Stricker, Sigmar
Max Planck Institute for Molecular Genetics · Freie Universität Berlin
5 papers on CoChatORCID 0000-0002-7174-5363
Most cited papers
- Verified
BMP signaling controls muscle mass
Sartori, R., Schirwis, E., Blaauw, B., Bortolanza, S., Zhao, J., Enzo, E., Stantzou, A., Mouisel, E., Toniolo, L., Ferry, A., et al. (2013) · Nature Genetics
Muscle Physiology and DisordersTGF-β signaling in diseases
Cited by 467
- Verified
PDE3A mutations cause autosomal dominant hypertension with brachydactyly
Maass, P. G., Aydin, A., Luft, F. C., Schächterle, C., Weise, A., Stricker, S., Lindschau, C., Vaegler, M., Qadri, F., Toka, H. R., et al. (2015) · Nature Genetics
Phosphodiesterase function and regulationBlood Pressure and Hypertension Studies
Cited by 166
- Verified
Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development
Vallecillo-García, P., Orgeur, M., vom Hofe-Schneider, S., Stumm, J., Kappert, V., Ibrahim, D. M., Börno, S. T., Hayashi, S., Relaix, F., Hildebrandt, K., et al. (2017) · Nature Communications
Muscle Physiology and DisordersDevelopmental Biology and Gene Regulation
Cited by 126
- Verified
Copy-Number Variations Involving the IHH Locus Are Associated with Syndactyly and Craniosynostosis
Klopocki, E., Lohan, S., Brancati, F., Koll, R., Brehm, A., Seemann, P., Dathe, K., Stricker, S., Hecht, J., Bosse, K., et al. (2011) · The American Journal of Human Genetics
Congenital limb and hand anomaliesCraniofacial Disorders and Treatments
Cited by 104
- Verified
Negative regulation of Wnt signaling mediated by CK1‐phosphorylated Dishevelled via Ror2
Witte, F., Bernatik, O., Kirchner, K., Masek, J., Mahl, A., Krejci, P., Mundlos, S., Schambony, A., Bryja, V., & Stricker, S. (2010) · The FASEB Journal
Wnt/β-catenin signaling in development and cancerDevelopmental Biology and Gene Regulation
Cited by 75
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