Showing results (11-20 of 28) with videos related to
Sort By:
Pageof 3
Cell Reports Methods|May 20, 2025
Highly quantitative measurement of differential protein-genome binding with PerCell chromatin sequencingAlexi Tallan, Jack Kucinski, Benjamin Sunkel, et al.Circulation. Cardiovascular Genetics|July 16, 2016
Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart DiseaseStephanie LaHaye, Don Corsmeier, Madhumita Basu, et al.JCI Insight|November 3, 2017
Notch1 haploinsufficiency causes ascending aortic aneurysms in miceSara N Koenig, Stephanie LaHaye, James D Feller, et al.JACC. Basic to Translational Science|August 1, 2025
Disruption of Notch1 and Gata5 in Mice Leads to Congenital Aortic Valve DiseaseJun Yasuhara, Mona Aljuhani, Talita Z Choudhury, et al.Journal of Molecular and Cellular Cardiology|April 16, 2013
Endothelial nitric oxide signaling regulates Notch1 in aortic valve diseaseKevin Bosse, Chetan P Hans, Ning Zhao, et al.Genes, Chromosomes & Cancer|April 24, 2021
Novel morphologic findings in PLAG1-rearranged soft tissue tumorsSuzanna J Logan, Kathleen M Schieffer, Miriam R Conces, et al.The Journal of Molecular Diagnostics : JMD|October 3, 2022
Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome-Based Resolution of Isoform ComplexityAnthony R Miller, Saranga Wijeratne, Sean D McGrath, et al.Genes, Chromosomes & Cancer|July 8, 2022
EGFR internal tandem duplications in fusion-negative congenital and neonatal spindle cell tumorsSelene C Koo, Kathleen M Schieffer, Kristy Lee, et al.Iscience|July 19, 2021
Endogenous retrovirus envelope as a tumor-associated immunotherapeutic target in murine osteosarcomaMary Frances Wedekind, Katherine E Miller, Chun-Yu Chen, et al.Genes, Chromosomes & Cancer|June 18, 2022
Infantile metastatic ependymoma with a novel molecular profile and favorable outcome to intensive chemotherapy without irradiation: Case-based reviewFlavia Watusi De Faria, Kathleen M Schieffer, Christopher R Pierson, et al.Pageof 3