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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 1
2004 1
2005 2
2010 3
2011 2
2012 2
2013 3
2014 2
2015 1
2016 4
2017 1
2018 2
2019 4
2020 1
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29 results
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Page 1
Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation.
Gurumurthy CB, O'Brien AR, Quadros RM, Adams J Jr, Alcaide P, Ayabe S, Ballard J, Batra SK, Beauchamp MC, Becker KA, Bernas G, Brough D, Carrillo-Salinas F, Chan W, Chen H, Dawson R, DeMambro V, D'Hont J, Dibb KM, Eudy JD, Gan L, Gao J, Gonzales A, Guntur AR, Guo H, Harms DW, Harrington A, Hentges KE, Humphreys N, Imai S, Ishii H, Iwama M, Jonasch E, Karolak M, Keavney B, Khin NC, Konno M, Kotani Y, Kunihiro Y, Lakshmanan I, Larochelle C, Lawrence CB, Li L, Lindner V, Liu XD, Lopez-Castejon G, Loudon A, Lowe J, Jerome-Majewska LA, Matsusaka T, Miura H, Miyasaka Y, Morpurgo B, Motyl K, Nabeshima YI, Nakade K, Nakashiba T, Nakashima K, Obata Y, Ogiwara S, Ouellet M, Oxburgh L, Piltz S, Pinz I, Ponnusamy MP, Ray D, Redder RJ, Rosen CJ, Ross N, Ruhe MT, Ryzhova L, Salvador AM, Alam SS, Sedlacek R, Sharma K, Smith C, Staes K, Starrs L, Sugiyama F, Takahashi S, Tanaka T, Trafford AW, Uno Y, Vanhoutte L, Vanrockeghem F, Willis BJ, Wright CS, Yamauchi Y, Yi X, Yoshimi K, Zhang X, Zhang Y, Ohtsuka M, Das S, Garry DJ, Hochepied T, Thomas P, Parker-Thornburg J, Adamson AD, Yoshiki A, Schmouth JF, Golovko A, Thompson WR, Lloyd KCK, Wood JA, Cowan M, Mashimo T, Mizuno S, Zhu H, Kasparek P, Liaw L, Miano JM, Burgio G. Gurumurthy CB, et al. Among authors: jerome majewska la. Genome Biol. 2019 Aug 26;20(1):171. doi: 10.1186/s13059-019-1776-2. Genome Biol. 2019. PMID: 31446895 Free PMC article. Clinical Trial.
Snap29 mutant mice recapitulate neurological and ophthalmological abnormalities associated with 22q11 and CEDNIK syndrome.
Keser V, Lachance JB, Alam SS, Lim Y, Scarlata E, Kaur A, Zhang TF, Lv S, Lachapelle P, O'Flaherty C, Golden JA, Jerome-Majewska LA. Keser V, et al. Among authors: jerome majewska la. Commun Biol. 2019 Oct 11;2:375. doi: 10.1038/s42003-019-0601-5. eCollection 2019. Commun Biol. 2019. PMID: 31633066 Free PMC article.
During embryogenesis, esrp1 expression is restricted to a subset of epithelial cells and is associated with splicing of a number of developmentally important genes.
Revil T, Jerome-Majewska LA. Revil T, et al. Among authors: jerome majewska la. Dev Dyn. 2013 Mar;242(3):281-90. doi: 10.1002/dvdy.23918. Epub 2013 Jan 30. Dev Dyn. 2013. PMID: 23233200 Free article.
Loss of function mutation of Eftud2, the gene responsible for mandibulofacial dysostosis with microcephaly (MFDM), leads to pre-implantation arrest in mouse.
Beauchamp MC, Djedid A, Daupin K, Clokie K, Kumar S, Majewski J, Jerome-Majewska LA. Beauchamp MC, et al. PLoS One. 2019 Jul 5;14(7):e0219280. doi: 10.1371/journal.pone.0219280. eCollection 2019. PLoS One. 2019. PMID: 31276534 Free PMC article.
Spliceosomopathies and neurocristopathies: Two sides of the same coin?
Beauchamp MC, Alam SS, Kumar S, Jerome-Majewska LA. Beauchamp MC, et al. Dev Dyn. 2020 Aug;249(8):924-945. doi: 10.1002/dvdy.183. Epub 2020 May 21. Dev Dyn. 2020. PMID: 32315467 Review.
Transmembrane emp24 domain proteins in development and disease.
Aber R, Chan W, Mugisha S, Jerome-Majewska LA. Aber R, et al. Among authors: jerome majewska la. Genet Res (Camb). 2019 Dec 27;101:e14. doi: 10.1017/S0016672319000090. Genet Res (Camb). 2019. PMID: 31878985 Free PMC article. Review.
Low Dietary Folate Interacts with MTHFD1 Synthetase Deficiency in Mice, a Model for the R653Q Variant, to Increase Incidence of Developmental Delays and Defects.
Christensen KE, Bahous RH, Hou W, Deng L, Malysheva OV, Arning E, Bottiglieri T, Caudill MA, Jerome-Majewska LA, Rozen R. Christensen KE, et al. Among authors: jerome majewska la. J Nutr. 2018 Apr 1;148(4):501-509. doi: 10.1093/jn/nxy013. J Nutr. 2018. PMID: 29659962
Non-alcoholic fatty liver disease in mice with heterozygous mutation in TMED2.
Hou W, Gupta S, Beauchamp MC, Yuan L, Jerome-Majewska LA. Hou W, et al. Among authors: jerome majewska la. PLoS One. 2017 Aug 10;12(8):e0182995. doi: 10.1371/journal.pone.0182995. eCollection 2017. PLoS One. 2017. PMID: 28797121 Free PMC article.
MTHFD1 formyltetrahydrofolate synthetase deficiency, a model for the MTHFD1 R653Q variant, leads to congenital heart defects in mice.
Christensen KE, Deng L, Bahous RH, Jerome-Majewska LA, Rozen R. Christensen KE, et al. Among authors: jerome majewska la. Birth Defects Res A Clin Mol Teratol. 2015 Dec;103(12):1031-8. doi: 10.1002/bdra.23451. Epub 2015 Sep 26. Birth Defects Res A Clin Mol Teratol. 2015. PMID: 26408344
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