Afadin and RhoA control pancreatic endocrine mass via lumen morphogenesis

por Azizoglu, D. Berfin, Braitsch, Caitlin, Marciano, Denise K., Cleaver, Ondine
Publicado 2017

In Vivo Assessment of Laboratory-Grown Kidney Tissue Grafts

por Chuang, Tinghsien, Bejar, Justin, Yue, Zhiwei, Slavinsky, Mary, Marciano, Denise, Drummond, Iain, Oxburgh, Leif
Publicado 2023

cor, a Novel Carbon Monoxide Resistance Gene, Is Essential for Mycobacterium tuberculosis Pathogenesis

por Zacharia, Vineetha M., Manzanillo, Paolo S., Nair, Vidhya R., Marciano, Denise K., Kinch, Lisa N., Grishin, Nick V., Cox, Jeffery S., Shiloh, Michael U.
Publicado 2013

Listeria monocytogenes InlP interacts with afadin and facilitates basement membrane crossing

por Faralla, Cristina, Bastounis, Effie E., Ortega, Fabian E., Light, Samuel H., Rizzuto, Gabrielle, Gao, Lei, Marciano, Denise K., Nocadello, Salvatore, Anderson, Wayne F., Robbins, Jennifer R., Theriot, Julie A., Bakardjiev, Anna I.
Publicado 2018

Disruption of the beclin 1/Bcl-2 autophagy regulatory complex promotes longevity in mice

por Fernández, Álvaro F., Sebti, Salwa, Wei, Yongjie, Zou, Zhongju, Shi, Mingjun, McMillan, Kathryn L., He, Congcong, Ting, Tabitha, Liu, Yang, Chiang, Wei-Chung, Marciano, Denise K., Schiattarella, Gabriele G., Bhagat, Govind, Moe, Orson W., Hu, Ming Chang, Levine, Beth
Publicado 2018

Endogenous renal adiponectin drives gluconeogenesis through enhancing pyruvate and fatty acid utilization

por Onodera, Toshiharu, Wang, May-Yun, Rutkowski, Joseph M., Deja, Stanislaw, Chen, Shiuhwei, Balzer, Michael S., Kim, Dae-Seok, Sun, Xuenan, An, Yu A., Field, Bianca C., Lee, Charlotte, Matsuo, Ei-ichi, Mizerska, Monika, Sanjana, Ina, Fujiwara, Naoto, Kusminski, Christine M., Gordillo, Ruth, Gautron, Laurent, Marciano, Denise K., Hu, Ming Chang, Burgess, Shawn C., Susztak, Katalin, Moe, Orson W., Scherer, Philipp E.
Publicado 2023

Light-Sheet Microscopy of Cleared Tissues with Isotropic, Subcellular Resolution

por Chakraborty, Tonmoy, Driscoll, Meghan K., Jeffery, Elise, Murphy, Malea M., Roudot, Philippe, Chang, Bo-Jui, Vora, Saumya, Wong, Wen Mai, Nielson, Cara D., Zhang, Hua, Zhemkov, Vladimir, Hiremath, Chitkale, De La Cruz, Estanislao Daniel, Yating, Yi, Bezprozvanny, Ilya, Zhao, Hu, Tomer, Raju, Heintzmann, Rainer, Meeks, Julian P., Marciano, Denise K., Morrison, Sean J., Danuser, Gaudenz, Dean, Kevin M., Fiolka, Reto
Publicado 2019

Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

por Alharatani, Reham, Ververi, Athina, Beleza-Meireles, Ana, Ji, Weizhen, Mis, Emily, Patterson, Quinten T, Griffin, John N, Bhujel, Nabina, Chang, Caitlin A, Dixit, Abhijit, Konstantino, Monica, Healy, Christopher, Hannan, Sumayyah, Neo, Natsuko, Cash, Alex, Li, Dong, Bhoj, Elizabeth, Zackai, Elaine H, Cleaver, Ruth, Baralle, Diana, McEntagart, Meriel, Newbury-Ecob, Ruth, Scott, Richard, Hurst, Jane A, Au, Ping Yee Billie, Hosey, Marie Therese, Khokha, Mustafa, Marciano, Denise K, Lakhani, Saquib A, Liu, Karen J
Publicado 2020