Publications
Showing all 29 journal articles & 1 books available
Journal Articles
12/10/2022
Alkhunaizi E, Martin N, Jelin AC, Rosner M, Bailey DJ, Steiner LA, Lakhani S, Ji W, Katzman PJ, Forster KR, Jarinova O, Shannon P, Chitayat D, . "Fetal akinesia deformation sequence syndrome associated with recessive TTN variants." American journal of medical genetics. Part A.. 2022 Dec 10; Epub 2022 Dec 10.
8/30/2022
Guo B, Friedland SC, Alexander W, Myers JA, Wang W, O'Dell MR, Getman M, Whitney-Miller CL, Agostini-Vulaj D, Huber AR, Mello SS, Vertino PM, Land HK, Steiner LA, Hezel AF. "Arid1a mutation suppresses TGF-? signaling and induces cholangiocarcinoma." Cell reports.. 2022 Aug 30; 40(9):111253.
1/18/2022
Dulmovits BM, Tang Y, Papoin J, He M, Li J, Yang H, Addorisio ME, Kennedy L, Khan M, Brindley EC, Ashley RJ, Ackert-Bicknell C, Hale J, Kurita RK, Nakamura Y, Diamond B, Barnes BJ, Hermine O, Gallagher PG, Steiner LA, Lipton JM, Taylor N, Mohandas N, Andersson U, Al-Abed Y, Tracey KJ, Blanc L. "HMGB1-Mediated Restriction of EPO Signaling Contributes to Anemia of Inflammation." Blood.. 2022 Jan 18; Epub 2022 Jan 18.
6/1/2021
Murphy Z, Murphy K, Myers JA, Getman MR, Couch T, Schulz V, Lezon-Geyda K, Palumbo C, Yan H, Narla M, Gallagher PG, Steiner LA. "Regulation of RNA Polymerase II Activity is Essential for Terminal Erythroid Maturation." Blood.. 2021 Jun 1; Epub 2021 Jun 01.
10/16/2020
Murphy ZC, Getman MR, Myers JA, Villar KNB, Leshen E, Kurita R, Nakamura Y, Steiner LA. "Codanin-1 Mutations Engineered in Human Erythroid Cells Demonstrate Role of CDAN1 in Terminal Erythroid Maturation." Experimental hematology.. 2020 Oct 16; Epub 2020 Oct 16.
3/16/2020
Myers JA, Couch T, Murphy Z, Malik J, Getman M, Steiner LA. "The histone methyltransferase Setd8 alters the chromatin landscape and regulates the expression of key transcription factors during erythroid differentiation." Epigenetics & chromatin. 2020 Mar 16; 13(1):16. Epub 2020 Mar 16.
10/29/2019
Steiner LA, Getman M, Schiralli Lester GM, Iqbal MA, Katzman P, Szafranski P, Stankiewicz P, Bhattacharya S, Mariani T, Pryhuber G, Lin X, Young JL, Dean DA, Scheible K. "Disruption of normal patterns of FOXF1 expression in a lethal disorder of lung development." Journal of medical genetics.. 2019 Oct 29; Epub 2019 Oct 29.
6/2019
Couch T, Murphy Z, Getman M, Kurita R, Nakamura Y, Steiner LA. "Human erythroblasts with c-Kit activating mutations have reduced cell culture costs and remain capable of terminal maturation." Experimental hematology.. 2019 Jun; 74:19-24.e4. Epub 2019 Apr 18.
9/18/2018
Wang W, Friedland SC, Guo B, O'Dell MR, Alexander WB, Whitney-Miller CL, Agostini-Vulaj D, Huber AR, Myers JR, Ashton JM, Dunne RF, Steiner LA, Hezel AF. "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." Gut.. 2018 Sep 18; Epub 2018 Sep 18.
11/28/2017
Malik J, Lillis JA, Couch T, Getman M, Steiner LA. "The Methyltransferase Setd8 Is Essential for Erythroblast Survival and Maturation." Cell reports.. 2017 Nov 28; 21(9):2376-2383.
9/6/2016
Li Y, Schulz VP, Deng C, Li G, Shen Y, Tusi BK, Ma G, Stees J, Qiu Y, Steiner LA, Zhou L, Zhao K, Bungert J, Gallagher PG, Huang S. "Setd1a and NURF mediate chromatin dynamics and gene regulation during erythroid lineage commitment and differentiation." Nucleic acids research.. 2016 Sep 6; 44(15):7173-88. Epub 2016 May 03.
2016
Steiner LA, Schulz V, Makismova Y, Lezon-Geyda K, Gallagher PG. "CTCF and CohesinSA-1 Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid Cells." PloS one.. 2016 11(5):e0155378. Epub 2016 May 24.
6/2015
Malik J, Getman M, Steiner LA. "Histone methyltransferase Setd8 represses Gata2 expression and regulates erythroid maturation." Molecular and cellular biology.. 2015 Jun; 35(12):2059-72. Epub 2015 Apr 06.
7/2014
Getman M, England SJ, Malik J, Peterson K, Palis J, Steiner LA. "Extensively self-renewing erythroblasts derived from transgenic ?-yac mice is a novel model system for studying globin switching and erythroid maturation." Experimental hematology.. 2014 Jul; 42(7):536-46.e8. Epub 2014 Apr 02.
3/22/2013
Su MY, Steiner LA, Bogardus H, Mishra T, Schulz VP, Hardison RC, Gallagher PG. "Identification of biologically relevant enhancers in human erythroid cells." The Journal of biological chemistry.. 2013 Mar 22; 288(12):8433-44. Epub 2013 Jan 22.
10/25/2012
Yocum AO, Steiner LA, Seidel NE, Cline AP, Rout ED, Lin JY, Wong C, Garrett LJ, Gallagher PG, Bodine DM. "A tissue-specific chromatin loop activates the erythroid ankyrin-1 promoter." Blood.. 2012 Oct 25; 120(17):3586-93. Epub 2012 Sep 11.
11/11/2011
Steiner LA, Schulz VP, Maksimova Y, Wong C, Gallagher PG. "Patterns of histone H3 lysine 27 monomethylation and erythroid cell type-specific gene expression." The Journal of biological chemistry.. 2011 Nov 11; 286(45):39457-65. Epub 2011 Sep 21.
10/27/2011
Pilon AM, Ajay SS, Kumar SA, Steiner LA, Cherukuri PF, Wincovitch S, Anderson SM, , Mullikin JC, Gallagher PG, Hardison RC, Margulies EH, Bodine DM. "Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiation." Blood.. 2011 Oct 27; 118(17):e139-48. Epub 2011 Sep 06.
8/4/2011
Li X, Wang S, Li Y, Deng C, Steiner LA, Xiao H, Wu C, Bungert J, Gallagher PG, Felsenfeld G, Qiu Y, Huang S. "Chromatin boundaries require functional collaboration between the hSET1 and NURF complexes." Blood.. 2011 Aug 4; 118(5):1386-94. Epub 2011 Jun 08.
8/2011
Hopewell B, Steiner LA, Ehrenkranz RA, Bizzarro MJ, Gallagher PG. "Partial exchange transfusion for polycythemia hyperviscosity syndrome." American journal of perinatology.. 2011 Aug; 28(7):557-64. Epub 2011 Mar 01.
2011
Steiner LA, Ehrenkranz RA, Peterec S, Steiner RD, Reyes-Múgica M, Gallagher P. "Perinatal onset mevalonate kinase deficiency." Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.. 2011 14(4):301-6. Epub 2011 Mar 22.
12/2010
Gallagher PG, Steiner LA, Liem RI, Owen AN, Cline AP, Seidel NE, Garrett LJ, Bodine DM. "Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis." The Journal of clinical investigation.. 2010 Dec; 120(12):4453-65. Epub 2010 Nov 22.
7/2010
Laflamme K, Owen AN, Devlin EE, Yang MQ, Wong C, Steiner LA, Garrett LJ, Elnitski L, Gallagher PG, Bodine DM. "Functional analysis of a novel cis-acting regulatory region within the human ankyrin gene (ANK-1) promoter." Molecular and cellular biology.. 2010 Jul; 30(14):3493-502. Epub 2010 May 17.
10/2009
Steiner LA, Maksimova Y, Schulz V, Wong C, Raha D, Mahajan MC, Weissman SM, Gallagher PG. "Chromatin architecture and transcription factor binding regulate expression of erythrocyte membrane protein genes." Molecular and cellular biology.. 2009 Oct; 29(20):5399-412. Epub 2009 Aug 17.
3/2009
Di Terlizzi R, Gallagher PG, Mohandas N, Steiner LA, Dolce KS, Guo X, Wilkerson MJ, Stockham SL. "Canine elliptocytosis due to a mutant beta-spectrin." Veterinary clinical pathology. 2009 Mar; 38(1):52-8. Epub 2008 Oct 28.
2/12/2009
Gallagher PG, Nilson DG, Steiner LA, Maksimova YD, Lin JY, Bodine DM. "An insulator with barrier-element activity promotes alpha-spectrin gene expression in erythroid cells." Blood.. 2009 Feb 12; 113(7):1547-54. Epub 2008 Nov 13.
8/2007
Steiner LA, Gallagher PG. "Erythrocyte disorders in the perinatal period." Seminars in perinatology.. 2007 Aug; 31(4):254-61.
7/2007
Steiner LA, Bizzarro MJ, Ehrenkranz RA, Gallagher PG. "A decline in the frequency of neonatal exchange transfusions and its effect on exchange-related morbidity and mortality." Pediatrics.. 2007 Jul; 120(1):27-32.
2007
Steiner LA, Van Hoff J, Kutlar F, Gallagher PG. "Aplastic crisis revealing the diagnosis of Hb Evans [alpha62(E11)Val-->Met, GTG-->ATG (alpha2)] in a Hispanic kindred: case report and review." Hemoglobin.. 2007 31(4):409-16.