Beier DR - Search Results

1

Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoskeletal defects.

Geister KA, Lopez-Jimenez AJ, Houghtaling S, Ho TH, Vanacore R, Beier DR. Geister KA, et al. Among authors: beier dr. Dis Model Mech. 2019 Jun 17;12(6):dmm037176. doi: 10.1242/dmm.037176. Dis Model Mech. 2019. PMID: 31101663 Free PMC article.

2

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. Among authors: beier dr. G3 (Bethesda). 2018 Feb 2;8(2):401-409. doi: 10.1534/g3.117.300292. G3 (Bethesda). 2018. PMID: 29208648 Free PMC article.

3

The arginine methyltransferase Carm1 is necessary for heart development.

Jamet S, Ha S, Ho TH, Houghtaling S, Timms A, Yu K, Paquette A, Maga AM, Greene NDE, Beier DR. Jamet S, et al. Among authors: beier dr. G3 (Bethesda). 2022 Jul 29;12(8):jkac155. doi: 10.1093/g3journal/jkac155. G3 (Bethesda). 2022. PMID: 35736367 Free PMC article.

4

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. Among authors: beier dr. BMC Genomics. 2015 Nov 9;16:913. doi: 10.1186/s12864-015-2173-1. BMC Genomics. 2015. PMID: 26552429 Free PMC article.

5

Generation of a multipurpose Prdm16 mouse allele by targeted gene trapping.

Strassman A, Schnütgen F, Dai Q, Jones JC, Gomez AC, Pitstick L, Holton NE, Moskal R, Leslie ER, von Melchner H, Beier DR, Bjork BC. Strassman A, et al. Among authors: beier dr. Dis Model Mech. 2017 Jul 1;10(7):909-922. doi: 10.1242/dmm.029561. Epub 2017 Apr 19. Dis Model Mech. 2017. PMID: 28424158 Free PMC article.

6

Dysfunction of intraflagellar transport-A causes hyperphagia-induced obesity and metabolic syndrome.

Jacobs DT, Silva LM, Allard BA, Schonfeld MP, Chatterjee A, Talbott GC, Beier DR, Tran PV. Jacobs DT, et al. Among authors: beier dr. Dis Model Mech. 2016 Jul 1;9(7):789-98. doi: 10.1242/dmm.025791. Epub 2016 May 11. Dis Model Mech. 2016. PMID: 27482817 Free PMC article.

7

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.

8

C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR, Causing Abnormal Development of the Cerebral Cortex and Hippocampus.

Ha S, Tripathi PP, Mihalas AB, Hevner RF, Beier DR. Ha S, et al. Among authors: beier dr. J Neurosci. 2017 Jan 25;37(4):960-971. doi: 10.1523/JNEUROSCI.1826-16.2016. J Neurosci. 2017. PMID: 28123028 Free PMC article.

9

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.

10

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.

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