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A STRAUSS

Showing results (421-430 of 453) with videos related to

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Journal of Controlled Release : Official Journal of the Controlled Release Society|July 21, 2015
Targeted diagnostic magnetic nanoparticles for medical imaging of pancreatic cancerI Rosenberger, A Strauss, S Dobiasch, et al.
American Journal of Human Genetics|January 10, 2015
CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon proteaseKevin A Strauss, Robert N Jinks, Erik G Puffenberger, et al.
Scientific Reports|March 19, 2021
Molecular and epidemiologic characterization of the diphtheria outbreak in VenezuelaRicardo A Strauss, Laura Herrera-Leon, Ana C Guillén, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
Genomic diagnostics within a medically underserved population: efficacy and implicationsKevin A Strauss, Claudia Gonzaga-Jauregui, Karlla W Brigatti, et al.
Plos One|May 20, 2014
External quality assurance of malaria nucleic acid testing for clinical trials and eradication surveillanceSean C Murphy, Cornelus C Hermsen, Alexander D Douglas, et al.
Nature Medicine|June 17, 2022
Onasemnogene abeparvovec for presymptomatic infants with two copies of SMN2 at risk for spinal muscular atrophy type 1: the Phase III SPR1NT trialKevin A Strauss, Michelle A Farrar, Francesco Muntoni, et al.
Nature Medicine|June 17, 2022
Onasemnogene abeparvovec for presymptomatic infants with three copies of SMN2 at risk for spinal muscular atrophy: the Phase III SPR1NT trialKevin A Strauss, Michelle A Farrar, Francesco Muntoni, et al.
Molecular Cell|December 23, 2021
APC7 mediates ubiquitin signaling in constitutive heterochromatin in the developing mammalian brainCole J Ferguson, Olivia Urso, Tatyana Bodrug, et al.
Geburtshilfe Und Frauenheilkunde|September 27, 2016
Indications and Route of Hysterectomy for Benign Diseases. Guideline of the DGGG, OEGGG and SGGG (S3 Level, AWMF Registry No. 015/070, April 2015)K J Neis, W Zubke, T Römer, et al.
Molecular Genetics and Metabolism|January 26, 2020
Branched-chain α-ketoacid dehydrogenase deficiency (maple syrup urine disease): Treatment, biomarkers, and outcomesKevin A Strauss, Vincent J Carson, Kyle Soltys, et al.
Pageof 46

Showing results (421-430 of 453) with videos related to

Sort By:
Pageof 46
Journal of Controlled Release : Official Journal of the Controlled Release Society|July 21, 2015
Targeted diagnostic magnetic nanoparticles for medical imaging of pancreatic cancerI Rosenberger, A Strauss, S Dobiasch, et al.
American Journal of Human Genetics|January 10, 2015
CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon proteaseKevin A Strauss, Robert N Jinks, Erik G Puffenberger, et al.
Scientific Reports|March 19, 2021
Molecular and epidemiologic characterization of the diphtheria outbreak in VenezuelaRicardo A Strauss, Laura Herrera-Leon, Ana C Guillén, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
Genomic diagnostics within a medically underserved population: efficacy and implicationsKevin A Strauss, Claudia Gonzaga-Jauregui, Karlla W Brigatti, et al.
Plos One|May 20, 2014
External quality assurance of malaria nucleic acid testing for clinical trials and eradication surveillanceSean C Murphy, Cornelus C Hermsen, Alexander D Douglas, et al.
Nature Medicine|June 17, 2022
Onasemnogene abeparvovec for presymptomatic infants with two copies of SMN2 at risk for spinal muscular atrophy type 1: the Phase III SPR1NT trialKevin A Strauss, Michelle A Farrar, Francesco Muntoni, et al.
Nature Medicine|June 17, 2022
Onasemnogene abeparvovec for presymptomatic infants with three copies of SMN2 at risk for spinal muscular atrophy: the Phase III SPR1NT trialKevin A Strauss, Michelle A Farrar, Francesco Muntoni, et al.
Molecular Cell|December 23, 2021
APC7 mediates ubiquitin signaling in constitutive heterochromatin in the developing mammalian brainCole J Ferguson, Olivia Urso, Tatyana Bodrug, et al.
Geburtshilfe Und Frauenheilkunde|September 27, 2016
Indications and Route of Hysterectomy for Benign Diseases. Guideline of the DGGG, OEGGG and SGGG (S3 Level, AWMF Registry No. 015/070, April 2015)K J Neis, W Zubke, T Römer, et al.
Molecular Genetics and Metabolism|January 26, 2020
Branched-chain α-ketoacid dehydrogenase deficiency (maple syrup urine disease): Treatment, biomarkers, and outcomesKevin A Strauss, Vincent J Carson, Kyle Soltys, et al.
Pageof 46