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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
January 28, 2010
Serum prognostic markers in head and neck cancer
François Meyer, Elodie Samson, Pierre Douville, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
May 31, 2022
Gastrointestinal Dysmotility as the First Manifestation of Myasthenia Gravis
Sara Alnajjar, Juan Fco Idiaquez Rios, Davood Fathi, et al.
BMC Proceedings
|
March 1, 2012
A pathway-based association analysis model using common and rare variants
Lu Cheng, Pingzhao Hu, Jenna Sykes, et al.
Cancer
|
April 2, 2025
Update advances in anaplastic lymphoma kinase-positive non-small cell lung cancer treatment
Beatriz E Jimenez Munarriz, Sam Khan, Yuchen Li, et al.
Neoplasia (New York, N.Y.)
|
February 23, 2012
Genome-wide DNA methylation profiling of cell-free serum DNA in esophageal adenocarcinoma and Barrett esophagus
Rihong Zhai, Yang Zhao, Li Su, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
August 4, 2010
Germline genetic variation, cancer outcome, and pharmacogenetics
Linda Coate, Sinead Cuffe, Anne Horgan, et al.
Oncology and Therapy
|
April 16, 2024
Correction: Real-World Treatment Patterns and Survival Among Patients with Stage I-III, Non-Squamous, Non-Small Cell Lung Cancer Receiving Surgery as Primary Treatment
Soo Jin Seung, Daniel Moldaver, Shazia Hassan, et al.
BMC Proceedings
|
December 19, 2014
Haplotype approach for association analysis on hypertension
Xiaowei Shen, Osvaldo Espin-Garcia, Xin Qiu, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer
|
April 29, 2018
Heritable Germline Variation and Lung Cancer Susceptibility: One Size Does not Fit All
Michael Herman, Matthew T Warkentin, Daniel Shepshelovich, et al.
BMC Proceedings
|
March 1, 2012
Addition of multiple rare SNPs to known common variants improves the association between disease and gene in the Genetic Analysis Workshop 17 data
Jenna Sykes, Lu Cheng, Wei Xu, et al.
Page
of 58
Search research articles
Search
Showing results (41-50 of 574) with videos related to
Sort By:
Page
of 58
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
January 28, 2010
Serum prognostic markers in head and neck cancer
François Meyer, Elodie Samson, Pierre Douville, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
May 31, 2022
Gastrointestinal Dysmotility as the First Manifestation of Myasthenia Gravis
Sara Alnajjar, Juan Fco Idiaquez Rios, Davood Fathi, et al.
BMC Proceedings
|
March 1, 2012
A pathway-based association analysis model using common and rare variants
Lu Cheng, Pingzhao Hu, Jenna Sykes, et al.
Cancer
|
April 2, 2025
Update advances in anaplastic lymphoma kinase-positive non-small cell lung cancer treatment
Beatriz E Jimenez Munarriz, Sam Khan, Yuchen Li, et al.
Neoplasia (New York, N.Y.)
|
February 23, 2012
Genome-wide DNA methylation profiling of cell-free serum DNA in esophageal adenocarcinoma and Barrett esophagus
Rihong Zhai, Yang Zhao, Li Su, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
August 4, 2010
Germline genetic variation, cancer outcome, and pharmacogenetics
Linda Coate, Sinead Cuffe, Anne Horgan, et al.
Oncology and Therapy
|
April 16, 2024
Correction: Real-World Treatment Patterns and Survival Among Patients with Stage I-III, Non-Squamous, Non-Small Cell Lung Cancer Receiving Surgery as Primary Treatment
Soo Jin Seung, Daniel Moldaver, Shazia Hassan, et al.
BMC Proceedings
|
December 19, 2014
Haplotype approach for association analysis on hypertension
Xiaowei Shen, Osvaldo Espin-Garcia, Xin Qiu, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer
|
April 29, 2018
Heritable Germline Variation and Lung Cancer Susceptibility: One Size Does not Fit All
Michael Herman, Matthew T Warkentin, Daniel Shepshelovich, et al.
BMC Proceedings
|
March 1, 2012
Addition of multiple rare SNPs to known common variants improves the association between disease and gene in the Genetic Analysis Workshop 17 data
Jenna Sykes, Lu Cheng, Wei Xu, et al.
Page
of 58