DNMTs and Impact of CpG Content, Transcription Factors, Consensus Motifs, lncRNAs, and Histone Marks on DNA Methylation

por Loaeza-Loaeza, Jaqueline, Beltran, Adriana S., Hernández-Sotelo, Daniel
Publicado 2020

Suppression of Breast Tumor Growth and Metastasis by an Engineered Transcription Factor

por Beltran, Adriana S., Russo, Angela, Lara, Haydee, Fan, Cheng, Lizardi, Paul M., Blancafort, Pilar
Publicado 2011

Targeted silencing of the oncogenic transcription factor SOX2 in breast cancer

por Stolzenburg, Sabine, Rots, Marianne G., Beltran, Adriana S., Rivenbark, Ashley G., Yuan, Xinni, Qian, Haili, Strahl, Brian D., Blancafort, Pilar
Publicado 2012

Expression of the Pluripotency Transcription Factor OCT4 in the Normal and Aberrant Mammary Gland

por Hassiotou, Foteini, Hepworth, Anna R., Beltran, Adriana S., Mathews, Michelle M., Stuebe, Alison M., Hartmann, Peter E., Filgueira, Luis, Blancafort, Pilar
Publicado 2013

Generation of tumor-initiating cells by exogenous delivery of OCT4 transcription factor

por Beltran, Adriana S, Rivenbark, Ashley G, Richardson, Bryan T, Yuan, Xinni, Quian, Haili, Hunt, John P, Zimmerman, Eric, Graves, Lee M, Blancafort, Pilar
Publicado 2011

Modulation of tau tubulin kinases (TTBK1 and TTBK2) impacts ciliogenesis

por Bashore, Frances M., Marquez, Ariana B., Chaikuad, Apirat, Howell, Stefanie, Dunn, Andrea S., Beltran, Alvaro A., Smith, Jeffery L., Drewry, David H., Beltran, Adriana S., Axtman, Alison D.
Publicado 2023

Breastmilk Is a Novel Source of Stem Cells with Multilineage Differentiation Potential

por Hassiotou, Foteini, Beltran, Adriana, Chetwynd, Ellen, Stuebe, Alison M, Twigger, Alecia-Jane, Metzger, Philipp, Trengove, Naomi, Lai, Ching Tat, Filgueira, Luis, Blancafort, Pilar, Hartmann, Peter E
Publicado 2012

Inheritance of OCT4 predetermines fate choice in human embryonic stem cells

por Wolff, Samuel C, Kedziora, Katarzyna M, Dumitru, Raluca, Dungee, Cierra D, Zikry, Tarek M, Beltran, Adriana S, Haggerty, Rachel A, Cheng, JrGang, Redick, Margaret A, Purvis, Jeremy E
Publicado 2018

Intermediate filament dysregulation and astrocytopathy in the human disease model of KLHL16 mutation in giant axonal neuropathy (GAN)

por Battaglia, Rachel, Faridounnia, Maryam, Beltran, Adriana, Robinson, Jasmine, Kinghorn, Karina, Ezzell, J. Ashley, Bharucha-Goebel, Diana, Bonnemann, Carsten, Hooper, Jody E., Opal, Puneet, Bouldin, Thomas W., Armao, Diane, Snider, Natasha
Publicado 2023

Organotypic 3D Cell-Architecture Impacts the Expression Pattern of miRNAs–mRNAs Network in Breast Cancer SKBR3 Cells

por Gastélum-López, María de los Ángeles, Aguilar-Medina, Maribel, García Mata, Cristina, López-Gutiérrez, Jorge, Romero-Quintana, Geovanni, Bermúdez, Mercedes, Avendaño-Felix, Mariana, López-Camarillo, César, Pérez-Plascencia, Carlos, Beltrán, Adriana S, Ramos-Payán, Rosalío
Publicado 2023

SOX9 knockout decreases stemness properties in colorectal cancer cells

por Avendaño-Felix, Mariana, Aguilar-Medina, Maribel, Romero-Quintana, José Geovanni, Ayala-Ham, Alfredo, Beltran, Adriana S., Olivares-Quintero, José F., López-Camarillo, César, Pérez-Plasencia, Carlos, Bermúdez, Mercedes, Lizárraga-Verdugo, Erik, López-Gutierrez, Jorge, Sanchez-Schmitz, Guzman, Ramos-Payán, Rosalío
Publicado 2023

Site-specific phosphorylation and caspase cleavage of GFAP are new markers of Alexander disease severity

por Battaglia, Rachel A, Beltran, Adriana S, Delic, Samed, Dumitru, Raluca, Robinson, Jasmine A, Kabiraj, Parijat, Herring, Laura E, Madden, Victoria J, Ravinder, Namritha, Willems, Erik, Newman, Rhonda A, Quinlan, Roy A, Goldman, James E, Perng, Ming-Der, Inagaki, Masaki, Snider, Natasha T
Publicado 2019

RNA-binding deficient TDP-43 drives cognitive decline in a mouse model of TDP-43 proteinopathy

por Necarsulmer, Julie C, Simon, Jeremy M, Evangelista, Baggio A, Chen, Youjun, Tian, Xu, Nafees, Sara, Marquez, Ariana B, Jiang, Huijun, Wang, Ping, Ajit, Deepa, Nikolova, Viktoriya D, Harper, Kathryn M, Ezzell, J Ashley, Lin, Feng-Chang, Beltran, Adriana S, Moy, Sheryl S, Cohen, Todd J
Publicado 2023

Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

por Cousin, Margot A., Creighton, Blake A., Breau, Keith A., Spillmann, Rebecca C., Torti, Erin, Dontu, Sruthi, Tripathi, Swarnendu, Ajit, Deepa, Edwards, Reginald J., Afriyie, Simone, Bay, Julia C., Harper, Kathryn M., Beltran, Alvaro A., Munoz, Lorena J., Rodriguez, Liset Falcon, Stankewich, Michael C., Person, Richard E., Si, Yue, Normand, Elizabeth A., Blevins, Amy, May, Alison S., Bier, Louise, Aggarwal, Vimla, Mancini, Grazia M. S., van Slegtenhorst, Marjon A., Cremer, Kirsten, Becker, Jessica, Engels, Hartmut, Aretz, Stefan, MacKenzie, Jennifer J., Brilstra, Eva, van Gassen, Koen L. I., van Jaarsveld, Richard H., Oegema, Renske, Parsons, Gretchen M., Mark, Paul, Helbig, Ingo, McKeown, Sarah E., Stratton, Robert, Cogne, Benjamin, Isidor, Bertrand, Cacheiro, Pilar, Smedley, Damian, Firth, Helen V., Bierhals, Tatjana, Kloth, Katja, Weiss, Deike, Fairley, Cecilia, Shieh, Joseph T., Kritzer, Amy, Jayakar, Parul, Kurtz-Nelson, Evangeline, Bernier, Raphael A., Wang, Tianyun, Eichler, Evan E., van de Laar, Ingrid M. B. H., McConkie-Rosell, Allyn, McDonald, Marie T., Kemppainen, Jennifer, Lanpher, Brendan C., Schultz-Rogers, Laura E., Gunderson, Lauren B., Pichurin, Pavel N., Yoon, Grace, Zech, Michael, Jech, Robert, Winkelmann, Juliane, Beltran, Adriana S., Zimmermann, Michael T., Temple, Brenda, Moy, Sheryl S., Klee, Eric W., Tan, Queenie K.-G., Lorenzo, Damaris N.
Publicado 2021