Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mirna Lechpamme"'
Autor:
Mirna Lechpammer, Austin Todd, Vivian Tang, Taryn Morningstar, Alexander Borowsky, Kiarash Shahlaie, John A. Kintner, John D. McPherson, John W. Bishop, Farzad Fereidouni, Zachary T. Harmany, Nicholas Coley, David Zagzag, Jason W. H. Wong, Jiang Tao, Luke B. Hesson, Leslie Burnett, Richard Levenson
Publikováno v:
Brain Sciences, Vol 14, Iss 1, p 108 (2024)
Whereas traditional histology and light microscopy require multiple steps of formalin fixation, paraffin embedding, and sectioning to generate images for pathologic diagnosis, Microscopy using Ultraviolet Surface Excitation (MUSE) operates through UV
Externí odkaz:
https://doaj.org/article/199e9290e30d41d68253f83c6c595d64
Autor:
Amir Ghorbani-Aghbolaghia, Mirna Lechpammer, Saba F. Ali, Nam K. Ku, Denis M. Dwyre, Hooman H. Rashidi
Publikováno v:
Autopsy and Case Reports, Vol 7, Iss 3 (2017)
BRAF protein is a serine/threonine kinase with 766 amino acids. Approximately 15% of human cancers harbor BRAF mutations as well as other BRAF anomalies (amplifications, fusions). Somatic mutations mainly occur in the catalytic kinase domain (CR3), a
Externí odkaz:
https://doaj.org/article/3289f737cb7242b6bece71830e542d3e
Publikováno v:
Autopsy and Case Reports, Vol 7, Iss 2 (2017)
Centronuclear myopathy (CNM) is a group of rare genetic muscle disorders characterized by muscle fibers with centrally located nuclei. The most common forms of CNM have been attributed to X-linked recessive mutations in the MTM1 gene; autosomal-domin
Externí odkaz:
https://doaj.org/article/6d2f94cc2afd4faca2a2afeec51a3287
Autor:
Audrey E. Arzamendi, Kiarash Shahlaie, Richard E. Latchaw, Mirna Lechpammer, Hasmik Arzumanyan
Publikováno v:
Journal of Neurological Surgery Reports, Vol 77, Iss 03, Pp e113-e117 (2016)
Abstract Objective To describe the work-up and treatment of rare ectopic acromegaly caused by a biopsy-proven somatotroph pituitary adenoma located within the bony intersphenoid septum of a patient with empty sella syndrome (ESS). Methods We repo
Externí odkaz:
https://doaj.org/article/9b870e89a0c04055ae0b1497446d4871
Autor:
Jonathan Liu, Arjang Ahmadpour, Arnaud F. Bewley, Mirna Lechpammer, Matthew Bobinski, Kiarash Shahlaie
Publikováno v:
Journal of Neurological Surgery Reports, Vol 76, Iss 02, Pp e258-e264 (2015)
Abstract Background and Importance Chondroblastoma is a benign primary bone tumor that typically develops in the epiphyses of long bones. Chondroblastoma of the craniofacial skeleton is extremely rare, with most cases occurring in the squamosal por
Externí odkaz:
https://doaj.org/article/b598f43d637247448c65bed1d409776c
Autor:
Vivian Tang, Peter Michael Conner, Jason Paul Tovar, Regina Frances Gandour-Edwards, Reuben Antony, Matthew Bobinsk, Michael Steven Brent Edwards, Mirna Lechpamme
Publikováno v:
Autopsy and Case Reports, Vol 10, Iss 4 (2021)
Atypical teratoid/rhabdoid tumor (AT/RT) is a rare central nervous system (CNS) tumor diagnosed primarily in infants and usually portends a poor prognosis. Despite being the most common embryonal tumor in children less than 1 year old, diagnosis is d
Externí odkaz:
https://doaj.org/article/b17f088a19534822b886dc96f0e9dee4
Autor:
Zachary Rabow, Taryn Morningstar, Megan Showalter, Hailey Heil, Krista Thongphanh, Sili Fan, Joanne Chan, Verónica Martínez‐Cerdeño, Robert Berman, David Zagzag, Evgeny Nudler, Oliver Fiehn, Mirna Lechpammer
Publikováno v:
Brain and Behavior, Vol 11, Iss 5, Pp n/a-n/a (2021)
Abstract Introduction Dimethyl sulfoxide (DMSO) is a widely used solvent to dissolve hydrophobic substances for clinical uses and experimental in vivo purposes. While usually regarded safe, our prior studies suggest changes to behavior following DMSO
Externí odkaz:
https://doaj.org/article/a4d815b214e5429eb73f8d5f28facfbb
Publikováno v:
PLoS Biology, Vol 1, Iss 3, p E83 (2003)
Biallelic inactivation of the von Hippel-Lindau tumor suppressor gene (VHL) is linked to the development of hereditary (VHL-associated) and sporadic clear-cell renal carcinomas as well as other abnormalities. The VHL gene product, pVHL, is part of an
Externí odkaz:
https://doaj.org/article/e63ad86c3bab49329d1b92b697a9a1d3