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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 Patients
Anna 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 trial
Roy W Beck, Jonathan D Trobe, Pamela S Moke, et al.
Archives of Neurology
|
September 15, 2004
Neurologic impairment 10 years after optic neuritis
Roy 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 trial
Roy 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 wheeze
Thomas 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 Targets
Damir 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 variants
Maria 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 applications
Patrick 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 syndromes
Erin 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 detector
G Aad, B Abbott, J Abdallah, et al.
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Search research articles
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Showing results (401-410 of 684) with videos related to
Sort By:
Page
of 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 Patients
Anna 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 trial
Roy W Beck, Jonathan D Trobe, Pamela S Moke, et al.
Archives of Neurology
|
September 15, 2004
Neurologic impairment 10 years after optic neuritis
Roy 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 trial
Roy 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 wheeze
Thomas 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 Targets
Damir 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 variants
Maria 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 applications
Patrick 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 syndromes
Erin 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 detector
G Aad, B Abbott, J Abdallah, et al.
Page
of 69