Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kumari Vadlamudi"'
Autor:
Veronica Ortega, Alka Chaubey, Christina Mendiola, William Ehman Jr., Kumari Vadlamudi, Barbara Dupont, Gopalrao Velagaleti
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 18, Iss 4, Pp 223-228 (2016)
Genomic instability is a well-known hallmark of cancer. Recent genome sequencing studies have led to the identification of novel phenomena called chromothripsis and chromoanasynthesis in which complex genomic rearrangements are thought to be derived
Externí odkaz:
https://doaj.org/article/51ddaeee4f054841adcfd6d5dd09b9dc
Autor:
Hongxin Fan, Alia Nazarullah, Preethi Dileep Menon, Kumari Vadlamudi, Daniel D. Mais, Hamza Tariq, Srilakshmi Pandeswara
Publikováno v:
Archives of Pathology & Laboratory Medicine. 146:749-754
Context.— Associations between granulomatous lobular mastitis (GLM) and Corynebacterium kroppenstedtii have been reported since 2002, but large-scale studies to assess the actual prevalence of this bacterium in GLM have not been performed. Objectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a0f892ed0103ec6a7357340955903d5
https://doi.org/10.5858/arpa.2021-0061-oa
https://doi.org/10.5858/arpa.2021-0061-oa
Autor:
Gopalrao V.N. Velagaleti, Kumari Vadlamudi, Christina Mendiola, Alka Chaubey, Veronica Ortega, Barbara Dupont, William Ehman
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 18, Iss 4, Pp 223-228 (2016)
Neoplasia (New York, N.Y.)
Neoplasia (New York, N.Y.)
Genomic instability is a well-known hallmark of cancer. Recent genome sequencing studies have led to the identification of novel phenomena called chromothripsis and chromoanasynthesis in which complex genomic rearrangements are thought to be derived
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56e550e3b3d7b69eac609a86ece86fe3
Autor:
Christina Mendiola, Gopalrao V.N. Velagaleti, Veronica Ortega, Kumari Vadlamudi, Russell A. Higgins, Gihan Mohamed, Kenneth N. Holder, Yao Wang, Hilal M. Fanasch, Hongxin Fan
Publikováno v:
European Journal of Haematology. 93:354-358
We describe a case of acute promyelocytic leukemia in a 61-yr-old woman with a cryptic insertion of RARA gene into PML gene. Using a combination of cytogenetic and molecular methods, we confirmed the insertion and presence of the PML-RARA transcript
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa0d4d433246e74084469d0230dda311
https://doi.org/10.1111/ejh.12326
https://doi.org/10.1111/ejh.12326