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Items: 1 to 20 of 70

1.

Brain and eye malformations resembling Walker-Warburg syndrome are recapitulated in mice by dystroglycan deletion in the epiblast.

Satz JS, Barresi R, Durbeej M, Willer T, Turner A, Moore SA, Campbell KP.

J Neurosci. 2008 Oct 15;28(42):10567-75. doi: 10.1523/JNEUROSCI.2457-08.2008.

2.

Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation.

Sato S, Omori Y, Katoh K, Kondo M, Kanagawa M, Miyata K, Funabiki K, Koyasu T, Kajimura N, Miyoshi T, Sawai H, Kobayashi K, Tani A, Toda T, Usukura J, Tano Y, Fujikado T, Furukawa T.

Nat Neurosci. 2008 Aug;11(8):923-31. doi: 10.1038/nn.2160. Epub 2008 Jul 20.

PMID:
18641643
3.

Divergent phenotypes of vision and accessory visual function in mice with visual cycle dysfunction (Rpe65 rd12) or retinal degeneration (rd/rd).

Thompson S, Mullins RF, Philp AR, Stone EM, Mrosovsky N.

Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2737-42. doi: 10.1167/iovs.07-1546.

PMID:
18515598
4.

N-myc coordinates retinal growth with eye size during mouse development.

Martins RA, Zindy F, Donovan S, Zhang J, Pounds S, Wey A, Knoepfler PS, Eisenman RN, Roussel MF, Dyer MA.

Genes Dev. 2008 Jan 15;22(2):179-93. doi: 10.1101/gad.1608008.

5.

Neuron-specific TGF-beta signaling deficiency results in retinal detachment and cataracts in mice.

Honjo Y, Nagineni CN, Larsson J, Nandula SR, Hooks JJ, Chan CC, Karlsson S, Kulkarni AB.

Biochem Biophys Res Commun. 2007 Jan 12;352(2):418-22. Epub 2006 Nov 16.

6.

Connexin43 is required for production of the aqueous humor in the murine eye.

Calera MR, Topley HL, Liao Y, Duling BR, Paul DL, Goodenough DA.

J Cell Sci. 2006 Nov 1;119(Pt 21):4510-9. Epub 2006 Oct 17.

7.

Dystroglycan: from biosynthesis to pathogenesis of human disease.

Barresi R, Campbell KP.

J Cell Sci. 2006 Jan 15;119(Pt 2):199-207. Review.

8.

Identification of a beta-dystroglycan immunoreactive subcompartment in photoreceptor terminals.

Jastrow H, Koulen P, Altrock WD, Kröger S.

Invest Ophthalmol Vis Sci. 2006 Jan;47(1):17-24.

PMID:
16384939
9.

Ocular abnormalities in Large(myd) and Large(vls) mice, spontaneous models for muscle, eye, and brain diseases.

Lee Y, Kameya S, Cox GA, Hsu J, Hicks W, Maddatu TP, Smith RS, Naggert JK, Peachey NS, Nishina PM.

Mol Cell Neurosci. 2005 Oct;30(2):160-72.

PMID:
16111892
10.

Basement membrane-dependent survival of retinal ganglion cells.

Halfter W, Willem M, Mayer U.

Invest Ophthalmol Vis Sci. 2005 Mar;46(3):1000-9.

PMID:
15728558
11.

Impaired motor performance and learning in glia maturation factor-knockout mice.

Lim R, Zaheer A, Khosravi H, Freeman JH Jr, Halverson HE, Wemmie JA, Yang B.

Brain Res. 2004 Oct 22;1024(1-2):225-32.

PMID:
15451385
12.

Contribution of Kir4.1 to the mouse electroretinogram.

Wu J, Marmorstein AD, Kofuji P, Peachey NS.

Mol Vis. 2004 Sep 1;10:650-4.

13.

The congenital muscular dystrophies in 2004: a century of exciting progress.

Muntoni F, Voit T.

Neuromuscul Disord. 2004 Oct;14(10):635-49. Review.

PMID:
15351421
14.

Cell type-specific effects of Rb deletion in the murine retina.

MacPherson D, Sage J, Kim T, Ho D, McLaughlin ME, Jacks T.

Genes Dev. 2004 Jul 15;18(14):1681-94. Epub 2004 Jul 1.

15.

The potassium channel Kir4.1 associates with the dystrophin-glycoprotein complex via alpha-syntrophin in glia.

Connors NC, Adams ME, Froehner SC, Kofuji P.

J Biol Chem. 2004 Jul 2;279(27):28387-92. Epub 2004 Apr 21.

16.

Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development.

Takeda S, Kondo M, Sasaki J, Kurahashi H, Kano H, Arai K, Misaki K, Fukui T, Kobayashi K, Tachikawa M, Imamura M, Nakamura Y, Shimizu T, Murakami T, Sunada Y, Fujikado T, Matsumura K, Terashima T, Toda T.

Hum Mol Genet. 2003 Jun 15;12(12):1449-59.

17.
18.

Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.

Cohn RD, Henry MD, Michele DE, Barresi R, Saito F, Moore SA, Flanagan JD, Skwarchuk MW, Robbins ME, Mendell JR, Williamson RA, Campbell KP.

Cell. 2002 Sep 6;110(5):639-48.

19.

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

Moore SA, Saito F, Chen J, Michele DE, Henry MD, Messing A, Cohn RD, Ross-Barta SE, Westra S, Williamson RA, Hoshi T, Campbell KP.

Nature. 2002 Jul 25;418(6896):422-5.

PMID:
12140559
20.

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.

Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kelley RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP.

Nature. 2002 Jul 25;418(6896):417-22.

PMID:
12140558
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