Resultats de la cerca - Alison A. Bertuch

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  1. 1
    EXO1 Contributes to Telomere Maintenance in Both Telomerase-Proficient and Telomerase-Deficient Saccharomyces cerevisiae

    EXO1 Contributes to Telomere Maintenance in Both Telomerase-Proficient and Telomerase-Deficient Saccharomyces cerevisiae per Alison A. Bertuch

    Publicat 2004
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  2. 2
    The molecular genetics of the telomere biology disorders

    The molecular genetics of the telomere biology disorders per Alison A. Bertuch

    Publicat 2015
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  3. 3
    The Ku Heterodimer Performs Separable Activities at Double-Strand Breaks and Chromosome Termini

    The Ku Heterodimer Performs Separable Activities at Double-Strand Breaks and Chromosome Termini per Alison A. Bertuch, Victoria Lundblad

    Publicat 2003
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  4. 4
    Dyskeratosis congenita as a disorder of telomere maintenance

    Dyskeratosis congenita as a disorder of telomere maintenance per Nya D. Nelson, Alison A. Bertuch

    Publicat 2011
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  5. 5
    Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

    Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy per M. Monica Gramatges, Alison A. Bertuch

    Publicat 2013
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  6. 6
    The genetics and clinical manifestations of telomere biology disorders

    The genetics and clinical manifestations of telomere biology disorders per Sharon A. Savage, Alison A. Bertuch

    Publicat 2010
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  7. 7
    Consider the workhorse: Nonhomologous end-joining in budding yeast

    Consider the workhorse: Nonhomologous end-joining in budding yeast per Charlene H. Emerson, Alison A. Bertuch

    Publicat 2016
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  8. 8
    Specific stimulation of simian virus 40 late transcription in vitro by a cellular factor binding the simian virus 40 21-base-pair repeat promoter element.

    Specific stimulation of simian virus 40 late transcription in vitro by a cellular factor binding the simian virus 40 21-base-pair repeat promoter element. per C.H. Kim, Christian Heath, Alison A. Bertuch, Ulla Hansen

    Publicat 1987
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  9. 9
    Three novel truncating <i>TINF2</i> mutations causing severe dyskeratosis congenita in early childhood

    Three novel truncating <i>TINF2</i> mutations causing severe dyskeratosis congenita in early childhood per GS Sasa, Albert Ribes‐Zamora, ND Nelson, Alison A. Bertuch

    Publicat 2011
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  10. 10
    TRF2 Interaction with Ku Heterotetramerization Interface Gives Insight into c-NHEJ Prevention at Human Telomeres

    TRF2 Interaction with Ku Heterotetramerization Interface Gives Insight into c-NHEJ Prevention at Human Telomeres per Albert Ribes‐Zamora, Sandra M. Indiviglio, Ivana Mihalek, Christopher L. Williams, Alison A. Bertuch

    Publicat 2013
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  11. 11
    A role for heterochromatin protein 1γ at human telomeres

    A role for heterochromatin protein 1γ at human telomeres per Sı́lvia Canudas, Benjamin R. Houghtaling, Monica Bhanot, Ghadir Sasa, Sharon A. Savage, Alison A. Bertuch, Susan Smith

    Publicat 2011
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  12. 12
    Consequences of mutations in the non-coding RMRP RNA in cartilage-hair hypoplasia

    Consequences of mutations in the non-coding RMRP RNA in cartilage-hair hypoplasia per Pia Hermanns, Alison A. Bertuch, Terry Bertin, Brian Dawson, Mark E. Schmitt, Chad A. Shaw, Bernhard Zabel, Brendan Lee

    Publicat 2005
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  13. 13
    Clinical, histopathologic, and genetic features of pediatric primary myelofibrosis—An entity different from adults

    Clinical, histopathologic, and genetic features of pediatric primary myelofibrosis—An entity different from adults per Melissa R. DeLario, Andrea M. Sheehan, Ramona Ataya, Alison A. Bertuch, Carlos Gabriel Briones Vega, C. Renee Webb, Dolores López‐Terrada, Lakshmi Venkateswaran

    Publicat 2012
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  14. 14
    Structural Insights into Yeast Telomerase Recruitment to Telomeres

    Structural Insights into Yeast Telomerase Recruitment to Telomeres per Hongwen Chen, Jing Xue, Dmitri Churikov, Evan P. Hass, Shaohua Shi, Laramie D. Lemon, Pierre Luciano, Alison A. Bertuch, David C. Zappulla, Vincent Géli, Jian Wu, Ming Lei

    Publicat 2017
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  15. 15
    Poly(ADP-ribose) polymerase inhibitor ABT-888 potentiates the cytotoxic activity of temozolomide in leukemia cells: influence of mismatch repair status and <i>O</i>6-methylguanine-DNA methyltransferase activity

    Poly(ADP-ribose) polymerase inhibitor ABT-888 potentiates the cytotoxic activity of temozolomide in leukemia cells: influence of mismatch repair status and <i>O</i>6-methylguanine-... per Terzah M. Horton, Gaye Jenkins, Debananda Pati, Linna Zhang, M. Eileen Dolan, Albert Ribes‐Zamora, Alison A. Bertuch, Susan M. Blaney, Shannon L. Delaney, Madhuri Hegde, Stacey L. Berg

    Publicat 2009
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  16. 16
    Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders

    Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders per Payal P. Khincha, Alison A. Bertuch, Suneet Agarwal, Danielle M. Townsley, Neal S. Young, Sioḃán Keel, Akiko Shimamura, Farid Boulad, Tregony Simoneau, Henri Justino, Christin S. Kuo, Steven E. Artandi, Charles McCaslin, D. Cox, Sara Chaffee, Bridget F. Collins, Neelam Giri, Blanche P. Alter, Ganesh Raghu, Sharon A. Savage

    Publicat 2016
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  17. 17
    Somatic mutations and clonal hematopoiesis in congenital neutropenia

    Somatic mutations and clonal hematopoiesis in congenital neutropenia per Jun Xia, Christopher A. Miller, Jack Baty, Amrita Ramesh, Matthew Jotte, Robert S. Fulton, Tiphanie P. Vogel, Megan A. Cooper, Kelly Walkovich, Vahagn Makaryan, Audrey Anna Bolyard, Mary C. Dinauer, David B. Wilson, Adrianna Vlachos, Kasiani C. Myers, Robert Rothbaum, Alison A. Bertuch, David C. Dale, Akiko Shimamura, Laurence A. Boxer, Daniel C. Link

    Publicat 2017
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  18. 18
    Compound Heterozygous CORO1A Mutations in Siblings with a Mucocutaneous-Immunodeficiency Syndrome of Epidermodysplasia Verruciformis-HPV, Molluscum Contagiosum and Granulomatous Tuberculoid Leprosy

    Compound Heterozygous CORO1A Mutations in Siblings with a Mucocutaneous-Immunodeficiency Syndrome of Epidermodysplasia Verruciformis-HPV, Molluscum Contagiosum and Granulomatous Tu... per Asbjørg Stray‐Pedersen, Emmanuelle Jouanguy, Amandine Créquer, Alison A. Bertuch, Betty S. Brown, Shalini N. Jhangiani, Donna M. Muzny, Tomasz Gambin, Hanne Sørmo Sorte, Ghadir Sasa, Denise W. Metry, Judith Campbell, Marianna Sockrider, Megan K. Dishop, David M. Scollard, Richard A. Gibbs, Emily M. Mace, Jordan S. Orange, James R. Lupski, Jean‐Laurent Casanova, Lenora M. Noroski

    Publicat 2014
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  19. 19
    Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC)

    Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC) per Courtney D. DiNardo, Sarah A. Bannon, Mark J. Routbort, Anna R. Franklin, Maureen E. Mork, Mary Armanios, Emily M. Mace, Jordan S. Orange, Meselle Jeff‐Eke, Jane E. Churpek, Koichi Takahashi, Jeffrey L. Jorgensen, Guillermo Garcia‐Manero, Steve Kornblau, Alison A. Bertuch, Hannah Cheung, Kapil N. Bhalla, P. Andrew Futreal, Lucy A. Godley, Keyur P. Patel

    Publicat 2016
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  20. 20
    Hematologic complications with age in Shwachman-Diamond syndrome

    Hematologic complications with age in Shwachman-Diamond syndrome per Elissa Furutani, Shanshan Liu, Ashley Galvin, Sarah K. Steltz, Maggie Malsch, Sara Loveless, Leann Mount, Jordan H. Larson, Kelan Queenan, Alison A. Bertuch, Mark D. Fleming, John M. Gansner, Amy E. Geddis, Rabi Hanna, Sioḃán Keel, Bonnie Lau, Jeffrey M. Lipton, Robert B. Lorsbach, Taizo A. Nakano, Adrianna Vlachos, Winfred C. Wang, Stella M. Davies, Edie Weller, Kasiani C. Myers, Akiko Shimamura

    Publicat 2021
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