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Przemko Tylzanowski

Showing results (1-10 of 40) with videos related to

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European Journal of Medical Genetics|July 26, 2011
Limb skeletal malformations - what the HOX is going on?Nathalie Brison, Przemko Tylzanowski, Philippe Debeer
Plos One|October 22, 2014
Orphan G-protein coupled receptor 22 (Gpr22) regulates cilia length and structure in the zebrafish Kupffer's vesicleDaphne Verleyen, Frank P Luyten, Przemko Tylzanowski
Cells|January 30, 2021
Appendage Regeneration in Vertebrates: What Makes This Possible?Valentina Daponte, Przemko Tylzanowski, Antonella Forlino
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 17, 2013
Joining the fingers: a HOXD13 StoryNathalie Brison, Philippe Debeer, Przemko Tylzanowski
International Journal of Molecular Sciences|January 21, 2022
Orofacial Cleft and Mandibular Prognathism-Human Genetics and Animal ModelsAnna Jaruga, Jakub Ksiazkiewicz, Krystian Kuzniarz, et al.
Scientific Reports|August 31, 2016
Noggin inactivation affects the number and differentiation potential of muscle progenitor cells in vivoDomiziana Costamagna, Hendrik Mommaerts, Maurilio Sampaolesi, et al.
Journal of Medical Genetics|December 21, 2019
Mutations in gene regulatory elements linked to human limb malformationsKarol Nowosad, Ewa Hordyjewska-Kowalczyk, Przemko Tylzanowski
The Journal of Cell Biology|December 2, 2009
delta-EF1 is a negative regulator of Ihh in the developing growth plateEllen Bellon, Frank P Luyten, Przemko Tylzanowski
Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 7, 2006
The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defectsPrzemko Tylzanowski, Liese Mebis, Frank P Luyten
Molecular Syndromology|September 8, 2017
Novel Mutation of the <i>RUNX2</i> Gene in Patients with Cleidocranial DysplasiaEwa Hordyjewska, Anna Jaruga, Grzegorz Kandzierski, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
European Journal of Medical Genetics|July 26, 2011
Limb skeletal malformations - what the HOX is going on?Nathalie Brison, Przemko Tylzanowski, Philippe Debeer
Plos One|October 22, 2014
Orphan G-protein coupled receptor 22 (Gpr22) regulates cilia length and structure in the zebrafish Kupffer's vesicleDaphne Verleyen, Frank P Luyten, Przemko Tylzanowski
Cells|January 30, 2021
Appendage Regeneration in Vertebrates: What Makes This Possible?Valentina Daponte, Przemko Tylzanowski, Antonella Forlino
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 17, 2013
Joining the fingers: a HOXD13 StoryNathalie Brison, Philippe Debeer, Przemko Tylzanowski
International Journal of Molecular Sciences|January 21, 2022
Orofacial Cleft and Mandibular Prognathism-Human Genetics and Animal ModelsAnna Jaruga, Jakub Ksiazkiewicz, Krystian Kuzniarz, et al.
Scientific Reports|August 31, 2016
Noggin inactivation affects the number and differentiation potential of muscle progenitor cells in vivoDomiziana Costamagna, Hendrik Mommaerts, Maurilio Sampaolesi, et al.
Journal of Medical Genetics|December 21, 2019
Mutations in gene regulatory elements linked to human limb malformationsKarol Nowosad, Ewa Hordyjewska-Kowalczyk, Przemko Tylzanowski
The Journal of Cell Biology|December 2, 2009
delta-EF1 is a negative regulator of Ihh in the developing growth plateEllen Bellon, Frank P Luyten, Przemko Tylzanowski
Developmental Dynamics : an Official Publication of the American Association of Anatomists|April 7, 2006
The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defectsPrzemko Tylzanowski, Liese Mebis, Frank P Luyten
Molecular Syndromology|September 8, 2017
Novel Mutation of the <i>RUNX2</i> Gene in Patients with Cleidocranial DysplasiaEwa Hordyjewska, Anna Jaruga, Grzegorz Kandzierski, et al.
Pageof 4