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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
November 27, 2024
Update on Cancer Screening in Children with Syndromes of Bone Lesions, Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome, and Other Rare Syndromes
Orli Michaeli, Sun Young Kim, Sarah G Mitchell, et al.
Cell Reports
|
June 15, 2017
The NOTCH1/SNAIL1/MEF2C Pathway Regulates Growth and Self-Renewal in Embryonal Rhabdomyosarcoma
Myron S Ignatius, Madeline N Hayes, Riadh Lobbardi, et al.
BMJ Open
|
November 24, 2024
Development of the Ontario Hereditary Cancer Research Network, a unified registry as a resource for individuals with inherited cancer syndromes: an observational registry creation protocol
Kirsten M Farncombe, Lauren K Hughes, Elif Tuzlali, et al.
Cancer Medicine
|
November 23, 2019
Medulloblastoma has a global impact on health related quality of life: Findings from an international cohort
Cynthia B de Medeiros, Iska Moxon-Emre, Nadia Scantlebury, et al.
Cancer
|
July 30, 2019
Provocative questions in osteosarcoma basic and translational biology: A report from the Children's Oncology Group
Ryan D Roberts, Michael M Lizardo, Damon R Reed, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
January 19, 2018
<i>DICER1</i> and Associated Conditions: Identification of At-risk Individuals and Recommended Surveillance Strategies
Kris Ann P Schultz, Gretchen M Williams, Junne Kamihara, et al.
Nature
|
June 15, 2022
Signatures of copy number alterations in human cancer
Christopher D Steele, Ammal Abbasi, S M Ashiqul Islam, et al.
Nature Communications
|
August 26, 2025
Peripheral blood DNA methylation predicts the early onset of primary tumor in TP53 mutation carriers
Vallijah Subasri, Benjamin Brew, Brianne Laverty, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 25, 2025
Updated Recommendations for Pediatric Surveillance in Hereditary Endocrine Neoplasia Syndromes: Multiple Endocrine Neoplasias, Hyperparathyroidism-Jaw Tumor Syndrome, and Carney Complex
Jonathan D Wasserman, Kami Wolfe Schneider, Maria-Isabel Achatz, et al.
Cell Death Discovery
|
February 16, 2023
Elephant TP53-RETROGENE 9 induces transcription-independent apoptosis at the mitochondria
Aidan J Preston, Aaron Rogers, Miranda Sharp, et al.
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of 27
Search research articles
Search
Showing results (191-200 of 270) with videos related to
Sort By:
Page
of 27
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
November 27, 2024
Update on Cancer Screening in Children with Syndromes of Bone Lesions, Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome, and Other Rare Syndromes
Orli Michaeli, Sun Young Kim, Sarah G Mitchell, et al.
Cell Reports
|
June 15, 2017
The NOTCH1/SNAIL1/MEF2C Pathway Regulates Growth and Self-Renewal in Embryonal Rhabdomyosarcoma
Myron S Ignatius, Madeline N Hayes, Riadh Lobbardi, et al.
BMJ Open
|
November 24, 2024
Development of the Ontario Hereditary Cancer Research Network, a unified registry as a resource for individuals with inherited cancer syndromes: an observational registry creation protocol
Kirsten M Farncombe, Lauren K Hughes, Elif Tuzlali, et al.
Cancer Medicine
|
November 23, 2019
Medulloblastoma has a global impact on health related quality of life: Findings from an international cohort
Cynthia B de Medeiros, Iska Moxon-Emre, Nadia Scantlebury, et al.
Cancer
|
July 30, 2019
Provocative questions in osteosarcoma basic and translational biology: A report from the Children's Oncology Group
Ryan D Roberts, Michael M Lizardo, Damon R Reed, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
January 19, 2018
<i>DICER1</i> and Associated Conditions: Identification of At-risk Individuals and Recommended Surveillance Strategies
Kris Ann P Schultz, Gretchen M Williams, Junne Kamihara, et al.
Nature
|
June 15, 2022
Signatures of copy number alterations in human cancer
Christopher D Steele, Ammal Abbasi, S M Ashiqul Islam, et al.
Nature Communications
|
August 26, 2025
Peripheral blood DNA methylation predicts the early onset of primary tumor in TP53 mutation carriers
Vallijah Subasri, Benjamin Brew, Brianne Laverty, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
June 25, 2025
Updated Recommendations for Pediatric Surveillance in Hereditary Endocrine Neoplasia Syndromes: Multiple Endocrine Neoplasias, Hyperparathyroidism-Jaw Tumor Syndrome, and Carney Complex
Jonathan D Wasserman, Kami Wolfe Schneider, Maria-Isabel Achatz, et al.
Cell Death Discovery
|
February 16, 2023
Elephant TP53-RETROGENE 9 induces transcription-independent apoptosis at the mitochondria
Aidan J Preston, Aaron Rogers, Miranda Sharp, et al.
Page
of 27