CHIP(−/−)-Mouse Liver: Adiponectin-AMPK-FOXO-Activation Overrides CYP2E1-Elicited JNK1-Activation, Delaying Onset of NASH: Therapeutic Implications

por Kim, Sung-Mi, Grenert, James P., Patterson, Cam, Correia, Maria Almira
Publicado 2016

Next-generation sequencing of a large uveal melanoma with whole genome doubling and a PBRM1 mutation

por Ahmad, Tessnim R., Pekmezci, Melike, Bloomer, Michele M., Grenert, James P., Afshar, Armin R.
Publicado 2023

Differential hepatotoxicity of dietary and DNL-derived palmitate in the methionine-choline-deficient model of steatohepatitis

por Pierce, Andrew A., Pickens, Michael K., Siao, Kevin, Grenert, James P., Maher, Jacquelyn J.
Publicado 2015

Heritable epigenetic mutation of MLHI in a mother and daughter with Lynch syndrome

por Blanco, Amie M, Chen, Yunn-Yi, Grenert, James P, Thibodeau, Stephen N, Terdiman, Jonathan P
Publicado 2010

TP53 structural variants in metastatic prostatic carcinoma

por Sirohi, Deepika, Devine, Patrick, Grenert, James P., van Ziffle, Jessica, Simko, Jeffry P., Stohr, Bradley A.
Publicado 2019

Racial/ethnic differences in fibrosis prevalence and progression in biopsy‐proven steatosis: A focus on the Asian American population

por Kim, Rebecca G., Chu, Janet N., Vittinghoff, Eric, Deng, Jasmine, Reaso, Jewel N., Grenert, James P., Khalili, Mandana
Publicado 2022

Well-differentiated papillary mesothelioma of the peritoneum is genetically defined by mutually exclusive mutations in TRAF7 and CDC42

por Stevers, Meredith, Rabban, Joseph T., Garg, Karuna, Van Ziffle, Jessica, Onodera, Courtney, Grenert, James P., Yeh, Iwei, Bastian, Boris C., Zaloudek, Charles, Solomon, David A.
Publicado 2018

Oligodendrogliomas, IDH-mutant and 1p/19q-codeleted, arising during teenage years often lack TERT promoter mutation that is typical of their adult counterparts

por Lee, Julieann, Putnam, Angelica R., Chesier, Samuel H., Banerjee, Anuradha, Raffel, Corey, Van Ziffle, Jessica, Onodera, Courtney, Grenert, James P., Bastian, Boris C., Perry, Arie, Solomon, David A.
Publicado 2018

Strain Background Modifies Phenotypes in the ATP8B1-Deficient Mouse

por Shah, Sohela, Sanford, Ukina R., Vargas, Julie C., Xu, Hongmei, Groen, Annamiek, Paulusma, Coen C., Grenert, James P., Pawlikowska, Ludmila, Sen, Saunak, Elferink, Ronald P. J. Oude, Bull, Laura N.
Publicado 2010

Specific Macronutrients Exert Unique Influences on the Adipose-Liver Axis to Promote Hepatic Steatosis in Mice

por Duwaerts, Caroline C., Amin, Amin M., Siao, Kevin, Her, Chris, Fitch, Mark, Beysen, Carine, Turner, Scott M., Goodsell, Amanda, Baron, Jody L., Grenert, James P., Cho, Soo-Jin, Maher, Jacquelyn J.
Publicado 2017

Adenomatoid tumors of the male and female genital tract are defined by TRAF7 mutations that drive aberrant NF-kB pathway activation

por Goode, Benjamin, Joseph, Nancy M., Stevers, Meredith, van Ziffle, Jessica, Onodera, Courtney, Talevich, Eric, Grenert, James P., Yeh, Iwei, Bastian, Boris C., Phillips, Joanna J., Garg, Karuna, Rabban, Joseph T., Zaloudek, Charles, Solomon, David A.
Publicado 2017

APOBEC Mutational Signature and Tumor Mutational Burden as Predictors of Clinical Outcomes and Treatment Response in Patients With Advanced Urothelial Cancer

por Natesan, Divya, Zhang, Li, Martell, Henry J., Jindal, Tanya, Devine, Patrick, Stohr, Bradley, Espinosa-Mendez, Carlos, Grenert, James, Van Ziffle, Jessica, Joseph, Nancy, Umetsu, Sarah, Onodera, Courtney, Turski, Michelle, Chan, Emily, Desai, Arpita, Aggarwal, Rahul, Wong, Anthony, Porten, Sima, Chou, Jonathan, Friedlander, Terence, Fong, Lawrence, Small, Eric J., Sweet-Cordero, Alejandro, Koshkin, Vadim S.
Publicado 2022

The genetic landscape of ganglioglioma

por Pekmezci, Melike, Villanueva-Meyer, Javier E., Goode, Benjamin, Van Ziffle, Jessica, Onodera, Courtney, Grenert, James P., Bastian, Boris C., Chamyan, Gabriel, Maher, Ossama M., Khatib, Ziad, Kleinschmidt-DeMasters, Bette K., Samuel, David, Mueller, Sabine, Banerjee, Anuradha, Clarke, Jennifer L., Cooney, Tabitha, Torkildson, Joseph, Gupta, Nalin, Theodosopoulos, Philip, Chang, Edward F., Berger, Mitchel, Bollen, Andrew W., Perry, Arie, Tihan, Tarik, Solomon, David A.
Publicado 2018

A recurrent kinase domain mutation in PRKCA defines chordoid glioma of the third ventricle

por Goode, Benjamin, Mondal, Gourish, Hyun, Michael, Ruiz, Diego Garrido, Lin, Yu-Hsiu, Van Ziffle, Jessica, Joseph, Nancy M., Onodera, Courtney, Talevich, Eric, Grenert, James P., Hewedi, Iman H., Snuderl, Matija, Brat, Daniel J., Kleinschmidt-DeMasters, Bette K., Rodriguez, Fausto J., Louis, David N., Yong, William H., Lopes, M. Beatriz, Rosenblum, Marc K., Butowski, Nicholas, Tihan, Tarik, Bollen, Andrew W., Phillips, Joanna J., Wiita, Arun P., Yeh, Iwei, Jacobson, Matthew P., Bastian, Boris C., Perry, Arie, Solomon, David A.
Publicado 2018