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Heike Olbrich

Showing results (11-20 of 80) with videos related to

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Human Molecular Genetics|July 23, 2004
Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formationInés Ibañez-Tallon, Axel Pagenstecher, Manfred Fliegauf, et al.
Human Reproduction (Oxford, England)|September 17, 2015
Ciliary function and motor protein composition of human fallopian tubesJohanna Raidt, Claudius Werner, Tabea Menchen, et al.
Cells|July 26, 2024
Primary Ciliary Dyskinesia Associated Disease-Causing Variants in <i>CCDC39</i> and <i>CCDC40</i> Cause Axonemal Absence of Inner Dynein Arm Heavy Chains DNAH1, DNAH6, and DNAH7Alina Wilken, Inga Marlena Höben, Alexander Wolter, et al.
Human Mutation|May 26, 2017
Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defectChristine Edelbusch, Sandra Cindrić, Gerard W Dougherty, et al.
Histochemistry and Cell Biology|April 22, 2009
Doxycycline accelerates renal cyst growth and fibrosis in the pcy/pcy mouse model of type 3 nephronophthisis, a form of recessive polycystic kidney diseaseLarissa Osten, Marion Kubitza, Anna Rachel Gallagher, et al.
Journal of the American Society of Nephrology : JASN|December 26, 2001
Identification of a gene locus for Senior-Løken syndrome in the region of the nephronophthisis type 3 geneHeymut Omran, GÜrsel Sasmaz, Karsten Häffner, et al.
The European Respiratory Journal|September 5, 2014
Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesiaJohanna Raidt, Julia Wallmeier, Rim Hjeij, et al.
American Journal of Respiratory Cell and Molecular Biology|September 1, 2022
Recessive Mutations in <i>CFAP74</i> Cause Primary Ciliary Dyskinesia with Normal Ciliary UltrastructureLuisa Biebach, Sandra Cindrić, Julia Koenig, et al.
NMR in Biomedicine|May 23, 2007
NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error of metabolismUdo F H Engelke, Jörn Oliver Sass, Rudy N Van Coster, et al.
Circulation. Genomic and Precision Medicine|October 23, 2019
Randomization of Left-right Asymmetry and Congenital Heart Defects: The Role of <i>DNAH5</i> in Humans and MiceTabea Nöthe-Menchen, Julia Wallmeier, Petra Pennekamp, et al.
Pageof 8

Showing results (11-20 of 80) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|July 23, 2004
Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formationInés Ibañez-Tallon, Axel Pagenstecher, Manfred Fliegauf, et al.
Human Reproduction (Oxford, England)|September 17, 2015
Ciliary function and motor protein composition of human fallopian tubesJohanna Raidt, Claudius Werner, Tabea Menchen, et al.
Cells|July 26, 2024
Primary Ciliary Dyskinesia Associated Disease-Causing Variants in <i>CCDC39</i> and <i>CCDC40</i> Cause Axonemal Absence of Inner Dynein Arm Heavy Chains DNAH1, DNAH6, and DNAH7Alina Wilken, Inga Marlena Höben, Alexander Wolter, et al.
Human Mutation|May 26, 2017
Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defectChristine Edelbusch, Sandra Cindrić, Gerard W Dougherty, et al.
Histochemistry and Cell Biology|April 22, 2009
Doxycycline accelerates renal cyst growth and fibrosis in the pcy/pcy mouse model of type 3 nephronophthisis, a form of recessive polycystic kidney diseaseLarissa Osten, Marion Kubitza, Anna Rachel Gallagher, et al.
Journal of the American Society of Nephrology : JASN|December 26, 2001
Identification of a gene locus for Senior-Løken syndrome in the region of the nephronophthisis type 3 geneHeymut Omran, GÜrsel Sasmaz, Karsten Häffner, et al.
The European Respiratory Journal|September 5, 2014
Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesiaJohanna Raidt, Julia Wallmeier, Rim Hjeij, et al.
American Journal of Respiratory Cell and Molecular Biology|September 1, 2022
Recessive Mutations in <i>CFAP74</i> Cause Primary Ciliary Dyskinesia with Normal Ciliary UltrastructureLuisa Biebach, Sandra Cindrić, Julia Koenig, et al.
NMR in Biomedicine|May 23, 2007
NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error of metabolismUdo F H Engelke, Jörn Oliver Sass, Rudy N Van Coster, et al.
Circulation. Genomic and Precision Medicine|October 23, 2019
Randomization of Left-right Asymmetry and Congenital Heart Defects: The Role of <i>DNAH5</i> in Humans and MiceTabea Nöthe-Menchen, Julia Wallmeier, Petra Pennekamp, et al.
Pageof 8