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Patrick Willems

Showing results (71-80 of 81) with videos related to

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Science (New York, N.Y.)|March 23, 2019
Damage on plants activates Ca<sup>2+</sup>-dependent metacaspases for release of immunomodulatory peptidesTim Hander, Álvaro D Fernández-Fernández, Robert P Kumpf, et al.
Scientific Reports|December 12, 2025
Increased plasma fibronectin mirrors intimal phenotypic switching of vascular smooth muscle cells in moyamoya arteriopathyCaroline Asselman, Jozefien Meersschaut, Patrick Willems, et al.
European Journal of Medical Genetics|June 11, 2022
Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular diseaseAnett Marais, Aida M Bertoli-Avella, Christian Beetz, et al.
Proteomics|August 10, 2024
TermineR: Extracting information on endogenous proteolytic processing from shotgun proteomics dataMiguel Cosenza-Contreras, Adrianna Seredynska, Daniel Vogele, et al.
Plant Physiology|May 27, 2016
Lack of GLYCOLATE OXIDASE1, but Not GLYCOLATE OXIDASE2, Attenuates the Photorespiratory Phenotype of CATALASE2-Deficient ArabidopsisPavel Kerchev, Cezary Waszczak, Aleksandra Lewandowska, et al.
Plant Physiology|February 8, 2017
The Transcription Factor MYB29 Is a Regulator of <i>ALTERNATIVE OXIDASE1a</i>Xinhua Zhang, Aneta Ivanova, Klaas Vandepoele, et al.
Bioinformatics (Oxford, England)|September 10, 2024
Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencingPeter De Rijk, Tijs Watzeels, Fahri Küçükali, et al.
Molecular & Cellular Proteomics : MCP|August 15, 2024
Immunopeptidomics Mapping of Listeria monocytogenes T Cell Epitopes in MiceAdillah Gul, Lecia L Pewe, Patrick Willems, et al.
Human Mutation|October 4, 2012
Novel mutations including deletions of the entire OFD1 gene in 30 families with type 1 orofaciodigital syndrome: a study of the extensive clinical variabilityIzak J Bisschoff, Christine Zeschnigk, Denise Horn, et al.
American Journal of Medical Genetics. Part A|January 8, 2019
Cornelia de Lange syndrome in diverse populationsLeah Dowsett, Antonio R Porras, Paul Kruszka, et al.
Pageof 9

Showing results (71-80 of 81) with videos related to

Sort By:
Pageof 9
Science (New York, N.Y.)|March 23, 2019
Damage on plants activates Ca<sup>2+</sup>-dependent metacaspases for release of immunomodulatory peptidesTim Hander, Álvaro D Fernández-Fernández, Robert P Kumpf, et al.
Scientific Reports|December 12, 2025
Increased plasma fibronectin mirrors intimal phenotypic switching of vascular smooth muscle cells in moyamoya arteriopathyCaroline Asselman, Jozefien Meersschaut, Patrick Willems, et al.
European Journal of Medical Genetics|June 11, 2022
Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular diseaseAnett Marais, Aida M Bertoli-Avella, Christian Beetz, et al.
Proteomics|August 10, 2024
TermineR: Extracting information on endogenous proteolytic processing from shotgun proteomics dataMiguel Cosenza-Contreras, Adrianna Seredynska, Daniel Vogele, et al.
Plant Physiology|May 27, 2016
Lack of GLYCOLATE OXIDASE1, but Not GLYCOLATE OXIDASE2, Attenuates the Photorespiratory Phenotype of CATALASE2-Deficient ArabidopsisPavel Kerchev, Cezary Waszczak, Aleksandra Lewandowska, et al.
Plant Physiology|February 8, 2017
The Transcription Factor MYB29 Is a Regulator of <i>ALTERNATIVE OXIDASE1a</i>Xinhua Zhang, Aneta Ivanova, Klaas Vandepoele, et al.
Bioinformatics (Oxford, England)|September 10, 2024
Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencingPeter De Rijk, Tijs Watzeels, Fahri Küçükali, et al.
Molecular & Cellular Proteomics : MCP|August 15, 2024
Immunopeptidomics Mapping of Listeria monocytogenes T Cell Epitopes in MiceAdillah Gul, Lecia L Pewe, Patrick Willems, et al.
Human Mutation|October 4, 2012
Novel mutations including deletions of the entire OFD1 gene in 30 families with type 1 orofaciodigital syndrome: a study of the extensive clinical variabilityIzak J Bisschoff, Christine Zeschnigk, Denise Horn, et al.
American Journal of Medical Genetics. Part A|January 8, 2019
Cornelia de Lange syndrome in diverse populationsLeah Dowsett, Antonio R Porras, Paul Kruszka, et al.
Pageof 9