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Janine Altmüller

Showing results (111-120 of 326) with videos related to

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Frontiers in Molecular Biosciences|January 19, 2016
Characterization of the Olfactory Receptors Expressed in Human SpermatozoaCaroline Flegel, Felix Vogel, Adrian Hofreuter, et al.
Cell & Bioscience|September 24, 2022
Reliable assessment of telomere maintenance mechanisms in neuroblastomaAlina Meeser, Christoph Bartenhagen, Lisa Werr, et al.
Clinical Genetics|February 26, 2022
Phenotypic spectrum of BLM- and RMI1-related Bloom syndromeIpek Ilgin Gönenc, Nursel H Elcioglu, Carolina Martinez Grijalva, et al.
The Journal of Biological Chemistry|September 24, 2021
Mitochondrial respiratory chain function promotes extracellular matrix integrity in cartilageKristina Bubb, Tatjana Holzer, Janica L Nolte, et al.
Neuropediatrics|August 31, 2018
Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech DevelopmentWalid Fazeli, Kerstin Becker, Peter Herkenrath, et al.
Genome Medicine|June 26, 2020
cfNOMe - A single assay for comprehensive epigenetic analyses of cell-free DNAFlorian Erger, Deborah Nörling, Domenica Borchert, et al.
Human Molecular Genetics|November 20, 2018
Mechanism suppressing H3K9 trimethylation in pluripotent stem cells and its demise by polyQ-expanded huntingtin mutationsDilber Irmak, Azra Fatima, Ricardo Gutiérrez-Garcia, et al.
Orphanet Journal of Rare Diseases|May 2, 2023
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continuedSimone Schröder, Gökhan Yigit, Yun Li, et al.
Plos One|September 17, 2013
RBFOX1 and RBFOX3 mutations in rolandic epilepsyDennis Lal, Eva M Reinthaler, Janine Altmüller, et al.
American Journal of Medical Genetics. Part A|January 11, 2021
Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal studyAndrea Gangfuß, Gökhan Yigit, Janine Altmüller, et al.
Pageof 33

Showing results (111-120 of 326) with videos related to

Sort By:
Pageof 33
Frontiers in Molecular Biosciences|January 19, 2016
Characterization of the Olfactory Receptors Expressed in Human SpermatozoaCaroline Flegel, Felix Vogel, Adrian Hofreuter, et al.
Cell & Bioscience|September 24, 2022
Reliable assessment of telomere maintenance mechanisms in neuroblastomaAlina Meeser, Christoph Bartenhagen, Lisa Werr, et al.
Clinical Genetics|February 26, 2022
Phenotypic spectrum of BLM- and RMI1-related Bloom syndromeIpek Ilgin Gönenc, Nursel H Elcioglu, Carolina Martinez Grijalva, et al.
The Journal of Biological Chemistry|September 24, 2021
Mitochondrial respiratory chain function promotes extracellular matrix integrity in cartilageKristina Bubb, Tatjana Holzer, Janica L Nolte, et al.
Neuropediatrics|August 31, 2018
Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech DevelopmentWalid Fazeli, Kerstin Becker, Peter Herkenrath, et al.
Genome Medicine|June 26, 2020
cfNOMe - A single assay for comprehensive epigenetic analyses of cell-free DNAFlorian Erger, Deborah Nörling, Domenica Borchert, et al.
Human Molecular Genetics|November 20, 2018
Mechanism suppressing H3K9 trimethylation in pluripotent stem cells and its demise by polyQ-expanded huntingtin mutationsDilber Irmak, Azra Fatima, Ricardo Gutiérrez-Garcia, et al.
Orphanet Journal of Rare Diseases|May 2, 2023
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continuedSimone Schröder, Gökhan Yigit, Yun Li, et al.
Plos One|September 17, 2013
RBFOX1 and RBFOX3 mutations in rolandic epilepsyDennis Lal, Eva M Reinthaler, Janine Altmüller, et al.
American Journal of Medical Genetics. Part A|January 11, 2021
Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal studyAndrea Gangfuß, Gökhan Yigit, Janine Altmüller, et al.
Pageof 33