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David R. Beier, MD, PhD

Affiliations: 
Harvard Medical School, Brigham and Women's Hospital, and Seattle Children's Research Institute 
Area:
ENU mutagenesis, forebrain and cerebral cortex development
Website:
http://www.seattlechildrens.org/medical-staff/David-Randolph-Beier/
Google:
"David Beier"
Mean distance: 16.53 (cluster 32)
 
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Publications

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Ha S, Tripathi PP, Daza RA, et al. (2020) Reelin Mediates Hippocampal Cajal-Retzius Cell Positioning and Infrapyramidal Blade Morphogenesis. Journal of Developmental Biology. 8
Bittermann E, Abdelhamed Z, Liegel RP, et al. (2019) Differential requirements of tubulin genes in mammalian forebrain development. Plos Genetics. 15: e1008243
Abdelhamed Z, Vuong SM, Hill L, et al. (2018) A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice. Development (Cambridge, England). 145
Geister KA, Timms AE, Beier DR. (2017) Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice. G3 (Bethesda, Md.)
Strassman A, Schnütgen F, Dai Q, et al. (2017) Generation of a multipurpose Prdm16 allele by targeted trapping. Disease Models & Mechanisms
Ha S, Tripathi PP, Mihalas AB, et al. (2017) C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR, Causing Abnormal Development of the Cerebral Cortex and Hippocampus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 37: 960-971
Ha S, Tripathi PP, Mihalas AB, et al. (2016) C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR Causing Abnormal Development of the Cerebral Cortex and Hippocampus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Jacobs DT, Silva LM, Allard BA, et al. (2016) Dysfunction of intraflagellar transport-A causes hyperphagia-induced obesity and metabolic syndrome. Disease Models & Mechanisms. 9: 789-98
Gallego-Llamas J, Timms AE, Pitstick R, et al. (2016) Improvement of ENU Mutagenesis Efficiency Using Serial Injection and Mismatch Repair Deficiency Mice. Plos One. 11: e0159377
Ha S, Lindsay AM, Timms AE, et al. (2016) Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice. G3 (Bethesda, Md.)
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