Search research articles
Contact Us
Filters
Showing results (291-300 of 493) with videos related to
Page
of 50
Sort By:
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 spectroscopy
Alistair 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 Cataract
Venkata Pulla Rao Vendra, Christian Ostrowski, Marzena A Dyba, et al.
Scientific Reports
|
June 5, 2015
Electron spin coherence near room temperature in magnetic quantum dots
Fabrizio 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 Group
A 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 GJA8
Lars 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 Indies
Dan 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 populations
Jessie 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 cataracts
Eran 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 sources
R 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 mutation
Qingjiong Zhang, Fareeha Zulfiqar, S Amer Riazuddin, et al.
Page
of 50
Search research articles
Search
Showing results (291-300 of 493) with videos related to
Sort By:
Page
of 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 spectroscopy
Alistair 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 Cataract
Venkata Pulla Rao Vendra, Christian Ostrowski, Marzena A Dyba, et al.
Scientific Reports
|
June 5, 2015
Electron spin coherence near room temperature in magnetic quantum dots
Fabrizio 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 Group
A 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 GJA8
Lars 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 Indies
Dan 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 populations
Jessie 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 cataracts
Eran 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 sources
R 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 mutation
Qingjiong Zhang, Fareeha Zulfiqar, S Amer Riazuddin, et al.
Page
of 50