Beier D - Search Results

1

A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice.

Abdelhamed Z, Vuong SM, Hill L, Shula C, Timms A, Beier D, Campbell K, Mangano FT, Stottmann RW, Goto J. Abdelhamed Z, et al. Among authors: beier d. Development. 2018 Jan 9;145(1):dev154500. doi: 10.1242/dev.154500. Development. 2018. PMID: 29317443 Free PMC article.

2

A forward genetic screen in mice identifies mutants with abnormal cortical patterning.

Ha S, Stottmann RW, Furley AJ, Beier DR. Ha S, et al. Cereb Cortex. 2015 Jan;25(1):167-79. doi: 10.1093/cercor/bht209. Epub 2013 Aug 22. Cereb Cortex. 2015. PMID: 23968836 Free PMC article.

3

Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice.

Ha S, Lindsay AM, Timms AE, Beier DR. Ha S, et al. G3 (Bethesda). 2016 Aug 9;6(8):2479-87. doi: 10.1534/g3.116.030791. G3 (Bethesda). 2016. PMID: 27261005 Free PMC article.

4

Differential requirements of tubulin genes in mammalian forebrain development.

Bittermann E, Abdelhamed Z, Liegel RP, Menke C, Timms A, Beier DR, Stottmann RW. Bittermann E, et al. PLoS Genet. 2019 Aug 6;15(8):e1008243. doi: 10.1371/journal.pgen.1008243. eCollection 2019 Aug. PLoS Genet. 2019. PMID: 31386652 Free PMC article.

5

ENU Mutagenesis in the Mouse.

Stottmann R, Beier D. Stottmann R, et al. Among authors: beier d. Curr Protoc Hum Genet. 2014 Jul 14;82:15.4.1-15.4.10. doi: 10.1002/0471142905.hg1504s82. Curr Protoc Hum Genet. 2014. PMID: 25042716 Free PMC article.

6

ENU mutagenesis in the mouse.

Stottmann R, Beier D. Stottmann R, et al. Among authors: beier d. Curr Protoc Mouse Biol. 2014 Jun 16;4(2):25-35. doi: 10.1002/9780470942390.mo140029. Curr Protoc Mouse Biol. 2014. PMID: 25723916

7

A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse.

Stottmann RW, Donlin M, Hafner A, Bernard A, Sinclair DA, Beier DR. Stottmann RW, et al. Among authors: beier dr. Hum Mol Genet. 2013 Oct 15;22(20):4053-63. doi: 10.1093/hmg/ddt255. Epub 2013 May 31. Hum Mol Genet. 2013. PMID: 23727838 Free PMC article.

8

Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice.

Geister KA, Timms AE, Beier DR. Geister KA, et al. G3 (Bethesda). 2018 Feb 2;8(2):401-409. doi: 10.1534/g3.117.300292. G3 (Bethesda). 2018. PMID: 29208648 Free PMC article.

9

Grhl2 is required in nonneural tissues for neural progenitor survival and forebrain development.

Menke C, Cionni M, Siggers T, Bulyk ML, Beier DR, Stottmann RW. Menke C, et al. Genesis. 2015 Sep;53(9):573-582. doi: 10.1002/dvg.22875. Epub 2015 Jul 22. Genesis. 2015. PMID: 26177923 Free PMC article.

10

Variant mapping and mutation discovery in inbred mice using next-generation sequencing.

Gallego-Llamas J, Timms AE, Geister KA, Lindsay A, Beier DR. Gallego-Llamas J, et al. BMC Genomics. 2015 Nov 9;16:913. doi: 10.1186/s12864-015-2173-1. BMC Genomics. 2015. PMID: 26552429 Free PMC article.

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