Early Life and Prevented by Blocking BAX
  29. Radiotherapy-Induced Neurocognitive Impairment Is Driven by Heightened Apoptotic Priming in Early Life and Prevented by Blocking BAX
  30. Targeting TBK1 to overcome resistance to cancer immunotherapy
  31. Heightened apoptotic priming of vascular cells across tissues and life span predisposes them to cancer therapy–induced toxicities
  32. Exploiting endogenous and therapy-induced apoptotic vulnerabilities in immunoglobulin light chain amyloidosis with BH3 mimetics
  33. Age and sex effects across the blood proteome after ionizing radiation exposure can bias biomarker screening and risk assessment
  34. Age-related long-term response in rat thyroid tissue and plasma after internal low dose exposure to 131I
  35. Age and Sex Effects across the Blood Proteome after Lonizing Radiation Exposure: Consequences for Biomarker Screening and Risk Assessment
  36. Correction: Long-term transcriptomic and proteomic effects in Sprague Dawley rat thyroid and plasma after internal low dose 131I exposure
  37. Neuroblastoma xenograft models demonstrate the therapeutic potential of 177Lu-octreotate
  38. Age-dependent regulation of SARS-CoV-2 cell entry genes and cell death programs correlates with COVID-19 severity
  39. Metabolic perturbations sensitize triple-negative breast cancers to apoptosis induced by BH3 mimetics
  40. Long-term transcriptomic and proteomic effects in Sprague Dawley rat thyroid and plasma after internal low dose 131I exposure
  41. Biodistribution of 131I in mice is influenced by circadian variations
  42. Age-dependent regulation of SARS-CoV-2 cell entry genes and cell death programs correlates with COVID-19 disease severity
  43. Increased therapeutic effect on medullary thyroid cancer using a combination of radiation and tyrosine kinase inhibitors
  44. Preface: Life through death—Key role of cellular suicide for colonial and organismal homeostasis
  45. Preface: Life through death—Key role of cellular suicide for colonial and organismal homeostasis
  46. Preface: Life through death—Key role of cellular suicide for colonial and organismal homeostasis
  47. Gemcitabine potentiates the anti-tumour effect of radiation on medullary thyroid cancer
  48. Transcriptional effects of 177Lu-octreotate therapy using a priming treatment schedule on GOT1 tumor in nude mice
  49. Multiparametric MR for non-invasive evaluation of tumour tissue histological characteristics after radionuclide therapy
  50. T Cells and Regulated Cell Death
  51. Deconvolution of expression microarray data reveals 131I-induced responses otherwise undetected in thyroid tissue
  52. Time-dependent transcriptional response of GOT1 human small intestine neuroendocrine tumor after 177 Lu[Lu]-octreotate therapy
  53. Identification of Potential MR-Derived Biomarkers for Tumor Tissue Response to 177Lu-Octreotate Therapy in an Animal Model of Small Intestine Neuroendocrine Tumor
  54. Radiation-Induced Cardiovascular Toxicity: Mechanisms, Prevention, and Treatment
  55. Hedgehog inhibitor sonidegib potentiates 177Lu-octreotate therapy of GOT1 human small intestine neuroendocrine tumors in nude mice
  56. Transcriptional response to 131I exposure of rat thyroid gland
  57. Priming increases the anti-tumor effect and therapeutic window of 177Lu-octreotate in nude mice bearing human small intestine neuroendocrine tumor GOT1
  58. Non-targeted transcriptomic effects upon thyroid irradiation: similarity between in-field and out-of-field responses varies with tissue type
  59. Gene expression signature in mouse thyroid tissue after 131I and 211At exposure
  60. Transcriptional Response in Mouse Thyroid Tissue after 211At Administration: Effects of Absorbed Dose, Initial Dose-Rate and Time after Administration
  61. Transcriptional response in normal mouse tissues after i.v. 211At administration - response related to absorbed dose, dose rate, and time
  62. Time- and dose rate-related effects of internal 177Lu exposure on gene expression in mouse kidney tissue
  63. Biodistribution and Dosimetry of Free 211At, 125I− and 131I− in Rats
  64. Radionuclide Therapy via SSTR: Future Aspects from Experimental Animal Studies
  65. Specific Binding and Uptake of 131I-MIBG and 111In-Octreotide in Metastatic Paraganglioma - Tools for Choice of Radionuclide Therapy
  66. Biodistribution of 177Lu-octreotate and 111In-minigastrin in female nude mice transplanted with human medullary thyroid carcinoma GOT2