Search Results - "Banaszak, Lauren G."

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    Circulating exosomal microRNAs in acquired aplastic anemia and myelodysplastic syndromes by Giudice, Valentina, Banaszak, Lauren G, Gutierrez-Rodrigues, Fernanda, Kajigaya, Sachiko, Panjwani, Reema, Ibanez, Maria Del Pilar Fernandez, Rios, Olga, Bleck, Christopher K, Stempinski, Erin S, Raffo, Diego Quinones, Townsley, Danielle M, Young, Neal S

    Published in Haematologica (Roma) (01-07-2018)
    “…Exosomal microRNAs modulate cancer cell metabolism and the immune response. Specific exosomal microRNAs have been reported to be reliable biomarkers of several…”
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    Neighborhood disadvantage, insurance status, and molecular profiling of patients with acute myeloid leukemia by Bade, Rory, Banaszak, Lauren G., Osman, Fauzia, Cabral, Paloma, Hassan, Ayesha, Stepanovic, Adam, Reinig, Erica, Mattison, Ryan J.

    Published in Leukemia research (01-08-2023)
    “…Next-generation sequencing (NGS) is important for prognostication and determining eligibility for targeted therapies in acute myeloid leukemia (AML). The use…”
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    Clinical utility and real-world application of molecular genetic sequencing in the management of patients with acute myeloid leukemia and myelodysplastic syndromes by Banaszak, Lauren G., Reinig, Erica, Lasarev, Michael R., Mattison, Ryan J.

    Published in Leukemia & lymphoma (23-02-2022)
    “…Recurrently mutated genes in acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS) have proven useful in risk stratification and clinical…”
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    Role of ASXL1 in hematopoiesis and myeloid diseases by Gao, Xin, You, Xiaona, Droin, Nathalie, Banaszak, Lauren G., Churpek, Jane, Padron, Eric, Geissler, Klaus, Solary, Eric, Patnaik, Mrinal M., Zhang, Jing

    Published in Experimental hematology (01-11-2022)
    “…•ASXL1 hotspot mutations around codon G646 are prevalent in myeloid diseases but are rarely identified in clonal hematopoiesis of indeterminate potential,…”
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    CRISPR/Cas9-mediated ASXL1 mutations in U937 cells disrupt myeloid differentiation by Wu, Zhi-Jie, Zhao, Xin, Banaszak, Lauren G, Gutierrez-Rodrigues, Fernanda, Keyvanear, Keyvan, Gao, Shou-Guo, Raffo, Diego Quinones, Kajigaya, Sachiko, Young, Neal S

    Published in International journal of oncology (01-04-2018)
    “…Additional sex combs-like 1 (ASXL1) is a well-known tumor suppressor gene and epigenetic modifier. ASXL1 mutations are frequent in myeloid malignances; these…”
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    A Comprehensive Microscopy and Peripheral Blood Smear Curriculum for Hematology Fellows by Banaszak, Lauren G, Brunner, Matthew James, Guenther, Chad, Williams, Eliot C.

    Published in Blood (02-11-2023)
    “…Background: Peripheral blood smear (PBS) analysis is an essential skill for the practicing hematologist and allows for the timely diagnosis of a variety of…”
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    Derivation of a Risk Prediction Model for Venous Thromboembolism in Adult Patients with Acute Myeloid Leukemia by McQuinn, Danielle, Banaszak, Lauren G, Cabral, Paloma L, Reinig, Erica, Hyun, Meredith, Mattison, Ryan J

    Published in Blood (02-11-2023)
    “…Background: Venous thromboembolism (VTE) is a well-established complication of malignancy associated with high morbidity. Many validated scoring systems exist…”
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    Prevalence and Spectrum of Autoimmune Diseases Among Patients with Telomere Biology Disorder by Kelly, Alaina M, Banaszak, Lauren G, Smith-Simmer, Kelcy, Shoger, Kyle, Donohue, Sarah M, Lowery, Erin, Churpek, Jane E

    Published in Blood (02-11-2023)
    “…Introduction Telomeres are the protective ends of linear chromosomes that prevent DNA degradation with each replication. Premature attrition or dysfunction of…”
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    Crispr/Cas9-Mediated ASXL1knockout in U937 Human Leukemic Cells Perturbs Myeloid Differentiation by Wu, Zhijie, Zhao, Xin, Banaszak, Lauren G., Keyvanfar, Keyvan, Kajigaya, Sachiko, Young, Neal S.

    Published in Blood (02-12-2016)
    “…Introduction.Mutations in the Additional Sex Combs Like1 (ASXL1) gene are frequent in myeloid malignances (myelodysplastic syndromes [MDS], myeloproliferative…”
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    Crispr/Cas9-Induced DNMT3A Mutations in the K562 Human Leukemic Cell Line As a Model of DNMT3A-Mutated Leukemogenesis by Banaszak, Lauren G., Giudice, Valentina, Zhao, Xin, Wu, Zhijie, Hosokawa, Kohei, Keyvanfar, Keyvan, Townsley, Danielle, Kajigaya, Sachiko, Young, Neal S.

    Published in Blood (02-12-2016)
    “…Background:DNA methyltransferase 3A(DNMT3A) is a member of the DNA methyltransferase family primarily involved in de novo gene methylation. Mutations in DNMT3A…”
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