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R Bochner

Showing results (31-40 of 37) with videos related to

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The British Journal of Dermatology|November 21, 2019
Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicinA Peled, L Samuelov, O Sarig, et al.
Plos One|April 2, 2011
Assay of the multiple energy-producing pathways of mammalian cellsBarry R Bochner, Mark Siri, Richard H Huang, et al.
The British Journal of Dermatology|September 19, 2017
A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENENM Pavlovsky, O Sarig, M Eskin-Schwartz, et al.
Journal of Bacteriology|December 31, 2005
Phenotype microarray profiling of Staphylococcus aureus menD and hemB mutants with the small-colony-variant phenotypeChristof von Eiff, Peter McNamara, Karsten Becker, et al.
Molecular Autism|June 5, 2013
Decreased tryptophan metabolism in patients with autism spectrum disordersLuigi Boccuto, Chin-Fu Chen, Ayla R Pittman, et al.
Epidemiology and Infection|October 15, 2015
Hantavirus pulmonary syndrome in a highly endemic area of BrazilR C Oliveira, M M Sant'ana, A Guterres, et al.
Nucleic Acids Research|November 17, 2014
GenoBase: comprehensive resource database of Escherichia coli K-12Yuta Otsuka, Ai Muto, Rikiya Takeuchi, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
The British Journal of Dermatology|November 21, 2019
Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicinA Peled, L Samuelov, O Sarig, et al.
Plos One|April 2, 2011
Assay of the multiple energy-producing pathways of mammalian cellsBarry R Bochner, Mark Siri, Richard H Huang, et al.
The British Journal of Dermatology|September 19, 2017
A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENENM Pavlovsky, O Sarig, M Eskin-Schwartz, et al.
Journal of Bacteriology|December 31, 2005
Phenotype microarray profiling of Staphylococcus aureus menD and hemB mutants with the small-colony-variant phenotypeChristof von Eiff, Peter McNamara, Karsten Becker, et al.
Molecular Autism|June 5, 2013
Decreased tryptophan metabolism in patients with autism spectrum disordersLuigi Boccuto, Chin-Fu Chen, Ayla R Pittman, et al.
Epidemiology and Infection|October 15, 2015
Hantavirus pulmonary syndrome in a highly endemic area of BrazilR C Oliveira, M M Sant'ana, A Guterres, et al.
Nucleic Acids Research|November 17, 2014
GenoBase: comprehensive resource database of Escherichia coli K-12Yuta Otsuka, Ai Muto, Rikiya Takeuchi, et al.
Pageof 4