Publications by authors named "David Beier"

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Centriolar protein PIBF1 is required for craniofacial and forebrain development.
Lylyan Pimentel, Seungshin Ha, Yanfen Yang, Kim Cochran, Ching-Fang Chang, David R Beier

Dev Biol· November 2025

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Inhibition of Hedgehog signaling does not mitigate polycystic kidney disease severity in a Pkd1 mutant mouse model.
Sean K Gombart, Scott Houghtaling, Tzu-Hua Ho, David R Beier

J Cell Sci· October 2025

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A systems genetics approach identifies roles for proteasome factors in heart development and congenital heart defects.
Gist H Farr, Whitaker Reid, Eva H Hasegawa, Azzam Azzam, Isabelle Young, David R Beier

PLoS Genet· August 2025

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Huntington's disease LIG1 modifier variant increases ligase fidelity and suppresses somatic CAG repeat expansion.
Eunhye Lee, Wonju Kim, David H Beier, Yejin Lee, Marina Kovalenko

bioRxiv· July 2025

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A conditional smoothened (smo) allele on an inbred C57BL/6J genetic background has a hypomorphic smo mutant phenotype.
Scott Houghtaling, Sean K Gombart, Tzu-Hua Ho, Grace Huang, David R Beier

Dev Biol· February 2025

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Single-cell, whole-embryo phenotyping of mammalian developmental disorders.
Xingfan Huang, Jana Henck, Chengxiang Qiu, Varun K A Sreenivasan, Saranya Balachandran, David R Beier

Nature· November 2023

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Genome Report: chromosome-scale genome assembly of the African spiny mouse (Acomys cahirinus).
Elizabeth Dong Nguyen, Vahid Nikoonejad Fard, Bernard Y Kim, Sarah Collins, Miranda Galey, David R Beier

G3 (Bethesda)· September 2023

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Mammalian organ regeneration in spiny mice.
Daryl M Okamura, Elizabeth D Nguyen, Sarah J Collins, Kevin Yoon, Joshua B Gere, David R Beier

J Muscle Res Cell Motil· June 2023

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GENOME REPORT: Chromosome-scale genome assembly of the African spiny mouse ( ).
Elizabeth Dong Nguyen, Vahid Nikoonejad Fard, Bernard Y Kim, Sarah Collins, Miranda Galey, David R Beier

bioRxiv· April 2023

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The arginine methyltransferase Carm1 is necessary for heart development.
Sophie Jamet, Seungshin Ha, Tzu-Hua Ho, Scott Houghtaling, Andrew Timms, David R Beier

G3 (Bethesda)· July 2022

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Wound healing and regeneration in spiny mice (Acomys cahirinus).
Daryl M Okamura, Elizabeth D Nguyen, David R Beier, Mark W Majesky

Curr Top Dev Biol· April 2022

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Spiny mice activate unique transcriptional programs after severe kidney injury regenerating organ function without fibrosis.
Daryl M Okamura, Chris M Brewer, Paul Wakenight, Nadia Bahrami, Kristina Bernardi, David R Beier

iScience· November 2021

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Reelin Mediates Hippocampal Cajal-Retzius Cell Positioning and Infrapyramidal Blade Morphogenesis.
Seungshin Ha, Prem P Tripathi, Ray A Daza, Robert F Hevner, David R Beier

J Dev Biol· September 2020

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Isolation and Characterization of Adult Cardiac Fibroblasts and Myofibroblasts.
Meiling Melzer, David Beier, Pampee P Young, Sarika Saraswati

J Vis Exp· March 2020

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Dynamics of the DEAD-box ATPase Prp5 RecA-like domains provide a conformational switch during spliceosome assembly.
David H Beier, Tucker J Carrocci, Clarisse van der Feltz, U Sandy Tretbar, Joshua C Paulson

Nucleic Acids Res· November 2019

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Applicability of the Mutation-Selection Balance Model to Population Genetics of Heterozygous Protein-Truncating Variants in Humans.
Donate Weghorn, Daniel J Balick, Christopher Cassa, Jack A Kosmicki, Mark J Daly, David R Beier

Mol Biol Evol· August 2019

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Differential requirements of tubulin genes in mammalian forebrain development.
Elizabeth Bittermann, Zakia Abdelhamed, Ryan P Liegel, Chelsea Menke, Andrew Timms, David R Beier

PLoS Genet· August 2019

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Loss of function of disrupts collagen post-translational modification and causes musculoskeletal defects.
Krista A Geister, Alberto Jose Lopez-Jimenez, Scott Houghtaling, Tzu-Hua Ho, Roberto Vanacore, David R Beier

Dis Model Mech· June 2019

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Reply to 'Selective effects of heterozygous protein-truncating variants'.
Christopher A Cassa, Donate Weghorn, Daniel J Balick, Daniel M Jordan, David Nusinow, David R Beier

Nat Genet· January 2019

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Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice.
Krista A Geister, Andrew E Timms, David R Beier

G3 (Bethesda)· February 2018

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A mutation in causes neonatal hydrocephalus with abnormal motile cilia development in mice.
Zakia Abdelhamed, Shawn M Vuong, Lauren Hill, Crystal Shula, Andrew Timms, David Beier

Development· January 2018

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Human Embryo Editing: Opportunities and Importance of Transnational Cooperation.
Duanqing Pei, David W Beier, Ephrat Levy-Lahad, Gary Marchant, Janet Rossant

Cell Stem Cell· October 2017

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Generation of a multipurpose mouse allele by targeted gene trapping.
Alexander Strassman, Frank Schnütgen, Qi Dai, Jennifer C Jones, Angela C Gomez, David R Beier

Dis Model Mech· July 2017

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Estimating the selective effects of heterozygous protein-truncating variants from human exome data.
Christopher A Cassa, Donate Weghorn, Daniel J Balick, Daniel M Jordan, David Nusinow, David R Beier

Nat Genet· May 2017

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Halting Zika's resurgence with new rapid tests for the virus.
Ranu S Dhillon, Devabhaktuni Srikrishna, David Beier

BMJ· May 2017

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