Channelpedia

Cav1.4 Channel

79 automatically matched literature references

3

Berkowitz BA et al. Genetic dissection of horizontal cell inhibitory signaling in mice in complete darkness in vivo.
Invest. Ophthalmol. Vis. Sci., 2015 May , 56 (3132-9).

12

Michalakis S et al. Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2.
Hum. Mol. Genet., 2014 Mar 15 , 23 (1538-50).

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Burtscher V et al. Spectrum of Cav1.4 dysfunction in congenital stationary night blindness type 2.
Biochim. Biophys. Acta, 2014 Aug , 1838 (2053-65).

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Tao Y et al. Visual signal pathway reorganization in the Cacna1f mutant rat model.
Invest. Ophthalmol. Vis. Sci., 2013 , 54 (1988-97).

23

Vincent A et al. Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.
Eye (Lond), 2012 Sep , 26 (1278-80).

32

Lodha N et al. Congenital stationary night blindness in mice - a tale of two Cacna1f mutants.
Adv. Exp. Med. Biol., 2010 , 664 (549-58).

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Griessmeier K et al. Calmodulin is a functional regulator of Cav1.4 L-type Ca2+ channels.
J. Biol. Chem., 2009 Oct 23 , 284 (29809-16).

35

Zeitz C et al. Genotyping microarray for CSNB-associated genes.
Invest. Ophthalmol. Vis. Sci., 2009 Dec , 50 (5919-26).

36

Peloquin JB et al. Temperature dependence of Cav1.4 calcium channel gating.
Neuroscience, 2008 Feb 19 , 151 (1066-83).

40

Doering CJ et al. The Ca(v)1.4 calcium channel: more than meets the eye.
Channels (Austin), 2007 Jan-Feb , 1 (3-10).

41

Yu M et al. Attenuation of oscillatory potentials in nob2 mice.
, 2007 Nov , 115 (173-86).

42

Jalkanen R et al. A novel CACNA1F gene mutation causes Aland Island eye disease.
Invest. Ophthalmol. Vis. Sci., 2007 Jun , 48 (2498-502).

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Wahl-Schott C et al. Switching off calcium-dependent inactivation in L-type calcium channels by an autoinhibitory domain.
Proc. Natl. Acad. Sci. U.S.A., 2006 Oct 17 , 103 (15657-62).

50

Wei J et al. A further study of a possible locus for schizophrenia on the X chromosome.
Biochem. Biophys. Res. Commun., 2006 Jun 16 , 344 (1241-5).

51

Jalkanen R et al. X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.
J. Med. Genet., 2006 Aug , 43 (699-704).

52

Morgans CW et al. Photoreceptor calcium channels: insight from night blindness.
Vis. Neurosci., 2005 Sep-Oct , 22 (561-8).

54

Doering CJ et al. Cav1.4 encodes a calcium channel with low open probability and unitary conductance.
Biophys. J., 2005 Nov , 89 (3042-8).

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Hemara-Wahanui A et al. A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.
Proc. Natl. Acad. Sci. U.S.A., 2005 May 24 , 102 (7553-8).

61

Nakamura M et al. [Molecular genetic study of congenital stationary night blindness]
Nippon Ganka Gakkai Zasshi, 2004 Nov , 108 (665-73).

63

Baumann L et al. Functional characterization of the L-type Ca2+ channel Cav1.4alpha1 from mouse retina.
Invest. Ophthalmol. Vis. Sci., 2004 Feb , 45 (708-13).

67

Nakamura M et al. Retinal and optic disc atrophy associated with a CACNA1F mutation in a Japanese family.
Arch. Ophthalmol., 2003 Jul , 121 (1028-33).

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Zito I et al. Mutations in the CACNA1F and NYX genes in British CSNBX families.
Hum. Mutat., 2003 Feb , 21 (169).

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Nakamura M et al. Incomplete congenital stationary night blindness associated with symmetrical retinal atrophy.
Am. J. Ophthalmol., 2002 Sep , 134 (463-5).

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Pietrobon D Calcium channels and channelopathies of the central nervous system.
Mol. Neurobiol., 2002 Feb , 25 (31-50).

72

Nakamura M et al. Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness.
Invest. Ophthalmol. Vis. Sci., 2001 Jun , 42 (1610-6).

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