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Heike Olbrich

Showing results (41-50 of 80) with videos related to

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Nature Genetics|January 15, 2002
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetryHeike Olbrich, Karsten Häffner, Andreas Kispert, et al.
Human Mutation|November 21, 2007
Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutationsGeorg C Schwabe, Katrin Hoffmann, Niki Tomas Loges, et al.
American Journal of Human Genetics|June 2, 2021
Mutations in TP73 cause impaired mucociliary clearance and lissencephalyJulia Wallmeier, Diana Bracht, Hessa S Alsaif, et al.
American Journal of Respiratory and Critical Care Medicine|April 22, 2006
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defectsNada Hornef, Heike Olbrich, Judit Horvath, et al.
American Journal of Human Genetics|January 3, 2017
Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm DefectsTamara Paff, Niki T Loges, Isabella Aprea, et al.
The Journal of Clinical Investigation|April 10, 2008
BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomasStefan Pfister, Wibke G Janzarik, Marc Remke, et al.
Nature|December 5, 2008
Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneinsHeymut Omran, Daisuke Kobayashi, Heike Olbrich, et al.
American Journal of Human Genetics|October 28, 2008
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armNiki Tomas Loges, Heike Olbrich, Lale Fenske, et al.
The European Respiratory Journal|July 11, 2024
A range of 30-62% of functioning multiciliated airway cells is sufficient to maintain ciliary airway clearanceNiki T Loges, June Kehlet Marthin, Johanna Raidt, et al.
American Journal of Human Genetics|October 2, 2012
Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetryHeike Olbrich, Miriam Schmidts, Claudius Werner, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Nature Genetics|January 15, 2002
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetryHeike Olbrich, Karsten Häffner, Andreas Kispert, et al.
Human Mutation|November 21, 2007
Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutationsGeorg C Schwabe, Katrin Hoffmann, Niki Tomas Loges, et al.
American Journal of Human Genetics|June 2, 2021
Mutations in TP73 cause impaired mucociliary clearance and lissencephalyJulia Wallmeier, Diana Bracht, Hessa S Alsaif, et al.
American Journal of Respiratory and Critical Care Medicine|April 22, 2006
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defectsNada Hornef, Heike Olbrich, Judit Horvath, et al.
American Journal of Human Genetics|January 3, 2017
Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm DefectsTamara Paff, Niki T Loges, Isabella Aprea, et al.
The Journal of Clinical Investigation|April 10, 2008
BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomasStefan Pfister, Wibke G Janzarik, Marc Remke, et al.
Nature|December 5, 2008
Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneinsHeymut Omran, Daisuke Kobayashi, Heike Olbrich, et al.
American Journal of Human Genetics|October 28, 2008
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armNiki Tomas Loges, Heike Olbrich, Lale Fenske, et al.
The European Respiratory Journal|July 11, 2024
A range of 30-62% of functioning multiciliated airway cells is sufficient to maintain ciliary airway clearanceNiki T Loges, June Kehlet Marthin, Johanna Raidt, et al.
American Journal of Human Genetics|October 2, 2012
Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetryHeike Olbrich, Miriam Schmidts, Claudius Werner, et al.
Pageof 8