Search research articles
Contact Us
Filters
Showing results (1141-1150 of 1,876) with videos related to
Page
of 188
Sort By:
BMC Health Services Research
|
April 1, 2008
Securing recruitment and obtaining informed consent in minority ethnic groups in the UK
Cathy E Lloyd, Mark R D Johnson, Shanaz Mughal, et al.
Journal of Clinical Epidemiology
|
October 28, 2023
Open science practices need substantial improvement in prognostic model studies in oncology using machine learning
Gary S Collins, Rebecca Whittle, Garrett S Bullock, et al.
Skeletal Radiology
|
June 15, 2023
Rhabdomyolysis: a review of imaging features across modalities
Allison B Rixey, Katrina N Glazebrook, Garret M Powell, et al.
Ciba Foundation Symposium
|
January 1, 1994
Strategies for studying mouse and human immune responses to human papillomavirus type 16
P C Beverley, E Sadovnikova, X Zhu, et al.
Plos One
|
March 4, 2014
A panel of diverse assays to interrogate the interaction between glucokinase and glucokinase regulatory protein, two vital proteins in human disease
Matthew G Rees, Mindy I Davis, Min Shen, et al.
Annals of the New York Academy of Sciences
|
January 1, 1990
Expression of human globin genes in transgenic mice carrying the beta-globin gene cluster with a mutation causing G gamma beta + hereditary persistence of fetal hemoglobin
M Tanaka, J A Nolan, A K Bhargava, et al.
Molecular Genetics and Metabolism
|
June 7, 2005
Evaluation of SLC2A10 (GLUT10) as a candidate gene for type 2 diabetes and related traits in Finns
Karen L Mohlke, Andrew D Skol, Laura J Scott, et al.
Nature Astronomy
|
September 23, 2024
An estimate of the impact rate on Mars from statistics of very-high-frequency marsquakes
Géraldine Zenhäusern, Natalia Wójcicka, Simon C Stähler, et al.
ACS Nano
|
November 9, 2020
Strongly Quantum-Confined Blue-Emitting Excitons in Chemically Configurable Multiquantum Wells
Kaiyuan Yao, Mary S Collins, Kara M Nell, et al.
Nature Genetics
|
December 17, 1997
Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders
B E Reuber, E Germain-Lee, C S Collins, et al.
Page
of 188
Search research articles
Search
Showing results (1141-1150 of 1,876) with videos related to
Sort By:
Page
of 188
BMC Health Services Research
|
April 1, 2008
Securing recruitment and obtaining informed consent in minority ethnic groups in the UK
Cathy E Lloyd, Mark R D Johnson, Shanaz Mughal, et al.
Journal of Clinical Epidemiology
|
October 28, 2023
Open science practices need substantial improvement in prognostic model studies in oncology using machine learning
Gary S Collins, Rebecca Whittle, Garrett S Bullock, et al.
Skeletal Radiology
|
June 15, 2023
Rhabdomyolysis: a review of imaging features across modalities
Allison B Rixey, Katrina N Glazebrook, Garret M Powell, et al.
Ciba Foundation Symposium
|
January 1, 1994
Strategies for studying mouse and human immune responses to human papillomavirus type 16
P C Beverley, E Sadovnikova, X Zhu, et al.
Plos One
|
March 4, 2014
A panel of diverse assays to interrogate the interaction between glucokinase and glucokinase regulatory protein, two vital proteins in human disease
Matthew G Rees, Mindy I Davis, Min Shen, et al.
Annals of the New York Academy of Sciences
|
January 1, 1990
Expression of human globin genes in transgenic mice carrying the beta-globin gene cluster with a mutation causing G gamma beta + hereditary persistence of fetal hemoglobin
M Tanaka, J A Nolan, A K Bhargava, et al.
Molecular Genetics and Metabolism
|
June 7, 2005
Evaluation of SLC2A10 (GLUT10) as a candidate gene for type 2 diabetes and related traits in Finns
Karen L Mohlke, Andrew D Skol, Laura J Scott, et al.
Nature Astronomy
|
September 23, 2024
An estimate of the impact rate on Mars from statistics of very-high-frequency marsquakes
Géraldine Zenhäusern, Natalia Wójcicka, Simon C Stähler, et al.
ACS Nano
|
November 9, 2020
Strongly Quantum-Confined Blue-Emitting Excitons in Chemically Configurable Multiquantum Wells
Kaiyuan Yao, Mary S Collins, Kara M Nell, et al.
Nature Genetics
|
December 17, 1997
Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders
B E Reuber, E Germain-Lee, C S Collins, et al.
Page
of 188