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Steffen Uebe

Showing results (1-10 of 88) with videos related to

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BMC Bioinformatics|September 23, 2010
GPFrontend and GPGraphics: graphical analysis tools for genetic association studiesSteffen Uebe, Francesca Pasutto, Mandy Krumbiegel, et al.
Plos One|May 19, 2015
Novel loci for non-syndromic coarctation of the aorta in sporadic and familial casesJulia Moosmann, Steffen Uebe, Sven Dittrich, et al.
Mutation Research|March 26, 2003
Identification of a novel mutation in WFS1 in a family affected by low-frequency hearing impairmentJürgen Kunz, Ben Marquez-Klaka, Steffen Uebe, et al.
Arthritis Research & Therapy|April 20, 2012
Identification of low-frequency TRAF3IP2 coding variants in psoriatic arthritis patients and functional characterizationBeate Böhm, Harald Burkhardt, Steffen Uebe, et al.
American Journal of Medical Genetics. Part A|November 20, 2018
Microphthalmia is not a mandatory finding in X-linked recessive syndromic microphthalmia caused by the recurrent BCOR variant p.Pro85LeuCornelia Kraus, Steffen Uebe, Christian T Thiel, et al.
Molecular and Cellular Probes|May 25, 2015
Recurrent null mutation in SPG20 leads to Troyer syndromeHasan Tawamie, Eva Wohlleber, Steffen Uebe, et al.
Development (Cambridge, England)|February 25, 2017
Transcriptome sequencing reveals <i>maelstrom</i> as a novel target gene of the terminal system in the red flour beetle <i>Tribolium castaneum</i>Fabian Pridöhl, Matthias Weißkopf, Nikolaus Koniszewski, et al.
BMC Medical Genomics|April 25, 2018
Integrative bioinformatics analysis characterizing the role of EDC3 in mRNA decay and its association to intellectual disabilityUte Scheller, Kathrin Pfisterer, Steffen Uebe, et al.
Biochemical Genetics|September 10, 2025
Exploring Differentially Expressed Genes and Understanding the Underlying Mechanisms in GlioblastomaDidem Seven, Arif Ekici, Steffen Uebe, et al.
JIMD Reports|January 29, 2017
A Homozygous Mutation in GPT2 Associated with Nonsyndromic Intellectual Disability in a Consanguineous Family from Costa RicaTanya Lobo-Prada, Heinrich Sticht, Sixto Bogantes-Ledezma, et al.
Pageof 9

Showing results (1-10 of 88) with videos related to

Sort By:
Pageof 9
BMC Bioinformatics|September 23, 2010
GPFrontend and GPGraphics: graphical analysis tools for genetic association studiesSteffen Uebe, Francesca Pasutto, Mandy Krumbiegel, et al.
Plos One|May 19, 2015
Novel loci for non-syndromic coarctation of the aorta in sporadic and familial casesJulia Moosmann, Steffen Uebe, Sven Dittrich, et al.
Mutation Research|March 26, 2003
Identification of a novel mutation in WFS1 in a family affected by low-frequency hearing impairmentJürgen Kunz, Ben Marquez-Klaka, Steffen Uebe, et al.
Arthritis Research & Therapy|April 20, 2012
Identification of low-frequency TRAF3IP2 coding variants in psoriatic arthritis patients and functional characterizationBeate Böhm, Harald Burkhardt, Steffen Uebe, et al.
American Journal of Medical Genetics. Part A|November 20, 2018
Microphthalmia is not a mandatory finding in X-linked recessive syndromic microphthalmia caused by the recurrent BCOR variant p.Pro85LeuCornelia Kraus, Steffen Uebe, Christian T Thiel, et al.
Molecular and Cellular Probes|May 25, 2015
Recurrent null mutation in SPG20 leads to Troyer syndromeHasan Tawamie, Eva Wohlleber, Steffen Uebe, et al.
Development (Cambridge, England)|February 25, 2017
Transcriptome sequencing reveals <i>maelstrom</i> as a novel target gene of the terminal system in the red flour beetle <i>Tribolium castaneum</i>Fabian Pridöhl, Matthias Weißkopf, Nikolaus Koniszewski, et al.
BMC Medical Genomics|April 25, 2018
Integrative bioinformatics analysis characterizing the role of EDC3 in mRNA decay and its association to intellectual disabilityUte Scheller, Kathrin Pfisterer, Steffen Uebe, et al.
Biochemical Genetics|September 10, 2025
Exploring Differentially Expressed Genes and Understanding the Underlying Mechanisms in GlioblastomaDidem Seven, Arif Ekici, Steffen Uebe, et al.
JIMD Reports|January 29, 2017
A Homozygous Mutation in GPT2 Associated with Nonsyndromic Intellectual Disability in a Consanguineous Family from Costa RicaTanya Lobo-Prada, Heinrich Sticht, Sixto Bogantes-Ledezma, et al.
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