A role for Ebi in neuronal cell cycle control

Por Boulton, Simon J., Brook, Adam, Staehling-Hampton, Karen, Heitzler, Pascal, Dyson, Nick
Publicado em 2000

A comprehensive library of histone mutants identifies nucleosomal residues required for H3K4 methylation

Por Nakanishi, Shima, Sanderson, Brian W, Delventhal, Kym M, Bradford, William D, Staehling-Hampton, Karen, Shilatifard, Ali
Publicado em 2008

Aneuploidy and polyploidy underlie adaptive evolution of yeast cells deprived of a conserved cytokinesis motor

Por Rancati, Giulia, Pavelka, Norman, Fleharty, Brian, Noll, Aaron, Allen, Rhonda, Walton, Kendra, Perera, Anoja, Staehling-Hampton, Karen, Seidel, Chris W., Li, Rong
Publicado em 2008

Identification of EMS-Induced Mutations in Drosophila melanogaster by Whole-Genome Sequencing

Por Blumenstiel, Justin P., Noll, Aaron C., Griffiths, Jennifer A., Perera, Anoja G., Walton, Kendra N., Gilliland, William D., Hawley, R. Scott, Staehling-Hampton, Karen
Publicado em 2009

RDH10 is essential for synthesis of embryonic retinoic acid and is required for limb, craniofacial, and organ development

Por Sandell, Lisa L., Sanderson, Brian W., Moiseyev, Gennadiy, Johnson, Teri, Mushegian, Arcady, Young, Kendra, Rey, Jean-Philippe, Ma, Jian-xing, Staehling-Hampton, Karen, Trainor, Paul A.
Publicado em 2007

A point mutation in the murine Hem1 gene reveals an essential role for Hematopoietic Protein 1 in lymphopoiesis and innate immunity

Por Park, Heon, Staehling-Hampton, Karen, Appleby, Mark W., Brunkow, Mary E., Habib, Tania, Zhang, Yi, Ramsdell, Fred, Liggitt, H. Denny, Freie, Brian, Tsang, Mark, Carlson, George, Friend, Sherree, Frevert, Charles, Iritani, Brian M.
Publicado em 2008

Osteocyte control of bone formation via sclerostin, a novel BMP antagonist

Por Winkler, David G., Sutherland, May Kung, Geoghegan, James C., Yu, Changpu, Hayes, Trenton, Skonier, John E., Shpektor, Diana, Jonas, Mechtild, Kovacevich, Brian R., Staehling-Hampton, Karen, Appleby, Mark, Brunkow, Mary E., Latham, John A.
Publicado em 2003

Mutations in the MESP2 Gene Cause Spondylothoracic Dysostosis/Jarcho-Levin Syndrome

Por Cornier, Alberto S., Staehling-Hampton, Karen, Delventhal, Kym M., Saga, Yumiko, Caubet, Jean-Francois, Sasaki, Nobuo, Ellard, Sian, Young, Elizabeth, Ramirez, Norman, Carlo, Simon E., Torres, Jose, Emans, John B., Turnpenny, Peter D., Pourquié, Olivier
Publicado em 2008