Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Stephanie A. Smoley"'
Autor:
Beth A. Pitel, Cinthya Zepeda-Mendoza, Zohar Sachs, Hongwei Tang, Suganti Shivaram, Neeraj Sharma, James B. Smadbeck, Stephanie A. Smoley, Kathryn E. Pearce, Ivy M. Luoma, Joselle Cook, Mark R. Litzow, Nicole L. Hoppman, David Viswanatha, Xinjie Xu, Rhett P. Ketterling, Patricia T. Greipp, Jess F. Peterson, Linda B. Baughn
Publikováno v:
Blood Cancer Journal, Vol 13, Iss 1, Pp 1-5 (2023)
Externí odkaz:
https://doaj.org/article/aeebb67adf5c4359bd02b1d433a4766a
Autor:
Cinthya J. Zepeda‐Mendoza, Anna Essendrup, Stephanie A. Smoley, Sarah H. Johnson, Nicole L Hoppman, George Vasmatzis, Daniel L. Jackson, Hutton M. Kearney, Linda B. Baughn
Publikováno v:
Clinical Case Reports, Vol 9, Iss 2, Pp 769-774 (2021)
Abstract This case report underlines the importance of molecular characterization of genomic duplications and other structural variants in the prenatal setting to guide clinical interpretation, genetic counseling, and perinatal medical care.
Externí odkaz:
https://doaj.org/article/b75342e9196e4580a66a44c90a6d35e5
Autor:
Rebecca L. King, Ellen D. McPhail, Reid G. Meyer, George Vasmatzis, Kathryn Pearce, James B. Smadbeck, Rhett P. Ketterling, Stephanie A. Smoley, Patricia T. Greipp, Nicole L. Hoppman, Jess F. Peterson, Linda B. Baughn
Publikováno v:
Haematologica, Vol 104, Iss 6 (2019)
Externí odkaz:
https://doaj.org/article/acb63e03c7564ff89768796ed27b31a1
Autor:
Wei Shen, Heidi L. Sellers, Lauren A. Choate, Mariam I. Stein, Pratyush P. Tandale, Jiayu Tan, Rohit Setlem, Yuta Sakai, Numrah Fadra, Carlos Sosa, Shawn P. McClelland, Sarah S. Barnett, Kristen J. Rasmussen, Cassandra K. Runke, Stephanie A. Smoley, Lori S. Tillmans, Cherisse A. Marcou, Ross A. Rowsey, Erik C. Thorland, Nicole J. Boczek, Hutton M. Kearney
Publikováno v:
The Journal of Molecular Diagnostics.
Autor:
Linda B. Baughn, Anna Essendrup, Cinthya J. Zepeda-Mendoza, Hutton M. Kearney, Daniel L. Jackson, Nicole L. Hoppman, George Vasmatzis, Stephanie A. Smoley, Sarah Johnson
Publikováno v:
Clinical Case Reports, Vol 9, Iss 2, Pp 769-774 (2021)
Clinical Case Reports
Clinical Case Reports
This case report underlines the importance of molecular characterization of genomic duplications and other structural variants in the prenatal setting to guide clinical interpretation, genetic counseling, and perinatal medical care.
Autor:
George Vasmatzis, Stephanie A. Smoley, Cynthia M. Williamson, Patricia T. Greipp, Yi Ning, Nicole L. Hoppman, Ross A. Rowsey, Jess F. Peterson, Linda B. Baughn, James B. Smadbeck, Rhett P. Ketterling
Publikováno v:
Blood Cancer Journal, Vol 9, Iss 10, Pp 1-8 (2019)
Blood Cancer Journal
Blood Cancer Journal
The TCF3/PBX1 gene fusion is a recurrent genetic abnormality in pediatric B-lymphoblastic leukemia/lymphoma (B-ALL/LBL). While dual-color, dual-fusion fluorescence in situ hybridization (D-FISH) probes can detect TCF3/PBX1 fusions, further characteri
Autor:
George Vasmatzis, Fiona E. Craig, Stephanie A. Smoley, James B. Smadbeck, Reid G. Meyer, Patricia T. Greipp, Linda B. Baughn, Rhett P. Ketterling, Matthew Webley, Kathryn E. Pearce, A. Keith Stewart, Jess F. Peterson
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 19:598-602
Autor:
James B. Smadbeck, Linda B. Baughn, Patricia T. Greipp, Ivy Luoma, Beth A. Pitel, George Vasmatzis, Stephanie A. Smoley, Jess F. Peterson, Jonna C. Benevides Demasi, Tong Yang, Rhett P. Ketterling, Christopher S. Rice
Publikováno v:
Journal of Hematopathology. 12:99-104
The detection of recurrent chromosomal rearrangements in B-lymphoblastic leukemia/lymphoma (B-ALL/LBL) is critical for patient management decisions. We present a newly diagnosed case of B-ALL in a young adult with a cryptic KMT2A/AFF1 fusion that was
Autor:
Beth A. Pitel, William R. Sukov, Nicole L. Hoppman, Reid G. Meyer, Kathryn E. Pearce, Rhett P. Ketterling, Linda B. Baughn, Patricia T. Greipp, Jess F. Peterson, George Vasmatzis, Stephanie A. Smoley, Cynthia M. Williamson, James B. Smadbeck
Publikováno v:
Genes, Chromosomes and Cancer. 58:567-577
The MLLT10 (formerly AF10) gene is the fourth most common KMT2A fusion partner across all acute leukemias and requires at least 3 breaks to form an in-frame KMT2A/MLLT10 fusion due to the opposite orientation of each gene. A 10-year retrospective rev
Autor:
Michelle K. Bianco, Jess F. Peterson, Prasuna Muppa, Beth A. Pitel, Daniel L. Van Dyke, William R. Sukov, James B. Smadbeck, Linda B. Baughn, George Vasmatzis, Stephanie A. Smoley, Rhett P. Ketterling, Patricia T. Greipp
Publikováno v:
Journal of Hematopathology. 12:85-90
Per the 2017 WHO, several translocations have been described that are sufficient for the diagnosis of acute myeloid leukemia with myelodysplasia-related changes (AML-MRC) (assuming no prior therapy and ≥ 20% myeloblasts present in blood or bone mar