T
Twala L. Hogg
Researcher at St. Jude Children's Research Hospital
Publications - 20
Citations - 4333
Twala L. Hogg is an academic researcher from St. Jude Children's Research Hospital. The author has contributed to research in topics: Sendai virus & Epitope. The author has an hindex of 16, co-authored 20 publications receiving 4085 citations. Previous affiliations of Twala L. Hogg include University of Newcastle.
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Journal ArticleDOI
A Perivascular Niche for Brain Tumor Stem Cells
Christopher Calabrese,Helen Poppleton,Mehmet Kocak,Twala L. Hogg,Christine E. Fuller,Blair Hamner,Eun Young Oh,M. Waleed Gaber,David Finklestein,Meredith Allen,Adrian J. Frank,Ildar T. Bayazitov,Stanislav S. Zakharenko,Amar Gajjar,Andrew M. Davidoff,Richard J. Gilbertson +15 more
TL;DR: This work shows that endothelial cells interact closely with self-renewing brain tumor cells and secrete factors that maintain these cells in a stem cell-like state, and proposes that brain CSCs are maintained within vascular niches that are important targets for therapeutic approaches.
Journal ArticleDOI
Subtypes of medulloblastoma have distinct developmental origins
Paul Gibson,Yiai Tong,Giles W. Robinson,Margaret C. Thompson,D. Spencer Currle,Christopher G Eden,Tanya A. Kranenburg,Twala L. Hogg,Helen Poppleton,Julie Martin,David B. Finkelstein,Stanley Pounds,Aaron Weiss,Zoltan Patay,Matthew A. Scoggins,Robert J. Ogg,Yanxin Pei,Zeng-Jie Yang,Sonja N. Brun,Youngsoo Lee,Frederique Zindy,Janet C. Lindsey,Makoto Mark Taketo,Frederick A. Boop,Robert A. Sanford,Amar Gajjar,Steven C. Clifford,Martine F. Roussel,Peter J. McKinnon,David H. Gutmann,David W. Ellison,Robert J. Wechsler-Reya,Richard J. Gilbertson +32 more
TL;DR: Evidence is provided that a discrete subtype of medulloblastoma that contains activating mutations in the WNT pathway effector CTNNB1 (hereafter, WNT subtype) arises outside the cerebellum from cells of the dorsal brainstem, the first evidence, to the authors' knowledge, that subtypes of medULLoblastomas have distinct cellular origins.
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Genomics Identifies Medulloblastoma Subgroups That Are Enriched for Specific Genetic Alterations
Margaret C. Thompson,Christine E. Fuller,Twala L. Hogg,James T. Dalton,David Finkelstein,Ching C. Lau,Murali Chintagumpala,Adekunle M. Adesina,David M. Ashley,Stewart J. Kellie,Michael D. Taylor,Tom Curran,Amar Gajjar,Richard J. Gilbertson +13 more
TL;DR: Genome-wide expression profiles can partition large tumor cohorts into subgroups that are enriched for specific genetic alterations that may assist ultimately in the selection of patients for future clinical trials of molecular targeted therapies.
Journal ArticleDOI
Cross-species genomics matches driver mutations and cell compartments to model ependymoma
Robert A. Johnson,Karen Wright,Helen Poppleton,Kumarasamypet M. Mohankumar,David Finkelstein,Stanley Pounds,Vikki Rand,Sarah Leary,Elsie White,Christopher J. Eden,Twala L. Hogg,Paul A. Northcott,Stephen C. Mack,Geoffrey Neale,Yong Dong Wang,Beth Coyle,Jennifer M. Atkinson,Mariko DeWire,Tanya A. Kranenburg,Yancey Gillespie,Jeffrey C. Allen,Thomas E. Merchant,F.A. Boop,Robert A. Sanford,Amar Gajjar,David W. Ellison,Michael D. Taylor,Richard Grundy,Richard J. Gilbertson +28 more
TL;DR: Comparison of matched mouse and human tumours revealed selective deregulation in the expression and copy number of genes that control synaptogenesis, pinpointing disruption of this pathway as a critical event in the production of this ependymoma subgroup.
Journal ArticleDOI
The MHC class l-restricted T cell response to Sendai virus infection in C57BL/6 mice: a single immunodominant epitope elicits an extremely diverse repertoire of T cells
TL;DR: The data demonstrate that a diverse repertoire of TCR is able to recognize a single MHC class I epitope and that mice make use of this potential diversity in the primary response to a natural viral infection.