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Items: 1 to 20 of 83

1.

Breaches of the pial basement membrane are associated with defective dentate gyrus development in mouse models of congenital muscular dystrophies.

Li J, Yu M, Feng G, Hu H, Li X.

Neurosci Lett. 2011 Nov 7;505(1):19-24. doi: 10.1016/j.neulet.2011.09.040. Epub 2011 Sep 29.

3.

Breaches of the pial basement membrane and disappearance of the glia limitans during development underlie the cortical lamination defect in the mouse model of muscle-eye-brain disease.

Hu H, Yang Y, Eade A, Xiong Y, Qi Y.

J Comp Neurol. 2007 Mar 1;501(1):168-83. Erratum in: J Comp Neurol. 2007 May 10;502(2):337. Corrected and republished in: J Comp Neurol. 2007 May 10;502(2):168-83.

PMID:
17206611
4.

Ectopia of meningeal fibroblasts and reactive gliosis in the cerebral cortex of the mouse model of muscle-eye-brain disease.

Yang Y, Zhang P, Xiong Y, Li X, Qi Y, Hu H.

J Comp Neurol. 2007 Dec 10;505(5):459-77.

PMID:
17924568
5.

FAK deficiency in cells contributing to the basal lamina results in cortical abnormalities resembling congenital muscular dystrophies.

Beggs HE, Schahin-Reed D, Zang K, Goebbels S, Nave KA, Gorski J, Jones KR, Sretavan D, Reichardt LF.

Neuron. 2003 Oct 30;40(3):501-14.

6.

Differentiation and developmental origin of cerebellar granule neuron ectopia in protein O-mannose UDP-N-acetylglucosaminyl transferase 1 knockout mice.

Li X, Zhang P, Yang Y, Xiong Y, Qi Y, Hu H.

Neuroscience. 2008 Mar 18;152(2):391-406. doi: 10.1016/j.neuroscience.2007.06.041. Epub 2007 Jul 17.

PMID:
18295407
7.
8.

Conditional knockout of protein O-mannosyltransferase 2 reveals tissue-specific roles of O-mannosyl glycosylation in brain development.

Hu H, Li J, Gagen CS, Gray NW, Zhang Z, Qi Y, Zhang P.

J Comp Neurol. 2011 May 1;519(7):1320-37. doi: 10.1002/cne.22572.

9.

POMGnT1, POMT1, and POMT2 mutations in congenital muscular dystrophies.

Endo T, Manya H, Seta N, Guicheney P.

Methods Enzymol. 2010;479:343-52. doi: 10.1016/S0076-6879(10)79019-4.

PMID:
20816175
10.

Biochemical and biophysical changes underlie the mechanisms of basement membrane disruptions in a mouse model of dystroglycanopathy.

Zhang P, Yang Y, Candiello J, Thorn TL, Gray N, Halfter WM, Hu H.

Matrix Biol. 2013 Apr 24;32(3-4):196-207. doi: 10.1016/j.matbio.2013.02.002. Epub 2013 Feb 27.

11.

Expression and localization of fukutin, POMGnT1, and POMT1 in the central nervous system: consideration for functions of fukutin.

Yamamoto T, Kato Y, Kawaguchi M, Shibata N, Kobayashi M.

Med Electron Microsc. 2004 Dec;37(4):200-7. Review.

PMID:
15614444
12.
13.

Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy.

Yamamoto T, Toyoda C, Kobayashi M, Kondo E, Saito K, Osawa M.

Brain Dev. 1997 Jan;19(1):35-42.

PMID:
9071488
14.

GPR56 regulates pial basement membrane integrity and cortical lamination.

Li S, Jin Z, Koirala S, Bu L, Xu L, Hynes RO, Walsh CA, Corfas G, Piao X.

J Neurosci. 2008 May 28;28(22):5817-26. doi: 10.1523/JNEUROSCI.0853-08.2008.

15.

Basement membrane abnormality in merosin-negative congenital muscular dystrophy.

Osari S, Kobayashi O, Yamashita Y, Matsuishi T, Goto M, Tanabe Y, Migita T, Nonaka I.

Acta Neuropathol. 1996;91(4):332-6.

PMID:
8928608
16.

Cellular and molecular characterization of abnormal brain development in protein o-mannose N-acetylglucosaminyltransferase 1 knockout mice.

Liu J, Yang Y, Li X, Zhang P, Qi Y, Hu H.

Methods Enzymol. 2010;479:353-66. doi: 10.1016/S0076-6879(10)79020-0.

PMID:
20816176
17.
18.
19.

Astroglial in vivo response to cocaine in mouse dentate gyrus: a quantitative and qualitative analysis by confocal microscopy.

Fattore L, Puddu MC, Picciau S, Cappai A, Fratta W, Serra GP, Spiga S.

Neuroscience. 2002;110(1):1-6.

PMID:
11882367
20.

[Defective O-mannosyl glycosylation causes congenital muscular dystrophies].

Manya H, Endo T.

Tanpakushitsu Kakusan Koso. 2004 Nov;49(15 Suppl):2451-6. Review. Japanese. No abstract available.

PMID:
15553000

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