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G Buckley

Showing results (401-410 of 684) with videos related to

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Human Mutation|July 30, 2015
Concurrent DNA Copy-Number Alterations and Mutations in Genes Related to Maintenance of Genome Stability in Uninvolved Mammary Glandular Tissue from Breast Cancer PatientsAnna Ronowicz, Anna Janaszak-Jasiecka, Jarosław Skokowski, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 16, 2003
High- and low-risk profiles for the development of multiple sclerosis within 10 years after optic neuritis: experience of the optic neuritis treatment trialRoy W Beck, Jonathan D Trobe, Pamela S Moke, et al.
Archives of Neurology|September 15, 2004
Neurologic impairment 10 years after optic neuritisRoy W Beck, Craig H Smith, Robin L Gal, et al.
American Journal of Ophthalmology|January 1, 2004
Visual function more than 10 years after optic neuritis: experience of the optic neuritis treatment trialRoy W Beck, Robin L Gal, M Tariq Bhatti, et al.
JCI Insight|March 26, 2020
Aberrant cell migration contributes to defective airway epithelial repair in childhood wheezeThomas Iosifidis, Erika N Sutanto, Alysia G Buckley, et al.
Journal of the National Cancer Institute|July 3, 2018
Transcriptome Characterization of Matched Primary Breast and Brain Metastatic Tumors to Detect Novel Actionable TargetsDamir Varešlija, Nolan Priedigkeit, Ailís Fagan, et al.
BMC Cancer|May 1, 2026
Beyond tumors: uninvolved breast tissue of breast cancer patients with adverse prognoses is enriched for pathogenic PIK3CA and TP53 post-zygotic variantsMaria Andreou, Katarzyna Chojnowska, Natalia Filipowicz, et al.
Human Molecular Genetics|November 22, 2002
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applicationsPatrick G Buckley, Kiran K Mantripragada, Magdalena Benetkiewicz, et al.
American Journal of Human Genetics|April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromesErin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
The European Physical Journal. C, Particles and Fields|August 14, 2015
Search for the Standard Model Higgs boson produced in association with top quarks and decaying into [Formula: see text] in [Formula: see text] collisions at [Formula: see text] with the ATLAS detectorG Aad, B Abbott, J Abdallah, et al.
Pageof 69

Showing results (401-410 of 684) with videos related to

Sort By:
Pageof 69
Human Mutation|July 30, 2015
Concurrent DNA Copy-Number Alterations and Mutations in Genes Related to Maintenance of Genome Stability in Uninvolved Mammary Glandular Tissue from Breast Cancer PatientsAnna Ronowicz, Anna Janaszak-Jasiecka, Jarosław Skokowski, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 16, 2003
High- and low-risk profiles for the development of multiple sclerosis within 10 years after optic neuritis: experience of the optic neuritis treatment trialRoy W Beck, Jonathan D Trobe, Pamela S Moke, et al.
Archives of Neurology|September 15, 2004
Neurologic impairment 10 years after optic neuritisRoy W Beck, Craig H Smith, Robin L Gal, et al.
American Journal of Ophthalmology|January 1, 2004
Visual function more than 10 years after optic neuritis: experience of the optic neuritis treatment trialRoy W Beck, Robin L Gal, M Tariq Bhatti, et al.
JCI Insight|March 26, 2020
Aberrant cell migration contributes to defective airway epithelial repair in childhood wheezeThomas Iosifidis, Erika N Sutanto, Alysia G Buckley, et al.
Journal of the National Cancer Institute|July 3, 2018
Transcriptome Characterization of Matched Primary Breast and Brain Metastatic Tumors to Detect Novel Actionable TargetsDamir Varešlija, Nolan Priedigkeit, Ailís Fagan, et al.
BMC Cancer|May 1, 2026
Beyond tumors: uninvolved breast tissue of breast cancer patients with adverse prognoses is enriched for pathogenic PIK3CA and TP53 post-zygotic variantsMaria Andreou, Katarzyna Chojnowska, Natalia Filipowicz, et al.
Human Molecular Genetics|November 22, 2002
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applicationsPatrick G Buckley, Kiran K Mantripragada, Magdalena Benetkiewicz, et al.
American Journal of Human Genetics|April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromesErin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
The European Physical Journal. C, Particles and Fields|August 14, 2015
Search for the Standard Model Higgs boson produced in association with top quarks and decaying into [Formula: see text] in [Formula: see text] collisions at [Formula: see text] with the ATLAS detectorG Aad, B Abbott, J Abdallah, et al.
Pageof 69