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Setd1a and NURF mediate chromatin dynamics and gene regulation during erythroid lineage commitment and differentiation.
Published in:
Nucleic Acids Research, 2016, v. 44, n. 15, p. 7173, doi. 10.1093/nar/gkw327
By:
- Ying Li;
- Schulz, Vincent P.;
- Changwang Deng;
- Guangyao Li;
- Yong Shen;
- Tusi, Betsabeh K.;
- Ma, Gina;
- Stees, Jared;
- Yi Qiu;
- Steiner, Laurie A.;
- Lei Zhou;
- Keji Zhao;
- Bungert, Jörg;
- Gallagher, Patrick G.;
- Huang, Suming
Publication type:
Article
You have free access to this contentA variant Sp1 (R218Q) transcription factor might enhance HbF expression in β<sup>0</sup>-thalassaemia homozygotes.
Published in:
British Journal of Haematology, 2018, v. 180, n. 5, p. 755, doi. 10.1111/bjh.14445
By:
- Jiang, Zhihua;
- Luo, Hong‐Yuan;
- Farrell, John J.;
- Zhang, Zhengjian;
- Schulz, Vincent P.;
- Albarawi, Dilan;
- Steinberg, Martin H.;
- Al‐Allawi, Nasir A.S.;
- Gallagher, Patrick G.;
- Forget, Bernard G.;
- Chui, David H.K.
Publication type:
Article
MKL1-actin pathway restricts chromatin accessibility and prevents mature pluripotency activation.
Published in:
Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09636-6
By:
- Hu, Xiao;
- Liu, Zongzhi Z.;
- Chen, Xinyue;
- Schulz, Vincent P.;
- Kumar, Abhishek;
- Hartman, Amaleah A.;
- Weinstein, Jason;
- Johnston, Jessica F.;
- Rodriguez, Elisa C.;
- Eastman, Anna E.;
- Cheng, Jijun;
- Min, Liz;
- Zhong, Mei;
- Carroll, Christopher;
- Gallagher, Patrick G.;
- Lu, Jun;
- Schwartz, Martin;
- King, Megan C.;
- Krause, Diane S.;
- Guo, Shangqin
Publication type:
Article
Aberrant splicing contributes to severe α-spectrin-linked congenital hemolytic anemia.
Published in:
2019
By:
- Gallagher, Patrick G.;
- Maksimova, Yelena;
- Lezon-Geyda, Kimberly;
- Newburger, Peter E.;
- Medeiros, Desiree;
- Hanson, Robin D.;
- Rothman, Jennifer;
- Israels, Sara;
- Wall, Donna A.;
- Sidonio Jr., Robert F.;
- Sieff, Colin;
- Gowans, L. Kate;
- Mittal, Nupur;
- Rivera-Santiago, Roland;
- Speicher, David W.;
- Baserga, Susan J.;
- Schulz, Vincent P.;
- Sidonio, Robert F Jr
Publication type:
journal article
Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability.
Published in:
Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 2, doi. 10.1186/1755-8166-7-4
By:
- Fang Xu;
- Lun Li;
- Schulz, Vincent P.;
- Gallagher, Patrick G.;
- Bixia Xiang;
- Hongyu Zhao;
- Peining Li
Publication type:
Article
Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosis.
Published in:
2017
By:
- Yang, Elizabeth;
- Voelkel, Erin B.;
- Lezon‐Geyda, Kimberly;
- Schulz, Vincent P.;
- Gallagher, Patrick G.
Publication type:
journal article
Tcf7 Is an Important Regulator of the Switch of Self-Renewal and Differentiation in a Multipotential Hematopoietic Cell Line.
Published in:
PLoS Genetics, 2012, v. 8, n. 3, p. 1, doi. 10.1371/journal.pgen.1002565
By:
- Jia Qian Wu;
- Seay, Montrell;
- Schulz, Vincent P.;
- Hariharan, Manoj;
- Tuck, David;
- Jin Lian;
- Jiang Du;
- Minyi Shi;
- Zhijia Ye;
- Gerstein, Mark;
- Snyder, Michael P.;
- Weissman, Sherman
Publication type:
Article
Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing.
Published in:
Movement Disorders, 2012, v. 27, n. 4, p. 539, doi. 10.1002/mds.24020
By:
- Walker, Ruth H.;
- Schulz, Vincent P.;
- Tikhonova, Irina R.;
- Mahajan, Milind C.;
- Mane, Shrikant;
- Arroyo Muniz, Maritza;
- Gallagher, Patrick G.
Publication type:
Article

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