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Results: 1 to 20 of 80

Similar articles for PubMed (Select 24096375)

1.

Crybb2 coding for βB2-crystallin affects sensorimotor gating and hippocampal function.

Sun M, Hölter SM, Stepan J, Garrett L, Genius J, Kremmer E, Hrabě de Angelis M, Wurst W, Lie DC, Bally-Cuif L, Eder M, Rujescu D, Graw J.

Mamm Genome. 2013 Oct;24(9-10):333-48. doi: 10.1007/s00335-013-9478-7. Epub 2013 Oct 6.

2.

Novel allele of crybb2 in the mouse and its expression in the brain.

Ganguly K, Favor J, Neuhäuser-Klaus A, Sandulache R, Puk O, Beckers J, Horsch M, Schädler S, Vogt Weisenhorn D, Wurst W, Graw J.

Invest Ophthalmol Vis Sci. 2008 Apr;49(4):1533-41. doi: 10.1167/iovs.07-0788.

PMID:
18385073
3.

Decreased levels of Ca²⁺-calmodulin-dependent protein kinase IV in the testis as a contributing factor to reduced fertility in male Crybb2⁻/⁻ mice.

Xiang F, Cui B, Gao Q, Zhang J, Zhang J, Li W.

Int J Mol Med. 2012 Nov;30(5):1145-51. doi: 10.3892/ijmm.2012.1116. Epub 2012 Sep 3.

PMID:
22948125
4.

Targeted knockout of the mouse betaB2-crystallin gene (Crybb2) induces age-related cataract.

Zhang J, Li J, Huang C, Xue L, Peng Y, Fu Q, Gao L, Zhang J, Li W.

Invest Ophthalmol Vis Sci. 2008 Dec;49(12):5476-83. doi: 10.1167/iovs.08-2179. Epub 2008 Aug 21.

PMID:
18719080
5.

Subfertility in mice harboring a mutation in betaB2-crystallin.

Duprey KM, Robinson KM, Wang Y, Taube JR, Duncan MK.

Mol Vis. 2007 Mar 14;13:366-73.

6.

A missense mutation in CRYBB2 leads to progressive congenital membranous cataract by impacting the solubility and function of βB2-crystallin.

Chen W, Chen X, Hu Z, Lin H, Zhou F, Luo L, Zhang X, Zhong X, Yang Y, Wu C, Lin Z, Ye S, Liu Y; Study Group of CCPMOH.

PLoS One. 2013 Nov 28;8(11):e81290. doi: 10.1371/journal.pone.0081290. eCollection 2013.

7.

Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse.

Graw J, Löster J, Soewarto D, Fuchs H, Reis A, Wolf E, Balling R, Hrabé de Angelis M.

Invest Ophthalmol Vis Sci. 2001 Jun;42(7):1574-80.

PMID:
11381063
8.

Molecular analysis of cataract families in India: new mutations in the CRYBB2 and GJA3 genes and rare polymorphisms.

Santhiya ST, Kumar GS, Sudhakar P, Gupta N, Klopp N, Illig T, Söker T, Groth M, Platzer M, Gopinath PM, Graw J.

Mol Vis. 2010 Sep 10;16:1837-47.

9.

Crybb2 deficiency impairs fertility in female mice.

Gao Q, Sun LL, Xiang FF, Gao L, Jia Y, Zhang JR, Tao HB, Zhang JJ, Li WJ.

Biochem Biophys Res Commun. 2014 Oct 10;453(1):37-42. doi: 10.1016/j.bbrc.2014.09.049. Epub 2014 Sep 20.

PMID:
25245288
10.

Binding of destabilized betaB2-crystallin mutants to alpha-crystallin: the role of a folding intermediate.

Sathish HA, Koteiche HA, McHaourab HS.

J Biol Chem. 2004 Apr 16;279(16):16425-32. Epub 2004 Feb 3.

11.

Gene conversion mutation in crystallin, beta-B2 (CRYBB2) in a Chilean family with autosomal dominant cataract.

Bateman JB, von-Bischhoffshaunsen FR, Richter L, Flodman P, Burch D, Spence MA.

Ophthalmology. 2007 Mar;114(3):425-32. Epub 2007 Jan 17.

PMID:
17234267
12.

Mutation analysis of congenital cataracts in Indian families: identification of SNPS and a new causative allele in CRYBB2 gene.

Santhiya ST, Manisastry SM, Rawlley D, Malathi R, Anishetty S, Gopinath PM, Vijayalakshmi P, Namperumalsamy P, Adamski J, Graw J.

Invest Ophthalmol Vis Sci. 2004 Oct;45(10):3599-607.

PMID:
15452067
13.
14.

A sensitive period for GABAergic interneurons in the dentate gyrus in modulating sensorimotor gating.

Guo N, Yoshizaki K, Kimura R, Suto F, Yanagawa Y, Osumi N.

J Neurosci. 2013 Apr 10;33(15):6691-704. doi: 10.1523/JNEUROSCI.0032-12.2013.

15.

The importance of the last strand at the C-terminus in βB2-crystallin stability and assembly.

Zhang K, Zhao WJ, Leng XY, Wang S, Yao K, Yan YB.

Biochim Biophys Acta. 2014 Jan;1842(1):44-55. doi: 10.1016/j.bbadis.2013.10.001. Epub 2013 Oct 9.

16.

Domain interaction sites of human lens betaB2-crystallin.

Liu BF, Liang JJ.

J Biol Chem. 2006 Feb 3;281(5):2624-30. Epub 2005 Nov 29.

17.

Creation of a new eye lens crystallin (Gambeta) through structure-guided mutagenic grafting of the surface of betaB2 crystallin onto the hydrophobic core of gammaB crystallin.

Kapoor D, Singh B, Subramanian K, Guptasarma P.

FEBS J. 2009 Jun;276(12):3341-53. doi: 10.1111/j.1742-4658.2009.07059.x. Epub 2009 May 7.

PMID:
19438717
18.
19.

Crystallin-β-b2-overexpressing NPCs support the survival of injured retinal ganglion cells and photoreceptors in rats.

Böhm MR, Pfrommer S, Chiwitt C, Brückner M, Melkonyan H, Thanos S.

Invest Ophthalmol Vis Sci. 2012 Dec 17;53(13):8265-79. doi: 10.1167/iovs.12-10334.

PMID:
23132806
20.

Identification of a novel CRYBB2 missense mutation causing congenital autosomal dominant cataract.

Weisschuh N, Aisenbrey S, Wissinger B, Riess A.

Mol Vis. 2012;18:174-80. Epub 2012 Jan 21.

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