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Jochen Hecht

Showing results (21-30 of 87) with videos related to

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The Journal of Clinical Investigation|December 17, 2008
Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesisPia Kuss, Pablo Villavicencio-Lorini, Florian Witte, et al.
The Journal of Clinical Investigation|May 12, 2010
Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formationPablo Villavicencio-Lorini, Pia Kuss, Julia Friedrich, et al.
Journal of Medical Genetics|November 20, 2012
Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type AUmm-e- Kalsoom, Eva Klopocki, Naveed Wasif, et al.
Journal of Molecular Microbiology and Biotechnology|October 26, 2013
Generation and analysis of draft sequences of 'stolbur' phytoplasma from multiple displacement amplification templatesJelena Mitrović, Christin Siewert, Bojan Duduk, et al.
Circulation|October 13, 2006
Induction of macrophage chemotaxis by aortic extracts of the mgR Marfan mouse model and a GxxPG-containing fibrillin-1 fragmentGao Guo, Patrick Booms, Marc Halushka, et al.
Digestion|December 17, 2013
Analysis of the intestinal microbiome of a recovered Clostridium difficile patient after fecal transplantationFelix Broecker, Michael Kube, Jochen Klumpp, et al.
Frontiers in Immunology|April 27, 2019
BKV Clearance Time Correlates With Exhaustion State and T-Cell Receptor Repertoire Shape of BKV-Specific T-Cells in Renal Transplant PatientsUlrik Stervbo, Mikalai Nienen, Benjamin J D Weist, et al.
BMC Genomics|March 26, 2011
Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healingMarten Jäger, Claus-Eric Ott, Johannes Grünhagen, et al.
Journal of Medical Genetics|May 28, 2013
Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusionAleksander Jamsheer, Tomasz Zemojtel, Mateusz Kolanczyk, et al.
American Journal of Medical Genetics. Part A|October 22, 2014
First description of a patient with Vici syndrome due to a mutation affecting the penultimate exon of EPG5 and review of the literatureNadja Ehmke, Nima Parvaneh, Peter Krawitz, et al.
Pageof 9

Showing results (21-30 of 87) with videos related to

Sort By:
Pageof 9
The Journal of Clinical Investigation|December 17, 2008
Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesisPia Kuss, Pablo Villavicencio-Lorini, Florian Witte, et al.
The Journal of Clinical Investigation|May 12, 2010
Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formationPablo Villavicencio-Lorini, Pia Kuss, Julia Friedrich, et al.
Journal of Medical Genetics|November 20, 2012
Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type AUmm-e- Kalsoom, Eva Klopocki, Naveed Wasif, et al.
Journal of Molecular Microbiology and Biotechnology|October 26, 2013
Generation and analysis of draft sequences of 'stolbur' phytoplasma from multiple displacement amplification templatesJelena Mitrović, Christin Siewert, Bojan Duduk, et al.
Circulation|October 13, 2006
Induction of macrophage chemotaxis by aortic extracts of the mgR Marfan mouse model and a GxxPG-containing fibrillin-1 fragmentGao Guo, Patrick Booms, Marc Halushka, et al.
Digestion|December 17, 2013
Analysis of the intestinal microbiome of a recovered Clostridium difficile patient after fecal transplantationFelix Broecker, Michael Kube, Jochen Klumpp, et al.
Frontiers in Immunology|April 27, 2019
BKV Clearance Time Correlates With Exhaustion State and T-Cell Receptor Repertoire Shape of BKV-Specific T-Cells in Renal Transplant PatientsUlrik Stervbo, Mikalai Nienen, Benjamin J D Weist, et al.
BMC Genomics|March 26, 2011
Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healingMarten Jäger, Claus-Eric Ott, Johannes Grünhagen, et al.
Journal of Medical Genetics|May 28, 2013
Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusionAleksander Jamsheer, Tomasz Zemojtel, Mateusz Kolanczyk, et al.
American Journal of Medical Genetics. Part A|October 22, 2014
First description of a patient with Vici syndrome due to a mutation affecting the penultimate exon of EPG5 and review of the literatureNadja Ehmke, Nima Parvaneh, Peter Krawitz, et al.
Pageof 9