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Oncotarget
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July 10, 2015
TCF21 hypermethylation in genetically quiescent clear cell sarcoma of the kidney
Saskia L Gooskens, Samantha Gadd, Jaime M Guidry Auvil, et al.
Biodiversity Data Journal
|
February 8, 2024
Biodiversity of aquatic organisms in the Mekong Delta, Vietnam
Dmitriy G Seleznev, Cu Nguyen Dinh, Truong Ba Hai, et al.
Nature Communications
|
December 5, 2015
MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours
Elizabeth J Perlman, Samantha Gadd, Stefan T Arold, et al.
Plos Medicine
|
December 7, 2016
Somatic Genomics and Clinical Features of Lung Adenocarcinoma: A Retrospective Study
Jianxin Shi, Xing Hua, Bin Zhu, et al.
Cancer Cell
|
February 12, 2015
Recurrent DGCR8, DROSHA, and SIX homeodomain mutations in favorable histology Wilms tumors
Amy L Walz, Ariadne Ooms, Samantha Gadd, et al.
Nature Genetics
|
August 22, 2017
A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor
Samantha Gadd, Vicki Huff, Amy L Walz, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 6, 2016
Significance of TP53 Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children's Oncology Group
Ariadne H A G Ooms, Samantha Gadd, Daniela S Gerhard, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 16, 2020
Cross-Site Concordance Evaluation of Tumor DNA and RNA Sequencing Platforms for the CIMAC-CIDC Network
Zexian Zeng, Jingxin Fu, Carrie Cibulskis, et al.
Nature Biotechnology
|
September 10, 2021
Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Li Tai Fang, Bin Zhu, Yongmei Zhao, et al.
Nature Biotechnology
|
September 10, 2021
Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing
Wenming Xiao, Luyao Ren, Zhong Chen, et al.
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Search research articles
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Showing results (51-60 of 60) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 60 results.
Oncotarget
|
July 10, 2015
TCF21 hypermethylation in genetically quiescent clear cell sarcoma of the kidney
Saskia L Gooskens, Samantha Gadd, Jaime M Guidry Auvil, et al.
Biodiversity Data Journal
|
February 8, 2024
Biodiversity of aquatic organisms in the Mekong Delta, Vietnam
Dmitriy G Seleznev, Cu Nguyen Dinh, Truong Ba Hai, et al.
Nature Communications
|
December 5, 2015
MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours
Elizabeth J Perlman, Samantha Gadd, Stefan T Arold, et al.
Plos Medicine
|
December 7, 2016
Somatic Genomics and Clinical Features of Lung Adenocarcinoma: A Retrospective Study
Jianxin Shi, Xing Hua, Bin Zhu, et al.
Cancer Cell
|
February 12, 2015
Recurrent DGCR8, DROSHA, and SIX homeodomain mutations in favorable histology Wilms tumors
Amy L Walz, Ariadne Ooms, Samantha Gadd, et al.
Nature Genetics
|
August 22, 2017
A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor
Samantha Gadd, Vicki Huff, Amy L Walz, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
October 6, 2016
Significance of TP53 Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children's Oncology Group
Ariadne H A G Ooms, Samantha Gadd, Daniela S Gerhard, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 16, 2020
Cross-Site Concordance Evaluation of Tumor DNA and RNA Sequencing Platforms for the CIMAC-CIDC Network
Zexian Zeng, Jingxin Fu, Carrie Cibulskis, et al.
Nature Biotechnology
|
September 10, 2021
Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
Li Tai Fang, Bin Zhu, Yongmei Zhao, et al.
Nature Biotechnology
|
September 10, 2021
Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing
Wenming Xiao, Luyao Ren, Zhong Chen, et al.
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of 6