Calpain 3 and CaMKIIβ signaling are required to induce HSP70 necessary for adaptive muscle growth after atrophy

por Kramerova, Irina, Torres, Jorge A, Eskin, Ascia, Nelson, Stanley F, Spencer, Melissa J
Publicado 2018

Characterization of three cell lines derived from fine needle biopsy of choroidal melanoma with metastatic outcome

por Burgess, Barry L., Rao, Nagesh P., Eskin, Ascia, Nelson, Stanley F., McCannel, Tara A.
Publicado 2011

U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line

por Clark, Michael James, Homer, Nils, O'Connor, Brian D., Chen, Zugen, Eskin, Ascia, Lee, Hane, Merriman, Barry, Nelson, Stanley F.
Publicado 2010

Correction: U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line

por Clark, Michael James, Homer, Nils, O'Connor, Brian D., Chen, Zugen, Eskin, Ascia, Lee, Hane, Merriman, Barry, Nelson, Stanley F.
Publicado 2018

Decitabine immunosensitizes human gliomas to NY-ESO-1 specific T lymphocyte targeting through the Fas/Fas Ligand pathway

por Konkankit, Veerauo V, Kim, Won, Koya, Richard C, Eskin, Ascia, Dam, Mai-Anh, Nelson, Stanley, Ribas, Antoni, Liau, Linda M, Prins, Robert M
Publicado 2011

Sex-Specific Effects of Testosterone on the Sexually Dimorphic Transcriptome and Epigenome of Embryonic Neural Stem/Progenitor Cells

por Bramble, Matthew S., Roach, Lara, Lipson, Allen, Vashist, Neerja, Eskin, Ascia, Ngun, Tuck, Gosschalk, Jason E., Klein, Steven, Barseghyan, Hayk, Arboleda, Valerie A., Vilain, Eric
Publicado 2016

Stem cell associated gene expression in glioblastoma multiforme: relationship to survival and the subventricular zone

por Kappadakunnel, Melanie, Eskin, Ascia, Dong, Jun, Nelson, Stanley F., Mischel, Paul S., Liau, Linda M., Ngheimphu, Phioanh, Lai, Albert, Cloughesy, Timothy F., Goldin, Jonathan, Pope, Whitney B.
Publicado 2009

Loss of the scavenger mRNA decapping enzyme DCPS causes syndromic intellectual disability with neuromuscular defects

por Ng, Calista K.L., Shboul, Mohammad, Taverniti, Valerio, Bonnard, Carine, Lee, Hane, Eskin, Ascia, Nelson, Stanley F., Al-Raqad, Mohammed, Altawalbeh, Samah, Séraphin, Bertrand, Reversade, Bruno
Publicado 2015

Downregulation of SATB1 by miRNAs reduces megakaryocyte/erythroid progenitor expansion in preclinical models of Diamond–Blackfan anemia

por Wilkes, Mark C., Scanlon, Vanessa, Shibuya, Aya, Cepika, Alma-Martina, Eskin, Ascia, Chen, Zugen, Narla, Anupama, Glader, Bert, Roncarolo, Maria Grazia, Nelson, Stanley F., Sakamoto, Kathleen M.
Publicado 2022

Feedback modulation of cholesterol metabolism by LeXis, a lipid-responsive non-coding RNA

por Sallam, Tamer, Jones, Marius, Gilliland, Thomas, Zhang, Li, Wu, Xiaohui, Eskin, Ascia, Sandhu, Jaspreet, Casero, David, de Aguiar Vallim, Thomas, Hong, Cynthia, Katz, Melanie, Lee, Richard, Whitelegge, Julian, Tontonoz, Peter
Publicado 2016

Identification of novel candidate genes for 46,XY disorders of sex development (DSD) using a C57BL/6J-Y(POS) mouse model

por Barseghyan, Hayk, Symon, Aleisha, Zadikyan, Mariam, Almalvez, Miguel, Segura, Eva E., Eskin, Ascia, Bramble, Matthew S., Arboleda, Valerie A., Baxter, Ruth, Nelson, Stanley F., Délot, Emmanuèle C., Harley, Vincent, Vilain, Eric
Publicado 2018

DMD genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtype

por Wang, Richard T., Barthelemy, Florian, Martin, Ann S., Douine, Emilie D., Eskin, Ascia, Lucas, Ann, Lavigne, Jenifer, Peay, Holly, Khanlou, Negar, Sweeney, Lee, Cantor, Rita M., Miceli, M. Carrie, Nelson, Stanley F.
Publicado 2018

Online Self-Report Data for Duchenne Muscular Dystrophy Confirms Natural History and Can Be Used to Assess for Therapeutic Benefits

por Wang, Richard T., Silverstein Fadlon, Cheri A., Ulm, J. Wes, Jankovic, Ivana, Eskin, Ascia, Lu, Ake, Rangel Miller, Vanessa, Cantor, Rita M., Li, Ning, Elashoff, Robert, Martin, Anne S., Peay, Holly L., Halnon, Nancy, Nelson, Stanley F.
Publicado 2014

A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability

por Chia, Poh Hui, Zhong, Franklin Lei, Niwa, Shinsuke, Bonnard, Carine, Utami, Kagistia Hana, Zeng, Ruizhu, Lee, Hane, Eskin, Ascia, Nelson, Stanley F, Xie, William H, Al-Tawalbeh, Samah, El-Khateeb, Mohammad, Shboul, Mohammad, Pouladi, Mahmoud A, Al-Raqad, Mohammed, Reversade, Bruno
Publicado 2018

IL-17A is increased in the serum and in spinal cord CD8 and mast cells of ALS patients

por Fiala, Milan, Chattopadhay, Madhuri, La Cava, Antonio, Tse, Eric, Liu, Guanghao, Lourenco, Elaine, Eskin, Ascia, Liu, Philip T, Magpantay, Larry, Tse, Stephen, Mahanian, Michelle, Weitzman, Rachel, Tong, Jason, Nguyen, Caroline, Cho, Tiffany, Koo, Patrick, Sayre, James, Martinez-Maza, Otoniel, Rosenthal, Mark J, Wiedau-Pazos, Martina
Publicado 2010

Metabolic characterization of isocitrate dehydrogenase (IDH) mutant and IDH wildtype gliomaspheres uncovers cell type-specific vulnerabilities

por Garrett, Matthew, Sperry, Jantzen, Braas, Daniel, Yan, Weihong, Le, Thuc M., Mottahedeh, Jack, Ludwig, Kirsten, Eskin, Ascia, Qin, Yue, Levy, Rachelle, Breunig, Joshua J., Pajonk, Frank, Graeber, Thomas G., Radu, Caius G., Christofk, Heather, Prins, Robert M., Lai, Albert, Liau, Linda M., Coppola, Giovanni, Kornblum, Harley I.
Publicado 2018

Transcriptional regulation of macrophage cholesterol efflux and atherogenesis by a long noncoding RNA

por Sallam, Tamer, Jones, Marius, Thomas, Brandon J, Wu, Xiaohui, Gilliland, Thomas, Qian, Kevin, Eskin, Ascia, Casero, David, Zhang, Zhengyi, Sandhu, Jaspreet, Salisbury, David, Rajbhandari, Prashant, Civelek, Mete, Hong, Cynthia, Ito, Ayaka, Liu, Xin, Daniel, Bence, Lusis, Aldons J, Whitelegge, Julian, Nagy, Laszlo, Castrillo, Antonio, Smale, Stephen, Tontonoz, Peter
Publicado 2018

A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome

por Oud, Machteld M., Bonnard, Carine, Mans, Dorus A., Altunoglu, Umut, Tohari, Sumanty, Ng, Alvin Yu Jin, Eskin, Ascia, Lee, Hane, Rupar, C. Anthony, de Wagenaar, Nathalie P., Wu, Ka Man, Lahiry, Piya, Pazour, Gregory J., Nelson, Stanley F., Hegele, Robert A., Roepman, Ronald, Kayserili, Hülya, Venkatesh, Byrappa, Siu, Victoria M., Reversade, Bruno, Arts, Heleen H.
Publicado 2016

Recessive ciliopathy mutations in primary endocardial fibroelastosis: a rare neonatal cardiomyopathy in a case of Alstrom syndrome

por Zhao, Yan, Wang, Lee-kai, Eskin, Ascia, Kang, Xuedong, Fajardo, Viviana M., Mehta, Zubin, Pineles, Stacy, Schmidt, Ryan J., Nagiel, Aaron, Satou, Gary, Garg, Meena, Federman, Myke, Reardon, Leigh C., Lee, Steven L., Biniwale, Reshma, Grody, Wayne W., Halnon, Nancy, Khanlou, Negar, Quintero-Rivera, Fabiola, Alejos, Juan C., Nakano, Atsushi, Fishbein, Gregory A., Van Arsdell, Glen S., Nelson, Stanley F., Touma, Marlin
Publicado 2021