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Halley

Showing results (1051-1060 of 1,394) with videos related to

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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-ERBαYuliya 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 disordersJennie 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 DirectionsPolina 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 chromosomesA 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 nicheMaria 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 TrialHeidi 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 SupportChirag 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 NetherlandsR 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 phenotypeStephen 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 defectsM C Y de Wit, J M Kros, D J J Halley, et al.
Pageof 140

Showing results (1051-1060 of 1,394) with videos related to

Sort By:
Pageof 140
Journal of Biological Methods|August 28, 2019
Development and implementation of a cell-based assay to discover agonists of the nuclear receptor REV-ERBαYuliya 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 disordersJennie 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 DirectionsPolina 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 chromosomesA 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 nicheMaria 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 TrialHeidi 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 SupportChirag 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 NetherlandsR 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 phenotypeStephen 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 defectsM C Y de Wit, J M Kros, D J J Halley, et al.
Pageof 140