Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Stephen J. Coleman"'
Gene Expression Analysis before and after the Pelvic Flexure in the Epithelium of the Equine Hindgut
Autor:
Cameron D. Moss, Amber L. Wilson, Kailee J. Reed, Kaysie J. Jennings, Isabelle G. Z. Kunz, Gabriele A. Landolt, Jessica Metcalf, Terry E. Engle, Stephen J. Coleman
Publikováno v:
Animals, Vol 14, Iss 16, p 2303 (2024)
Previous research demonstrated the distribution of distinct microbial communities in the equine hindgut surrounding the pelvic flexure. The current study evaluated gene expression in epithelial tissues surrounding the pelvic flexure to characterize p
Externí odkaz:
https://doaj.org/article/a34ba6260e1f46c0b6feb19634086162
Autor:
Kailee J. Reed, Isabelle G. Z. Kunz, Jessica A. Scare, Martin K. Nielsen, Philip J. Turk, Robert J. Coleman, Stephen J. Coleman
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract As hindgut fermenters, horses are especially dependent on the microbiota residing in their cecum and large intestines. Interactions between these microbial populations and the horse are critical for maintaining gut homeostasis, which support
Externí odkaz:
https://doaj.org/article/3fe2af425fb74195a2d754f6ee8ebbac
Publikováno v:
PLoS ONE, Vol 8, Iss 9 (2013)
Externí odkaz:
https://doaj.org/article/8930204a177445f9a428e7f4abc7818d
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0144302 (2015)
Cellular mechanisms that achieve protein diversity in eukaryotes are multifaceted, including transcriptional components such as RNA splicing. Through alternative splicing, a single protein-coding gene can generate multiple mRNA transcripts and protei
Externí odkaz:
https://doaj.org/article/84e16b53a9ed4fb6839e22a4405adb8e
Autor:
Matthew S Hestand, Theodore S Kalbfleisch, Stephen J Coleman, Zheng Zeng, Jinze Liu, Ludovic Orlando, James N MacLeod
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0124375 (2015)
Current gene annotation of the horse genome is largely derived from in silico predictions and cross-species alignments. Only a small number of genes are annotated based on equine EST and mRNA sequences. To expand the number of equine genes annotated
Externí odkaz:
https://doaj.org/article/524dbe9465f8483bacf21ad9da477fda
Autor:
Kristin M. Klohonatz, Stephen J. Coleman, Ashley D. Cameron, Ann M. Hess, Kailee J. Reed, Angela Canovas, Juan F. Medrano, Alma D. Islas-Trejo, Ted Kalbfleisch, Gerrit J. Bouma, Jason E. Bruemmer
Publikováno v:
Genes, Vol 10, Iss 10, p 821 (2019)
Genes, vol 10, iss 10
Genes
Volume 10
Issue 10
Genes, vol 10, iss 10
Genes
Volume 10
Issue 10
Maternal recognition of pregnancy (MRP) in the mare is not well defined. In a non-pregnant mare, prostaglandin F2&alpha
(PGF) is released on day 14 post-ovulation (PO) to cause luteal regression, resulting in loss of progesterone production. Equ
(PGF) is released on day 14 post-ovulation (PO) to cause luteal regression, resulting in loss of progesterone production. Equ
Publikováno v:
Calcified Tissue International. 31:21-28
This is a study of the fine structure of cells of the 20-day fetal rat calvarium. Special attention is given to identifying and characterizing preosteoclasts. These cells are relatively common and located largely, but not exclusively, at the endocran
Publikováno v:
Cell and tissue research. 207(2)
Bone cultures exposed to prostaglandin E2 (PGE2) and revealed an increase in 45Ca release from bone to medium and an increase in osteoclast number compared to control bones. In addition, PGE2-treated osteoclasts contained a more extensive ruffled bor
Autor:
Martha J. Somerman, Susan E. Pointon, Richard L. Baker, Stephen J. Coleman, Barry R. Rifkin, William Y. W. Au
Publikováno v:
Cell and tissue research. 210(3)
For the first time, mononuclear cell-mediated ingestion of osteoid in cultures of long bones of fetal rats is described and characterized. The mononuclear cells, located at sites of osteoid deposition, ingest collagen fibrils and clumps of mineral cr
Publikováno v:
Cell and Tissue Research. 202
Ultrastructural observations on macrophage-mediated resorption of calcified tissue of killed fetal long bones are described and correlated with increased 45Ca release into the medium. Macrophages disrupt calcified tissue extracellularly and appear to