Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Michael J. Hamilton"'
Publikováno v:
AIMS Biophysics, Vol 2, Iss 4, Pp 794-809 (2015)
Long non-coding RNAs (lncRNAs) are a class of RNA molecules that are changing how researchers view eukaryotic gene regulation. Once considered to be non-functional products of low-level aberrant transcription from non-coding regions of the genome, ln
Externí odkaz:
https://doaj.org/article/022f3a629a4c41c3a01df83342377bb5
HOTAIRM1 lncRNA is downregulated in clear cell renal cell carcinoma and inhibits the hypoxia pathway
Autor:
Michael J. Hamilton, Thomas Girke, Kay Jang, Alexia T. King, Ernest Martinez, Silvia Sauer, Matthew D. Young, Vanessa E. Neang
Publikováno v:
Cancer Lett
HOXA Transcript Antisense RNA, Myeloid-Specific 1 (HOTAIRM1) is a conserved long non-coding RNA (lncRNA) involved in myeloid and neural differentiation that is deregulated in acute myeloid leukemia and other cancers. Previous studies focused on the n
Autor:
Joan R. Coates, Leslie A. Lyons, Robert A. Grahn, John R. Middleton, Barbara Gandolfi, N.A. Villani, Derek B. Fox, Michael J. Hamilton, S.T. Sellers, Lisa G. Britt, Reuben M. Buckley, Kari L. Chesney, S. Pfleuger
Despite the contribution of a few major genes for disproportionate dwarfism in humans, many dwarf patients are yet genetically undiagnosed. In domestic cats, disproportionate dwarfism has led to the development of a defined breed, the Munchkin or Min
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a067509764929886d249bd7b3b817c4
https://doi.org/10.1101/687210
https://doi.org/10.1101/687210
Autor:
Erica K. Creighton, Michael J. Hamilton, Clare Rusbridge, Nicholas H. Dodman, Leslie H. Bach, Richard Malik, Mona Abdi, Rashid Saif, Jared E. Decker, Jennifer D. Kurushima, Jennifer C. Grahn, Carlyn B. Peterson, G. Diane Shelton, Christopher R Helps, Maria Longeri, Leslie A. Lyons, James C. Mullikin, Hannes Lohi, Wesley C. Warren, Barbara Gandolfi, William J. Murphy, Kathryn M. Meurs, Michael J. Montague, Hasan Alhaddad, Brian W. Davis, Edward I. Ginns, Jens Häggström, Niels C Pedersen, Bianca Haase, Sara M. Nilson, Robert A. Grahn, Muhammad Wasim
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-2 (2019)
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-2 (2018)
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-2 (2018)
A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has been fixed in the paper.
Publikováno v:
Oncotarget, vol 9, iss 34
Oncotarget
Oncotarget
Extensive genome-wide analyses of deregulated gene expression have now been performed for many types of cancer. However, most studies have focused on deregulation at the gene-level, which may overlook the alterations of specific transcripts for a giv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b41e7b7fd3d2275aa4195fb24ede05b
https://escholarship.org/uc/item/2hp802xm
https://escholarship.org/uc/item/2hp802xm
Publikováno v:
Cell Transplantation, Vol 15 (2006)
As part of ongoing work to develop a method of cytokine delivery for use as an intratumoral depot, we noted that HEK293 cells, encapsulated in alginate, died within 24–48 h after in vivo, intratumoral implantation. We hypothesized that the highly h
Publikováno v:
Molecular bioSystems, vol 10, iss 4
Exploration of the ubiquitin system in eukaryotes has shown that the chemical modification of proteins by ubiquitin, known as ubiquitylation, is an incredibly important post-translational event that is crucial to numerous cellular processes. Ubiquity
Autor:
Michael J. Hamilton, Hasan Alhaddad, Barbara Gandolfi, Leslie A. Lyons, Christopher R Helps, Robert A. Grahn, Carolyn A. Erdman, Michael Carter
Publikováno v:
Lyons, L A, Erdman, C, Grahn, R, Hamilton, M, Carter, M, Helps, C R, Alhaddad, H & Gandolfi, B 2016, ' Aristaless-like homeobox protein 1 (ALX1) variant associated with craniofacial structure and frontonasal dysplasia in Burmese cats ', Developmental Biology, vol. 409, no. 2, pp. 451-458 . https://doi.org/10.1016/j.ydbio.2015.11.015
Developmental biology, vol 409, iss 2
Developmental biology, vol 409, iss 2
Frontonasal dysplasia (FND) can have severe presentations that are medically and socially debilitating. Several genes are implicated in FND conditions, including Aristaless-Like Homeobox 1 (ALX1), which is associated with FND3. Breeds of cats are sel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc27abd344b789313681eb1d72c750cf
https://hdl.handle.net/1983/71d90ec8-3416-428a-a576-2f05c3457dbe
https://hdl.handle.net/1983/71d90ec8-3416-428a-a576-2f05c3457dbe
Publikováno v:
Inorganica Chimica Acta. 369:190-196
The oxidative addition of I 2 , PhCH 2 Br and MeI with [Pt(CH 2 SiMe 3 ) 2 (DPK)], 1 , DPK = di-2-pyridyl ketone, occurred with trans stereochemistry to give [PtI 2 (CH 2 SiMe 3 ) 2 (DPK)], [PtBr(CH 2 Ph)(CH 2 SiMe 3 ) 2 (DPK)] and [PtIMe(CH 2 SiMe 3
Autor:
M. L. Wagner, Danika L. Bannasch, M. Cecilia T. Penedo, Mark Jackson, Robert C. Tryon, Michael J. Hamilton, Thomas R. Famula, Sabine Nooteboom, Stephanie J. Valberg, James R. Mickelson, Molly E. McCue
Publikováno v:
Journal of the American Veterinary Medical Association. 234:120-125
Objective—To estimate allele frequencies of the hyperkalaemic periodic paralysis (HYPP), lethal white foal syndrome (LWFS), glycogen branching enzyme deficiency (GBED), hereditary equine regional dermal asthenia (HERDA), and type 1 polysaccharide s