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Personal profile

Keywords

  • muscular dystrophy
  • development
  • facioscapulohumeral muscular dystrophy
  • embryonic stem cells
  • developmental biology
  • fshd
  • adult stem cells

Fingerprint The Fingerprint is created by mining the titles and abstracts of the person's research outputs and projects/funding awards to create an index of weighted terms from discipline-specific thesauri.

  • 56 Similar Profiles
Embryonic Stem Cells Medicine & Life Sciences
Stem cells Chemical Compounds
Facioscapulohumeral Muscular Dystrophy Medicine & Life Sciences
Mesoderm Medicine & Life Sciences
Stem Cells Medicine & Life Sciences
Genes Medicine & Life Sciences
Hematopoietic Stem Cells Medicine & Life Sciences
Transcription Factors Medicine & Life Sciences

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Projects 2008 2020

Selected Research Output 1997 2018

69 Citations

Mesp1 patterns mesoderm into cardiac, hematopoietic, or skeletal myogenic progenitors in a context-dependent manner

Chan, S. S. K., Shi, X., Toyama, A., Arpke, R. W., Dandapat, A., Iacovino, M., Kang, J., Le, G., Hagen, H. R., Garry, D. J. & Kyba, M., May 2 2013, In : Cell Stem Cell. 12, 5, p. 587-601 15 p.

Research output: Contribution to journalArticle

Mesoderm
Yolk Sac
Embryonic Stem Cells
Cell Differentiation
Transcription Factors
55 Citations

HoxA3 is an apical regulator of haemogenic endothelium

Iacovino, M., Chong, D., Szatmari, I., Hartweck, L., Rux, D., Caprioli, A., Cleaver, O. & Kyba, M., Jan 1 2011, In : Nature Cell Biology. 13, 1, p. 72-78 7 p.

Research output: Contribution to journalArticle

Endothelium
Yolk Sac
Endothelial Cells
Hematopoiesis
Hematopoietic Stem Cells
33 Citations

Dominant Lethal Pathologies in Male Mice Engineered to Contain an X-Linked DUX4 Transgene

Dandapat, A., Bosnakovski, D., Hartweck, L. M., Arpke, R. W., Baltgalvis, K. A., Vang, D., Baik, J., Darabi, R., Perlingeiro, R. C. R., Hamra, F. K., Gupta, K., Lowe, D. A. & Kyba, M., Jan 1 2014, In : Cell Reports. 8, 5, p. 1484-1496 13 p.

Research output: Contribution to journalArticle

Facioscapulohumeral Muscular Dystrophy
Doxycycline
Pathology
Transgenes
Retinal Vessels
33 Citations

A focal domain of extreme demethylation within D4Z4 in FSHD2

Hartweck, L. M., Anderson, L. J., Lemmers, R. J., Dandapat, A., Toso, E. A., Dalton, J. C., Tawil, R., Day, J. W., Van Der Maarel, S. M. & Kyba, M., Jan 22 2013, In : Neurology. 80, 4, p. 392-399 8 p.

Research output: Contribution to journalArticle

Facioscapulohumeral Muscular Dystrophy
Methylation
Chromatin
Alleles
Neuromuscular Diseases
143 Citations

An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies

Bosnakovski, D., Xu, Z., Ji Gang, E., Galindo, C. L., Liu, M., Simsek, T., Garner, H. R., Agha-Mohammadi, S., Tassin, A., Coppée, F., Belayew, A., Perlingeiro, R. R. & Kyba, M., Oct 22 2008, In : EMBO Journal. 27, 20, p. 2766-2779 14 p.

Research output: Contribution to journalArticle

Facioscapulohumeral Muscular Dystrophy
Molecular Pathology
Myoblasts
Pathology
Genes
19 Citations

High-throughput screening identifies inhibitors of DUX4-induced myoblast toxicity

Bosnakovski, D., Choi, S. H., Strasser, J. M., Toso, E. A., Walters, M. A. & Kyba, M., Feb 1 2014, In : Skeletal Muscle. 4, 1, 4.

Research output: Contribution to journalArticle

Myoblasts
Facioscapulohumeral Muscular Dystrophy
Oxidative Stress
Chromosomes, Human, Pair 4
Proteins