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Lars Hansen

Showing results (161-170 of 178) with videos related to

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The Journal of Pharmacology and Experimental Therapeutics|September 28, 2025
Preclinical evaluation and first-in-human phase 1 trial of AZD0186, a novel, oral small molecule glucagon-like peptide-1 receptor agonistWeier Qi, Simina M Boca, Alessandro Boianelli, et al.
Plos One|July 30, 2013
Complete genome sequence of the cystic fibrosis pathogen Achromobacter xylosoxidans NH44784-1996 complies with important pathogenic phenotypesTim Holm Jakobsen, Martin Asser Hansen, Peter Østrup Jensen, et al.
American Journal of Medical Genetics. Part A|May 4, 2011
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairmentNanna D Rendtorff, Marianne Lodahl, Houda Boulahbel, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 2023
The SHDRA syndrome-associated gene <i>TMEM260</i> encodes a protein-specific O-mannosyltransferaseIda Signe Bohse Larsen, Lorenzo Povolo, Luping Zhou, et al.
Nature Metabolism|December 8, 2023
Cotadutide promotes glycogenolysis in people with overweight or obesity diagnosed with type 2 diabetesVictoria E R Parker, Darren Robertson, Edmundo Erazo-Tapia, et al.
The Journal of Biological Chemistry|May 26, 2019
Site-specific <i>O</i>-glycosylation of members of the low-density lipoprotein receptor superfamily enhances ligand interactionsShengjun Wang, Yang Mao, Yoshiki Narimatsu, et al.
The Journal of Biological Chemistry|March 22, 2018
Site-specific <i>O</i>-glycosylation of members of the low-density lipoprotein receptor superfamily enhances ligand interactionsShengjun Wang, Yang Mao, Yoshiki Narimatsu, et al.
Nature Communications|November 17, 2020
RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesisMuhammad Farooq, Louise Lindbæk, Nicolai Krogh, et al.
Molecular Cell|June 23, 2019
An Atlas of Human Glycosylation Pathways Enables Display of the Human Glycome by Gene Engineered CellsYoshiki Narimatsu, Hiren J Joshi, Rebecca Nason, et al.
American Journal of Medical Genetics. Part A|August 17, 2019
Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior yearsAngela E Lin, Siddharth K Prakash, Niels H Andersen, et al.
Pageof 18

Showing results (161-170 of 178) with videos related to

Sort By:
Pageof 18
The Journal of Pharmacology and Experimental Therapeutics|September 28, 2025
Preclinical evaluation and first-in-human phase 1 trial of AZD0186, a novel, oral small molecule glucagon-like peptide-1 receptor agonistWeier Qi, Simina M Boca, Alessandro Boianelli, et al.
Plos One|July 30, 2013
Complete genome sequence of the cystic fibrosis pathogen Achromobacter xylosoxidans NH44784-1996 complies with important pathogenic phenotypesTim Holm Jakobsen, Martin Asser Hansen, Peter Østrup Jensen, et al.
American Journal of Medical Genetics. Part A|May 4, 2011
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairmentNanna D Rendtorff, Marianne Lodahl, Houda Boulahbel, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 2023
The SHDRA syndrome-associated gene <i>TMEM260</i> encodes a protein-specific O-mannosyltransferaseIda Signe Bohse Larsen, Lorenzo Povolo, Luping Zhou, et al.
Nature Metabolism|December 8, 2023
Cotadutide promotes glycogenolysis in people with overweight or obesity diagnosed with type 2 diabetesVictoria E R Parker, Darren Robertson, Edmundo Erazo-Tapia, et al.
The Journal of Biological Chemistry|May 26, 2019
Site-specific <i>O</i>-glycosylation of members of the low-density lipoprotein receptor superfamily enhances ligand interactionsShengjun Wang, Yang Mao, Yoshiki Narimatsu, et al.
The Journal of Biological Chemistry|March 22, 2018
Site-specific <i>O</i>-glycosylation of members of the low-density lipoprotein receptor superfamily enhances ligand interactionsShengjun Wang, Yang Mao, Yoshiki Narimatsu, et al.
Nature Communications|November 17, 2020
RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesisMuhammad Farooq, Louise Lindbæk, Nicolai Krogh, et al.
Molecular Cell|June 23, 2019
An Atlas of Human Glycosylation Pathways Enables Display of the Human Glycome by Gene Engineered CellsYoshiki Narimatsu, Hiren J Joshi, Rebecca Nason, et al.
American Journal of Medical Genetics. Part A|August 17, 2019
Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior yearsAngela E Lin, Siddharth K Prakash, Niels H Andersen, et al.
Pageof 18