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Nature Medicine
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May 26, 2022
A cellular hierarchy framework for understanding heterogeneity and predicting drug response in acute myeloid leukemia
Andy G X Zeng, Suraj Bansal, Liqing Jin, et al.
The Oncologist
|
November 18, 2018
Applying Artificial Intelligence to Address the Knowledge Gaps in Cancer Care
George Simon, Courtney D DiNardo, Koichi Takahashi, et al.
Nature
|
February 19, 2010
Signatures of mutation and selection in the cancer genome
Graham R Bignell, Chris D Greenman, Helen Davies, et al.
Journal of Medical Genetics
|
March 21, 2007
The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene
Charles E Schwartz, Patrick S Tarpey, Herbert A Lubs, et al.
Science Advances
|
July 22, 2021
FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translation
Nicol Birsa, Agnieszka M Ule, Maria Giovanna Garone, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
May 13, 2022
Immunogenomic intertumor heterogeneity across primary and metastatic sites in a patient with lung adenocarcinoma
Runzhe Chen, Jun Li, Junya Fujimoto, et al.
Leukemia
|
July 6, 2026
Decreased TXNRD1 is associated with resistance to tagraxofusp in blastic plasmacytoid dendritic cell neoplasms, as seen in phase II
Hannah C Beird, Sankaranarayanan Kannan, Jingjing Liu, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 21, 2020
Evolution of Genomic and T-cell Repertoire Heterogeneity of Malignant Pleural Mesothelioma Under Dasatinib Treatment
Runzhe Chen, Won-Chul Lee, Junya Fujimoto, et al.
Blood
|
January 24, 2018
Clinical implications of cancer gene mutations in patients with chronic lymphocytic leukemia treated with lenalidomide
Koichi Takahashi, Boyu Hu, Feng Wang, et al.
Nature Genetics
|
May 18, 2010
Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability
Cheryl Shoubridge, Patrick S Tarpey, Fatima Abidi, et al.
Page
of 87
Search research articles
Search
Showing results (711-720 of 866) with videos related to
Sort By:
Page
of 87
Nature Medicine
|
May 26, 2022
A cellular hierarchy framework for understanding heterogeneity and predicting drug response in acute myeloid leukemia
Andy G X Zeng, Suraj Bansal, Liqing Jin, et al.
The Oncologist
|
November 18, 2018
Applying Artificial Intelligence to Address the Knowledge Gaps in Cancer Care
George Simon, Courtney D DiNardo, Koichi Takahashi, et al.
Nature
|
February 19, 2010
Signatures of mutation and selection in the cancer genome
Graham R Bignell, Chris D Greenman, Helen Davies, et al.
Journal of Medical Genetics
|
March 21, 2007
The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene
Charles E Schwartz, Patrick S Tarpey, Herbert A Lubs, et al.
Science Advances
|
July 22, 2021
FUS-ALS mutants alter FMRP phase separation equilibrium and impair protein translation
Nicol Birsa, Agnieszka M Ule, Maria Giovanna Garone, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
May 13, 2022
Immunogenomic intertumor heterogeneity across primary and metastatic sites in a patient with lung adenocarcinoma
Runzhe Chen, Jun Li, Junya Fujimoto, et al.
Leukemia
|
July 6, 2026
Decreased TXNRD1 is associated with resistance to tagraxofusp in blastic plasmacytoid dendritic cell neoplasms, as seen in phase II
Hannah C Beird, Sankaranarayanan Kannan, Jingjing Liu, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 21, 2020
Evolution of Genomic and T-cell Repertoire Heterogeneity of Malignant Pleural Mesothelioma Under Dasatinib Treatment
Runzhe Chen, Won-Chul Lee, Junya Fujimoto, et al.
Blood
|
January 24, 2018
Clinical implications of cancer gene mutations in patients with chronic lymphocytic leukemia treated with lenalidomide
Koichi Takahashi, Boyu Hu, Feng Wang, et al.
Nature Genetics
|
May 18, 2010
Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability
Cheryl Shoubridge, Patrick S Tarpey, Fatima Abidi, et al.
Page
of 87