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Janine Altmüller

Showing results (61-70 of 326) with videos related to

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Genome Biology and Evolution|July 2, 2022
De Novo-Whole Genome Assembly of the Roborovski Dwarf Hamster (Phodopus roborovskii) Genome: An Animal Model for Severe/Critical COVID-19Sandro Andreotti, Janine Altmüller, Claudia Quedenau, et al.
Haematologica|February 5, 2021
Micro-RNA networks in T-cell prolymphocytic leukemia reflect T-cell activation and shape DNA damage response and survival pathwaysTill Braun, Markus Glass, Linus Wahnschaffe, et al.
European Journal of Human Genetics : EJHG|October 11, 2021
Familial cleft tongue caused by a unique translation initiation codon variant in TP63Julia Schmidt, Gudrun Schreiber, Janine Altmüller, et al.
Frontiers in Oncology|March 3, 2018
Olfactory Receptors as Biomarkers in Human Breast Carcinoma TissuesLea Weber, Désirée Maßberg, Christian Becker, et al.
Nucleus (Austin, Tex.)|September 18, 2018
Depletion of Nesprin-2 is associated with an embryonic lethal phenotype in miceCarmen Mroß, Marija Marko, Martina Munck, et al.
Scientific Reports|May 5, 2017
A deep intronic CLRN1 (USH3A) founder mutation generates an aberrant exon and underlies severe Usher syndrome on the Arabian PeninsulaArif O Khan, Elvir Becirovic, Christian Betz, et al.
Neurology. Genetics|May 2, 2019
Novel PNKP mutations causing defective DNA strand break repair and PARP1 hyperactivity in MCSZIlona Kalasova, Hana Hanzlikova, Neerja Gupta, et al.
Scientific Reports|January 1, 2021
Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1BTim Becker, Andreas Pich, Stephanie Tamm, et al.
Journal of Medical Genetics|August 19, 2018
Homozygosity for the c.428delG variant in <i>KIAA0586</i> in a healthy individual: implications for molecular testing in patients with Joubert syndromeSilke Pauli, Janine Altmüller, Simone Schröder, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 2, 2017
Association of a synonymous SCN1B variant affecting splicing efficiency with Benign Familial Infantile Epilepsy (BFIE)Sunay Usluer, Melek Aslı Kayserili, Aslı Gündoğdu Eken, et al.
Pageof 33

Showing results (61-70 of 326) with videos related to

Sort By:
Pageof 33
Genome Biology and Evolution|July 2, 2022
De Novo-Whole Genome Assembly of the Roborovski Dwarf Hamster (Phodopus roborovskii) Genome: An Animal Model for Severe/Critical COVID-19Sandro Andreotti, Janine Altmüller, Claudia Quedenau, et al.
Haematologica|February 5, 2021
Micro-RNA networks in T-cell prolymphocytic leukemia reflect T-cell activation and shape DNA damage response and survival pathwaysTill Braun, Markus Glass, Linus Wahnschaffe, et al.
European Journal of Human Genetics : EJHG|October 11, 2021
Familial cleft tongue caused by a unique translation initiation codon variant in TP63Julia Schmidt, Gudrun Schreiber, Janine Altmüller, et al.
Frontiers in Oncology|March 3, 2018
Olfactory Receptors as Biomarkers in Human Breast Carcinoma TissuesLea Weber, Désirée Maßberg, Christian Becker, et al.
Nucleus (Austin, Tex.)|September 18, 2018
Depletion of Nesprin-2 is associated with an embryonic lethal phenotype in miceCarmen Mroß, Marija Marko, Martina Munck, et al.
Scientific Reports|May 5, 2017
A deep intronic CLRN1 (USH3A) founder mutation generates an aberrant exon and underlies severe Usher syndrome on the Arabian PeninsulaArif O Khan, Elvir Becirovic, Christian Betz, et al.
Neurology. Genetics|May 2, 2019
Novel PNKP mutations causing defective DNA strand break repair and PARP1 hyperactivity in MCSZIlona Kalasova, Hana Hanzlikova, Neerja Gupta, et al.
Scientific Reports|January 1, 2021
Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1BTim Becker, Andreas Pich, Stephanie Tamm, et al.
Journal of Medical Genetics|August 19, 2018
Homozygosity for the c.428delG variant in <i>KIAA0586</i> in a healthy individual: implications for molecular testing in patients with Joubert syndromeSilke Pauli, Janine Altmüller, Simone Schröder, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 2, 2017
Association of a synonymous SCN1B variant affecting splicing efficiency with Benign Familial Infantile Epilepsy (BFIE)Sunay Usluer, Melek Aslı Kayserili, Aslı Gündoğdu Eken, et al.
Pageof 33