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Steffen Uebe

Showing results (41-50 of 88) with videos related to

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Theranostics|January 4, 2021
Network- and systems-based re-engineering of dendritic cells with non-coding RNAs for cancer immunotherapyXin Lai, Florian S Dreyer, Martina Cantone, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
HIBCH deficiency in a patient with phenotypic characteristics of mitochondrial disordersMiriam S Reuter, Jörn Oliver Sass, Thomas Leis, et al.
Human Mutation|October 18, 2014
MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and Golgi architecture as a central mechanism in growth regulationDiana Zahnleiter, Nadine N Hauer, Kristin Kessler, et al.
American Journal of Human Genetics|March 5, 2017
Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and MicrocephalyHasan Tawamie, Igor Martianov, Natalie Wohlfahrt, et al.
The Journal of Investigative Dermatology|January 1, 2022
Transcriptomes of MPO-Deficient Patients with Generalized Pustular Psoriasis Reveals Expansion of CD4<sup>+</sup> Cytotoxic T Cells and an Involvement of the Complement SystemStefan Haskamp, Benjamin Frey, Ina Becker, et al.
American Journal of Human Genetics|December 3, 2014
A peroxisomal disorder of severe intellectual disability, epilepsy, and cataracts due to fatty acyl-CoA reductase 1 deficiencyRebecca Buchert, Hasan Tawamie, Christopher Smith, et al.
BMC Medical Genetics|August 25, 2017
Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patientsSteffen Uebe, Maria Ehrlicher, Arif Bülent Ekici, et al.
European Journal of Medical Genetics|May 22, 2026
A multi-omics approach to characterize a deep intronic ARID1A deletion in Coffin-Siris SyndromeSarah Schuhmann, Elisabeth Bosch, Andreas Fink, et al.
Arthritis Research & Therapy|March 31, 2017
DNA methylation mediates genotype and smoking interaction in the development of anti-citrullinated peptide antibody-positive rheumatoid arthritisWeida Meng, Zaihua Zhu, Xia Jiang, et al.
Scientific Reports|July 2, 2015
DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defectsKristin Kessler, Ina Wunderlich, Steffen Uebe, et al.
Pageof 9

Showing results (41-50 of 88) with videos related to

Sort By:
Pageof 9
Theranostics|January 4, 2021
Network- and systems-based re-engineering of dendritic cells with non-coding RNAs for cancer immunotherapyXin Lai, Florian S Dreyer, Martina Cantone, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
HIBCH deficiency in a patient with phenotypic characteristics of mitochondrial disordersMiriam S Reuter, Jörn Oliver Sass, Thomas Leis, et al.
Human Mutation|October 18, 2014
MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and Golgi architecture as a central mechanism in growth regulationDiana Zahnleiter, Nadine N Hauer, Kristin Kessler, et al.
American Journal of Human Genetics|March 5, 2017
Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and MicrocephalyHasan Tawamie, Igor Martianov, Natalie Wohlfahrt, et al.
The Journal of Investigative Dermatology|January 1, 2022
Transcriptomes of MPO-Deficient Patients with Generalized Pustular Psoriasis Reveals Expansion of CD4<sup>+</sup> Cytotoxic T Cells and an Involvement of the Complement SystemStefan Haskamp, Benjamin Frey, Ina Becker, et al.
American Journal of Human Genetics|December 3, 2014
A peroxisomal disorder of severe intellectual disability, epilepsy, and cataracts due to fatty acyl-CoA reductase 1 deficiencyRebecca Buchert, Hasan Tawamie, Christopher Smith, et al.
BMC Medical Genetics|August 25, 2017
Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patientsSteffen Uebe, Maria Ehrlicher, Arif Bülent Ekici, et al.
European Journal of Medical Genetics|May 22, 2026
A multi-omics approach to characterize a deep intronic ARID1A deletion in Coffin-Siris SyndromeSarah Schuhmann, Elisabeth Bosch, Andreas Fink, et al.
Arthritis Research & Therapy|March 31, 2017
DNA methylation mediates genotype and smoking interaction in the development of anti-citrullinated peptide antibody-positive rheumatoid arthritisWeida Meng, Zaihua Zhu, Xia Jiang, et al.
Scientific Reports|July 2, 2015
DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defectsKristin Kessler, Ina Wunderlich, Steffen Uebe, et al.
Pageof 9