Radiation takes its Toll

Por Ratikan, Josephine A., Micewicz, Ewa D., Xie, Michael W., Schaue, Dörthe
Publicado no Cancer Lett (2015)

Regulatory T Cells in Radiotherapeutic Responses

Por Schaue, Dörthe, Xie, Michael W., Ratikan, Josephine A., McBride, William H.
Publicado em 2012

Insights into TOR function and rapamycin response: Chemical genomic profiling by using a high-density cell array method

Por Xie, Michael W., Jin, Fulai, Hwang, Heejun, Hwang, Seungmin, Anand, Vikram, Duncan, Mara C., Huang, Jing
Publicado em 2005

LC-MS characterization and purity assessment of a prototype bispecific antibody

Por Woods, R. Jeremy, Xie, Michael Hongwei, Von Kreudenstein, Thomas Spreter, Ng, Gordon Y., Dixit, Surjit B.
Publicado em 2013

Radiation & Inflammation

Por Schaue, Dörthe, Micewicz, Ewa D., Ratikan, Josephine A., Xie, Michael W., Cheng, Genhong, McBride, William H.
Publicado no Semin Radiat Oncol (2015)

Marrow-Derived Stromal Cell Delivery on Fibrin Microbeads Can Correct Radiation-Induced Wound Healing Deficits

Por Xie, Michael W, Gorodetsky, Raphael, Micevicz, Ewa, Mackenzie, Natalia C., Gaberman, Elena, Levdansky, Lilia, McBride, William H.
Publicado em 2012

Novel functions of the phosphatidylinositol metabolic pathway discovered by a chemical genomics screen with wortmannin

Por Zewail, Amani, Xie, Michael W., Xing, Yi, Lin, Lan, Zhang, P. Fred, Zou, Wei, Saxe, Jonathan P., Huang, Jing
Publicado em 2003

Mitochondrial Disease Genetic Diagnostics: Optimized whole-exome analysis for all MitoCarta nuclear genes and the mitochondrial genome

Por Falk, Marni J., Pierce, Eric A., Consugar, Mark, Xie, Michael H., Guadalupe, Moraima, Hardy, Owen, Rappaport, Eric F., Wallace, Douglas C., LeProust, Emily, Gai, Xiaowu
Publicado em 2012

Improving biophysical properties of a bispecific antibody scaffold to aid developability: Quality by molecular design

Por Von Kreudenstein, Thomas Spreter, Escobar-Carbrera, Eric, Lario, Paula I., D’Angelo, Igor, Brault, Karine, Kelly, John F, Durocher, Yves, Baardsnes, Jason, Woods, R. Jeremy, Xie, Michael Hongwei, Girod, Pierre-Alain, Suits, Michael D. L., Boulanger, Martin J., Poon, David K. Y., Ng, Gordon Y., Dixit, Surjit B.
Publicado em 2013

Cutaneous wound healing through paradoxical MAPK activation by BRAF inhibitors

Por Escuin-Ordinas, Helena, Li, Shuoran, Xie, Michael W., Sun, Lu, Hugo, Willy, Huang, Rong Rong, Jiao, Jing, de-Faria, Felipe Meira, Realegeno, Susan, Krystofinski, Paige, Azhdam, Ariel, Komenan, Sara Marie D., Atefi, Mohammad, Comin-Anduix, Begoña, Pellegrini, Matteo, Cochran, Alistair J., Modlin, Robert L., Herschman, Harvey R., Lo, Roger S., McBride, William H., Segura, Tatiana, Ribas, Antoni
Publicado no Nat Commun (2016)

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

Por Mlynarski, Elisabeth E., Xie, Michael, Taylor, Deanne, Sheridan, Molly B., Guo, Tingwei, Racedo, Silvia E., McDonald-McGinn, Donna M., Chow, Eva W. C., Vorstman, Jacob, Swillen, Ann, Devriendt, Koen, Breckpot, Jeroen, Digilio, Maria Cristina, Marino, Bruno, Dallapiccola, Bruno, Philip, Nicole, Simon, Tony J., Roberts, Amy E., Piotrowicz, Małgorzata, Bearden, Carrie E., Eliez, Stephan, Gothelf, Doron, Coleman, Karlene, Kates, Wendy R., Devoto, Marcella, Zackai, Elaine, Heine-Suñer, Damian, Goldmuntz, Elizabeth, Bassett, Anne S., Morrow, Bernice E., Emanuel, Beverly S.
Publicado no Hum Genet (2016)

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome

Por Mlynarski, Elisabeth E., Sheridan, Molly B., Xie, Michael, Guo, Tingwei, Racedo, Silvia E., McDonald-McGinn, Donna M., Gai, Xiaowu, Chow, Eva W.C., Vorstman, Jacob, Swillen, Ann, Devriendt, Koen, Breckpot, Jeroen, Digilio, Maria Cristina, Marino, Bruno, Dallapiccola, Bruno, Philip, Nicole, Simon, Tony J., Roberts, Amy E., Piotrowicz, Małgorzata, Bearden, Carrie E., Eliez, Stephan, Gothelf, Doron, Coleman, Karlene, Kates, Wendy R., Devoto, Marcella, Zackai, Elaine, Heine-Suñer, Damian, Shaikh, Tamim H., Bassett, Anne S., Goldmuntz, Elizabeth, Morrow, Bernice E., Emanuel, Beverly S.
Publicado no Am J Hum Genet (2015)