Kathryn V Anderson
7PUBLICATIONS
14CO-AUTHORS
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Publications (7)
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|Jul 25, 2022
A hypomorphic mutation in Pold1 disrupts the coordination of embryo size expansion and morphogenesis during gastrulation.Tingxu Chen, Heather Alcorn, Sujan Devbhandari
|Nov 28, 2020
β-Pix-dependent cellular protrusions propel collective mesoderm migration in the mouse embryo.Tatiana Omelchenko, Alan Hall, Kathryn V Anderson
|Dec 12, 2018
Spinocerebellar ataxia type 11-associated alleles of Ttbk2 dominantly interfere with ciliogenesis and cilium stability.Emily Bowie, Ryan Norris, Kathryn V Anderson
|Oct 18, 2017
The small GTPase RSG1 controls a final step in primary cilia initiation.Stephanie O Agbu, Yinwen Liang, Aimin Liu
|Aug 31, 2017
rahu is a mutant allele of Dnmt3c, encoding a DNA methyltransferase homolog required for meiosis and transposon repression in the mouse male germline.Devanshi Jain, Cem Meydan, Julian Lange
|Mar 15, 2017
The Meckel syndrome- associated protein MKS1 functionally interacts with components of the BBSome and IFT complexes to mediate ciliary trafficking and hedgehog signaling.Sarah C Goetz, Fiona Bangs, Chloe L Barrington
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Frequent Collaborators
2 joint publications
Sarah C Goetz
1 joint publications
Fiona Bangs
1 joint publications
Devanshi Jain
1 joint publications
Cem Meydan
1 joint publications
Corentin Claeys Bouuaert
1 joint publications
Christopher E Mason
1 joint publications
Scott Keeney
1 joint publications
Yinwen Liang
1 joint publications
Aimin Liu
1 joint publications
Tatiana Omelchenko
