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The Journal of Pediatrics
|
February 1, 1996
Pleuropulmonary blastoma: a marker for familial disease
J R Priest, J Watterson, L Strong, et al.
Human Genetics
|
March 29, 2008
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease
Themistocles L Assimes, Joshua W Knowles, James R Priest, et al.
Human Mutation
|
September 2, 2011
Extending the phenotypes associated with DICER1 mutations
William D Foulkes, Amin Bahubeshi, Nancy Hamel, et al.
Atherosclerosis
|
October 26, 2007
A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease
Themistocles L Assimes, Joshua W Knowles, James R Priest, et al.
JACC. Basic to Translational Science
|
November 1, 2025
Mendelian Randomization Suggests a Causal Link Between Glycemic Traits and Thoracic Aortic Structures and Diseases
Tselmen Daria, Kruthika Iyer, Hasan Alkhairo, et al.
Nature Communications
|
May 15, 2023
Author Correction: Ultra-high-resolution observations of persistent null-point reconnection in the solar corona
X Cheng, E R Priest, H T Li, et al.
Nature Communications
|
April 13, 2023
Ultra-high-resolution observations of persistent null-point reconnection in the solar corona
X Cheng, E R Priest, H T Li, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 25, 2020
Clinical Outcomes and Complications of Pituitary Blastoma
Anthony P Y Liu, Megan M Kelsey, Nelly Sabbaghian, et al.
Frontiers in Cardiovascular Medicine
|
August 12, 2025
Identification of candidate cardiomyopathy modifier genes through genome sequencing and RNA profiling
Malene E Lindholm, Sarah Abramowitz, Daryl M Waggott, et al.
JAMA
|
January 6, 2011
DICER1 mutations in familial multinodular goiter with and without ovarian Sertoli-Leydig cell tumors
Thomas Rio Frio, Amin Bahubeshi, Chryssa Kanellopoulou, et al.
Page
of 22
Search research articles
Search
Showing results (191-200 of 216) with videos related to
Sort By:
Page
of 22
The Journal of Pediatrics
|
February 1, 1996
Pleuropulmonary blastoma: a marker for familial disease
J R Priest, J Watterson, L Strong, et al.
Human Genetics
|
March 29, 2008
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease
Themistocles L Assimes, Joshua W Knowles, James R Priest, et al.
Human Mutation
|
September 2, 2011
Extending the phenotypes associated with DICER1 mutations
William D Foulkes, Amin Bahubeshi, Nancy Hamel, et al.
Atherosclerosis
|
October 26, 2007
A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease
Themistocles L Assimes, Joshua W Knowles, James R Priest, et al.
JACC. Basic to Translational Science
|
November 1, 2025
Mendelian Randomization Suggests a Causal Link Between Glycemic Traits and Thoracic Aortic Structures and Diseases
Tselmen Daria, Kruthika Iyer, Hasan Alkhairo, et al.
Nature Communications
|
May 15, 2023
Author Correction: Ultra-high-resolution observations of persistent null-point reconnection in the solar corona
X Cheng, E R Priest, H T Li, et al.
Nature Communications
|
April 13, 2023
Ultra-high-resolution observations of persistent null-point reconnection in the solar corona
X Cheng, E R Priest, H T Li, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 25, 2020
Clinical Outcomes and Complications of Pituitary Blastoma
Anthony P Y Liu, Megan M Kelsey, Nelly Sabbaghian, et al.
Frontiers in Cardiovascular Medicine
|
August 12, 2025
Identification of candidate cardiomyopathy modifier genes through genome sequencing and RNA profiling
Malene E Lindholm, Sarah Abramowitz, Daryl M Waggott, et al.
JAMA
|
January 6, 2011
DICER1 mutations in familial multinodular goiter with and without ovarian Sertoli-Leydig cell tumors
Thomas Rio Frio, Amin Bahubeshi, Chryssa Kanellopoulou, et al.
Page
of 22