George Chalmers' portrait of James Lind, 1783–2008: a reconstruction

Por Peters, Linda, Hepner, John
Publicado em 2012

Nurses’ perceptions of and satisfaction with the use of automated dispensing cabinets at the Heart and Cancer Centers in Qatar: a cross-sectional study

Por Zaidan, Manal, Rustom, Fatma, Kassem, Nancy, Al Yafei, Sumaya, Peters, Linda, Ibrahim, Mohamed Izham M.
Publicado no BMC Nurs (2016)

Signatures from Tissue-specific MPSS Libraries Identify Transcripts Preferentially Expressed in the Mouse Inner Ear

Por Peters, Linda M., Belyantseva, Inna A., Lagziel, Ayala, Battey, James F., Friedman, Thomas B., Morell, Robert J.
Publicado em 2006

Development of a qPCR Method to Measure Mitochondrial and Genomic DNA Damage with Application to Chemotherapy-Induced DNA Damage and Cryopreserved Cells

Por Evans, Stephen O., Jameson, Michael B., Cursons, Ray T. M., Peters, Linda M., Bird, Steve, Jacobson, Gregory M.
Publicado no Biology (Basel) (2016)

Selection of oleaginous yeasts for fatty acid production

Por Lamers, Dennis, van Biezen, Nick, Martens, Dirk, Peters, Linda, van de Zilver, Eric, Jacobs-van Dreumel, Nicole, Wijffels, René H., Lokman, Christien
Publicado no BMC Biotechnol (2016)

Complete genome sequence of the phenanthrene-degrading soil bacterium Delftia acidovorans Cs1-4

Por Shetty, Ameesha R., de Gannes, Vidya, Obi, Chioma C., Lucas, Susan, Lapidus, Alla, Cheng, Jan-Fang, Goodwin, Lynne A., Pitluck, Samuel, Peters, Linda, Mikhailova, Natalia, Teshima, Hazuki, Han, Cliff, Tapia, Roxanne, Land, Miriam, Hauser, Loren J., Kyrpides, Nikos, Ivanova, Natalia, Pagani, Ioanna, Chain, Patrick S. G., Denef, Vincent J, Woyke, Tanya, Hickey, William J.
Publicado no Stand Genomic Sci (2015)

Mutations in Grxcr1 Are The Basis for Inner Ear Dysfunction in the Pirouette Mouse

Por Odeh, Hana, Hunker, Kristina L., Belyantseva, Inna A., Azaiez, Hela, Avenarius, Matthew R., Zheng, Lili, Peters, Linda M., Gagnon, Leona H., Hagiwara, Nobuko, Skynner, Michael J., Brilliant, Murray H., Allen, Nicholas D., Riazuddin, Saima, Johnson, Kenneth R., Raphael, Yehoash, Najmabadi, Hossein, Friedman, Thomas B., Bartles, James R., Smith, Richard J.H., Kohrman, David C.
Publicado em 2010

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

Por Bork, Julie M., Peters, Linda M., Riazuddin, Saima, Bernstein, Steve L., Ahmed, Zubair M., Ness, Seth L., Polomeno, Robert, Ramesh, Arabandi, Schloss, Melvin, Srisailpathy, C. R. Srikumari, Wayne, Sigrid, Bellman, Susan, Desmukh, Dilip, Ahmed, Zahoor, Khan, Shaheen N., Kaloustian, Vazken M. Der, Li, X. Cindy, Lalwani, Anil, Riazuddin, Sheikh, Bitner-Glindzicz, Maria, Nance, Walter E., Liu, Xue-Zhong, Wistow, Graeme, Smith, Richard J. H., Griffith, Andrew J., Wilcox, Edward R., Friedman, Thomas B., Morell, Robert J.
Publicado em 2001