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Gregor Andelfinger

Showing results (91-100 of 110) with videos related to

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European Journal of Human Genetics : EJHG|March 2, 2019
Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing geneIlse Luyckx, Ajay A Kumar, Edwin Reyniers, et al.
JCI Insight|February 15, 2022
Triglyceride-derived fatty acids reduce autophagy in a model of retinal angiomatous proliferationEmilie Heckel, Gael Cagnone, Tapan Agnihotri, et al.
Nature Medicine|September 14, 2014
Subcellular localization of coagulation factor II receptor-like 1 in neurons governs angiogenesisJean-Sébastien Joyal, Satra Nim, Tang Zhu, et al.
American Journal of Human Genetics|May 1, 2012
Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndromeFrancois P Bernier, Oana Caluseriu, Sarah Ng, et al.
Nature Communications|June 25, 2025
Metabolic reprogramming of the neovascular niche promotes regenerative angiogenesis in proliferative retinopathyGael Cagnone, Sheetal Pundir, Charlotte Betus, et al.
Nature Genetics|December 18, 2019
Loss of ADAMTS19 causes progressive non-syndromic heart valve diseaseFlorian Wünnemann, Asaf Ta-Shma, Christoph Preuss, et al.
Plos Genetics|September 13, 2012
Rare copy number variants contribute to congenital left-sided heart diseaseMarc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, et al.
Science (New York, N.Y.)|August 22, 2020
Neutrophil extracellular traps target senescent vasculature for tissue remodeling in retinopathyFrançois Binet, Gael Cagnone, Sergio Crespo-Garcia, et al.
Science Advances|June 30, 2023
<i>N</i>-acetylneuraminate pyruvate lyase controls sialylation of muscle glycoproteins essential for muscle regeneration and functionAfitz Da Silva, Junio Dort, Zakaria Orfi, et al.
Nature Genetics|October 6, 2014
Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythmPhilippe Chetaille, Christoph Preuss, Silja Burkhard, et al.
Pageof 11

Showing results (91-100 of 110) with videos related to

Sort By:
Pageof 11
European Journal of Human Genetics : EJHG|March 2, 2019
Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing geneIlse Luyckx, Ajay A Kumar, Edwin Reyniers, et al.
JCI Insight|February 15, 2022
Triglyceride-derived fatty acids reduce autophagy in a model of retinal angiomatous proliferationEmilie Heckel, Gael Cagnone, Tapan Agnihotri, et al.
Nature Medicine|September 14, 2014
Subcellular localization of coagulation factor II receptor-like 1 in neurons governs angiogenesisJean-Sébastien Joyal, Satra Nim, Tang Zhu, et al.
American Journal of Human Genetics|May 1, 2012
Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndromeFrancois P Bernier, Oana Caluseriu, Sarah Ng, et al.
Nature Communications|June 25, 2025
Metabolic reprogramming of the neovascular niche promotes regenerative angiogenesis in proliferative retinopathyGael Cagnone, Sheetal Pundir, Charlotte Betus, et al.
Nature Genetics|December 18, 2019
Loss of ADAMTS19 causes progressive non-syndromic heart valve diseaseFlorian Wünnemann, Asaf Ta-Shma, Christoph Preuss, et al.
Plos Genetics|September 13, 2012
Rare copy number variants contribute to congenital left-sided heart diseaseMarc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, et al.
Science (New York, N.Y.)|August 22, 2020
Neutrophil extracellular traps target senescent vasculature for tissue remodeling in retinopathyFrançois Binet, Gael Cagnone, Sergio Crespo-Garcia, et al.
Science Advances|June 30, 2023
<i>N</i>-acetylneuraminate pyruvate lyase controls sialylation of muscle glycoproteins essential for muscle regeneration and functionAfitz Da Silva, Junio Dort, Zakaria Orfi, et al.
Nature Genetics|October 6, 2014
Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythmPhilippe Chetaille, Christoph Preuss, Silja Burkhard, et al.
Pageof 11