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Genome Medicine|October 29, 2021
Novel temporal and spatial patterns of metastatic colonization from breast cancer rapid-autopsy tumor biopsiesXiaomeng Huang, Yi Qiao, Samuel W Brady, et al.
Journal of Medical Genetics|September 24, 2018
Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic TelangiectasiaWhitney L Wooderchak-Donahue, Jamie McDonald, Andrew Farrell, et al.
Oncogene|February 20, 2022
TSPAN6 is a suppressor of Ras-driven cancerPatrick O Humbert, Tamara Zoranovic Pryjda, Blanka Pranjic, et al.
Cold Spring Harbor Molecular Case Studies|November 15, 2022
Rapid genome sequencing identifies a novel de novo SNAP25 variant for neonatal congenital myasthenic syndromeHayley M Reynolds, Ting Wen, Andrew Farrell, et al.
Journal of Experimental & Clinical Cancer Research : CR|January 6, 2026
High-throughput drug screening identifies EGFR/MAPK pathway targeting sensitivities in organoid models of ovarian carcinosarcomaAndrew Farrell, Genevieve Dall, Cassandra J Vandenberg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 15, 2019
Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)?Whitney L Wooderchak-Donahue, Gulsen Akay, Kevin Whitehead, et al.
NPJ Precision Oncology|May 22, 2026
Molecular features unique to circulating tumor DNA enable the tumor-naïve liquid biopsy of glioblastomaHunter R Underhill, Drew L Sellers, Sabine Hellwig, et al.
Molecular Genetics & Genomic Medicine|February 4, 2022
Comprehensive variant calling from whole-genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic herniaThomas J Nicholas, Najla Al-Sweel, Andrew Farrell, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
BRCA1 secondary splice-site mutations drive exon-skipping and PARP inhibitor resistanceKsenija Nesic, John J Krais, Cassandra J Vandenberg, et al.
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