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J Fielding

Showing results (291-300 of 493) with videos related to

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Biochemistry|August 21, 2008
Intramolecular electron transfer versus substrate oxidation in lactoperoxidase: investigation of radical intermediates by stopped-flow absorption spectrophotometry and (9-285 GHz) electron paramagnetic resonance spectroscopyAlistair J Fielding, Rahul Singh, Barbara Boscolo, et al.
International Journal of Molecular Sciences|September 28, 2023
Human γS-Crystallin Mutation F10_Y11delinsLN in the First Greek Key Pair Destabilizes and Impairs Tight Packing Causing Cortical Lamellar CataractVenkata Pulla Rao Vendra, Christian Ostrowski, Marzena A Dyba, et al.
Scientific Reports|June 5, 2015
Electron spin coherence near room temperature in magnetic quantum dotsFabrizio Moro, Lyudmila Turyanska, James Wilman, et al.
British Journal of Cancer|April 3, 1999
Patient survival after D1 and D2 resections for gastric cancer: long-term results of the MRC randomized surgical trial. Surgical Co-operative GroupA Cuschieri, S Weeden, J Fielding, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8Lars Hansen, Wenliang Yao, Hans Eiberg, et al.
Plos One|July 5, 2012
CDKN2B polymorphism is associated with primary open-angle glaucoma (POAG) in the Afro-Caribbean population of Barbados, West IndiesDan Cao, Xiaodong Jiao, Xing Liu, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
TyCHE enables time-resolved lineage tracing of heterogeneously-evolving populationsJessie J Fielding, Sherry Wu, Hunter J Melton, et al.
Investigative Ophthalmology & Visual Science|May 27, 2004
A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataractsEran Pras, Judith Raz, Vered Yahalom, et al.
Biochemistry|April 24, 1973
Cofactor activity of protein components of human very low density lipoproteins in the hydrolysis of triglycerides by lipoproteins lipase from different sourcesR J Havel, C J Fielding, T Olivecrona, et al.
Molecular Vision|December 1, 2004
Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutationQingjiong Zhang, Fareeha Zulfiqar, S Amer Riazuddin, et al.
Pageof 50

Showing results (291-300 of 493) with videos related to

Sort By:
Pageof 50
Biochemistry|August 21, 2008
Intramolecular electron transfer versus substrate oxidation in lactoperoxidase: investigation of radical intermediates by stopped-flow absorption spectrophotometry and (9-285 GHz) electron paramagnetic resonance spectroscopyAlistair J Fielding, Rahul Singh, Barbara Boscolo, et al.
International Journal of Molecular Sciences|September 28, 2023
Human γS-Crystallin Mutation F10_Y11delinsLN in the First Greek Key Pair Destabilizes and Impairs Tight Packing Causing Cortical Lamellar CataractVenkata Pulla Rao Vendra, Christian Ostrowski, Marzena A Dyba, et al.
Scientific Reports|June 5, 2015
Electron spin coherence near room temperature in magnetic quantum dotsFabrizio Moro, Lyudmila Turyanska, James Wilman, et al.
British Journal of Cancer|April 3, 1999
Patient survival after D1 and D2 resections for gastric cancer: long-term results of the MRC randomized surgical trial. Surgical Co-operative GroupA Cuschieri, S Weeden, J Fielding, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8Lars Hansen, Wenliang Yao, Hans Eiberg, et al.
Plos One|July 5, 2012
CDKN2B polymorphism is associated with primary open-angle glaucoma (POAG) in the Afro-Caribbean population of Barbados, West IndiesDan Cao, Xiaodong Jiao, Xing Liu, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
TyCHE enables time-resolved lineage tracing of heterogeneously-evolving populationsJessie J Fielding, Sherry Wu, Hunter J Melton, et al.
Investigative Ophthalmology & Visual Science|May 27, 2004
A nonsense mutation in the glucosaminyl (N-acetyl) transferase 2 gene (GCNT2): association with autosomal recessive congenital cataractsEran Pras, Judith Raz, Vered Yahalom, et al.
Biochemistry|April 24, 1973
Cofactor activity of protein components of human very low density lipoproteins in the hydrolysis of triglycerides by lipoproteins lipase from different sourcesR J Havel, C J Fielding, T Olivecrona, et al.
Molecular Vision|December 1, 2004
Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutationQingjiong Zhang, Fareeha Zulfiqar, S Amer Riazuddin, et al.
Pageof 50