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Haematologica|March 7, 2024
Prognostic impact of SF3B1 mutation and multilineage dysplasia in myelodysplastic syndromes with ring sideroblasts: a Mayo Clinic study of 170 informative casesFaiqa Farrukh, Maymona Abdelmagid, Abhishek Mangaonkar, et al.British Journal of Haematology|August 4, 2021
De novo isolated myeloid sarcoma: comparative analysis of survival in 19 consecutive casesKebede H Begna, Jaya Kittur, Jennifer Yui, et al.British Journal of Haematology|May 5, 2023
The clinical and molecular spectrum of ETV6 mutated myeloid neoplasmsMark Gurney, Ismahene Chekkaf, Anmol Baranwal, et al.Cell Death & Disease|November 7, 2025
The RNA N6-methyladenosine methylome coordinates long non-coding RNAs to mediate cancer drug resistance by activating PI3K signalingYanhong Tan, Changli Zhou, Sicheng Bian, et al.Leukemia & Lymphoma|October 24, 2012
Comparison of complication rates of Hickman(®) catheters versus peripherally inserted central catheters in patients with acute myeloid leukemia undergoing induction chemotherapyMing Y Lim, Aref Al-Kali, Aneel A Ashrani, et al.American Journal of Hematology|September 27, 2024
PHF6 mutations in chronic myelomonocytic leukemia identify a unique subset of patients with distinct phenotype and superior prognosisAyalew Tefferi, Saubia Fathima, Ali Khalid A Alsugair, et al.Matrix Biology : Journal of the International Society for Matrix Biology|April 2, 2018
A novel mouse model of intervertebral disc degeneration shows altered cell fate and matrix homeostasisHyowon Choi, Steven Tessier, Elizabeth S Silagi, et al.Cancer|March 19, 2016
Activity of the oral mitogen-activated protein kinase kinase inhibitor trametinib in RAS-mutant relapsed or refractory myeloid malignanciesGautam Borthakur, Leslie Popplewell, Michael Boyiadzis, et al.Blood Cancer Journal|March 3, 2021
Mayo Clinic experience with 1123 adults with acute myeloid leukemiaKebede H Begna, Walid Ali, Naseema Gangat, et al.American Journal of Clinical Pathology|May 12, 2021
Pathologic Spectrum and Molecular Landscape of Myeloid Disorders Harboring SF3B1 MutationsElise R Venable, Dong Chen, Constance P Chen, et al.Pageof 18