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Journal of Biological Methods
|
August 28, 2019
Development and implementation of a cell-based assay to discover agonists of the nuclear receptor REV-ERBα
Yuliya Hering, Alexandre Berthier, Helene Duez, et al.
The Journal of Allergy and Clinical Immunology
|
June 11, 2019
Supporting caregivers during hematopoietic cell transplantation for children with primary immunodeficiency disorders
Jennie Yoo, Meghan C Halley, E Anne Lown, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium
|
May 9, 2015
Clinical Decision Support-based Quality Measurement (CDS-QM) Framework: Prototype Implementation, Evaluation, and Future Directions
Polina V Kukhareva, Kensaku Kawamoto, David E Shields, et al.
Human Molecular Genetics
|
October 1, 1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes
A M van den Ouweland, W H Deelen, C B Kunst, et al.
Nature Medicine
|
March 24, 2019
Author Correction: Adrenergic nerve degeneration in bone marrow drives aging of the hematopoietic stem cell niche
Maria Maryanovich, Ali H Zahalka, Halley Pierce, et al.
JMIR Research Protocols
|
November 13, 2024
Collaborative Care to Improve Quality of Life for Anxiety and Depression in Posttraumatic Epilepsy (CoCarePTE): Protocol for a Randomized Hybrid Effectiveness-Implementation Trial
Heidi M Munger Clary, Beverly M Snively, Christian Cagle, et al.
Journal of Cardiac Failure
|
October 10, 2024
Anticoagulation Medications, Monitoring, and Outcomes in Patients with Cardiogenic Shock Requiring Temporary Mechanical Circulatory Support
Chirag Mehta, Brian Osorio, Neel R Sodha, et al.
Clinical Genetics
|
May 10, 2013
A clinical and genetic overview of 18 years neurofibromatosis type 1 molecular diagnostics in the Netherlands
R van Minkelen, Y van Bever, J N R Kromosoeto, et al.
Plos One
|
March 12, 2010
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype
Stephen C Collins, Brad Coffee, Paul J Benke, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 18, 2009
Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects
M C Y de Wit, J M Kros, D J J Halley, et al.
Page
of 140
Search research articles
Search
Showing results (1051-1060 of 1,394) with videos related to
Sort By:
Page
of 140
Journal of Biological Methods
|
August 28, 2019
Development and implementation of a cell-based assay to discover agonists of the nuclear receptor REV-ERBα
Yuliya Hering, Alexandre Berthier, Helene Duez, et al.
The Journal of Allergy and Clinical Immunology
|
June 11, 2019
Supporting caregivers during hematopoietic cell transplantation for children with primary immunodeficiency disorders
Jennie Yoo, Meghan C Halley, E Anne Lown, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium
|
May 9, 2015
Clinical Decision Support-based Quality Measurement (CDS-QM) Framework: Prototype Implementation, Evaluation, and Future Directions
Polina V Kukhareva, Kensaku Kawamoto, David E Shields, et al.
Human Molecular Genetics
|
October 1, 1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes
A M van den Ouweland, W H Deelen, C B Kunst, et al.
Nature Medicine
|
March 24, 2019
Author Correction: Adrenergic nerve degeneration in bone marrow drives aging of the hematopoietic stem cell niche
Maria Maryanovich, Ali H Zahalka, Halley Pierce, et al.
JMIR Research Protocols
|
November 13, 2024
Collaborative Care to Improve Quality of Life for Anxiety and Depression in Posttraumatic Epilepsy (CoCarePTE): Protocol for a Randomized Hybrid Effectiveness-Implementation Trial
Heidi M Munger Clary, Beverly M Snively, Christian Cagle, et al.
Journal of Cardiac Failure
|
October 10, 2024
Anticoagulation Medications, Monitoring, and Outcomes in Patients with Cardiogenic Shock Requiring Temporary Mechanical Circulatory Support
Chirag Mehta, Brian Osorio, Neel R Sodha, et al.
Clinical Genetics
|
May 10, 2013
A clinical and genetic overview of 18 years neurofibromatosis type 1 molecular diagnostics in the Netherlands
R van Minkelen, Y van Bever, J N R Kromosoeto, et al.
Plos One
|
March 12, 2010
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype
Stephen C Collins, Brad Coffee, Paul J Benke, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 18, 2009
Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects
M C Y de Wit, J M Kros, D J J Halley, et al.
Page
of 140