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Journal articles on the topic 'Mouse brain development'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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1

Cecchi, Chiara, and Edoardo Boncinelli. "Emx homeogenes and mouse brain development." Trends in Neurosciences 23, no. 8 (2000): 347–52. http://dx.doi.org/10.1016/s0166-2236(00)01608-8.

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2

LOMBROSO, PAUL J., and DANIEL GOLDOWITZ. "Brain Development, VIII: The Reeler Mouse." American Journal of Psychiatry 155, no. 12 (1998): 1660. http://dx.doi.org/10.1176/ajp.155.12.1660.

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3

Chanderkar, L. P., W. K. Paik, and S. Kim. "Studies on myelin-basic-protein methylation during mouse brain development." Biochemical Journal 240, no. 2 (1986): 471–79. http://dx.doi.org/10.1042/bj2400471.

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The synthesis and methylation in vivo of myelin basic protein (MBP) during the mouse brain development has been investigated. When mice ranging in age from 13 to 60 days were injected intracerebrally with L-[methyl-3H]methionine, the incorporation of radioactivity into MBP isolated from youngest brain was found to be the highest and declined progressively in mature brains. This pattern of radioactivity incorporation was inversely correlated with the total amount of MBP in the brains, suggesting a higher ratio of MBP methylation to synthesis in younger brain. To differentiate the relative rate

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4

Schiffmann, S. N., B. Bernier, and A. M. Goffinet. "Reelin mRNA Expression During Mouse Brain Development." European Journal of Neuroscience 9, no. 5 (1997): 1055–71. http://dx.doi.org/10.1111/j.1460-9568.1997.tb01456.x.

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5

Booler, H. S., J. Williams, and S. C. Brown. "Brain Development in a Mouse Model of Muscle–Eye–Brain Disease." Journal of Comparative Pathology 150, no. 1 (2014): 118. http://dx.doi.org/10.1016/j.jcpa.2013.11.176.

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6

Laeremans, Annelies, Babs Van De Plas, Stefan Clerens, Gert Van Den Bergh, Lutgarde Arckens, and Tjing-Tjing Hu. "Protein Expression Dynamics during Postnatal Mouse Brain Development." Journal of Experimental Neuroscience 7 (January 2013): JEN.S12453. http://dx.doi.org/10.4137/jen.s12453.

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We explored differential protein expression profiles in the mouse forebrain at different stages of postnatal development, including 10-day (P10), 30-day (P30), and adult (Ad) mice, by large-scale screening of proteome maps using two-dimensional difference gel electrophoresis. Mass spectrometry analysis resulted in the identification of 251 differentially expressed proteins. Most molecular changes were observed between P10 compared to both P30 and Ad. Computational ingenuity pathway analysis (IPA) confirmed these proteins as crucial molecules in the biological function of nervous system develop

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7

Ishii, Kayoko, Keiichi Uyemura, and Jean-Christophe Renauld. "Neocortical development in IL-9 transgenic mouse brain." Neuroscience Research 31 (January 1998): S287. http://dx.doi.org/10.1016/s0168-0102(98)82221-9.

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8

Shin, Incheol, Hyun J. Kim, Jae E. Lee, and Myung C. Gye. "Aquaporin7 expression during perinatal development of mouse brain." Neuroscience Letters 409, no. 2 (2006): 106–11. http://dx.doi.org/10.1016/j.neulet.2006.09.075.

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9

Seyfried, Thomas N. "Mouse Brain Development. Andre M. Goffinet , Pasko Rakic." Quarterly Review of Biology 76, no. 2 (2001): 265–66. http://dx.doi.org/10.1086/393966.

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10

Gompers, Andrea L., Linda Su-Feher, Jacob Ellegood, et al. "Germline Chd8 haploinsufficiency alters brain development in mouse." Nature Neuroscience 20, no. 8 (2017): 1062–73. http://dx.doi.org/10.1038/nn.4592.

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11

Liscovitch, Noa, and Gal Chechik. "Specialization of Gene Expression during Mouse Brain Development." PLoS Computational Biology 9, no. 9 (2013): e1003185. http://dx.doi.org/10.1371/journal.pcbi.1003185.

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12

Pareek, S., A. Saraswat, and A. L. Bhatia. "Biochemical changes in mouse brain during postnatal development." Cell Differentiation and Development 27 (August 1989): 193. http://dx.doi.org/10.1016/0922-3371(89)90580-7.

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13

Klein, R. M., T. M. Burns, J. A. Cloug, G. W. Wood, M. De, and N. E. J. Berman. "Differential expression of cytokines during mouse brain development." Journal of Neuroimmunology 35 (January 1991): 62. http://dx.doi.org/10.1016/0165-5728(91)90950-c.

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14

Guidi, Sandra, Fiorenza Stagni, Patrizia Bianchi, et al. "Prenatal pharmacotherapy rescues brain development in a Down’s syndrome mouse model." Brain 137, no. 2 (2013): 380–401. http://dx.doi.org/10.1093/brain/awt340.

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15

Ikeda, Yayoi, Yuko Tamura, and Masa-Aki Ikeda. "Localization of cyclin E during development of mouse brain." Neuroscience Research 31 (January 1998): S283. http://dx.doi.org/10.1016/s0168-0102(98)82211-6.

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16

Zhang, Jiangyang, Michael I. Miller, Celine Plachez, et al. "Mapping postnatal mouse brain development with diffusion tensor microimaging." NeuroImage 26, no. 4 (2005): 1042–51. http://dx.doi.org/10.1016/j.neuroimage.2005.03.009.

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17

Holmes-Hampton, Gregory P., Mrinmoy Chakrabarti, Allison L. Cockrell, et al. "Changing iron content of the mouse brain during development." Metallomics 4, no. 8 (2012): 761. http://dx.doi.org/10.1039/c2mt20086d.

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18

Du, Xiaonan, Bobbi Fleiss, Hongfu Li, et al. "Systemic Stimulation of TLR2 Impairs Neonatal Mouse Brain Development." PLoS ONE 6, no. 5 (2011): e19583. http://dx.doi.org/10.1371/journal.pone.0019583.

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19

Escamez, Teresa, Olga Bahamonde, Rafael Tabares-Seisdedos, Eduard Vieta, Salvador Martinez, and Diego Echevarria. "Developmental dynamics of PAFAH1B subunits during mouse brain development." Journal of Comparative Neurology 520, no. 17 (2012): 3877–94. http://dx.doi.org/10.1002/cne.23128.

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20

Hasegawa, Yuta, Daisuke Yoshida, Yuki Nakamura, and Shin-ichi Sakakibara. "Spatiotemporal distribution of SUMOylation components during mouse brain development." Journal of Comparative Neurology 522, no. 13 (2014): 3020–36. http://dx.doi.org/10.1002/cne.23563.

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21

Bi, Weimin, Tamar Sapir, Oleg A. Shchelochkov, et al. "Increased LIS1 expression affects human and mouse brain development." Nature Genetics 41, no. 2 (2009): 168–77. http://dx.doi.org/10.1038/ng.302.

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22

Talan, Jamie. "In Mouse Study, Methylphenidate Rewires Brain During Early Development." Neurology Today 7, no. 16 (2007): 18–19. http://dx.doi.org/10.1097/01.nt.0000288863.71568.54.

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23

Yan, Runchuan, Xinde Hu, Qi Zhang, et al. "Spag6 Negatively Regulates Neuronal Migration During Mouse Brain Development." Journal of Molecular Neuroscience 57, no. 4 (2015): 463–69. http://dx.doi.org/10.1007/s12031-015-0608-4.

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24

Brüning, Gerold, Orfeas Liangos, and Hans Georg Baumgarten. "Prenatal development of the serotonin transporter in mouse brain." Cell and Tissue Research 289, no. 2 (1997): 211–21. http://dx.doi.org/10.1007/s004410050868.

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25

Su, Li-Da, Ya-Jun Xie, Liang Zhou, Ying Shen, and Ying-Hong Hu. "LGI1 is Involved in the Development of Mouse Brain." Cerebellum 14, no. 1 (2014): 12–14. http://dx.doi.org/10.1007/s12311-014-0628-6.

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26

Hewitt, John K., Martin E. Hahn, and Laura M. Karkowski. "Genetic selection disrupts stability of mouse brain weight development." Brain Research 417, no. 2 (1987): 225–31. http://dx.doi.org/10.1016/0006-8993(87)90446-x.

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27

Galton, Valerie Anne, Emily T. Wood, Emily A. St. Germain, et al. "Thyroid Hormone Homeostasis and Action in the Type 2 Deiodinase-Deficient Rodent Brain during Development." Endocrinology 148, no. 7 (2007): 3080–88. http://dx.doi.org/10.1210/en.2006-1727.

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Considerable indirect evidence suggests that the type 2 deiodinase (D2) generates T3 from T4 for local use in specific tissues such as pituitary, brown fat, and brain, and studies with a D2-deficent mouse, the D2 knockout (D2KO) mouse, have shown this to be the case in pituitary and brown fat. The present study employs the D2KO mouse to determine the role of D2 in the developing brain. As expected, the T3 content in the neonatal D2KO brain was markedly reduced to a level comparable with that seen in the hypothyroid neonatal wild-type mouse. However, the mRNA levels of several T3-responsive gen

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28

Riederer, BM, IS Zagon, and SR Goodman. "Brain spectrin(240/235) and brain spectrin(240/235E): differential expression during mouse brain development." Journal of Neuroscience 7, no. 3 (1987): 864–74. http://dx.doi.org/10.1523/jneurosci.07-03-00864.1987.

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29

Fullston, Tod, Megan Mitchell, Sarah Wakefield, and Michelle Lane. "Mitochondrial inhibition during preimplantation embryogenesis shifts the transcriptional profile of fetal mouse brain." Reproduction, Fertility and Development 23, no. 5 (2011): 691. http://dx.doi.org/10.1071/rd10292.

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Environmental stress results in perturbations to mitochondrial function in the preimplantation embryo and hinders subsequent embryo and possibly offspring development. Global gene expression in fetal mouse brain was investigated following targeted mitochondrial inhibition by amino-oxyacetate (AOA) from the 2-cell to the blastocyst stage. Blastocysts were transferred to pseudopregnant recipients and RNA extracted from Day 18 fetal brains for microarray interrogation. Exposure to 5 μM AOA during preimplantation embryo development induced differential expression of 166 genes (>1.25 fold) in th

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30

Inaguma, Yutaka, Hidenori Ito, Akira Hara, et al. "Morphological characterization of mammalian Timeless in the mouse brain development." Neuroscience Research 92 (March 2015): 21–28. http://dx.doi.org/10.1016/j.neures.2014.10.017.

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31

Prohaska, Joseph R., and William R. Bailey. "Copper deficiency during neonatal development alters mouse brain catecholamine levels." Nutrition Research 13, no. 3 (1993): 331–38. http://dx.doi.org/10.1016/s0271-5317(05)80429-4.

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32

Szulc, Kamila U., Jason P. Lerch, Brian J. Nieman, et al. "4D MEMRI atlas of neonatal FVB/N mouse brain development." NeuroImage 118 (September 2015): 49–62. http://dx.doi.org/10.1016/j.neuroimage.2015.05.029.

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33

Funakoshi, Eishi, Masaki Fukui, Ayako Hamano, et al. "Expression of m-Golsyn/Syntabulin gene during mouse brain development." Neuroscience Letters 403, no. 3 (2006): 244–49. http://dx.doi.org/10.1016/j.neulet.2006.04.061.

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34

Frank, Marcus, Matthias Ebert, Weisong Shan, et al. "Differential expression of individual gamma-protocadherins during mouse brain development." Molecular and Cellular Neuroscience 29, no. 4 (2005): 603–16. http://dx.doi.org/10.1016/j.mcn.2005.05.001.

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35

Zhou, Dapeng, Chun Chen, Songmin Jiang, Zonghou Shen, Zhengwu Chi та Jianxin Gu. "Expression of β1,4-galactosyltransferase in the development of mouse brain". Biochimica et Biophysica Acta (BBA) - General Subjects 1425, № 1 (1998): 204–8. http://dx.doi.org/10.1016/s0304-4165(98)00070-1.

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36

Ogden, Kevin K., Emin D. Ozkan, and Gavin Rumbaugh. "Prioritizing the development of mouse models for childhood brain disorders." Neuropharmacology 100 (January 2016): 2–16. http://dx.doi.org/10.1016/j.neuropharm.2015.07.029.

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37

Hannah, Judy, and A. T. Campagnoni. "Effects of Essential Fatty Acid Deficiency on Mouse Brain Development." Developmental Neuroscience 9, no. 2 (1987): 120–27. http://dx.doi.org/10.1159/000111614.

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38

Inatani, Masaru, and Yu Yamaguchi. "Gene expression of EXT1 and EXT2 during mouse brain development." Developmental Brain Research 141, no. 1-2 (2003): 129–36. http://dx.doi.org/10.1016/s0165-3806(03)00010-5.

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39

Turnbull, D. H., T. S. Bloomfield, H. S. Baldwin, F. S. Foster, and A. L. Joyner. "Ultrasound backscatter microscope analysis of early mouse embryonic brain development." Proceedings of the National Academy of Sciences 92, no. 6 (1995): 2239–43. http://dx.doi.org/10.1073/pnas.92.6.2239.

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40

Hartl, Daniela, Martin Irmler, Irmgard Römer, et al. "Transcriptome and proteome analysis of early embryonic mouse brain development." PROTEOMICS 8, no. 6 (2008): 1257–65. http://dx.doi.org/10.1002/pmic.200700724.

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41

Knaus, Petra, Heinrich Betz, and Hubert Rehm. "Expression of Synaptophysin During Postnatal Development of the Mouse Brain." Journal of Neurochemistry 47, no. 4 (2006): 1302–4. http://dx.doi.org/10.1111/j.1471-4159.1986.tb00754.x.

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42

Fiedler, Eric P., Michael J. Marks, and Allan C. Collins. "Postnatal Development of Cholinergic Enzymes and Receptors in Mouse Brain." Journal of Neurochemistry 49, no. 3 (1987): 983–90. http://dx.doi.org/10.1111/j.1471-4159.1987.tb00990.x.

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43

Ribeiro, Patrícia A. O., Lourenço Sbragia, Rovilson Gilioli, Francesco Langone, Fábio F. Conte, and Iscia Lopes-Cendes. "Expression Profile of Lgi1 Gene in Mouse Brain During Development." Journal of Molecular Neuroscience 35, no. 3 (2008): 323–29. http://dx.doi.org/10.1007/s12031-008-9096-0.

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44

Van de Kamp, Jennifer L., and Allan C. Collins. "Prenatal nicotine alters nicotinic receptor development in the mouse brain." Pharmacology Biochemistry and Behavior 47, no. 4 (1994): 889–900. http://dx.doi.org/10.1016/0091-3057(94)90293-3.

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45

Marshall, Jonothon J., and John O. Mason. "Mouse vs man: Organoid models of brain development & disease." Brain Research 1724 (December 2019): 146427. http://dx.doi.org/10.1016/j.brainres.2019.146427.

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46

Wadghiri, Youssef Zaim, Jeffrey A. Blind, Xiaohong Duan, et al. "Manganese-enhanced magnetic resonance imaging (MEMRI) of mouse brain development." NMR in Biomedicine 17, no. 8 (2004): 613–19. http://dx.doi.org/10.1002/nbm.932.

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47

Hamden, Jordan E., Katherine M. Gray, Melody Salehzadeh, et al. "Steroid profiling of glucocorticoids in microdissected mouse brain across development." Developmental Neurobiology 81, no. 2 (2021): 189–206. http://dx.doi.org/10.1002/dneu.22808.

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48

Zhu, Jiangwen, Karin Motejlek, Denan Wang, Keling Zang, Andrea Schmidt та Louis F. Reichardt. "β8 integrins are required for vascular morphogenesis in mouse embryos". Development 129, № 12 (2002): 2891–903. http://dx.doi.org/10.1242/dev.129.12.2891.

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In order to assess the in vivo function of integrins containing the β8 subunit, we have generated integrin β8-deficient mice. Ablation of β8 results in embryonic or perinatal lethality with profound defects in vascular development. Sixty-five percent of integrin β8-deficient embryos die at midgestation, with evidence of insufficient vascularization of the placenta and yolk sac. The remaining 35% die shortly after birth with extensive intracerebral hemorrhage. Examination of brain tissue from integrin β8-deficient embryos reveals abnormal vascular morphogenesis resulting in distended and leaky

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49

Zhang, Wenjie, Yueling Zhang, Yuanjia Zheng, et al. "Progress in Research on Brain Development and Function of Mice During Weaning." Current Protein & Peptide Science 20, no. 7 (2019): 705–12. http://dx.doi.org/10.2174/1389203720666190125095819.

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Lactation is a critical phase for brain function development. New dietary experiences of mouse caused by weaning can regulate brain development and function, increase their response to food and environment, and eventually give rise to corresponding behavioral changes. Changes in weaning time induce the alteration of brain tissues morphology and molecular characteristics, glial cell activity and behaviors in the offspring. In addition, it is also sensitive to the intervention of environment and drugs during this period. That is to say, the study focused on brain development and function based o

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50

Yuen, Nili, Kamila U. Szulc-Lerch, Yu-Qing Li, et al. "Metformin effects on brain development following cranial irradiation in a mouse model." Neuro-Oncology 23, no. 9 (2021): 1523–36. http://dx.doi.org/10.1093/neuonc/noab131.

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Abstract Background Cranial radiation therapy (CRT) is a mainstay of treatment for malignant pediatric brain tumors and high-risk leukemia. Although CRT improves survival, it has been shown to disrupt normal brain development and result in cognitive impairments in cancer survivors. Animal studies suggest that there is potential to promote brain recovery after injury using metformin. Our aim was to evaluate whether metformin can restore brain volume outcomes in a mouse model of CRT. Methods C57BL/6J mice were irradiated with a whole-brain radiation dose of 7 Gy during infancy. Two weeks of metf

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