Zobrazeno 1 - 10
of 859
pro vyhledávání: '"and Andrew D. Hamilton"'
Autor:
L. Palanikumar, Laura Karpauskaite, Mohamed Al-Sayegh, Ibrahim Chehade, Maheen Alam, Sarah Hassan, Debabrata Maity, Liaqat Ali, Mona Kalmouni, Yamanappa Hunashal, Jemil Ahmed, Tatiana Houhou, Shake Karapetyan, Zackary Falls, Ram Samudrala, Renu Pasricha, Gennaro Esposito, Ahmed J. Afzal, Andrew D. Hamilton, Sunil Kumar, Mazin Magzoub
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-24 (2021)
Amyloid aggregation of mutant p53 contributes to its loss of tumor suppressor function and oncogenic gain-of-function. Here, the authors use a protein mimetic to abrogate mutant p53 aggregation and rescue p53 function, which inhibits cancer cell prol
Externí odkaz:
https://doaj.org/article/aabfbc8d47544f739652c54bd2eb3f1f
Autor:
Anja Henning-Knechtel, Sunil Kumar, Cecilia Wallin, Sylwia Król, Sebastian K.T.S. Wärmländer, Jüri Jarvet, Gennaro Esposito, Serdal Kirmizialtin, Astrid Gräslund, Andrew D. Hamilton, Mazin Magzoub
Publikováno v:
Cell Reports Physical Science, Vol 1, Iss 2, Pp 100014- (2020)
Summary: Amyloid proteins and peptides are a major contributing factor to the development of various neurodegenerative disorders, including Alzheimer’s and prion diseases. Previously, a designed cell-penetrating peptide (CPP) comprising a hydrophob
Externí odkaz:
https://doaj.org/article/5d236af9e01344af9941d4946465ac90
Autor:
Saïd M. Sebti, Jin Q. Cheng, Andrew D. Hamilton, Domenico Coppola, William J. Fulp, Y. Ann Chen, Kara D. Forinash, Maria E. Balasis
Supplementary Figures S1-S2; Supplementary Tables S1-S3.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d216809b2095fee2b72c1cb81311aac1
https://doi.org/10.1158/1078-0432.22442673
https://doi.org/10.1158/1078-0432.22442673
Autor:
Saïd M. Sebti, Jin Q. Cheng, Andrew D. Hamilton, Domenico Coppola, William J. Fulp, Y. Ann Chen, Kara D. Forinash, Maria E. Balasis
The Akt activation inhibitor triciribine and the farnesyltransferase inhibitor tipifarnib have modest to little activity in clinical trials when used as single agents. In this article, preclinical data show that the combination is more effective than
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e0895cd4b3d0ea341e7f26ac360ffdb
https://doi.org/10.1158/1078-0432.c.6519345
https://doi.org/10.1158/1078-0432.c.6519345
Autor:
Said M. Sebti, Andrew D. Hamilton, Jose G. Trevino, Jason B. Fleming, Patrick W. Underwood, Andrea Delitto, Michael P. Kim, Ya'an Kang, Francisca Beato, Harshani R. Lawrence, Christopher Cummings, Steven Fletcher, Muhammad Ayaz, Perry Kennedy, Liwei Chen, Hua Yang, Shengyan Xiang, Aslamuzzaman Kazi
Purpose:Mutant KRAS is a major driver of pancreatic oncogenesis and therapy resistance, yet KRAS inhibitors are lacking in the clinic. KRAS requires farnesylation for membrane localization and cancer-causing activity prompting the development of farn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22fe9b119d20d64790f763c5df4d19fc
https://doi.org/10.1158/1078-0432.c.6528320.v1
https://doi.org/10.1158/1078-0432.c.6528320.v1
Publikováno v:
Molecules, Vol 19, Iss 8, Pp 11316-11332 (2014)
Herein we describe the design and synthesis of a redox-dependent single-molecule switch. Appending a ferrocene unit to a diphenylacetylene scaffold gives a redox-sensitive handle, which undergoes reversible one-electron oxidation, as demonstrated by
Externí odkaz:
https://doaj.org/article/848dcffc5a534ed78552bb2299b7f17b
Autor:
Laura Karpauskaite, Ahmed J. Afzal, Ibrahim Chehade, Jemil Ahmed, Renu Pasricha, Mazin Magzoub, Andrew D. Hamilton, Debabrata Maity, Mona Kalmouni, Loganathan Palanikumar, Sunil Kumar, Maheen Alam, Tatiana Houhou, Gennaro Esposito, Zackary Falls, Shake Karapetyan, Yamanappa Hunashal, Ram Samudrala, Mohamed Al-Sayegh, Liaqat Ali, Sarah Hassan
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-24 (2021)
Nature Communications
Nature Communications
Missense mutations in p53 are severely deleterious and occur in over 50% of all human cancers. The majority of these mutations are located in the inherently unstable DNA-binding domain (DBD), many of which destabilize the domain further and expose it
Publikováno v:
Journal of the American Chemical Society. 143:3086-3093
An interruption in Aβ homeostasis leads to the deposit of neurotoxic amyloid plaques and is associated with Alzheimer's disease. A supramolecular strategy based on the assembly of peptidomimetic agents into functional vesicles has been conceived for
Autor:
Debabrata Maity, Yujeong Oh, Lothar Gremer, Wolfgang Hoyer, Mazin Magzoub, Andrew D. Hamilton
Publikováno v:
Chemistry – A European Journal. 28
Autor:
Debabrata Maity, Yujeong Oh, Lothar Gremer, Wolfgang Hoyer, Mazin Magzoub, Andrew D. Hamilton
Publikováno v:
Chemistry-a European journal 28(38), na/na (2022). doi:10.1002/chem.202201698
Two "hot segments" within an islet amyloid polypeptide are responsible for its self-assembly, which in turn is linked to the decline of β-cells in type 2 diabetes (T2D). A readily available water-soluble, macrocyclic host, cucurbit[7]uril (CB[7]), e