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Peter Nürnberg

Showing results (131-140 of 517) with videos related to

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Human Mutation|May 10, 2005
Application of genomewide SNP arrays for detection of simulated susceptibility lociBettina Kulle, Markus Schirmer, Mohammad R Toliat, et al.
Journal of Inherited Metabolic Disease|February 4, 2010
A novel mutation in LMBRD1 causes the cblF defect of vitamin B(12) metabolism in a Turkish patientSusann Gailus, Terttu Suormala, Ayse Gül Malerczyk-Aktas, et al.
American Journal of Medical Genetics. Part A|July 4, 2014
Atypical Aicardi-Goutieres syndrome: is the WRN locus a modifier?Davor Lessel, Bidisha Saha, Fuki Hisama, et al.
European Journal of Dermatology : EJD|August 29, 2006
Investigation of the HLA-DRB1 locus in alopecia areataPatricia Entz, Bettina Blaumeiser, Regina C Betz, et al.
Pediatric Research|September 1, 2021
Verification of immunology-related genetic associations in BPD supports ABCA3 and five other genesFelix Blume, Holger Kirsten, Peter Ahnert, et al.
Audiology & Neuro-Otology|June 12, 2017
AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant InheritanceRuth Lang-Roth, Eva Fischer-Krall, Cornelia Kornblum, et al.
Journal of Hepatology|October 9, 2012
Next generation sequencing of the Ago2 interacting transcriptome identified chemokine family members as novel targets of neuronal microRNAs in hepatic stellate cellsAndrea Noetel, Natalia Elfimova, Janine Altmüller, et al.
Carcinogenesis|June 30, 2012
Replication of genetic susceptibility loci for testicular germ cell cancer in the Croatian populationDavor Lessel, Marija Gamulin, Tomislav Kulis, et al.
Acta Neuropathologica|March 20, 2016
Neuropathological signs of inflammation correlate with mitochondrial DNA deletions in mesial temporal lobe epilepsyElisa Volmering, Pitt Niehusmann, Viktoriya Peeva, et al.
Investigative Ophthalmology & Visual Science|May 2, 2009
A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?Oliver Puk, Irene Esposito, Torben Söker, et al.
Pageof 52

Showing results (131-140 of 517) with videos related to

Sort By:
Pageof 52
Human Mutation|May 10, 2005
Application of genomewide SNP arrays for detection of simulated susceptibility lociBettina Kulle, Markus Schirmer, Mohammad R Toliat, et al.
Journal of Inherited Metabolic Disease|February 4, 2010
A novel mutation in LMBRD1 causes the cblF defect of vitamin B(12) metabolism in a Turkish patientSusann Gailus, Terttu Suormala, Ayse Gül Malerczyk-Aktas, et al.
American Journal of Medical Genetics. Part A|July 4, 2014
Atypical Aicardi-Goutieres syndrome: is the WRN locus a modifier?Davor Lessel, Bidisha Saha, Fuki Hisama, et al.
European Journal of Dermatology : EJD|August 29, 2006
Investigation of the HLA-DRB1 locus in alopecia areataPatricia Entz, Bettina Blaumeiser, Regina C Betz, et al.
Pediatric Research|September 1, 2021
Verification of immunology-related genetic associations in BPD supports ABCA3 and five other genesFelix Blume, Holger Kirsten, Peter Ahnert, et al.
Audiology & Neuro-Otology|June 12, 2017
AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant InheritanceRuth Lang-Roth, Eva Fischer-Krall, Cornelia Kornblum, et al.
Journal of Hepatology|October 9, 2012
Next generation sequencing of the Ago2 interacting transcriptome identified chemokine family members as novel targets of neuronal microRNAs in hepatic stellate cellsAndrea Noetel, Natalia Elfimova, Janine Altmüller, et al.
Carcinogenesis|June 30, 2012
Replication of genetic susceptibility loci for testicular germ cell cancer in the Croatian populationDavor Lessel, Marija Gamulin, Tomislav Kulis, et al.
Acta Neuropathologica|March 20, 2016
Neuropathological signs of inflammation correlate with mitochondrial DNA deletions in mesial temporal lobe epilepsyElisa Volmering, Pitt Niehusmann, Viktoriya Peeva, et al.
Investigative Ophthalmology & Visual Science|May 2, 2009
A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?Oliver Puk, Irene Esposito, Torben Söker, et al.
Pageof 52