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Peter Bauer

Showing results (261-270 of 585) with videos related to

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Journal of Neuroscience Research|June 20, 2003
Gene expression profiling of ciliary neurotrophic factor-overexpressing rat striatal progenitor cells (ST14A) indicates improved stress response during the early stage of differentiationTobias Böttcher, Eilhard Mix, Dirk Koczan, et al.
International Journal of Molecular Sciences|February 15, 2022
Gaucher Disease Diagnosis Using Lyso-Gb1 on Dry Blood Spot Samples: Time to Change the Paradigm?Tama Dinur, Peter Bauer, Christian Beetz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
Prevalence of THAP1 sequence variants in German patients with primary dystoniaAnne S Söhn, Nicola Glöckle, Andrea Duarte Doetzer, et al.
Clinical Nutrition (Edinburgh, Scotland)|January 30, 2010
Effect of hydrolysed formula feeding on taste preferences at 10 years. Data from the German Infant Nutritional Intervention Program Plus StudyStefanie Sausenthaler, Sibylle Koletzko, Berthold Koletzko, et al.
The European Respiratory Journal|July 14, 2018
Lung function trajectories using different reference equations in a birth cohort study up to the age of 20 yearsChristiane Lex, Marvin Reuter, Antje Schuster, et al.
Journal of Proteomics|January 10, 2012
How many spots with missing values can be tolerated in quantitative two-dimensional gel electrophoresis when applying univariate statistics?Maria Zellner, Alexandra Graf, Sonja Zehetmayer, et al.
European Journal of Human Genetics : EJHG|January 4, 2020
Unraveling the genetic cause of hereditary ophthalmic disorders in Arab societies from Israel and the Palestinian AuthorityAnja K Mayer, Ghassan Balousha, Rajech Sharkia, et al.
Clinical Genetics|December 23, 2020
Biallelic loss-of-function HACD1 variants are a bona fide cause of congenital myopathyLia Abbasi-Moheb, Ana Westenberger, Maha Alotaibi, et al.
International Journal of Dentistry|December 23, 2011
Analysis of polymorphisms in the lactotransferrin gene promoter and dental cariesJoão Armando Brancher, Giovana Daniela Pecharki, Andrea Duarte Doetzer, et al.
BMC Pediatrics|November 26, 2014
Serum 25(OH)D concentrations and atopic diseases at age 10: results from the GINIplus and LISAplus birth cohort studiesNina Wawro, Joachim Heinrich, Elisabeth Thiering, et al.
Pageof 59

Showing results (261-270 of 585) with videos related to

Sort By:
Pageof 59
Journal of Neuroscience Research|June 20, 2003
Gene expression profiling of ciliary neurotrophic factor-overexpressing rat striatal progenitor cells (ST14A) indicates improved stress response during the early stage of differentiationTobias Böttcher, Eilhard Mix, Dirk Koczan, et al.
International Journal of Molecular Sciences|February 15, 2022
Gaucher Disease Diagnosis Using Lyso-Gb1 on Dry Blood Spot Samples: Time to Change the Paradigm?Tama Dinur, Peter Bauer, Christian Beetz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
Prevalence of THAP1 sequence variants in German patients with primary dystoniaAnne S Söhn, Nicola Glöckle, Andrea Duarte Doetzer, et al.
Clinical Nutrition (Edinburgh, Scotland)|January 30, 2010
Effect of hydrolysed formula feeding on taste preferences at 10 years. Data from the German Infant Nutritional Intervention Program Plus StudyStefanie Sausenthaler, Sibylle Koletzko, Berthold Koletzko, et al.
The European Respiratory Journal|July 14, 2018
Lung function trajectories using different reference equations in a birth cohort study up to the age of 20 yearsChristiane Lex, Marvin Reuter, Antje Schuster, et al.
Journal of Proteomics|January 10, 2012
How many spots with missing values can be tolerated in quantitative two-dimensional gel electrophoresis when applying univariate statistics?Maria Zellner, Alexandra Graf, Sonja Zehetmayer, et al.
European Journal of Human Genetics : EJHG|January 4, 2020
Unraveling the genetic cause of hereditary ophthalmic disorders in Arab societies from Israel and the Palestinian AuthorityAnja K Mayer, Ghassan Balousha, Rajech Sharkia, et al.
Clinical Genetics|December 23, 2020
Biallelic loss-of-function HACD1 variants are a bona fide cause of congenital myopathyLia Abbasi-Moheb, Ana Westenberger, Maha Alotaibi, et al.
International Journal of Dentistry|December 23, 2011
Analysis of polymorphisms in the lactotransferrin gene promoter and dental cariesJoão Armando Brancher, Giovana Daniela Pecharki, Andrea Duarte Doetzer, et al.
BMC Pediatrics|November 26, 2014
Serum 25(OH)D concentrations and atopic diseases at age 10: results from the GINIplus and LISAplus birth cohort studiesNina Wawro, Joachim Heinrich, Elisabeth Thiering, et al.
Pageof 59