Irina A Lubensky
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Explore the profile of Irina A Lubensky including associated specialties, affiliations and a list of published articles.
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25
Citations
437
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Recent Articles
1.
McCall S, Lubensky I, Moskaluk C, Parwani A, Radin K, Ramirez N, et al.
Mol Cancer Ther
. 2023 Jul;
22(10):1144-1153.
PMID: 37523711
The Cooperative Human Tissue Network was created by the NCI in 1987 to support a coordinated national effort to collect and distribute high quality, pathologist-validated human tissues for cancer research....
2.
Zhuang Z, Yang C, Ryska A, Ji Y, Hou Y, Graybill S, et al.
Endocr Relat Cancer
. 2016 May;
23(5):L13-6.
PMID: 27130043
No abstract available.
3.
Xu D, Dirks M, Quezado M, Lubensky I, Zhuang Z, Lonser R, et al.
Neurosurgery
. 2011 May;
69(4):E1017-21.
PMID: 21572360
Background And Importance: We present a unique case of an anterior cranial base von Hippel-Lindau disease (VHL)-associated microcystic neoplasm. To determine the lesion's relationship with VHL and its appropriate management,...
4.
Helgager J, Li J, Lubensky I, Lonser R, Zhuang Z
J Oncol
. 2010 May;
2010:373491.
PMID: 20454582
Despite resistance of most gliomas to chemotherapy, approximately 2/3 of oligodendrogliomas show sensitivity to such agents. This sensitivity has been associated with deletions on chromosome 1p alone or in combination...
5.
Lai E, Joshi B, Martiniova L, Dogra R, Fujisawa T, Leland P, et al.
J Clin Endocrinol Metab
. 2009 Jun;
94(8):2952-7.
PMID: 19491224
Context: Pheochromocytomas and paragangliomas are rare catecholamine-secreting neuroendocrine tumors arising from the adrenal medulla and sympathetic tissues. When complete surgical resection is not an option, the treatment of pheochromocytoma is...
6.
Shen H, Adem A, Ylaya K, Wilson A, He M, Lorang D, et al.
PLoS One
. 2009 Apr;
4(4):e4897.
PMID: 19340311
The von Hippel-Lindau (VHL) syndrome is a pleomorphic familial disease characterized by the development of highly vascularized tumors, such as hemangioblastomas of the central nervous system, pheochromocytomas, renal cell carcinomas,...
7.
Martiniova L, Lai E, Elkahloun A, Abu-Asab M, Wickremasinghe A, Solis D, et al.
Clin Exp Metastasis
. 2009 Jan;
26(3):239-50.
PMID: 19169894
Pheochromocytomas are chromaffin cell-derived neuroendocrine tumors. There is presently no cure for metastatic pheochromocytoma and no reliable way to distinguish malignant from benign tumors before the development of metastases. In...
8.
Lubensky I, Zhuang Z
Endocr Pathol
. 2007 Nov;
18(3):156-62.
PMID: 18041590
Gastrointestinal and pancreatic neuroendocrine tumors originate from the cells of the diffuse endocrine system. Their molecular genetic mechanism of development and progression is complex and remains largely unknown, and they...
9.
Lai E, Rodriguez O, Aventian M, Cromelin C, Fricke S, Martiniova L, et al.
Cell Cycle
. 2007 Aug;
6(15):1946-50.
PMID: 17671425
Pheochromocytoma (PCC) is a rare catecholamine-producing tumor that arises from the adrenal medulla and is often familial. The genetic basis for familial PCC involves mutations of RET, VHL, SHDx or...
10.
Park D, Zhuang Z, Chen L, Szerlip N, Maric I, Li J, et al.
PLoS Med
. 2007 Feb;
4(2):e60.
PMID: 17298169
Background: To determine the origin of the neoplastic cell in central nervous system (CNS) hemangioblastomas in von Hippel-Lindau disease (VHL) and its role in tumor formation and distribution, we characterized...