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Cancer Genetics|February 2, 2022
Neurotrophic tyrosine receptor kinase fusion in pediatric central nervous system tumorsShih-Shan Lang, Nankee K Kumar, Peter Madsen, et al.Cancer Genetics|March 14, 2022
Somatic tumor testing implications for Lynch syndrome germline genetic testingKathleen Barrus, Natasha Purington, Nicolette Chun, et al.Cancer Genetics|October 19, 2021
Molecular profiling of osteosarcoma in children and adolescents from different age groups using a next-generation sequencing panelG M Guimarães, F Tesser-Gamba, A S Petrilli, et al.Cancer Genetics|January 29, 2022
The clinical aspect of NTRK-fusions in pediatric papillary thyroid cancerJulio C Ricarte-Filho, Stephen Halada, Alison O'Neill, et al.Cancer Genetics|October 23, 2021
Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2)Lisa J McReynolds, Kajal Biswas, Neelam Giri, et al.Cancer Genetics|October 24, 2021
Multi-region sequencing reveals genetic correlation between esophageal squamous cell carcinoma and matched cell-free DNAZuyang Yuan, Xinfeng Wang, Xiao Geng, et al.Cancer Genetics|March 9, 2022
PTEN alterations in sporadic and BRCA1-associated triple negative breast carcinomasNatalie Jones, Audrey Gros, Valérie Velasco, et al.Cancer Genetics|September 22, 2021
Novel genomic signature predictive of response to immune checkpoint blockade: A pan-cancer analysis from project Genomics Evidence Neo-plasia Information Exchange (GENIE)Nishwant Swami, William L Hwang, Jimmy A Guo, et al.Cancer Genetics|January 14, 2023
Over-expression of USP15/MMP3 predict poor prognosis and promote growth, migration in non-small cell lung cancer cellsWeiwei Chen, Daguang Ni, Hailin Zhang, et al.Cancer Genetics|May 19, 2015
Whole exome sequencing in a case of sporadic multiple meningioma reveals shared NF2, FAM109B, and TPRXL mutations, together with unique SMARCB1 alterations in a subset of tumor nodulesMiguel Torres-Martín, M Elena Kusak, Alberto Isla, et al.Pageof 113