Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Victoria Stinnett"'
Autor:
Eitan Halper-Stromberg, Victoria Stinnett, Laura Morsberger, Aparna Pallavajjala, Mark J. Levis, Amy E. DeZern, Michelle Lei, Brian Phan, Rena R. Xian, Christopher D. Gocke, Guilin Tang, Ying S. Zou
Publikováno v:
Experimental Hematology & Oncology, Vol 13, Iss 1, Pp 1-5 (2024)
Abstract 1q jumping translocation (JT) is rare and its molecular profiles in myeloid malignancies are not well-known. This study evaluated gene mutations in 1q-JT cohorts (0.38%) from hematological malignant specimens that underwent genetic analysis
Externí odkaz:
https://doaj.org/article/77a46d40981d4860855f1a65cee2f637
Autor:
Ying S. Zou, Melanie Klausner, Jen Ghabrial, Victoria Stinnett, Patty Long, Laura Morsberger, Jaclyn B. Murry, Katie Beierl, Christopher D. Gocke, Rena R. Xian, Kevin H. Toomer, Jing Christine Ye, Robert Z. Orlowski, Carol Ann Huff, Syed Abbas Ali, Philip H. Imus, Christian B. Gocke, Guilin Tang
Publikováno v:
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-5 (2024)
Externí odkaz:
https://doaj.org/article/cab7ab5369954ec9946ccb2755f77a59
Autor:
Ying Zou, Melanie Klausner, Jen Ghabrial, Victoria Stinnett, Laura Morsberger, Patty Long, Katie Beierl, Jaclyn Murry, Christian Gocke, Christopher Gocke
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100969- (2024)
Externí odkaz:
https://doaj.org/article/fc9ce602782c41a99c5331572cd3f80d
Autor:
Anita Madison, Carolyn Applegate, Victoria Stinnett, Chantal Cross, Kamaria Cayton Vaught, Jaclyn Murry
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101558- (2024)
Externí odkaz:
https://doaj.org/article/a1f36310735c4eb78fa7aba818c5eae5
Autor:
Michael Phan, Maria A. Gomes, Victoria Stinnett, Laura Morsberger, Nicole L. Hoppman, Kathryn E. Pearce, Kirstin Smith, Brian Phan, Liqun Jiang, Ying S. Zou
Publikováno v:
Biomedicines, Vol 12, Iss 3, p 598 (2024)
Complex structural chromosome abnormalities such as chromoanagenesis have been reported in acute myeloid leukemia (AML). They are usually not well characterized by conventional genetic methods, and the characterization of chromoanagenesis structural
Externí odkaz:
https://doaj.org/article/8b773efe20884d7cacf0d9bc3f123143
Autor:
Ying S. Zou, Laura Morsberger, Melanie Hardy, Jen Ghabrial, Victoria Stinnett, Jaclyn B. Murry, Patty Long, Andrew Kim, Christine A. Pratilas, Nicolas J. Llosa, Brian H. Ladle, Kathryn M. Lemberg, Adam S. Levin, Carol D. Morris, Lisa Haley, Christopher D. Gocke, John M. Gross
Publikováno v:
Genes; Volume 14; Issue 6; Pages: 1139
Ewing sarcomas (ES) are rare small round cell sarcomas often affecting children and characterized by gene fusions involving one member of the FET family of genes (usually EWSR1) and a member of the ETS family of transcription factors (usually FLI1 or
Autor:
Aparna Pallavajjala, Lisa Haley, Victoria Stinnett, Emily Adams, Roshni Pallavajjala, Jialing Huang, Laura Morsberger, Melanie Hardy, Patty Long, Christopher D. Gocke, James R. Eshleman, Fausto J. Rodriguez, Ying S. Zou
Publikováno v:
Human pathology. 126
Molecular classification of brain neoplasms is important for diagnosis, prognosis, and treatment outcome of histologically similar tumors. Oligodendroglioma is a glioma subtype characterized by 1p/19q co-deletion and IDH1/IDH2 mutations, which predic
Autor:
Jialing Huang, Victoria Stinnett, Liqun Jiang, Supin Chen, Fausto Rodriguez, Christopher D. Gocke, Ying S. Zou
Publikováno v:
Cancer genetics.
Lynch syndrome (LS) is the most common hereditary cancer syndrome involving multiple organ systems. The mutation patterns of the involved major DNA mismatch repair (MMR) genes, namely MLH1, MSH2, MSH6, and PMS2, have not been fully elucidated. Herein
Publikováno v:
Journal of Clinical & Anatomic Pathology. 6
Autor:
Sam Dougaparsad, Lori Long, Liqun Jiang, Aparna Pallavajjala, Victoria Stinnett, Candice Ament, Alexandra Finch, Jialing Huang, Laura Morsberger, Patty Long, Rebecca Parish, Kirstin Smith, Ying S. Zou, Azin Nozari, Lisa Haley, Rebecca Park, Alison Shane, Vamsi Parimi, Melanie Hardy, Christopher D. Gocke, Emily A. Adams
Publikováno v:
The Journal of molecular diagnostics : JMD. 23(4)
Copy number variants (CNVs) and gene mutations are important for diagnosis and treatment of myeloid malignancies. In a routine clinical setting, somatic gene mutations are detected by targeted next-generation sequencing (NGS) assay, but CNVs are comm