Erythrocyte Disorders in the Perinatal Period in Adverse Pregnancy Outcome and the Fetus/Neonate

di Steiner, Laurie A., Gallagher, Patrick G.
Pubblicazione 2007

Histone Methyltransferase Setd8 Represses Gata2 Expression and Regulates Erythroid Maturation

di Malik, Jeffrey, Getman, Michael, Steiner, Laurie A.
Pubblicato in Mol Cell Biol (2015)

Erythropoietin Signaling Regulates Key Epigenetic and Transcription Networks in Fetal Neural Progenitor Cells

di Sollinger, Christina, Lillis, Jacquelyn, Malik, Jeffrey, Getman, Michael, Proschel, Chris, Steiner, Laurie
Pubblicato in Sci Rep (2017)

The Methyltransferase Setd8 is Essential for Erythroblast Survival and Maturation

di Malik, Jeffrey, Lillis, Jacquelyn A., Couch, Tyler, Getman, Michael, Steiner, Laurie A.
Pubblicato in Cell Rep (2017)

Patterns of Histone H3 Lysine 27 Monomethylation and Erythroid Cell Type-specific Gene Expression

di Steiner, Laurie A., Schulz, Vincent P., Maksimova, Yelena, Wong, Clara, Gallagher, Patrick G.
Pubblicazione 2011

CTCF and Cohesin(SA-1) Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid Cells

di Steiner, Laurie A., Schulz, Vincent, Makismova, Yelena, Lezon-Geyda, Kimberly, Gallagher, Patrick G.
Pubblicato in PLoS One (2016)

Extensively self-renewing erythroblasts derived from transgenic β-yac mice is a novel model system for studying globin switching and erythroid maturation

di Getman, Michael, England, Samantha J., Malik, Jeffery, Peterson, Kenneth, Palis, James, Steiner, Laurie A.
Pubblicato in Exp Hematol (2014)

The histone methyltransferase Setd8 alters the chromatin landscape and regulates the expression of key transcription factors during erythroid differentiation

di Myers, Jacquelyn A., Couch, Tyler, Murphy, Zachary, Malik, Jeffrey, Getman, Michael, Steiner, Laurie A.
Pubblicato in Epigenetics Chromatin (2020)

An insulator with barrier-element activity promotes α-spectrin gene expression in erythroid cells

di Gallagher, Patrick G., Nilson, Douglas G., Steiner, Laurie A., Maksimova, Yelena D., Lin, Jolinta Y., Bodine, David M.
Pubblicazione 2009

Identification of Biologically Relevant Enhancers in Human Erythroid Cells

di Su, Mack Y., Steiner, Laurie A., Bogardus, Hannah, Mishra, Tejaswini, Schulz, Vincent P., Hardison, Ross C., Gallagher, Patrick G.
Pubblicazione 2013

Chromatin Architecture and Transcription Factor Binding Regulate Expression of Erythrocyte Membrane Protein Genes

di Steiner, Laurie A., Maksimova, Yelena, Schulz, Vincent, Wong, Clara, Raha, Debasish, Mahajan, Milind C., Weissman, Sherman M., Gallagher, Patrick G.
Pubblicazione 2009

Codanin-1 Mutations Engineered in Human Erythroid Cells Demonstrate Role of CDAN1 in Terminal Erythroid Maturation

di Murphy, Zachary C., Getman, Michael R, Myers, Jaquelyn A, Villar, Kimberly N Burgos, Leshen, Emily, Kurita, Ryo, Nakamura, Yukio, Steiner, Laurie A
Pubblicato in Exp Hematol (2020)

Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis

di Gallagher, Patrick G., Steiner, Laurie A., Liem, Robert I., Owen, Ashley N., Cline, Amanda P., Seidel, Nancy E., Garrett, Lisa J., Bodine, David M.
Pubblicazione 2010

Chromatin boundaries require functional collaboration between the hSET1 and NURF complexes

di Li, Xingguo, Wang, Shaohua, Li, Ying, Deng, Changwang, Steiner, Laurie A., Xiao, Hua, Wu, Carl, Bungert, Jörg, Gallagher, Patrick G., Felsenfeld, Gary, Qiu, Yi, Huang, Suming
Pubblicazione 2011

Functional Analysis of a Novel cis-Acting Regulatory Region within the Human Ankyrin Gene (ANK-1) Promoter

di Laflamme, Karina, Owen, Ashley N., Devlin, Emily E., Yang, Mary Q., Wong, Clara, Steiner, Laurie A., Garrett, Lisa J., Elnitski, Laura, Gallagher, Patrick G., Bodine, David M.
Pubblicazione 2010

A tissue-specific chromatin loop activates the erythroid ankyrin-1 promoter

di Yocum, Ashley O., Steiner, Laurie A., Seidel, Nancy E., Cline, Amanda P., Rout, Emily D., Lin, Jolinta Y., Wong, Clara, Garrett, Lisa J., Gallagher, Patrick G., Bodine, David M.
Pubblicazione 2012

Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiation

di Pilon, Andre M., Ajay, Subramanian S., Kumar, Swathi Ashok, Steiner, Laurie A., Cherukuri, Praveen F., Wincovitch, Stephen, Anderson, Stacie M., Mullikin, James C., Gallagher, Patrick G., Hardison, Ross C., Margulies, Elliott H., Bodine, David M.
Pubblicazione 2011

Setd1a and NURF mediate chromatin dynamics and gene regulation during erythroid lineage commitment and differentiation

di Li, Ying, Schulz, Vincent P., Deng, Changwang, Li, Guangyao, Shen, Yong, Tusi, Betsabeh K., Ma, Gina, Stees, Jared, Qiu, Yi, Steiner, Laurie A., Zhou, Lei, Zhao, Keji, Bungert, Jörg, Gallagher, Patrick G., Huang, Suming
Pubblicato in Nucleic Acids Res (2016)

ARID1A, a SWI/SNF subunit, is critical to acinar cell homeostasis and regeneration and is a barrier to transformation and epithelial-mesenchymal transition in the pancreas.

di Wang, Wenjia, Friedland, Scott C, Guo, Bing, O’Dell, Michael R, Alexander, William B, Whitney-Miller, Christa L, Agostini-Vulaj, Diana, Huber, Aaron R, Myers, Jason R, Ashton, John M, Dunne, Richard F, Steiner, Laurie A, Hezel, Aram F
Pubblicato in Gut (2018)

Pathogenetics of Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins

di Szafranski, Przemyslaw, Gambin, Tomasz, Dharmadhikari, Avinash V., Akdemir, Kadir Caner, Jhangiani, Shalini N., Schuette, Jennifer, Godiwala, Nihal, Yatsenko, Svetlana A., Sebastian, Jessica, Madan-Khetarpal, Suneeta, Surti, Urvashi, Abellar, Rosanna G., Bateman, David A., Wilson, Ashley L., Markham, Melinda H., Slamon, Jill, Santos-Simarro, Fernando, Palomares, María, Nevado, Julián, Lapunzina, Pablo, Hon-Yin, Brian Chung, Wai-Lap, Wong, Chu, Yoyo Wing Yiu, Mok, Gary Tsz Kin, Eitan, Kerem, Reiter, Joel, Ambalavanan, Namasivayam, Anderson, Scott A., Kelly, David R., Shieh, Joseph, Rosenthal, Taryn C., Scheible, Kristin, Steiner, Laurie, Iqbal, M. Anwar, McKinnon, Margaret, Hamilton, Sara Jane, Schlade-Bartusiak, Kamilla, English, Dawn, Hendson, Glenda, Roeder, Elizabeth R., DeNapoli, Thomas S., Littlejohn, Rebecca Okashah, Wolff, Daynna J., Wagner, Carol L., Yeung, Alison, Francis, David, Fiorino, Elizabeth K., Edelman, Morris, Fox, Joyce, Hayes, Denise A., Janssens, Sandra, De Baere, Elfride, Menten, Bjorn, Loccufier, Anne, Van Walleghem, Lieve, Moerman, Philippe, Sznajer, Yves, Lay, Amy S., Kussmann, Jennifer L., Chawla, Jasneek, Payton, Diane J., Phillips, Gael E., Brosens, Erwin, Tibboel, Dick, de Klein, Annelies, Maystadt, Isabelle, Fisher, Richard, Sebire, Neil, Male, Alison, Chopra, Maya, Pinner, Jason, Malcolm, Girvan, Peters, Gregory, Arbuckle, Susan, Lees, Melissa, Mead, Zoe, Quarrell, Oliver, Sayers, Richard, Owens, Martina, Shaw-Smith, Charles, Lioy, Janet, McKay, Eileen, de Leeuw, Nicole, Feenstra, Ilse, Spruijt, Liesbeth, Elmslie, Frances, Thiruchelvam, Timothy, Bacino, Carlos A., Langston, Claire, Lupski, James R., Sen, Partha, Popek, Edwina, Stankiewicz, Paweł
Pubblicato in Hum Genet (2016)