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Ute Felbor

Showing results (1-10 of 71) with videos related to

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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Cellular models of genetic diseasesMatthias Rath, Ute Felbor
Stroke|August 5, 2006
Controversial molecular classification of human cerebrovascular malformationsSonja Stahl, Ute Felbor
Journal of Medical Genetics|August 26, 2019
Postzygotic mosaicism in cerebral cavernous malformationMatthias Rath, Axel Pagenstecher, Alexander Hoischen, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 23, 2004
Non-heparan sulfate-binding interactions of endostatin/collagen XVIII in murine developmentNatalia Rychkova, Sonja Stahl, Sabine Gaetzner, et al.
Human Genetics|July 24, 2002
Centromeric association of chromosome 16- and 18-derived microchromosomesUte Felbor, Désirée Rutschow, Thomas Haaf, et al.
Hamostaseologie|September 28, 2018
Diagnostic Single Gene Analyses Beyond SangerJuliane Najm, Matthias Rath, Winnie Schröder, et al.
Molecular Syndromology|March 30, 2018
Cerebral Cavernous Malformations: An Update on Prevalence, Molecular Genetic Analyses, and Genetic CounsellingStefanie Spiegler, Matthias Rath, Christin Paperlein, et al.
Journal of Negative Results in Biomedicine|June 2, 2006
VEGF receptors on PC12 cells mediate transient activation of ERK1/2 and Akt: comparison of nerve growth factor and vascular endothelial growth factorIngrid Berger, Sonja Stahl, Natalia Rychkova, et al.
Human Molecular Genetics|December 18, 2008
A two-hit mechanism causes cerebral cavernous malformations: complete inactivation of CCM1, CCM2 or CCM3 in affected endothelial cellsAxel Pagenstecher, Sonja Stahl, Ulrich Sure, et al.
Deutsches Arzteblatt International|March 18, 2020
Disorders Caused by Genetic MosaicismUte Moog, Ute Felbor, Cristina Has, et al.
Pageof 8

Showing results (1-10 of 71) with videos related to

Sort By:
Pageof 8
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Cellular models of genetic diseasesMatthias Rath, Ute Felbor
Stroke|August 5, 2006
Controversial molecular classification of human cerebrovascular malformationsSonja Stahl, Ute Felbor
Journal of Medical Genetics|August 26, 2019
Postzygotic mosaicism in cerebral cavernous malformationMatthias Rath, Axel Pagenstecher, Alexander Hoischen, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|December 23, 2004
Non-heparan sulfate-binding interactions of endostatin/collagen XVIII in murine developmentNatalia Rychkova, Sonja Stahl, Sabine Gaetzner, et al.
Human Genetics|July 24, 2002
Centromeric association of chromosome 16- and 18-derived microchromosomesUte Felbor, Désirée Rutschow, Thomas Haaf, et al.
Hamostaseologie|September 28, 2018
Diagnostic Single Gene Analyses Beyond SangerJuliane Najm, Matthias Rath, Winnie Schröder, et al.
Molecular Syndromology|March 30, 2018
Cerebral Cavernous Malformations: An Update on Prevalence, Molecular Genetic Analyses, and Genetic CounsellingStefanie Spiegler, Matthias Rath, Christin Paperlein, et al.
Journal of Negative Results in Biomedicine|June 2, 2006
VEGF receptors on PC12 cells mediate transient activation of ERK1/2 and Akt: comparison of nerve growth factor and vascular endothelial growth factorIngrid Berger, Sonja Stahl, Natalia Rychkova, et al.
Human Molecular Genetics|December 18, 2008
A two-hit mechanism causes cerebral cavernous malformations: complete inactivation of CCM1, CCM2 or CCM3 in affected endothelial cellsAxel Pagenstecher, Sonja Stahl, Ulrich Sure, et al.
Deutsches Arzteblatt International|March 18, 2020
Disorders Caused by Genetic MosaicismUte Moog, Ute Felbor, Cristina Has, et al.
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