Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Samuel M. Peterson"'
Autor:
Eric J. Vallender, Charlotte E. Hotchkiss, Anne D. Lewis, Jeffrey Rogers, Joshua A. Stern, Samuel M. Peterson, Betsy Ferguson, Ken Sayers
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-13 (2023)
Abstract Pre-clinical research and development relies heavily upon translationally valid models of disease. A major difficulty in understanding the biology of, and developing treatments for, rare disease is the lack of animal models. It is important
Externí odkaz:
https://doaj.org/article/e2a4767fceee4ba6815e4c365ae0cc94
Autor:
Aparna N. Govindan, Kristin S. Fitzpatrick, Minsha Manoharan, Ian Tagge, Steven G. Kohama, Betsy Ferguson, Samuel M. Peterson, Grayson S. Wong, William D. Rooney, Byung Park, Michael K. Axthelm, Dennis N. Bourdette, Larry S. Sherman, Scott W. Wong
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 8, Iss 2, Pp 456-470 (2021)
Abstract Objective To determine whether animals with Japanese macaque encephalomyelitis (JME), a spontaneous demyelinating disease similar to multiple sclerosis (MS), harbor myelin‐specific T cells in their central nervous system (CNS) and peripher
Externí odkaz:
https://doaj.org/article/e3983dd963594c35b1d381ed7a651083
Autor:
Larry S. Sherman, Weiping Su, Amanda L. Johnson, Samuel M. Peterson, Cassandra Cullin, Tiffany Lavinder, Betsy Ferguson, Anne D. Lewis
Publikováno v:
Neurobiology of Disease, Vol 158, Iss , Pp 105465- (2021)
Pelizaeus-Merzbacher disease (PMD) is a severe hypomyelinating disorder of the central nervous system (CNS) linked to mutations in the proteolipid protein-1 (PLP1) gene. Although there are multiple animal models of PMD, few of them fully mimic the hu
Externí odkaz:
https://doaj.org/article/2d2d3e20c3af4b85b3ae0e3f5c95a2cb
Publikováno v:
BMC Genomics, Vol 20, Iss 1, Pp 1-9 (2019)
Abstract Background Non-human primates (NHPs), particularly macaques, serve as critical and highly relevant pre-clinical models of human disease. The similarity in human and macaque natural disease susceptibility, along with parallel genetic risk all
Externí odkaz:
https://doaj.org/article/27cc4cb837b947afb695e71f014464a7
Autor:
Byung Park, Dennis Bourdette, Steven G. Kohama, Samuel M. Peterson, Betsy Ferguson, Ian J. Tagge, Michael K. Axthelm, Larry S. Sherman, Kristin S. Fitzpatrick, Aparna N. Govindan, Scott W. Wong, William D. Rooney, Minsha Manoharan, Grayson S. Wong
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 8, Iss 2, Pp 456-470 (2021)
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology
Objective To determine whether animals with Japanese macaque encephalomyelitis (JME), a spontaneous demyelinating disease similar to multiple sclerosis (MS), harbor myelin‐specific T cells in their central nervous system (CNS) and periphery. Method
Autor:
Anne D. Lewis, Samuel M. Peterson, Betsy Ferguson, Lois M. A. Colgin, Margaret M L Terry, Amanda L. Johnson
Publikováno v:
Veterinary Pathology. 57:344-348
Epidermolysis bullosa simplex (EBS) is an inherited skin disorder characterized by increased skin and mucous membrane fragility. Most cases are caused by mutations in keratin 5 ( KRT5) and keratin 14 ( KRT14). Mutations of these genes result in cytos
Autor:
E. Elizabeth Patton, Alessandro Brombin, Samuel M. Peterson, John H. Postlethwait, Hannah Brunsdon
Publikováno v:
Brunsdon, H, Brombin, A, Peterson, S, Postlethwait, J H & Patton, E E 2022, ' Aldh2 is a lineage-specific metabolic gatekeeper in melanocyte stem cells ', Development . https://doi.org/10.1242/dev.200277
Development
Development
Melanocyte stem cells (McSCs) in zebrafish serve as an on-demand source of melanocytes during growth and regeneration, but metabolic programs associated with their activation and regenerative processes are not well known. Here, using live imaging cou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b278224dc94f14050dbbc0cab823f2e8
https://doi.org/10.1101/2021.09.23.461061
https://doi.org/10.1101/2021.09.23.461061
Autor:
Tiffany Lavinder, Cassandra Cullin, Anne D. Lewis, Betsy Ferguson, Larry S. Sherman, Samuel M. Peterson, Weiping Su, Amanda L. Johnson
Publikováno v:
Neurobiol Dis
Neurobiology of Disease, Vol 158, Iss, Pp 105465-(2021)
Neurobiology of Disease, Vol 158, Iss, Pp 105465-(2021)
Pelizaeus-Merzbacher disease (PMD) is a severe hypomyelinating disorder of the central nervous system (CNS) linked to mutations in the proteolipid protein-1 (PLP1) gene. Although there are multiple animal models of PMD, few of them fully mimic the hu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c920258f1bb575a24feef05673d7d18
https://europepmc.org/articles/PMC8442247/
https://europepmc.org/articles/PMC8442247/
Publikováno v:
Frontiers in Genetics, Vol 5 (2014)
The relationship between ionizing radiation (IR) and carcinogenesis is long established, but recently the association between IR and other diseases is starting to be recognized. Currently, there is limited information on the genetic mechanisms govern
Externí odkaz:
https://doaj.org/article/f831649f1186425da625c9d37baa810a
Autor:
Amanda L, Johnson, Samuel M, Peterson, Margaret M L, Terry, Betsy, Ferguson, Lois M, Colgin, Anne D, Lewis
Publikováno v:
Vet Pathol
Epidermolysis bullosa simplex (EBS) is an inherited skin disorder characterized by increased skin and mucous membrane fragility. The majority of cases are caused by mutations in keratin 5 (KRT5) and keratin 14 (KRT14). Mutations of these genes result