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Heike Olbrich

Showing results (21-30 of 80) with videos related to

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Frontiers in Molecular Biosciences|December 25, 2025
Limitations of PICADAR as a diagnostic predictive tool for primary ciliary dyskinesiaAndre Schramm, Johanna Raidt, Sarah Riepenhausen, et al.
Molecular Human Reproduction|February 9, 2021
Motility of efferent duct cilia aids passage of sperm cells through the male reproductive systemIsabella Aprea, Tabea Nöthe-Menchen, Gerard W Dougherty, et al.
Journal of the American Society of Nephrology : JASN|August 4, 2006
Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting ciliaManfred Fliegauf, Judit Horvath, Christian von Schnakenburg, et al.
International Journal of Cancer|December 31, 2010
Functional characterization of a BRAF insertion mutant associated with pilocytic astrocytomaAnja E Eisenhardt, Heike Olbrich, Michael Röring, et al.
American Journal of Respiratory Cell and Molecular Biology|April 23, 2005
Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patientsJudit Horváth, Manfred Fliegauf, Heike Olbrich, et al.
Annals of the American Thoracic Society|February 24, 2022
Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal UltrastructureJohanna Raidt, Henrike Krenz, Johannes Tebbe, et al.
The European Respiratory Journal|October 3, 2024
Pathogenic variants in <i>CFAP46</i>, <i>CFAP54</i>, <i>CFAP74</i> and <i>CFAP221</i> cause primary ciliary dyskinesia with a defective C1d projection of the central apparatusKai Wohlgemuth, Niklas Hoersting, Julia Koenig, et al.
Cells|June 26, 2024
Biallelic Variants in <i>MNS1</i> Are Associated with Laterality Defects and Respiratory InvolvementRim Hjeij, Joseph Leslie, Hoda Rizk, et al.
American Journal of Human Genetics|February 9, 2006
Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolismJorn Oliver Sass, Verena Mohr, Heike Olbrich, et al.
Plos Genetics|February 26, 2021
Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertilityIsabella Aprea, Johanna Raidt, Inga Marlena Höben, et al.
Pageof 8

Showing results (21-30 of 80) with videos related to

Sort By:
Pageof 8
Frontiers in Molecular Biosciences|December 25, 2025
Limitations of PICADAR as a diagnostic predictive tool for primary ciliary dyskinesiaAndre Schramm, Johanna Raidt, Sarah Riepenhausen, et al.
Molecular Human Reproduction|February 9, 2021
Motility of efferent duct cilia aids passage of sperm cells through the male reproductive systemIsabella Aprea, Tabea Nöthe-Menchen, Gerard W Dougherty, et al.
Journal of the American Society of Nephrology : JASN|August 4, 2006
Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting ciliaManfred Fliegauf, Judit Horvath, Christian von Schnakenburg, et al.
International Journal of Cancer|December 31, 2010
Functional characterization of a BRAF insertion mutant associated with pilocytic astrocytomaAnja E Eisenhardt, Heike Olbrich, Michael Röring, et al.
American Journal of Respiratory Cell and Molecular Biology|April 23, 2005
Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patientsJudit Horváth, Manfred Fliegauf, Heike Olbrich, et al.
Annals of the American Thoracic Society|February 24, 2022
Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal UltrastructureJohanna Raidt, Henrike Krenz, Johannes Tebbe, et al.
The European Respiratory Journal|October 3, 2024
Pathogenic variants in <i>CFAP46</i>, <i>CFAP54</i>, <i>CFAP74</i> and <i>CFAP221</i> cause primary ciliary dyskinesia with a defective C1d projection of the central apparatusKai Wohlgemuth, Niklas Hoersting, Julia Koenig, et al.
Cells|June 26, 2024
Biallelic Variants in <i>MNS1</i> Are Associated with Laterality Defects and Respiratory InvolvementRim Hjeij, Joseph Leslie, Hoda Rizk, et al.
American Journal of Human Genetics|February 9, 2006
Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolismJorn Oliver Sass, Verena Mohr, Heike Olbrich, et al.
Plos Genetics|February 26, 2021
Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertilityIsabella Aprea, Johanna Raidt, Inga Marlena Höben, et al.
Pageof 8