Rezultaty - Bekim Sadiković

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  1. 1
    Complexity in Genetic Epilepsies: A Comprehensive Review

    Complexity in Genetic Epilepsies: A Comprehensive Review od Cassandra Rastin, Laila C. Schenkel, Bekim Sadiković

    Wydane 2023
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  2. 2
    Cause and Consequences of Genetic and Epigenetic Alterations in Human Cancer

    Cause and Consequences of Genetic and Epigenetic Alterations in Human Cancer od Bekim Sadiković, Khaldoun Al‐Romaih, Jeremy A. Squire, Maria Zieleńska

    Wydane 2008
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  3. 3
    Genome-wide H3K9 Histone Acetylation Profiles Are Altered in Benzopyrene-treated MCF7 Breast Cancer Cells

    Genome-wide H3K9 Histone Acetylation Profiles Are Altered in Benzopyrene-treated MCF7 Breast Cancer Cells od Bekim Sadiković, Joseph Andrews, David M. Carter, J. Wesley Robinson, David I. Rodenhiser

    Wydane 2007
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  4. 4
    In Vitro Analysis of Integrated Global High-Resolution DNA Methylation Profiling with Genomic Imbalance and Gene Expression in Osteosarcoma

    In Vitro Analysis of Integrated Global High-Resolution DNA Methylation Profiling with Genomic Imbalance and Gene Expression in Osteosarcoma od Bekim Sadiković, Maisa Yoshimoto, Khaldoun Al‐Romaih, Georges Maire, Maria Zieleńska, Jeremy A. Squire

    Wydane 2008
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  5. 5
    Identification of interactive networks of gene expression associated with osteosarcoma oncogenesis by integrated molecular profiling

    Identification of interactive networks of gene expression associated with osteosarcoma oncogenesis by integrated molecular profiling od Bekim Sadiković, Maisa Yoshimoto, Susan Chilton‐MacNeill, Paul S. Thorner, Jeremy A. Squire, Maria Zieleńska

    Wydane 2009
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  6. 6
    Epigenetic mapping and functional analysis in a breast cancer metastasis model using whole-genome promoter tiling microarrays

    Epigenetic mapping and functional analysis in a breast cancer metastasis model using whole-genome promoter tiling microarrays od David I. Rodenhiser, Joseph Andrews, Wendy Kennette, Bekim Sadiković, Ariel Mendlowitz, Alan B. Tuck, Ann F. Chambers

    Wydane 2008
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  7. 7
    Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array

    Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array od Laila C. Schenkel, Charles E. Schwartz, Cindy Skinner, David I. Rodenhiser, Peter Ainsworth, Guillaume Paré, Bekim Sadiković

    Wydane 2016
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  8. 8
    Genomic DNA Methylation-Derived Algorithm Enables Accurate Detection of Malignant Prostate Tissues

    Genomic DNA Methylation-Derived Algorithm Enables Accurate Detection of Malignant Prostate Tissues od Erfan Aref‐Eshghi, Laila C. Schenkel, Peter Ainsworth, Hanxin Lin, David I. Rodenhiser, Jean‐Claude Cutz, Bekim Sadiković

    Wydane 2018
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  9. 9
    MALAT1: An Epigenetic Regulator of Inflammation in Diabetic Retinopathy

    MALAT1: An Epigenetic Regulator of Inflammation in Diabetic Retinopathy od Saumik Biswas, Anu Thomas, Shali Chen, Erfan Aref‐Eshghi, Biao Feng, John R. Gonder, Bekim Sadiković, Subrata Chakrabarti

    Wydane 2018
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  10. 10
    Expression analysis of genes associated with human osteosarcoma tumors shows correlation of RUNX2 overexpression with poor response to chemotherapy

    Expression analysis of genes associated with human osteosarcoma tumors shows correlation of RUNX2 overexpression with poor response to chemotherapy od Bekim Sadiković, Paul S. Thorner, Susan Chilton‐MacNeill, Jeff W. Martin, Nilva K. Cervigne, Jeremy A. Squire, Maria Zieleńska

    Wydane 2010
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  11. 11
    The Long Non-Coding RNA <i>HOTAIR</i> Is a Critical Epigenetic Mediator of Angiogenesis in Diabetic Retinopathy

    The Long Non-Coding RNA <i>HOTAIR</i> Is a Critical Epigenetic Mediator of Angiogenesis in Diabetic Retinopathy od Saumik Biswas, Biao Feng, Shali Chen, Jieting Liu, Erfan Aref‐Eshghi, John R. Gonder, Vy Ngo, Bekim Sadiković, Subrata Chakrabarti

    Wydane 2021
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  12. 12
    The defining DNA methylation signature of Floating-Harbor Syndrome

    The defining DNA methylation signature of Floating-Harbor Syndrome od Rebecca L. Hood, Laila C. Schenkel, Sarah M. Nikkel, Peter Ainsworth, Guillaume Paré, Kym M. Boycott, Dennis E. Bulman, Bekim Sadiković

    Wydane 2016
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  13. 13
    The Impact of Artificial Intelligence on Health Equity in Oncology: Scoping Review

    The Impact of Artificial Intelligence on Health Equity in Oncology: Scoping Review od Paul Istasy, Wen Shen Lee, Alla Iansavichene, Ross Upshur, Bishal Gyawali, Jacquelyn Burkell, Bekim Sadiković, Alejandro Lazo‐Langner, Benjamin Chin‐Yee

    Wydane 2022
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  14. 14
    Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy

    Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy od Kristin D. Kernohan, Laila C. Schenkel, Lijia Huang, Amanda Smith, Guillaume Paré, Peter Ainsworth, Kym M. Boycott, Jodi Warman‐Chardon, Bekim Sadiković

    Wydane 2016
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  15. 15
    The defining DNA methylation signature of Kabuki syndrome enables functional assessment of genetic variants of unknown clinical significance

    The defining DNA methylation signature of Kabuki syndrome enables functional assessment of genetic variants of unknown clinical significance od Erfan Aref‐Eshghi, Laila C. Schenkel, Hanxin Lin, Cindy Skinner, Peter Ainsworth, Guillaume Paré, David I. Rodenhiser, Charles E. Schwartz, Bekim Sadiković

    Wydane 2017
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  16. 16
    Peripheral blood epi-signature of Claes-Jensen syndrome enables sensitive and specific identification of patients and healthy carriers with pathogenic mutations in KDM5C

    Peripheral blood epi-signature of Claes-Jensen syndrome enables sensitive and specific identification of patients and healthy carriers with pathogenic mutations in KDM5C od Laila C. Schenkel, Erfan Aref‐Eshghi, Cindy Skinner, Peter Ainsworth, Hanxin Lin, Guillaume Paré, David I. Rodenhiser, Charles E. Schwartz, Bekim Sadiković

    Wydane 2018
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  17. 17
    An Approach to the Investigation of Thrombocytosis: Differentiating between Essential Thrombocythemia and Secondary Thrombocytosis

    An Approach to the Investigation of Thrombocytosis: Differentiating between Essential Thrombocythemia and Secondary Thrombocytosis od Ala Almanaseer, Benjamin Chin‐Yee, Jenny Ho, Alejandro Lazo‐Langner, Laila C. Schenkel, Pratibha Bhai, Bekim Sadiković, Ian Chin‐Yee, Cyrus C. Hsia

    Wydane 2024
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  18. 18
    Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes

    Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes od Bekim Sadiković, Jing Wang, Ayman W. El‐Hattab, Megan Landsverk, Ganka Douglas, Ellen K. Brundage, William J. Craigen, Eric Schmitt, Lee‐Jun C. Wong

    Wydane 2010
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  19. 19
    Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders

    Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders od Erfan Aref‐Eshghi, Laila C. Schenkel, Hanxin Lin, Cindy Skinner, Peter Ainsworth, Guillaume Paré, Victoria Mok Siu, David I. Rodenhiser, Charles E. Schwartz, Bekim Sadiković

    Wydane 2017
    Dokumenty pełnotekstowe Dokumenty pełnotekstowe
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  20. 20
    Mutation Update for UBE3A Variants in Angelman Syndrome

    Mutation Update for UBE3A Variants in Angelman Syndrome od Bekim Sadiković, Priscilla H. Fernandes, Victor Wei Zhang, Patricia A. Ward, Irene Miloslavskaya, William J. Rhead, Richard B. Rosenbaum, Robert Gin, Benjamin B. Roa, Ping Fang

    Wydane 2014
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