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Bolz

Showing results (621-630 of 866) with videos related to

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Plos One|February 21, 2012
Evidence for conserved function of γ-glutamyltranspeptidase in Helicobacter genusMirko Rossi, Christian Bolz, Joana Revez, et al.
Therapeutic Advances in Neurological Disorders|October 12, 2018
Feasibility and safety of intrathecal treatment with nusinersen in adult patients with spinal muscular atrophyBenjamin Stolte, Andreas Totzeck, Kathrin Kizina, et al.
Journal of the American Society of Nephrology : JASN|May 23, 2003
Oxidized LDL and its compound lysophosphatidylcholine potentiate AngII-induced vasoconstriction by stimulation of RhoAJan Galle, Alexander Mameghani, Steffen-Sebastian Bolz, et al.
Scientific Reports|May 5, 2017
A deep intronic CLRN1 (USH3A) founder mutation generates an aberrant exon and underlies severe Usher syndrome on the Arabian PeninsulaArif O Khan, Elvir Becirovic, Christian Betz, et al.
BMC Infectious Diseases|December 1, 2014
Primary cultivation: factors affecting contamination and Mycobacterium ulcerans growth after long turnover time of clinical specimensMartin W Bratschi, Miriam Bolz, Leticia Grize, et al.
Human Mutation|March 12, 2014
Targeted and genomewide NGS data disqualify mutations in MYO1A, the "DFNA48 gene", as a cause of deafnessTobias Eisenberger, Nataliya Di Donato, Shahid M Baig, et al.
Orphanet Journal of Rare Diseases|September 4, 2012
Targeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3Tobias Eisenberger, Rima Slim, Ahmad Mansour, et al.
Frontiers in Microbiology|July 15, 2021
Quorum Sensing and Cyclic di-GMP Exert Control Over Motility of <i>Vibrio fischeri</i> KB2B1Courtney N Dial, Steven J Eichinger, Randi Foxall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2018
A C-terminal nonsense mutation links PTPRQ with autosomal-dominant hearing loss, DFNA73Tobias Eisenberger, Nataliya Di Donato, Christian Decker, et al.
Frontiers in Physiology|August 21, 2025
Blood pressure is elevated in the absence of resistance artery dysfunction in a mouse model of diet-induced obesityDarcy Lidington, Danny D Dinh, Nan Chen, et al.
Pageof 87

Showing results (621-630 of 866) with videos related to

Sort By:
Pageof 87
Plos One|February 21, 2012
Evidence for conserved function of γ-glutamyltranspeptidase in Helicobacter genusMirko Rossi, Christian Bolz, Joana Revez, et al.
Therapeutic Advances in Neurological Disorders|October 12, 2018
Feasibility and safety of intrathecal treatment with nusinersen in adult patients with spinal muscular atrophyBenjamin Stolte, Andreas Totzeck, Kathrin Kizina, et al.
Journal of the American Society of Nephrology : JASN|May 23, 2003
Oxidized LDL and its compound lysophosphatidylcholine potentiate AngII-induced vasoconstriction by stimulation of RhoAJan Galle, Alexander Mameghani, Steffen-Sebastian Bolz, et al.
Scientific Reports|May 5, 2017
A deep intronic CLRN1 (USH3A) founder mutation generates an aberrant exon and underlies severe Usher syndrome on the Arabian PeninsulaArif O Khan, Elvir Becirovic, Christian Betz, et al.
BMC Infectious Diseases|December 1, 2014
Primary cultivation: factors affecting contamination and Mycobacterium ulcerans growth after long turnover time of clinical specimensMartin W Bratschi, Miriam Bolz, Leticia Grize, et al.
Human Mutation|March 12, 2014
Targeted and genomewide NGS data disqualify mutations in MYO1A, the "DFNA48 gene", as a cause of deafnessTobias Eisenberger, Nataliya Di Donato, Shahid M Baig, et al.
Orphanet Journal of Rare Diseases|September 4, 2012
Targeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3Tobias Eisenberger, Rima Slim, Ahmad Mansour, et al.
Frontiers in Microbiology|July 15, 2021
Quorum Sensing and Cyclic di-GMP Exert Control Over Motility of <i>Vibrio fischeri</i> KB2B1Courtney N Dial, Steven J Eichinger, Randi Foxall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2018
A C-terminal nonsense mutation links PTPRQ with autosomal-dominant hearing loss, DFNA73Tobias Eisenberger, Nataliya Di Donato, Christian Decker, et al.
Frontiers in Physiology|August 21, 2025
Blood pressure is elevated in the absence of resistance artery dysfunction in a mouse model of diet-induced obesityDarcy Lidington, Danny D Dinh, Nan Chen, et al.
Pageof 87