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Marcel Dinger

Showing results (1-10 of 8) with videos related to

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Astrobiology|January 18, 2003
Archaeal genome organization and stress responses: implications for the origin and evolution of cellular lifeDavid Musgrave, Xiaoying Zhang, Marcel Dinger
The Journal of Pathology|November 3, 2009
Non-coding RNAs: regulators of diseaseRyan J Taft, Ken C Pang, Timothy R Mercer, et al.
Frontiers in Neurology|April 15, 2021
Destination Amyotrophic Lateral SclerosisMatt Keon, Benjamin Musrie, Marcel Dinger, et al.
Experimental Eye Research|January 7, 2018
Identification of OAF and PVRL1 as candidate genes for an ocular anomaly characterized by Peters anomaly type 2 and ectopia lentisDezső David, Deepti Anand, Carlos Araújo, et al.
Journal of Medical Genetics|May 27, 2019
Pathogenic variants in <i>PLOD3</i> result in a Stickler syndrome-like connective tissue disorder with vascular complicationsLisa Jean Ewans, Alison Colley, Carles Gaston-Massuet, et al.
The Journal of Experimental Medicine|July 9, 2020
Mutations in the exocyst component EXOC2 cause severe defects in human brain developmentNicole J Van Bergen, Syed Mukhtar Ahmed, Felicity Collins, et al.
Nucleic Acids Research|October 30, 2014
RNAcentral: an international database of ncRNA sequences, Anton I Petrov, Simon J E Kay, et al.
American Journal of Human Genetics|March 5, 2019
De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-Progressive Neurocognitive SyndromeElizabeth E Palmer, Seungbeom Hong, Fatema Al Zahrani, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Astrobiology|January 18, 2003
Archaeal genome organization and stress responses: implications for the origin and evolution of cellular lifeDavid Musgrave, Xiaoying Zhang, Marcel Dinger
The Journal of Pathology|November 3, 2009
Non-coding RNAs: regulators of diseaseRyan J Taft, Ken C Pang, Timothy R Mercer, et al.
Frontiers in Neurology|April 15, 2021
Destination Amyotrophic Lateral SclerosisMatt Keon, Benjamin Musrie, Marcel Dinger, et al.
Experimental Eye Research|January 7, 2018
Identification of OAF and PVRL1 as candidate genes for an ocular anomaly characterized by Peters anomaly type 2 and ectopia lentisDezső David, Deepti Anand, Carlos Araújo, et al.
Journal of Medical Genetics|May 27, 2019
Pathogenic variants in <i>PLOD3</i> result in a Stickler syndrome-like connective tissue disorder with vascular complicationsLisa Jean Ewans, Alison Colley, Carles Gaston-Massuet, et al.
The Journal of Experimental Medicine|July 9, 2020
Mutations in the exocyst component EXOC2 cause severe defects in human brain developmentNicole J Van Bergen, Syed Mukhtar Ahmed, Felicity Collins, et al.
Nucleic Acids Research|October 30, 2014
RNAcentral: an international database of ncRNA sequences, Anton I Petrov, Simon J E Kay, et al.
American Journal of Human Genetics|March 5, 2019
De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-Progressive Neurocognitive SyndromeElizabeth E Palmer, Seungbeom Hong, Fatema Al Zahrani, et al.
Pageof 1