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Andrew Orr

Showing results (11-20 of 26) with videos related to

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American Journal of Human Genetics|July 7, 2009
Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2Duane L Guernsey, Haiyan Jiang, Susan C Evans, et al.
Communications Earth & Environment|June 9, 2025
Thin and ephemeral snow shapes melt and runoff dynamics in the Peruvian AndesCatriona L Fyffe, Emily Potter, Evan Miles, et al.
Plos One|August 2, 2007
Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophyAndrew Orr, Marie-Pierre Dubé, Julien Marcadier, et al.
American Journal of Pharmaceutical Education|May 9, 2024
The Role of Consumerism in Pharmacy EducationRiley Bowers, Kayla R Stover, Dana A Strachan, et al.
NPJ Climate and Atmospheric Science|June 5, 2026
Unprecedented 2024 East Antarctic winter heatwave driven by polar vortex weakening and amplified by anthropogenic warmingHaosu Tang, Sihan Li, Julie M Jones, et al.
Plos Genetics|September 25, 2010
Mutation in the gene encoding ubiquitin ligase LRSAM1 in patients with Charcot-Marie-Tooth diseaseDuane L Guernsey, Haiyan Jiang, Karen Bedard, et al.
Nature Communications|April 3, 2026
Föhn-induced melting over Larsen C modulated by atmospheric river shape, direction and landfall locationXun Zou, Penny M Rowe, Irina V Gorodetskaya, et al.
Human Genetics|June 25, 2013
A novel rearrangement of occludin causes brain calcification and renal dysfunctionMarissa A LeBlanc, Lynette S Penney, Daniel Gaston, et al.
Molecular Vision|August 19, 2011
Mutations in a novel serine protease PRSS56 in families with nanophthalmosAndrew Orr, Marie-Pierre Dubé, Juan C Zenteno, et al.
Nature Genetics|May 5, 2009
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemiaDuane L Guernsey, Haiyan Jiang, Dean R Campagna, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
American Journal of Human Genetics|July 7, 2009
Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2Duane L Guernsey, Haiyan Jiang, Susan C Evans, et al.
Communications Earth & Environment|June 9, 2025
Thin and ephemeral snow shapes melt and runoff dynamics in the Peruvian AndesCatriona L Fyffe, Emily Potter, Evan Miles, et al.
Plos One|August 2, 2007
Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophyAndrew Orr, Marie-Pierre Dubé, Julien Marcadier, et al.
American Journal of Pharmaceutical Education|May 9, 2024
The Role of Consumerism in Pharmacy EducationRiley Bowers, Kayla R Stover, Dana A Strachan, et al.
NPJ Climate and Atmospheric Science|June 5, 2026
Unprecedented 2024 East Antarctic winter heatwave driven by polar vortex weakening and amplified by anthropogenic warmingHaosu Tang, Sihan Li, Julie M Jones, et al.
Plos Genetics|September 25, 2010
Mutation in the gene encoding ubiquitin ligase LRSAM1 in patients with Charcot-Marie-Tooth diseaseDuane L Guernsey, Haiyan Jiang, Karen Bedard, et al.
Nature Communications|April 3, 2026
Föhn-induced melting over Larsen C modulated by atmospheric river shape, direction and landfall locationXun Zou, Penny M Rowe, Irina V Gorodetskaya, et al.
Human Genetics|June 25, 2013
A novel rearrangement of occludin causes brain calcification and renal dysfunctionMarissa A LeBlanc, Lynette S Penney, Daniel Gaston, et al.
Molecular Vision|August 19, 2011
Mutations in a novel serine protease PRSS56 in families with nanophthalmosAndrew Orr, Marie-Pierre Dubé, Juan C Zenteno, et al.
Nature Genetics|May 5, 2009
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemiaDuane L Guernsey, Haiyan Jiang, Dean R Campagna, et al.
Pageof 3