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53. Identification and characterization of immunogenic neoantigens in biliary cancer (BC) and pancreatic cancer (PC).

54. Molecular differences with therapeutic implications in early-onset compared to average-onset cholangiocarcinoma.

55. Molecular and immune landscape by cyclin dependent kinase (CDK) 4/6 expression and TP53 mutational status in mismatch repair deficient/microsatellite instability-high (dMMR/MSI-H) colorectal cancer (CRC).

56. Characterization of the cachexia pathway in pancreatic ductal adenocarcinoma.

57. LMTK3 gene expression and the molecular landscape of colorectal cancer (CRC).

58. APC as a high-utility mutational biomarker that may identify subpopulations of patients with mutant RAS/BRAF and right-sided colorectal cancer (CRC) who derive benefit from EGFR inhibitors (EGFRi).

61. Mesothelin expression correlates with elevated inhibitory immune activity in patients with colorectal cancer

62. Cross-Level Peer Mentoring

63. Nurturing Creative, Thinking Engineers

64. An Overview of Selected Theories about Student Learning

66. Design of Interventions for Instructional Reform in Software Development Education for Competency Enhancement

71. What Do Engineers Want? Examining Engineering Education through Bloom's Taxonomy

72. The Genomic, Transcriptomic, and Immunologic Landscape of HRAS Mutations in Solid Tumors.

75. 611 XTX202–01/02–001, Phase 1/2 first-in human study of XTX202, a masked, tumor-activated IL-2βγ, in patients with advanced solid tumors: results from phase 1

79. Security Challenges in Smart Grid Implementation

84. Outcomes of Helicobacter pylori (HP) infection in esophageal cancer (EC): A 5-year nationwide analysis.

85. Phase 1 dose-escalation study of SEA-CD40: a non-fucosylated CD40 agonist, in advanced solid tumors and lymphomas

90. Introduction

96. Supplementary Figure from The Genomics of Colorectal Cancer in Populations with African and European Ancestry

98. Data from The Genomics of Colorectal Cancer in Populations with African and European Ancestry

100. Data from RICTOR Amplification Defines a Novel Subset of Patients with Lung Cancer Who May Benefit from Treatment with mTORC1/2 Inhibitors

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