Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Katie L Uhl"'
Autor:
Chad R. Schultz, Ryan D. Sheldon, Huirong Xie, Elena Y. Demireva, Katie L. Uhl, Dalen W. Agnew, Dirk Geerts, André S. Bachmann
Publikováno v:
Biology Open, Vol 12, Iss 3 (2023)
Externí odkaz:
https://doaj.org/article/ff03a24cbd904c6da12eb4d5b15a39df
Autor:
Akansha S. Das, Emily C. Sherry, Robert M. Vaughan, Marian L. Henderson, Jacob Zieba, Katie L. Uhl, Olivia Koehn, Caleb P. Bupp, Surender Rajasekaran, Xiaopeng Li, Surya B. Chhetri, Sahar Nissim, Carol L. Williams, Jeremy W. Prokop
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
The small GTPase family is well-studied in cancer and cellular physiology. With 162 annotated human genes, the family has a broad expression throughout cells of the body. Members of the family have multiple exons that require splicing. Yet, the role
Externí odkaz:
https://doaj.org/article/c07fd91f53d941d8a816a9e1ed070660
Autor:
Gregory R. Keele, Jeremy W. Prokop, Hong He, Katie Holl, John Littrell, Aaron W. Deal, Yunjung Kim, Patrick B. Kyle, Esinam Attipoe, Ashley C. Johnson, Katie L. Uhl, Olivia L. Sirpilla, Seyedehameneh Jahanbakhsh, Melanie Robinson, Shawn Levy, William Valdar, Michael R. Garrett, Leah C. Solberg Woods
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Abstract Chronic kidney disease (CKD), which can ultimately progress to kidney failure, is influenced by genetics and the environment. Genes identified in human genome wide association studies (GWAS) explain only a small proportion of the heritable v
Externí odkaz:
https://doaj.org/article/6d41003b7a614d5f9d1574c3f69d76e1
Publikováno v:
Cancer Cell International, Vol 18, Iss 1, Pp 1-14 (2018)
Abstract Background Neuroblastoma (NB) is an early childhood malignancy that arises from the developing sympathetic nervous system. Harmine is a tricyclic β-carboline alkaloid isolated from the harmal plant that exhibits both cytostatic and cytotoxi
Externí odkaz:
https://doaj.org/article/034a949a8dae47a8a05142e7fd3f8755
Autor:
Sophia Y. Lunt, Dominic Sanfilippo, André S. Bachmann, Ruchir Gupta, Mara L. Leimanis, Jeremy W. Prokop, Sarah S. Comstock, Eric J. Kort, Rosemary Olivero, Nicholas L. Hartog, Katie L. Uhl, Marie Adams, Surender Rajasekaran, Caleb Bupp
Publikováno v:
Am J Physiol Lung Cell Mol Physiol
Viral infections affecting the lower respiratory tract place enormous burdens on hospitals. As neither vaccines nor antiviral agents exist for many viruses, understanding risk factors and outcomes in each patient using minimally invasive analysis, su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66131fd607c890a1c75f3ac51defb23b
https://doi.org/10.1152/ajplung.00440.2020
https://doi.org/10.1152/ajplung.00440.2020
Publikováno v:
Medical Sciences, Vol 6, Iss 3, p 65 (2018)
Osteosarcoma (OS) is the most common bone tumor in children. Polyamines (PAs) are ubiquitous cations involved in many cell processes including tumor development, invasion and metastasis. In other pediatric cancer models, inhibition of the PA biosynth
Externí odkaz:
https://doaj.org/article/70a38a54a3964e36a5ef76985e81210c
Publikováno v:
The FASEB Journal. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1782d292b74b35ed63c2f516e74e084c
https://doi.org/10.1096/fasebj.2021.35.s1.03755
https://doi.org/10.1096/fasebj.2021.35.s1.03755
Autor:
Seungtaek Kim, Jeremy Haskins, Ke Liu, Jing Xing, Xiaopeng Li, Shreya Paithankar, Meehyun Ko, Katie L. Uhl, Bin Chen
Publikováno v:
Briefings in Bioinformatics
bioRxiv
article-version (status) pre
article-version (number) 1
bioRxiv
article-version (status) pre
article-version (number) 1
The global efforts in the past few months have led to the discovery of around 200 drug repurposing candidates for COVID-19. Although most of them only exhibited moderate anti- SARS-CoV-2 activity, gaining more insights into their mechanisms of action
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42c521b9e9953e8d76520be2d9f6748a
https://doi.org/10.1101/2021.03.04.433931
https://doi.org/10.1101/2021.03.04.433931
Autor:
André S. Bachmann, Chad R. Schultz, Elizabeth VanSickle, Daniel Vogt, Austin Frisch, Daniel B. Campbell, Jeremy W. Prokop, Stephanie M. Bilinovich, Surender Rajasekaran, Katie L. Uhl, Caleb Bupp
Publikováno v:
Genes, Vol 12, Iss 470, p 470 (2021)
Genes
Volume 12
Issue 4
Genes
Volume 12
Issue 4
Ornithine decarboxylase 1 (ODC1 gene) has been linked through gain-of-function variants to a rare disease featuring developmental delay, alopecia, macrocephaly, and structural brain anomalies. ODC1 has been linked to additional diseases like cancer,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30a455b1a5300459a1fd11459f876b5e
https://www.mdpi.com/2073-4425/12/4/470
https://www.mdpi.com/2073-4425/12/4/470
Autor:
Katie L. Uhl, Esinam M. Attipoe, Shawn Levy, Katie Holl, William Valdar, Aaron Deal, Gregory R. Keele, Olivia Sirpilla, Yunjung Kim, Michael R. Garrett, Melanie Robinson, Hong He, Ashley C. Johnson, Patrick B. Kyle, John Littrell, Jeremy W. Prokop, Leah C. Solberg Woods, Seyedehameneh Jahanbakhsh
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Chronic kidney disease (CKD), which can ultimately progress to kidney failure, is influenced by genetics and the environment. Genes identified in human genome wide association studies (GWAS) explain only a small proportion of the heritable variation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fb3184cffbb906369b94679a04b581f
http://europepmc.org/articles/PMC7822875
http://europepmc.org/articles/PMC7822875