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Molecular mechanisms underlying FSHD Identification of genetic regulators of satellite cell biology

1997 …2024
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Personal profile

Research interests

  • 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.

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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 2024

Muscle Cells
Skeletal Muscle
Stem Cells
Clinical Studies
Protein Domains

Research Output 1997 2019

89 Citations (Scopus)

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

Yolk Sac
Embryonic Stem Cells
Cell Differentiation
Transcription Factors
58 Citations (Scopus)

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

Yolk Sac
Endothelial Cells
Hematopoietic Stem Cells
40 Citations (Scopus)

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
Retinal Vessels
38 Citations (Scopus)

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
Neuromuscular Diseases
160 Citations (Scopus)

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