Search Results - Speck, Maren E

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  1. 1
    Runx1 dose-dependently regulates endochondral ossification during skeletal development and fracture healing

    Runx1 dose-dependently regulates endochondral ossification during skeletal development and fracture healing by Soung, Do Y, Talebian, Laleh, Matheny, Christina J, Guzzo, Rosa, Speck, Maren E, Lieberman, Jay R, Speck, Nancy A, Drissi, Hicham

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  2. 2
    Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles

    Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles by Matheny, Christina J, Speck, Maren E, Cushing, Patrick R, Zhou, Yunpeng, Corpora, Takeshi, Regan, Michael, Newman, Miki, Roudaia, Liya, Speck, Caroline L, Gu, Ting-Lei, Griffey, Stephen M, Bushweller, John H, Speck, Nancy A

    Published in The EMBO journal
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  3. 3
    T-lymphoid, megakaryocyte, and granulocyte development are sensitive to decreases in CBFβ dosage

    T-lymphoid, megakaryocyte, and granulocyte development are sensitive to decreases in CBFβ dosage by Talebian, Laleh, Li, Zhe, Guo, Yalin, Gaudet, Justin, Speck, Maren E., Sugiyama, Daisuke, Kaur, Prabhjot, Pear, Warren S., Maillard, Ivan, Speck, Nancy A.

    Published in Blood
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  4. 4
    T-lymphoid, megakaryocyte, and granulocyte development are sensitive to decreases in CBFbeta dosage

    T-lymphoid, megakaryocyte, and granulocyte development are sensitive to decreases in CBFbeta dosage by Talebian, Laleh, Li, Zhe, Guo, Yalin, Gaudet, Justin, Speck, Maren E, Sugiyama, Daisuke, Kaur, Prabhjot, Pear, Warren S, Maillard, Ivan, Speck, Nancy A

    Published in Blood
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  5. 5
    A Hypomorphic Cbfb Allele Reveals a Critical Dosage-Sensitive Function of Core Binding Factors at the Earliest Stages of T Cell Development

    A Hypomorphic Cbfb Allele Reveals a Critical Dosage-Sensitive Function of Core Binding Factors at the Earliest Stages of T Cell Development by Maillard, Ivan, Talebian, Laleh, Li, Zhe, Guo, Yalin, Sugiyama, Daisuke, Speck, Maren E., Pear, Warren S., Speck, Nancy A.

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  6. 6
    Biochemical and In Vivo Characterization of Amino Acid Substitutions in the Runx1 (AML1) Runt Domain Found in FPD/AML, AML M0, and Cleidocranial Dysplasia (CCD) Patients

    Biochemical and In Vivo Characterization of Amino Acid Substitutions in the Runx1 (AML1) Runt Domain Found in FPD/AML, AML M0, and Cleidocranial Dysplasia (CCD) Patients by Matheny, Christina J., Corpora, Takeshi, Speck, Maren E., Gu, Ting-Lei, Bushweller, John H., Speck, Nancy A.

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