Matteson P - Search Results

1

Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex.

Salamon I, Park Y, Miškić T, Kopić J, Matteson P, Page NF, Roque A, McAuliffe GW, Favate J, Garcia-Forn M, Shah P, Judaš M, Millonig JH, Kostović I, De Rubeis S, Hart RP, Krsnik Ž, Rasin MR. Salamon I, et al. Among authors: matteson p. Nat Commun. 2023 Sep 27;14(1):6025. doi: 10.1038/s41467-023-41730-8. Nat Commun. 2023. PMID: 37758766 Free PMC article.

2

The orphan G protein-coupled receptor, Gpr161, encodes the vacuolated lens locus and controls neurulation and lens development.

Matteson PG, Desai J, Korstanje R, Lazar G, Borsuk TE, Rollins J, Kadambi S, Joseph J, Rahman T, Wink J, Benayed R, Paigen B, Millonig JH. Matteson PG, et al. Proc Natl Acad Sci U S A. 2008 Feb 12;105(6):2088-93. doi: 10.1073/pnas.0705657105. Epub 2008 Feb 4. Proc Natl Acad Sci U S A. 2008. PMID: 18250320 Free PMC article.

3

Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.

Wratten NS, Memoli H, Huang Y, Dulencin AM, Matteson PG, Cornacchia MA, Azaro MA, Messenger J, Hayter JE, Bassett AS, Buyske S, Millonig JH, Vieland VJ, Brzustowicz LM. Wratten NS, et al. Am J Psychiatry. 2009 Apr;166(4):434-41. doi: 10.1176/appi.ajp.2008.08081266. Epub 2009 Mar 2. Am J Psychiatry. 2009. PMID: 19255043 Free PMC article.

4

Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2.

Benayed R, Choi J, Matteson PG, Gharani N, Kamdar S, Brzustowicz LM, Millonig JH. Benayed R, et al. Biol Psychiatry. 2009 Nov 15;66(10):911-7. doi: 10.1016/j.biopsych.2009.05.027. Epub 2009 Jul 17. Biol Psychiatry. 2009. PMID: 19615670 Free PMC article.

5

Cut-like homeobox 1 and nuclear factor I/B mediate ENGRAILED2 autism spectrum disorder-associated haplotype function.

Choi J, Ababon MR, Matteson PG, Millonig JH. Choi J, et al. Hum Mol Genet. 2012 Apr 1;21(7):1566-80. doi: 10.1093/hmg/ddr594. Epub 2011 Dec 16. Hum Mol Genet. 2012. PMID: 22180456 Free PMC article.

6

Autism associated gene, engrailed2, and flanking gene levels are altered in post-mortem cerebellum.

Choi J, Ababon MR, Soliman M, Lin Y, Brzustowicz LM, Matteson PG, Millonig JH. Choi J, et al. PLoS One. 2014 Feb 10;9(2):e87208. doi: 10.1371/journal.pone.0087208. eCollection 2014. PLoS One. 2014. PMID: 24520327 Free PMC article.

7

The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation.

Li BI, Matteson PG, Ababon MF, Nato AQ Jr, Lin Y, Nanda V, Matise TC, Millonig JH. Li BI, et al. Dev Biol. 2015 Jun 1;402(1):17-31. doi: 10.1016/j.ydbio.2015.02.007. Epub 2015 Mar 6. Dev Biol. 2015. PMID: 25753732 Free article.

8

Engrailed-2 (En2) deletion produces multiple neurodevelopmental defects in monoamine systems, forebrain structures and neurogenesis and behavior.

Genestine M, Lin L, Durens M, Yan Y, Jiang Y, Prem S, Bailoor K, Kelly B, Sonsalla PK, Matteson PG, Silverman J, Crawley JN, Millonig JH, DiCicco-Bloom E. Genestine M, et al. Hum Mol Genet. 2015 Oct 15;24(20):5805-27. doi: 10.1093/hmg/ddv301. Epub 2015 Jul 28. Hum Mol Genet. 2015. PMID: 26220976 Free PMC article.

9

Quantitative Measurement of Relative Retinoic Acid Levels in E8.5 Embryos and Neurosphere Cultures Using the F9 RARE-Lacz Cell-based Reporter Assay.

Ababon MR, Li BI, Matteson PG, Millonig JH. Ababon MR, et al. J Vis Exp. 2016 Sep 6;(115):54443. doi: 10.3791/54443. J Vis Exp. 2016. PMID: 27684594 Free PMC article.

10

Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

Li BI, Ababon MR, Matteson PG, Lin Y, Nanda V, Millonig JH. Li BI, et al. Among authors: matteson pg. PLoS One. 2017 Jan 30;12(1):e0170724. doi: 10.1371/journal.pone.0170724. eCollection 2017. PLoS One. 2017. PMID: 28135291 Free PMC article.

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