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The Journal of Urology
|
June 20, 2019
Identification and Characterization of Circulating Tumor Cells in Men Who have Undergone Prostatectomy for Clinically Localized, High Risk Prostate Cancer
Terence W Friedlander, Christopher Welty, Archana Anantharaman, et al.
Annals of Neurology
|
September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutations
Naomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Scientific Reports
|
September 28, 2021
Integrated genomics point to immune vulnerabilities in pleural mesothelioma
Anca Nastase, Amit Mandal, Shir Kiong Lu, et al.
Scientific Reports
|
March 22, 2022
Author Correction: Integrated genomics point to immune vulnerabilities in pleural mesothelioma
Anca Nastase, Amit Mandal, Shir Kiong Lu, et al.
Human Molecular Genetics
|
December 10, 2019
Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants
Gavin Chapman, Julie L M Moreau, Eddie I P, et al.
Ebiomedicine
|
April 5, 2017
A Comprehensive Evaluation of Nasal and Bronchial Cytokines and Chemokines Following Experimental Rhinovirus Infection in Allergic Asthma: Increased Interferons (IFN-γ and IFN-λ) and Type 2 Inflammation (IL-5 and IL-13)
Trevor T Hansel, Tanushree Tunstall, Maria-Belen Trujillo-Torralbo, et al.
Clinical Epigenetics
|
September 1, 2018
Genetic variation affecting DNA methylation and the human imprinting disorder, Beckwith-Wiedemann syndrome
Vinod Dagar, Wendy Hutchison, Andrea Muscat, et al.
American Journal of Human Genetics
|
June 9, 2004
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35
Mary L Marazita, Jeffrey C Murray, Andrew C Lidral, et al.
Circulation
|
May 5, 2021
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy
Elizabeth Jordan, Laiken Peterson, Tomohiko Ai, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 17, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions
Katherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.
Page
of 13
Search research articles
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Showing results (111-120 of 130) with videos related to
Sort By:
Page
of 13
The Journal of Urology
|
June 20, 2019
Identification and Characterization of Circulating Tumor Cells in Men Who have Undergone Prostatectomy for Clinically Localized, High Risk Prostate Cancer
Terence W Friedlander, Christopher Welty, Archana Anantharaman, et al.
Annals of Neurology
|
September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutations
Naomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Scientific Reports
|
September 28, 2021
Integrated genomics point to immune vulnerabilities in pleural mesothelioma
Anca Nastase, Amit Mandal, Shir Kiong Lu, et al.
Scientific Reports
|
March 22, 2022
Author Correction: Integrated genomics point to immune vulnerabilities in pleural mesothelioma
Anca Nastase, Amit Mandal, Shir Kiong Lu, et al.
Human Molecular Genetics
|
December 10, 2019
Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants
Gavin Chapman, Julie L M Moreau, Eddie I P, et al.
Ebiomedicine
|
April 5, 2017
A Comprehensive Evaluation of Nasal and Bronchial Cytokines and Chemokines Following Experimental Rhinovirus Infection in Allergic Asthma: Increased Interferons (IFN-γ and IFN-λ) and Type 2 Inflammation (IL-5 and IL-13)
Trevor T Hansel, Tanushree Tunstall, Maria-Belen Trujillo-Torralbo, et al.
Clinical Epigenetics
|
September 1, 2018
Genetic variation affecting DNA methylation and the human imprinting disorder, Beckwith-Wiedemann syndrome
Vinod Dagar, Wendy Hutchison, Andrea Muscat, et al.
American Journal of Human Genetics
|
June 9, 2004
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35
Mary L Marazita, Jeffrey C Murray, Andrew C Lidral, et al.
Circulation
|
May 5, 2021
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy
Elizabeth Jordan, Laiken Peterson, Tomohiko Ai, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 17, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions
Katherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.
Page
of 13