2000
DOI: 10.1006/geno.2000.6204
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Isolation and Characterization of a Calcium Channel Gene, Cacna1f, the Murine Orthologue of the Gene for Incomplete X-Linked Congenital Stationary Night Blindness

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Cited by 26 publications
(16 citation statements)
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“…The full-length cDNA of Ca v 1.4␣1 was determined to be 6111 bp with an open reading frame encoding a protein of 1984 amino acid residues (GenBank accession number of murine Ca v 1.4␣1: AJ579852; available by ftp at zippy.nimh.nih.gov/ or at http://rsb.info.nih.gov/nih-image; developed by Wayne Rasband, National Institutes of Health, Bethesda, MD). The sequence is nearly identical with the mouse sequence published by Naylor et al23 with the notable exception of a strongly diverging sequence stretch in the C terminus (amino acid residues 1768-1807). Inspection of the nucleotide sequences revealed that the profound differences in this stretch arise from frame shifts in the cDNA.…”
mentioning
confidence: 50%
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“…The full-length cDNA of Ca v 1.4␣1 was determined to be 6111 bp with an open reading frame encoding a protein of 1984 amino acid residues (GenBank accession number of murine Ca v 1.4␣1: AJ579852; available by ftp at zippy.nimh.nih.gov/ or at http://rsb.info.nih.gov/nih-image; developed by Wayne Rasband, National Institutes of Health, Bethesda, MD). The sequence is nearly identical with the mouse sequence published by Naylor et al23 with the notable exception of a strongly diverging sequence stretch in the C terminus (amino acid residues 1768-1807). Inspection of the nucleotide sequences revealed that the profound differences in this stretch arise from frame shifts in the cDNA.…”
mentioning
confidence: 50%
“…Sequences and Localization of PCR Primers Used for Cloning of Ca v 1.4␣1Coding sequences are represented in uppercase letters, 5Ј-and 3Ј-untranslated sequences are shown in lowercase letters.Molecular Cloning of Murine Ca v 1.4␣1To clone murine Ca v 1.4␣1 we designed specific primer pairs based on the previously published sequence of this channel(Table 1)23 and performed RT-PCR with retinal cDNA from mouse strain C57Bl6. The full-length cDNA of Ca v 1.4␣1 was determined to be 6111 bp with an open reading frame encoding a protein of 1984 amino acid residues (GenBank accession number of murine Ca v 1.4␣1: AJ579852; available by ftp at zippy.nimh.nih.gov/ or at http://rsb.info.nih.gov/nih-image; developed by Wayne Rasband, National Institutes of Health, Bethesda, MD).…”
mentioning
confidence: 99%
“…8,9 In situ hybridization revealed the presence of Ca v 1.4 transcript in the outer plexiform, outer nuclear, inner nuclear, and ganglion cell layers of the retina, 9 although the presence in the outer plexiform layer was not found in other studies. 10 Immunohistochemical experiments using different antibodies have shown multiple calcium channel subtypes expressed throughout the retina. [11][12][13][14] However, experiments designed to determine the localization of the Ca v 1.4 channel have led to varying results.…”
Section: Characterization Of the Cacna1f Genementioning
confidence: 99%
“…Amplification of cDNA for ␣ 1F and ␤ 4 Subunits-cDNA for ␣ 1F and ␤ 4 subunits of L-type VDCCs was amplified from mouse brain cDNA by polymerase chain reaction using a set of oligonucleotides (␣ 1F , TTC-GACTCTTGTTGGGTCTTG and TCAAAGCGGGAAAGAATAGA; ␤ 4 , CTATAAACTCTCATCATTTCAC and TCATAACGGGTTGCACATAC) specific for the cDNA sequence of mouse ␣ 1F and ␤ 4 subunits of L-type VDCC (26,27). After the amplification, the cDNA was ligated with EcoRI adapter and inserted into the EcoRI site of pUC18.…”
Section: Camentioning
confidence: 99%