U42RR024244/RR/NCRR NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2012	2
2013	3
2014	9
2015	7
2016	4
2024	0

1

Notch4 reveals a novel mechanism regulating Notch signal transduction.

James AC, Szot JO, Iyer K, Major JA, Pursglove SE, Chapman G, Dunwoodie SL. James AC, et al. Biochim Biophys Acta. 2014 Jul;1843(7):1272-84. doi: 10.1016/j.bbamcr.2014.03.015. Epub 2014 Mar 22. Biochim Biophys Acta. 2014. PMID: 24667410 Free article.

2

Swiprosin-1/EFhd2 limits germinal center responses and humoral type 2 immunity.

Brachs S, Turqueti-Neves A, Stein M, Reimer D, Brachvogel B, Bösl M, Winkler T, Voehringer D, Jäck HM, Mielenz D. Brachs S, et al. Eur J Immunol. 2014 Nov;44(11):3206-19. doi: 10.1002/eji.201444479. Epub 2014 Sep 16. Eur J Immunol. 2014. PMID: 25092375 Free article.

3

Aldolase-B knockout in mice phenocopies hereditary fructose intolerance in humans.

Oppelt SA, Sennott EM, Tolan DR. Oppelt SA, et al. Mol Genet Metab. 2015 Mar;114(3):445-50. doi: 10.1016/j.ymgme.2015.01.001. Epub 2015 Jan 22. Mol Genet Metab. 2015. PMID: 25637246

4

Deletion of cavin genes reveals tissue-specific mechanisms for morphogenesis of endothelial caveolae.

Hansen CG, Shvets E, Howard G, Riento K, Nichols BJ. Hansen CG, et al. Nat Commun. 2013;4:1831. doi: 10.1038/ncomms2808. Nat Commun. 2013. PMID: 23652019 Free PMC article.

5

ESCRT-II/Vps25 constrains digit number by endosome-mediated selective modulation of FGF-SHH signaling.

Handschuh K, Feenstra J, Koss M, Ferretti E, Risolino M, Zewdu R, Sahai MA, Bénazet JD, Peng XP, Depew MJ, Quintana L, Sharpe J, Wang B, Alcorn H, Rivi R, Butcher S, Manak JR, Vaccari T, Weinstein H, Anderson KV, Lacy E, Selleri L. Handschuh K, et al. Cell Rep. 2014 Oct 23;9(2):674-87. doi: 10.1016/j.celrep.2014.09.019. Epub 2014 Oct 16. Cell Rep. 2014. PMID: 25373905 Free PMC article.

6

Heterozygous caveolin-3 mice show increased susceptibility to palmitate-induced insulin resistance.

Talukder MA, Preda M, Ryzhova L, Prudovsky I, Pinz IM. Talukder MA, et al. Physiol Rep. 2016 Mar;4(6):e12736. doi: 10.14814/phy2.12736. Epub 2016 Mar 31. Physiol Rep. 2016. PMID: 27033451 Free PMC article.

7

Novel genetic tools facilitate the study of cortical neuron migration.

Cionni M, Menke C, Stottmann RW. Cionni M, et al. Mamm Genome. 2016 Feb;27(1-2):8-16. doi: 10.1007/s00335-015-9615-6. Epub 2015 Dec 12. Mamm Genome. 2016. PMID: 26662625 Free PMC article.

8

No obvious phenotypic abnormalities in mice lacking the Pate4 gene.

Heckt T, Keller J, Reusch R, Hartmann K, Krasemann S, Hermans-Borgmeyer I, Amling M, Schinke T. Heckt T, et al. Biochem Biophys Res Commun. 2016 Jan 22;469(4):1069-74. doi: 10.1016/j.bbrc.2015.12.104. Epub 2015 Dec 28. Biochem Biophys Res Commun. 2016. PMID: 26731031

9

GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility.

Judson MC, Wallace ML, Sidorov MS, Burette AC, Gu B, van Woerden GM, King IF, Han JE, Zylka MJ, Elgersma Y, Weinberg RJ, Philpot BD. Judson MC, et al. Neuron. 2016 Apr 6;90(1):56-69. doi: 10.1016/j.neuron.2016.02.040. Epub 2016 Mar 24. Neuron. 2016. PMID: 27021170 Free PMC article.

10

Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology.

Orosco LA, Ross AP, Cates SL, Scott SE, Wu D, Sohn J, Pleasure D, Pleasure SJ, Adamopoulos IE, Zarbalis KS. Orosco LA, et al. Nat Commun. 2014 Sep 8;5:4692. doi: 10.1038/ncomms5692. Nat Commun. 2014. PMID: 25198012 Free PMC article.

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