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Showing results (531-540 of 644) with videos related to

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American Journal of Medical Genetics. Part A|September 24, 2018
22q and two: 22q11.2 deletion syndrome and coexisting conditionsJennifer L Cohen, Terrence B Crowley, Daniel E McGinn, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 12, 2009
AAV1/2-mediated CNS gene delivery of dominant-negative CCL2 mutant suppresses gliosis, beta-amyloidosis, and learning impairment of APP/PS1 miceTomomi Kiyota, Masaru Yamamoto, Bryce Schroder, et al.
Annals of Translational Medicine|June 19, 2018
Optimization of a microfluidics-based next generation sequencing assay for clinical oncology diagnosticsChristine Henzler, Matthew Schomaker, Rendong Yang, et al.
American Journal of Clinical Pathology|December 29, 2016
Rapid Evaluation of Platelet Function With T2 Magnetic ResonanceAdam Cuker, Holleh Husseinzadeh, Tatiana Lebedeva, et al.
Journal of the Advanced Practitioner in Oncology|April 13, 2026
Enhancing Immune Thrombocytopenia Education and Support: Insights From a Learning Exchange ProgramMichael Tarantino, David Dubinski, Corey Falcon, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Transcription Factor RUNX1 Regulates Coagulation Factor XIII-A ( <i>F13A1</i> ): Decreased Platelet-Megakaryocyte <i>F13A1</i> Expression and Clot Contraction in <i>RUNX1</i> HaplodeficiencyFabiola Del Carpio-Cano, Natthapol Songdej, Liying Guan, et al.
Biomaterials|May 8, 2021
Platelet heterogeneity enhances blood clot volumetric contraction: An example of asynchrono-mechanical amplificationYueyi Sun, David R Myers, Svetoslav V Nikolov, et al.
Nature Communications|August 31, 2019
Impaired mitochondrial calcium efflux contributes to disease progression in models of Alzheimer's diseasePooja Jadiya, Devin W Kolmetzky, Dhanendra Tomar, et al.
Research and Practice in Thrombosis and Haemostasis|February 25, 2025
Transcription factor RUNX1 regulates coagulation factor XIII-A (<i>F13A1</i>): decreased platelet-megakaryocyte <i>F13A1</i> expression and clot contraction in <i>RUNX1</i> haplodeficiencyFabiola Del Carpio-Cano, Natthapol Songdej, Liying Guan, et al.
Platelets|December 15, 2023
A case-control study of bleeding risk in children with 22q11.2 deletion syndrome undergoing cardiac surgeryT Blaine Crowley, Ian Campbell, Abinaya Arulselvan, et al.
Pageof 65

Showing results (531-540 of 644) with videos related to

Sort By:
Pageof 65
American Journal of Medical Genetics. Part A|September 24, 2018
22q and two: 22q11.2 deletion syndrome and coexisting conditionsJennifer L Cohen, Terrence B Crowley, Daniel E McGinn, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 12, 2009
AAV1/2-mediated CNS gene delivery of dominant-negative CCL2 mutant suppresses gliosis, beta-amyloidosis, and learning impairment of APP/PS1 miceTomomi Kiyota, Masaru Yamamoto, Bryce Schroder, et al.
Annals of Translational Medicine|June 19, 2018
Optimization of a microfluidics-based next generation sequencing assay for clinical oncology diagnosticsChristine Henzler, Matthew Schomaker, Rendong Yang, et al.
American Journal of Clinical Pathology|December 29, 2016
Rapid Evaluation of Platelet Function With T2 Magnetic ResonanceAdam Cuker, Holleh Husseinzadeh, Tatiana Lebedeva, et al.
Journal of the Advanced Practitioner in Oncology|April 13, 2026
Enhancing Immune Thrombocytopenia Education and Support: Insights From a Learning Exchange ProgramMichael Tarantino, David Dubinski, Corey Falcon, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Transcription Factor RUNX1 Regulates Coagulation Factor XIII-A ( <i>F13A1</i> ): Decreased Platelet-Megakaryocyte <i>F13A1</i> Expression and Clot Contraction in <i>RUNX1</i> HaplodeficiencyFabiola Del Carpio-Cano, Natthapol Songdej, Liying Guan, et al.
Biomaterials|May 8, 2021
Platelet heterogeneity enhances blood clot volumetric contraction: An example of asynchrono-mechanical amplificationYueyi Sun, David R Myers, Svetoslav V Nikolov, et al.
Nature Communications|August 31, 2019
Impaired mitochondrial calcium efflux contributes to disease progression in models of Alzheimer's diseasePooja Jadiya, Devin W Kolmetzky, Dhanendra Tomar, et al.
Research and Practice in Thrombosis and Haemostasis|February 25, 2025
Transcription factor RUNX1 regulates coagulation factor XIII-A (<i>F13A1</i>): decreased platelet-megakaryocyte <i>F13A1</i> expression and clot contraction in <i>RUNX1</i> haplodeficiencyFabiola Del Carpio-Cano, Natthapol Songdej, Liying Guan, et al.
Platelets|December 15, 2023
A case-control study of bleeding risk in children with 22q11.2 deletion syndrome undergoing cardiac surgeryT Blaine Crowley, Ian Campbell, Abinaya Arulselvan, et al.
Pageof 65