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Katrin Voss

Showing results (1-10 of 12) with videos related to

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The Journal of Experimental Biology|December 24, 2003
Acoustic communication in noise: regulation of call characteristics in a New World monkeyHenrik Brumm, Katrin Voss, Ireen Köllmer, et al.
Neurogenetics|July 28, 2007
CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformationsKatrin Voss, Sonja Stahl, Elisa Schleider, et al.
European Journal of Immunology|April 29, 2004
Inhibition of Notch signaling biases rat thymocyte development towards the NK cell lineageJens van den Brandt, Katrin Voss, Melanie Schott, et al.
Human Mutation|April 17, 2009
Functional analyses of human and zebrafish 18-amino acid in-frame deletion pave the way for domain mapping of the cerebral cavernous malformation 3 proteinKatrin Voss, Sonja Stahl, Benjamin M Hogan, et al.
Genome Research|April 11, 2013
Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait lociDirk S Paul, Cornelis A Albers, Augusto Rendon, et al.
Nature Genetics|February 26, 2008
G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growthSandra M Pasternack, Ivar von Kügelgen, Khalid Al Aboud, et al.
Human Mutation|February 27, 2008
Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complexSonja Stahl, Sabine Gaetzner, Katrin Voss, et al.
Blood|September 14, 2012
A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding siteSylvia T Nürnberg, Augusto Rendon, Peter A Smethurst, et al.
Nature Genetics|July 19, 2011
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndromeCornelis A Albers, Ana Cvejic, Rémi Favier, et al.
Science (New York, N.Y.)|September 27, 2014
Transcriptional diversity during lineage commitment of human blood progenitorsLu Chen, Myrto Kostadima, Joost H A Martens, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
The Journal of Experimental Biology|December 24, 2003
Acoustic communication in noise: regulation of call characteristics in a New World monkeyHenrik Brumm, Katrin Voss, Ireen Köllmer, et al.
Neurogenetics|July 28, 2007
CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformationsKatrin Voss, Sonja Stahl, Elisa Schleider, et al.
European Journal of Immunology|April 29, 2004
Inhibition of Notch signaling biases rat thymocyte development towards the NK cell lineageJens van den Brandt, Katrin Voss, Melanie Schott, et al.
Human Mutation|April 17, 2009
Functional analyses of human and zebrafish 18-amino acid in-frame deletion pave the way for domain mapping of the cerebral cavernous malformation 3 proteinKatrin Voss, Sonja Stahl, Benjamin M Hogan, et al.
Genome Research|April 11, 2013
Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait lociDirk S Paul, Cornelis A Albers, Augusto Rendon, et al.
Nature Genetics|February 26, 2008
G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growthSandra M Pasternack, Ivar von Kügelgen, Khalid Al Aboud, et al.
Human Mutation|February 27, 2008
Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complexSonja Stahl, Sabine Gaetzner, Katrin Voss, et al.
Blood|September 14, 2012
A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding siteSylvia T Nürnberg, Augusto Rendon, Peter A Smethurst, et al.
Nature Genetics|July 19, 2011
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndromeCornelis A Albers, Ana Cvejic, Rémi Favier, et al.
Science (New York, N.Y.)|September 27, 2014
Transcriptional diversity during lineage commitment of human blood progenitorsLu Chen, Myrto Kostadima, Joost H A Martens, et al.
Pageof 2