Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Neetha Paul Eduthan"'
Autor:
Micah G. Donovan, Angela L. Rachubinski, Keith P. Smith, Paula Araya, Katherine A. Waugh, Belinda Enriquez-Estrada, Eleanor C. Britton, Hannah R. Lyford, Ross E. Granrath, Kyndal A. Schade, Kohl T. Kinning, Neetha Paul Eduthan, Kelly D. Sullivan, Matthew D. Galbraith, Joaquin M. Espinosa
Publikováno v:
Cell Reports, Vol 43, Iss 8, Pp 114599- (2024)
Summary: Down syndrome (DS), the genetic condition caused by trisomy 21 (T21), is characterized by delayed neurodevelopment, accelerated aging, and increased risk of many co-occurring conditions. Hypoxemia and dysregulated hematopoiesis have been doc
Externí odkaz:
https://doaj.org/article/899484d6d7604ee5ad8c1bd6d67a98fd
Autor:
Michael P. Ludwig, Matthew D. Galbraith, Neetha Paul. Eduthan, Amanda A. Hill, Michael R. Clay, Cristiam Moreno Tellez, Breelyn A. Wilky, Anthony Elias, Joaquín Maximiliano. Espinosa, Kelly D. Sullivan
Publikováno v:
Cancer Research.
Liposarcoma is the most commonly occurring soft tissue sarcoma and is frequently characterized by amplification of chromosome region 12q13-15 harboring the oncogenes MDM2 and CDK4. This unique genetic profile makes liposarcoma an attractive candidate
Autor:
Edward J. Evans, Neetha Paul-Eduthan, Junxiao Hu, Dexiang Gao, Matthew Galbraith, Joaquin Espinosa, James DeGregori
Publikováno v:
Cancer Research. 83:1510-1510
In cancer-free tissues, somatic mutations accumulate in all of us over time. In most instances, these mutations are inconsequential to cellular fitness or to overall health. However, some mutations can result in a cell having a fitness advantage over
Autor:
Marisa Gallant Stahl, Jessica R Shaw, Neetha Paul Eduthan, Angela L Rachubinski, Keith P Smith, Belinda Enriquez Estrada, Matthew D Galbraith, Ronald J Sokol, Sameer Chavan, Laura Ann Leaton, Katherine M Kichula, Paul J Norman, Jill M Norris, Edwin Liu, Joaquin M Espinosa
ObjectivesIndividuals with Down syndrome (DS) display high risk of celiac disease (CD), but the mechanisms underlying this increased susceptibility await elucidation. Here, we examined the prevalence of HLA genotypes associated with CD risk in the ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::042a99f01fa3916a7ca9b977f1767b7c
https://doi.org/10.1101/2022.09.27.22280436
https://doi.org/10.1101/2022.09.27.22280436
Publikováno v:
Health & Medicine Week; 7/21/2023, p7766-7766, 1p