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L Christian

Showing results (431-440 of 478) with videos related to

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Scientific Reports|May 12, 2026
Comparative analysis of bypass vs. stent for coronary revascularization using an ex-vivo organ care system in an animal modelPhilipp Lindenhahn, Rabea Hinkel, L Christian Napp, et al.
Molecular and Cellular Biology|December 31, 2005
Fanconi anemia proteins are required to prevent accumulation of replication-associated DNA double-strand breaksAlexandra Sobeck, Stacie Stone, Vincenzo Costanzo, et al.
Eurointervention : Journal of Europcr in Collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology|August 23, 2013
Rationale and design of a large registry on renal denervation: the Global SYMPLICITY registryMichael Böhm, Felix Mahfoud, Christian Ukena, et al.
Cell Reports|November 25, 2020
DNMT3A Haploinsufficiency Results in Behavioral Deficits and Global Epigenomic Dysregulation Shared across Neurodevelopmental DisordersDiana L Christian, Dennis Y Wu, Jenna R Martin, et al.
JAMA Cardiology|July 21, 2016
Differences in the Clinical Profile and Outcomes of Typical and Atypical Takotsubo Syndrome: Data From the International Takotsubo RegistryJelena R Ghadri, Victoria L Cammann, L Christian Napp, et al.
Circulation. Heart Failure|January 20, 2025
Validity and Accuracy of the Derived Left Ventricular End-Diastolic Pressure in Impella 5.5Reza Poyanmehr, Jasmin S Hanke, Dietmar Boethig, et al.
Kidney International|March 4, 2011
A phase 1, single-dose study of fresolimumab, an anti-TGF-β antibody, in treatment-resistant primary focal segmental glomerulosclerosisHoward Trachtman, Fernando C Fervenza, Debbie S Gipson, et al.
Nature Genetics|January 24, 2009
Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellumJuliane Najm, Denise Horn, Isabella Wimplinger, et al.
European Journal of Nuclear Medicine and Molecular Imaging|July 4, 2018
Imaging of chemokine receptor CXCR4 expression in culprit and nonculprit coronary atherosclerotic plaque using motion-corrected [<sup>68</sup>Ga]pentixafor PET/CTThorsten Derlin, Daniel G Sedding, Jochen Dutzmann, et al.
Human Molecular Genetics|January 15, 1999
The spectrum of mutations in UBE3A causing Angelman syndromeP Fang, E Lev-Lehman, T F Tsai, et al.
Pageof 48

Showing results (431-440 of 478) with videos related to

Sort By:
Pageof 48
Scientific Reports|May 12, 2026
Comparative analysis of bypass vs. stent for coronary revascularization using an ex-vivo organ care system in an animal modelPhilipp Lindenhahn, Rabea Hinkel, L Christian Napp, et al.
Molecular and Cellular Biology|December 31, 2005
Fanconi anemia proteins are required to prevent accumulation of replication-associated DNA double-strand breaksAlexandra Sobeck, Stacie Stone, Vincenzo Costanzo, et al.
Eurointervention : Journal of Europcr in Collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology|August 23, 2013
Rationale and design of a large registry on renal denervation: the Global SYMPLICITY registryMichael Böhm, Felix Mahfoud, Christian Ukena, et al.
Cell Reports|November 25, 2020
DNMT3A Haploinsufficiency Results in Behavioral Deficits and Global Epigenomic Dysregulation Shared across Neurodevelopmental DisordersDiana L Christian, Dennis Y Wu, Jenna R Martin, et al.
JAMA Cardiology|July 21, 2016
Differences in the Clinical Profile and Outcomes of Typical and Atypical Takotsubo Syndrome: Data From the International Takotsubo RegistryJelena R Ghadri, Victoria L Cammann, L Christian Napp, et al.
Circulation. Heart Failure|January 20, 2025
Validity and Accuracy of the Derived Left Ventricular End-Diastolic Pressure in Impella 5.5Reza Poyanmehr, Jasmin S Hanke, Dietmar Boethig, et al.
Kidney International|March 4, 2011
A phase 1, single-dose study of fresolimumab, an anti-TGF-β antibody, in treatment-resistant primary focal segmental glomerulosclerosisHoward Trachtman, Fernando C Fervenza, Debbie S Gipson, et al.
Nature Genetics|January 24, 2009
Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellumJuliane Najm, Denise Horn, Isabella Wimplinger, et al.
European Journal of Nuclear Medicine and Molecular Imaging|July 4, 2018
Imaging of chemokine receptor CXCR4 expression in culprit and nonculprit coronary atherosclerotic plaque using motion-corrected [<sup>68</sup>Ga]pentixafor PET/CTThorsten Derlin, Daniel G Sedding, Jochen Dutzmann, et al.
Human Molecular Genetics|January 15, 1999
The spectrum of mutations in UBE3A causing Angelman syndromeP Fang, E Lev-Lehman, T F Tsai, et al.
Pageof 48