Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Martin R. Graf"'
Autor:
Martin R. Graf, Shruti Apte, Esteban Terzo, Simran Padhye, Shuhao Shi, Megan K. Cox, Roger B. Clark, Vijay Modur, Vasudeo Badarinarayana
Publikováno v:
Journal of Molecular Medicine. 101:375-385
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f15234d1587adb9352abe4d77020c45
https://doi.org/10.1007/s00109-023-02291-x
https://doi.org/10.1007/s00109-023-02291-x
Autor:
Martin R. Graf
Publikováno v:
Encyclopedia of Clinical Neuropsychology ISBN: 9783319567822
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c3c6550c7133213d1b1981889fe916c
https://doi.org/10.1007/978-3-319-56782-2_292-2
https://doi.org/10.1007/978-3-319-56782-2_292-2
Autor:
Martin R. Graf
Publikováno v:
Encyclopedia of Clinical Neuropsychology ISBN: 9783319567822
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cafae3bb5664931fb4e5c7d77873f41
https://doi.org/10.1007/978-3-319-56782-2_351-2
https://doi.org/10.1007/978-3-319-56782-2_351-2
Autor:
Martin R. Graf, Roger M. Loria
Publikováno v:
Annals of the New York Academy of Sciences. 1262:127-133
Δ5-androstene-3β,17α-diol (17α-AED) mediates oncophagy of human myeloid, glioma, and breast tumor cells by apoptotic- and autophagic-programmed cell death pathways, whereas the 17β-epimer does not. In hematologically derived myeloid tumor cells,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b2ccf3c1d68f934ddbdd13608e76f64
https://doi.org/10.1111/j.1749-6632.2012.06602.x
https://doi.org/10.1111/j.1749-6632.2012.06602.x
Publikováno v:
Purinergic Signalling. 8:181-190
In the central nervous system, the formation of the myelin sheath and the differentiation of the myelinating cells, namely oligodendrocytes, are regulated by complex signaling networks that involve purinergic receptors and the extracellular matrix. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12f89068166f8a37bd81344093c2238d
https://doi.org/10.1007/s11302-011-9283-2
https://doi.org/10.1007/s11302-011-9283-2
Publikováno v:
The International Journal of Biochemistry & Cell Biology. 42:2019-2029
In this study, we identified a mechanism by which the neuro-steroid, 5-androstene 3β,17α diol (17α-AED) induces autophagy in human malignant glioma cells and transformed fibroblasts. 17α-AED treatment induced endoplasmic reticulum (ER) stress, id
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::793e0290156ad0f2fe77f55e0a8e25d7
https://doi.org/10.1016/j.biocel.2010.09.003
https://doi.org/10.1016/j.biocel.2010.09.003
Autor:
Mike Y. Chen, Wagner G. dos Santos, Joy L. Ware, Martin R. Graf, Aaron J. Clark, Timothy E. Van Meter, William C. Broaddus, Helen L. Fillmore
Publikováno v:
Journal of Neurosurgery. 112:18-25
Object Wilms tumor 1 (WT1) is overexpressed in many human cancers, including glioblastoma multiforme (GBM). In another study, the authors showed that transient WT1 silencing increases the radiosensitivity of glioma cells. Studies of nonglioma cell li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e566b7ab9cae83c6de3e3a0702a81c7
https://doi.org/10.3171/2008.11.jns08368
https://doi.org/10.3171/2008.11.jns08368
Publikováno v:
Chemical Biology & Drug Design. 74:625-629
Androstene steroids are metabolites of dehydroepiandrosterone and exist as androstene-diols or -triols in alpha- and beta-epimeric forms based upon the placement of the hydroxyl groups relative to the plane of the Delta(5)cycloperhydrophenanthrene ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::342f5d1e6ac7a1a57871a4d70601eb08
https://doi.org/10.1111/j.1747-0285.2009.00900.x
https://doi.org/10.1111/j.1747-0285.2009.00900.x
Autor:
Hossein A. Hamed, Martin R. Graf, Mohammed Rahmani, Paul Dent, Guo Zhang, Ray Lee, David T. Curiel, Adly Yacoub, Paul B. Fisher, Aditi Pandya Martin, Steven Grant, Clint Mitchell, John D. Roberts, Margaret A. Park
Publikováno v:
Clinical Cancer Research. 14:5385-5399
Purpose and Design: Mechanism(s) by which the multikinase inhibitor sorafenib and the histone deacetylase inhibitor vorinostat interact to kill hepatic, renal, and pancreatic adenocarcinoma cells has been defined. Results: Low doses of sorafenib and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2eb5df6eee0c358a481608816c8fd31
https://doi.org/10.1158/1078-0432.ccr-08-0469
https://doi.org/10.1158/1078-0432.ccr-08-0469