Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Lukas D, Wartman"'
Autor:
Francesca Ferraro, Agata Gruszczynska, Marianna B. Ruzinova, Christopher A. Miller, Mary Elizabeth Percival, Geoffrey L. Uy, Iskra Pusic, Meagan A. Jacoby, Mathew J. Christopher, Miriam Y. Kim, Peter Westervelt, Amanda F. Cashen, Mark A. Schroeder, John F. DiPersio, Camille N. Abboud, Lukas D. Wartman, Feng Gao, Daniel C. Link, Timothy J. Ley, John S. Welch
Publikováno v:
Haematologica, Vol 107, Iss 7 (2022)
Externí odkaz:
https://doaj.org/article/a2116fd8e43648e69c98851780c8a622
Autor:
Matthew J. Christopher, Casey D. S. Katerndahl, Hayley R. LeBlanc, Tyler T. Elmendorf, Vaishali Basu, Margery Gang, Andrew J. Menssen, David H. Spencer, Eric J. Duncavage, Shamika Ketkar, Lukas D. Wartman, Sai Mukund Ramakrishnan, Christopher A. Miller, Timothy J. Ley
Publikováno v:
Haematologica, Vol 107, Iss 1 (2021)
Externí odkaz:
https://doaj.org/article/3db7069ffa6a432d938d4fd62f49a828
Autor:
Ling Tian, Monique Chavez, Gue Su Chang, Nichole M. Helton, Casey D. S. Katerndahl, Christopher A. Miller, Lukas D. Wartman
Publikováno v:
PLoS ONE, Vol 16, Iss 11 (2021)
Kdm6a/Utx, a gene on the X chromosome, encodes a histone H3K27me3 demethylase that has an orthologue on the Y chromosome (Uty) (Zheng et al. 2018). We previously identified inactivating mutations of Kdm6a in approximately 50% of mouse acute promyeloc
Externí odkaz:
https://doaj.org/article/66701aace8f94cd5834da0a895bd2866
Autor:
Christopher A. Miller, Christopher Tricarico, Zachary L. Skidmore, Geoffrey L. Uy, Yi-Shan Lee, Anjum Hassan, Michelle D. O'Laughlin, Heather Schmidt, Ling Tian, Eric J. Duncavage, Malachi Griffith, Obi L. Griffith, John S. Welch, Lukas D. Wartman
Publikováno v:
Blood Advances, Vol 2, Iss 11, Pp 1295-1299 (2018)
Externí odkaz:
https://doaj.org/article/77dac94e86d74c30978bfc528a44e654
Autor:
Timothy J. Ley, Vaishali Basu, Christopher A. Miller, Matthew J. Christopher, David H. Spencer, Eric J. Duncavage, Casey D.S. Katerndahl, Hayley R LeBlanc, Lukas D. Wartman, Margery Gang, Andrew J. Menssen, Tyler T Elmendorf, Sai Mukund Ramakrishnan, Shamika Ketkar
Publikováno v:
Haematologica. 107:342-346
Autor:
Michelle A Cai, Timothy J. Ley, Lukas D. Wartman, Sridhar Nonavinkere Srivatsan, Timothy P Rooney, Sai Mukund Ramakrishnan, Christopher A. Miller, Nichole M. Helton, Casey D.S. Katerndahl, Ryan B. Day, Olivia R S Rogers, Mieke Hoock
Publikováno v:
Blood
Most patients with acute promyelocytic leukemia (APL) can be cured with combined all-trans retinoic acid (ATRA) and arsenic trioxide therapy, which induces the destruction of PML-RARA, the initiating fusion protein for this disease. However, the unde
Autor:
Angela M Halstead, Chiraag D Kapadia, Jennifer Bolzenius, Clarence E Chu, Andrew Schriefer, Lukas D Wartman, Gregory R Bowman, Vivek K Arora
Publikováno v:
eLife, Vol 6 (2017)
RXRA regulates transcription as part of a heterodimer with 14 other nuclear receptors, including the peroxisome proliferator-activated receptors (PPARs). Analysis from TCGA raised the possibility that hyperactive PPAR signaling, either due to PPAR ga
Externí odkaz:
https://doaj.org/article/5e55d396266f41bb8f7c93bd06a58047
Autor:
Erica K. Barnell, Zachary L. Skidmore, Kenneth F. Newcomer, Monique Chavez, Katie M. Campbell, Kelsy C. Cotto, Nicholas C. Spies, Marianna B. Ruzinova, Tianjiao Wang, Brooj Abro, Friederike Kreisel, Bijal A. Parikh, Eric J. Duncavage, John L. Frater, Yi-Shan Lee, Anjum Hassan, Justin A. King, Daniel R. Kohnen, Mark A. Fiala, John S. Welch, Geoffrey L. Uy, Kiran Vij, Ravi Vij, Malachi Griffith, Obi L. Griffith, Lukas D. Wartman
Publikováno v:
Blood advances.
Patients with multiple myeloma (MM) who are treated with lenalidomide rarely develop a secondary B-cell acute lymphoblastic leukemia (B-ALL). The clonal and biological relationship between these sequential malignancies is not yet clear. We identified
Autor:
Lauren K. Shea, Neal S. Akhave, Leslie A. Sutton, Leigh A. Compton, Conner York, Sai Mukund Ramakrishnan, Christopher A. Miller, Lukas D. Wartman, David Y. Chen
Publikováno v:
The Journal of investigative dermatology.
Cutaneous squamous cell carcinoma (cSCC) has among the highest mutation burdens of all cancers, reflecting its pathogenic association with the mutagenic effects of UV light exposure. Although mutations in cancer-relevant genes such as TP53 and NOTCH1
Autor:
Francesca Ferraro, Jacqueline E. Payton, Keegan A. Christensen, Lukas D. Wartman, Ann-Kathrin Eisfeld, Sai Mukund Ramakrishnan, Ryan B. Day, Matthew J. Christopher, Geoffrey L. Uy, Michael P. Rettig, Peter Westervelt, Matthew J. Schuelke, Catrina Fronick, Robert S. Fulton, Jack Baty, Clara D. Bloomfield, David H. Spencer, Timothy J. Ley, Christopher A. Miller, Margaret O’Laughlin, Sharon Heath, Jessica Kohlschmidt, Nichole M. Helton, John F. DiPersio, Matthew J. Walter, John S. Welch, Daniel C. Link
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Significance Current acute myeloid leukemia (AML) risk assessment relies on cytogenetics and gene-sequencing studies but is imperfect, especially for patients with normal karyotypes and intermediate risk. To understand factors associated with excelle