Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nicole B. Halmai"'
Autor:
Margaret O’Brien, Ruth Duerr, Riley Taitingfong, Andrew Martinez, Lourdes Vera, Lydia L. Jennings, Robert R. Downs, Erin Antognoli, Talya ten Brink, Nicole B. Halmai, Dominique David-Chavez, Stephanie Russo Carroll, Maui Hudson, Pier Luigi Buttigieg
Publikováno v:
Data Science Journal, Vol 23, Pp 37-37 (2024)
Datasets carry cultural and political context at all parts of the data life cycle. Historically, Earth science data repositories have taken their guidance and policies as a combination of mandates from their funding agencies and the needs of their us
Externí odkaz:
https://doaj.org/article/6ca7b6518c0a4fef822a5a3c698dfdf7
Publikováno v:
Frontiers in Genome Editing, Vol 4 (2022)
An extensive arsenal of biosensing tools has been developed based on the clustered regularly interspaced short palindromic repeat (CRISPR) platform, including those that detect specific DNA sequences both in vitro and in live cells. To date, DNA imag
Externí odkaz:
https://doaj.org/article/20d965019e1643b1abd364af6fdf42ec
Publikováno v:
The Journal of pathology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e833ea757d01cc0084077264c499f34
https://pubmed.ncbi.nlm.nih.gov/36541926
https://pubmed.ncbi.nlm.nih.gov/36541926
Autor:
Isabelle Marty, John Rendu, Dave J. Segal, Nicole B. Halmai, Anne Petiot, Amandine Tourel, Mathilde Beaufils
Publikováno v:
Journal of Visualized Experiments.
One important application of clustered regulatory interspaced short palindromic repeats (CRISPR)/Cas 9 is the development of knock-out cell lines, specifically to study the function of new genes/proteins associated with a disease, identified during t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7f5481dbc6def57ed7e92a3cb72d7cd
https://doi.org/10.3791/64114-v
https://doi.org/10.3791/64114-v
Publikováno v:
Trends in cancer. 8(4)
Cancer health disparities define a critical healthcare issue for racial/ethnic minorities in the USA. Key findings have led to cancer treatment improvements tailored to minority patients, but such successes have been rare. Here, we highlight how the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a39b7a04376efa3ad6965228e24da50
https://pubmed.ncbi.nlm.nih.gov/35125330
https://pubmed.ncbi.nlm.nih.gov/35125330
Autor:
Graciela Molina, Carol Parra, Nicole B Halmai, Ana P Estrada, Alma Poceros, Paul Lott, Rasika Venkatesh, Enrique Norero, Osvaldo Torres, Alejandro Corvalán, Luis Carvajal-Carmona
Publikováno v:
Cancer Research. 82:5899-5899
The purpose of this study is to describe two Chilean families having Hereditary Gastric Cancer (GC). Both families present variants of uncertain significance (VUS), that could be pathogenic, but show incomplete penetrance. GC is the leading cause of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f72816bde10520b97a99f6ce2656a919
https://doi.org/10.1158/1538-7445.am2022-5899
https://doi.org/10.1158/1538-7445.am2022-5899