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Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.
Cereb Cortex. 2015 Oct;25(10):3977-93. doi: 10.1093/cercor/bhu285. Epub 2014 Dec 1.
Cereb Cortex. 2015.
PMID: 25452572
Free PMC article.
22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development.
Maynard TM, Gopalakrishna D, Meechan DW, Paronett EM, Newbern JM, LaMantia AS.
Maynard TM, et al. Among authors: paronett em.
Hum Mol Genet. 2013 Jan 15;22(2):300-12. doi: 10.1093/hmg/dds429. Epub 2012 Oct 16.
Hum Mol Genet. 2013.
PMID: 23077214
Free PMC article.
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A cellular and molecular mosaic establishes growth and differentiation states for cranial sensory neurons.
Karpinski BA, Bryan CA, Paronett EM, Baker JL, Fernandez A, Horvath A, Maynard TM, Moody SA, LaMantia AS.
Karpinski BA, et al. Among authors: paronett em.
Dev Biol. 2016 Jul 15;415(2):228-241. doi: 10.1016/j.ydbio.2016.03.015. Epub 2016 Mar 15.
Dev Biol. 2016.
PMID: 26988119
Free PMC article.
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Mitochondrial Dysfunction Leads to Cortical Under-Connectivity and Cognitive Impairment.
Fernandez A, Meechan DW, Karpinski BA, Paronett EM, Bryan CA, Rutz HL, Radin EA, Lubin N, Bonner ER, Popratiloff A, Rothblat LA, Maynard TM, LaMantia AS.
Fernandez A, et al. Among authors: paronett em.
Neuron. 2019 Jun 19;102(6):1127-1142.e3. doi: 10.1016/j.neuron.2019.04.013. Epub 2019 May 9.
Neuron. 2019.
PMID: 31079872
Free PMC article.
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Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome.
Yitsege G, Stokes BA, Sabatino JA, Sugrue KF, Banyai G, Paronett EM, Karpinski BA, Maynard TM, LaMantia AS, Zohn IE.
Yitsege G, et al. Among authors: paronett em.
Birth Defects Res. 2020 Oct;112(16):1194-1208. doi: 10.1002/bdr2.1709. Epub 2020 May 20.
Birth Defects Res. 2020.
PMID: 32431076
Free PMC article.
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Identity, lineage and fates of a temporally distinct progenitor population in the embryonic olfactory epithelium.
Paronett EM, Bryan CA, Maynard TM, LaMantia AS.
Paronett EM, et al.
Dev Biol. 2023 Mar;495:76-91. doi: 10.1016/j.ydbio.2023.01.001. Epub 2023 Jan 7.
Dev Biol. 2023.
PMID: 36627077
Free PMC article.
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Ranbp1 modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndrome.
Paronett EM, Bryan CA, Maynard ME, Goroff JA, Meechan DW, LaMantia AS, Maynard TM.
Paronett EM, et al.
Hum Mol Genet. 2023 Jun 5;32(12):1959-1974. doi: 10.1093/hmg/ddad030.
Hum Mol Genet. 2023.
PMID: 36790128
Free PMC article.
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