Beier DR - Search Results

1

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

Ha S, Stottmann RW, Furley AJ, Beier DR. Ha S, et al. Among authors: beier dr. 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.

2

ENU Mutagenesis in the Mouse.

Stottmann R, Beier D. Stottmann R, et al. 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.

3

Using ENU mutagenesis for phenotype-driven analysis of the mouse.

Stottmann RW, Beier DR. Stottmann RW, et al. Among authors: beier dr. Methods Enzymol. 2010;477:329-48. doi: 10.1016/S0076-6879(10)77017-8. Methods Enzymol. 2010. PMID: 20699149

4

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.

5

ENU mutagenesis in the mouse.

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

6

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. Development. 2018 Jan 9;145(1):dev154500. doi: 10.1242/dev.154500. Development. 2018. PMID: 29317443 Free PMC article.

7

Cholesterol metabolism is required for intracellular hedgehog signal transduction in vivo.

Stottmann RW, Turbe-Doan A, Tran P, Kratz LE, Moran JL, Kelley RI, Beier DR. Stottmann RW, et al. Among authors: beier dr. PLoS Genet. 2011 Sep;7(9):e1002224. doi: 10.1371/journal.pgen.1002224. Epub 2011 Sep 1. PLoS Genet. 2011. PMID: 21912524 Free PMC article.

8

Mutation mapping and identification by whole-genome sequencing.

Leshchiner I, Alexa K, Kelsey P, Adzhubei I, Austin-Tse CA, Cooney JD, Anderson H, King MJ, Stottmann RW, Garnaas MK, Ha S, Drummond IA, Paw BH, North TE, Beier DR, Goessling W, Sunyaev SR. Leshchiner I, et al. Among authors: beier dr. Genome Res. 2012 Aug;22(8):1541-8. doi: 10.1101/gr.135541.111. Epub 2012 May 3. Genome Res. 2012. PMID: 22555591 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. Among authors: beier dr. Genesis. 2015 Sep;53(9):573-582. doi: 10.1002/dvg.22875. Epub 2015 Jul 22. Genesis. 2015. PMID: 26177923 Free PMC article.

10

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. Among authors: beier dr. G3 (Bethesda). 2016 Aug 9;6(8):2479-87. doi: 10.1534/g3.116.030791. G3 (Bethesda). 2016. PMID: 27261005 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

182 results

Search Page

Filters