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Annette M Payne

Showing results (1-10 of 5) with videos related to

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Algorithms for Molecular Biology : AMB|September 24, 2011
Multi-membership gene regulation in pathway based microarray analysisStelios P Pavlidis, Annette M Payne, Stephen M Swift
Cancers|August 7, 2021
Statistical Meta-Analysis of Risk Factors for Endometrial Cancer and Development of a Risk Prediction Model Using an Artificial Neural Network AlgorithmSuzanna Hutt, Denis Mihaies, Emmanouil Karteris, et al.
Advances in Experimental Medicine and Biology|February 25, 2003
Guanylate cyclase activating proteins, guanylate cyclase and diseaseRichard J Newbold, Evelyne C Deery, Annette M Payne, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 11, 2003
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL geneDavid A R Bessant, Graham E Holder, Frederick W Fitzke, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 14, 2004
The phenotype of Leber congenital amaurosis in patients with AIPL1 mutationsSharola Dharmaraj, Bart P Leroy, Melanie M Sohocki, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Algorithms for Molecular Biology : AMB|September 24, 2011
Multi-membership gene regulation in pathway based microarray analysisStelios P Pavlidis, Annette M Payne, Stephen M Swift
Cancers|August 7, 2021
Statistical Meta-Analysis of Risk Factors for Endometrial Cancer and Development of a Risk Prediction Model Using an Artificial Neural Network AlgorithmSuzanna Hutt, Denis Mihaies, Emmanouil Karteris, et al.
Advances in Experimental Medicine and Biology|February 25, 2003
Guanylate cyclase activating proteins, guanylate cyclase and diseaseRichard J Newbold, Evelyne C Deery, Annette M Payne, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 11, 2003
Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL geneDavid A R Bessant, Graham E Holder, Frederick W Fitzke, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 14, 2004
The phenotype of Leber congenital amaurosis in patients with AIPL1 mutationsSharola Dharmaraj, Bart P Leroy, Melanie M Sohocki, et al.
Pageof 1