Martin Blum

Affiliations: 
University of Hohenheim 
Google:
"Martin Blum"
Mean distance: (not calculated yet)
 
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Szenker-Ravi E, Ott T, Khatoo M, et al. (2022) Publisher Correction: Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates. Nature Genetics
Szenker-Ravi E, Ott T, Khatoo M, et al. (2021) Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates. Nature Genetics
Maerker M, Getwan M, Dowdle ME, et al. (2021) Bicc1 and Dicer regulate left-right patterning through post-transcriptional control of the Nodal inhibitor Dand5. Nature Communications. 12: 5482
Beckers A, Fuhl F, Ott T, et al. (2021) The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus. Scientific Reports. 11: 13333
Beckers A, Adis C, Schuster-Gossler K, et al. (2020) The FOXJ1 target is required for sperm motility, mucociliary clearance of the airways and brain development. Development (Cambridge, England)
Kalev-Altman R, Hanael E, Zelinger E, et al. (2020) Conserved role of matrix metalloproteases 2 and 9 in promoting the migration of neural crest cells in avian and mammalian embryos. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology
Rachev E, Schuster-Gossler K, Fuhl F, et al. (2019) CFAP43 modulates ciliary beating in mouse and Xenopus. Developmental Biology
Blum M, Ott T. (2019) Mechanical strain, novel genes and evolutionary insights: news from the frog left-right organizer. Current Opinion in Genetics & Development. 56: 8-14
Schneider I, Kreis J, Schweickert A, et al. (2019) A dual function of FGF signaling in left-right axis formation. Development (Cambridge, England)
Ott T, Kaufmann L, Granzow M, et al. (2019) The Frog as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in . Frontiers in Physiology. 10: 134
See more...