Publications by authors named "Tim Ott"

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CIROZ is dispensable in ancestral vertebrates but essential for left-right patterning in humans.
Emmanuelle Szenker-Ravi, Tim Ott, Amirah Yusof, Maya Chopra, Muznah Khatoo

Am J Hum Genet· February 2025

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Identification of novel genes including associated with isolated tall stature.
Birgit Weiss, Tim Ott, Philipp Vick, Julian C Lui, Ralph Roeth

Front Endocrinol (Lausanne)· December 2023

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Expression and cilia associated localization of Histone deacetylases 6 in .
Matthias Tisler, Tim Ott, Martin Blum, Axel Schweickert

MicroPubl Biol· August 2023

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Publisher Correction: Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates.
Emmanuelle Szenker-Ravi, Tim Ott, Muznah Khatoo, Anne Moreau de Bellaing, Wei Xuan Goh

Nat Genet· June 2022

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Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates.
Emmanuelle Szenker-Ravi, Tim Ott, Muznah Khatoo, Anne Moreau de Bellaing, Wei Xuan Goh

Nat Genet· January 2022

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The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus.
Anja Beckers, Franziska Fuhl, Tim Ott, Karsten Boldt, Magdalena Maria Brislinger

Sci Rep· June 2021

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The FOXJ1 target is required for sperm motility, mucociliary clearance of the airways and brain development.
Anja Beckers, Christian Adis, Karin Schuster-Gossler, Lena Tveriakhina, Tim Ott

Development· June 2020

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CFAP43 modulates ciliary beating in mouse and Xenopus.
Ev Rachev, Karin Schuster-Gossler, Franziska Fuhl, Tim Ott, Lena Tveriakhina

Dev Biol· March 2020

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Xenopus: An Undervalued Model Organism to Study and Model Human Genetic Disease.
Martin Blum, Tim Ott

Cells Tissues Organs· August 2019

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Mechanical strain, novel genes and evolutionary insights: news from the frog left-right organizer.
Martin Blum, Tim Ott

Curr Opin Genet Dev· June 2019

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The Frog as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in .
Tim Ott, Lilian Kaufmann, Martin Granzow, Katrin Hinderhofer, Claus R Bartram

Front Physiol· February 2019

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The evolutionary conserved FOXJ1 target gene Fam183b is essential for motile cilia in Xenopus but dispensable for ciliary function in mice.
Anja Beckers, Tim Ott, Karin Schuster-Gossler, Karsten Boldt, Leonie Alten

Sci Rep· October 2018

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The Power of Strain: Organizing Left-Right Cilia.
Martin Blum, Tim Ott

Dev Cell· May 2018

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Animal left-right asymmetry.
Martin Blum, Tim Ott

Curr Biol· April 2018

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A Conserved Role of the Unconventional Myosin 1d in Laterality Determination.
Melanie Tingler, Sabrina Kurz, Markus Maerker, Tim Ott, Franziska Fuhl

Curr Biol· March 2018

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Vertebrate Left-Right Asymmetry: What Can Nodal Cascade Gene Expression Patterns Tell Us?
Axel Schweickert, Tim Ott, Sabrina Kurz, Melanie Tingler, Markus Maerker

J Cardiovasc Dev Dis· December 2017

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hmmr mediates anterior neural tube closure and morphogenesis in the frog Xenopus.
Angela Prager, Cathrin Hagenlocher, Tim Ott, Alexandra Schambony, Kerstin Feistel

Dev Biol· October 2017

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CFAP157 is a murine downstream effector of FOXJ1 that is specifically required for flagellum morphogenesis and sperm motility.
Marina Weidemann, Karin Schuster-Gossler, Michael Stauber, Christoph Wrede, Jan Hegermann, Tim Ott

Development· December 2016

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Symmetry breakage in the frog Xenopus: role of Rab11 and the ventral-right blastomere.
Melanie Tingler, Tim Ott, Janos Tözser, Sabrina Kurz, Maike Getwan

Genesis· June 2014

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