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A Botta

Showing results (41-50 of 177) with videos related to

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Mutation Research|June 28, 2008
Micronuclei frequency in peripheral blood lymphocytes of cancer patients: a meta-analysisG Iarmarcovai, M Ceppi, A Botta, et al.
Indian Journal of Medical Microbiology|August 17, 2006
Detection of Helicobacter pylori cagA gene in gastric biopsies, clinical isolates and faecesK M Bindayna, W A Al Baker, G A Botta
The Journal of Communicable Diseases|February 4, 2003
Rapid diagnosis of Mycobacterium tuberculosis by multiplex polymerase chain reaction from clinical specimensK M Bindayna, A Thani, B Baig, et al.
Molecular and Cellular Probes|January 18, 2005
Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian populationL Vallo, E Bonifazi, P Borgiani, et al.
The Journal of Infection|July 1, 1988
Evaluation of a computer-assisted method of analysing SDS-PAGE protein profiles in tracing a hospital outbreak of Serratia marcescensA Arzese, G A Botta, G P Gesu, et al.
The Cochrane Database of Systematic Reviews|October 13, 2009
Probiotics for the treatment of bacterial vaginosisAbiola C Senok, Hans Verstraelen, Marleen Temmerman, et al.
Virology|November 18, 2000
Naturally occurring woodchuck hepatitis virus (WHV) deletion mutants in chronically WHV-infected woodchucksA Botta, M Lu, X Zhen, et al.
Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|February 18, 2006
Neonatal sepsis 1991-2001: prevalent bacterial agents and antimicrobial susceptibilities in BahrainKhalid M Bindayna, Afaf Jamsheer, Eman Farid, et al.
Mutation Research|November 29, 2005
Comparison of the relative sensitivity of human lymphocytes and mouse splenocytes to two spindle poisonsG Steiblen, T Orsière, C Pallen, et al.
Clinical Genetics|December 20, 2016
Myotonic dystrophy type 1: role of CCG, CTC and CGG interruptions within DMPK alleles in the pathogenesis and molecular diagnosisM Santoro, M Masciullo, G Silvestri, et al.
Pageof 18

Showing results (41-50 of 177) with videos related to

Sort By:
Pageof 18
Mutation Research|June 28, 2008
Micronuclei frequency in peripheral blood lymphocytes of cancer patients: a meta-analysisG Iarmarcovai, M Ceppi, A Botta, et al.
Indian Journal of Medical Microbiology|August 17, 2006
Detection of Helicobacter pylori cagA gene in gastric biopsies, clinical isolates and faecesK M Bindayna, W A Al Baker, G A Botta
The Journal of Communicable Diseases|February 4, 2003
Rapid diagnosis of Mycobacterium tuberculosis by multiplex polymerase chain reaction from clinical specimensK M Bindayna, A Thani, B Baig, et al.
Molecular and Cellular Probes|January 18, 2005
Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian populationL Vallo, E Bonifazi, P Borgiani, et al.
The Journal of Infection|July 1, 1988
Evaluation of a computer-assisted method of analysing SDS-PAGE protein profiles in tracing a hospital outbreak of Serratia marcescensA Arzese, G A Botta, G P Gesu, et al.
The Cochrane Database of Systematic Reviews|October 13, 2009
Probiotics for the treatment of bacterial vaginosisAbiola C Senok, Hans Verstraelen, Marleen Temmerman, et al.
Virology|November 18, 2000
Naturally occurring woodchuck hepatitis virus (WHV) deletion mutants in chronically WHV-infected woodchucksA Botta, M Lu, X Zhen, et al.
Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|February 18, 2006
Neonatal sepsis 1991-2001: prevalent bacterial agents and antimicrobial susceptibilities in BahrainKhalid M Bindayna, Afaf Jamsheer, Eman Farid, et al.
Mutation Research|November 29, 2005
Comparison of the relative sensitivity of human lymphocytes and mouse splenocytes to two spindle poisonsG Steiblen, T Orsière, C Pallen, et al.
Clinical Genetics|December 20, 2016
Myotonic dystrophy type 1: role of CCG, CTC and CGG interruptions within DMPK alleles in the pathogenesis and molecular diagnosisM Santoro, M Masciullo, G Silvestri, et al.
Pageof 18