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Displaying 9 of 9 results for "CACNA1F"
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  1. CAC1F_MOUSE UniProt:Swiss-Prot

    ID: Q9JIS7

    Description: Voltage-dependent L-type calcium channel

  2. Crystal Structure of the catalytic domain of xylanase A from Streptomyces halstedii JM8 PDB

    ID: PDB:1NQ6

    Description: Xys1(E.C.3.2.1.8)

  3. Functional and Mechanistic Studies of XPC DNA-Repair Complex as Transcriptional Coactivator in Embryonic Stem Cells ArrayExpress

    ID: E-GEOD-64040

    Description: urine ESCs by mapping regions bound by its RAD23B subunit in wild type and Xpc-/- ESCs, and analyzing transcriptional profiles of SCC-depleted ESCs. RAD23B ChIP-seq in wild type murine ESCs was performed in two replicates; normal IgG were used as controls. RAD23B ChIP-seq in Xpc-/- mESCs was compared to normal IgG. Antibodies to immunoprecipita...

  4. Functional and Mechanistic Studies of XPC DNA-Repair Complex as Transcriptional Coactivator in Embryonic Stem Cells BioProject

    ID: PRJNA269957

    Keywords: Other

    Access Type: download

    dataset.description: urine ESCs by mapping regions bound by its RAD23B subunit in wild type and Xpc-/- ESCs, and analyzing transcriptional profiles of SCC-depleted ESCs. Overall design: RAD23B ChIP-seq in wild type murine ESCs was performed in two replicates; normal IgG were used as controls. RAD23B ChIP-seq in Xpc-/- mESCs was compared to normal IgG. Antibodies to...
  5. Analysis_of_microRNA_expression_within_ES_cells_with_targeted_microRNA_deletions BioProject

    ID: PRJEB1363

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: Cluster miR-106a~363 on the X chromosome (A) Wild type JM8.A3, (B,C) miR-106a~363 null with selection cassette, (D) miR-106a~363 conditional, (E,F) miR-106a~363 null without selection cassette.. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/...
  6. CGH analysis of mouse embryonic stem cells trisomic for chromosome 6, 8, 11,12 and 15 BioProject

    ID: PRJNA239949

    Keywords: Variation

    Access Type: download

    dataset.description: ced colony formation efficiencies. They were less dependent on growth factors for self-renewal and showed a reduced capacity to differentiate in vitro. Moreover, xenografted aneuploid stem cells formed teratomas more efficiently, with features of neoplastic progression. These findings demonstrate that aneuploidy enhances the self-renewal capacities of stem cells and reduces their differentiation abilities. Overall design: Array comparative genomic hybridization (aCGH) was performed to detect the DNA copy number variants of the trisomic mES cells on a genome-wide scale. For Ts6, Ts8, Ts11 and Ts15 ES cells, we used the wild-type AB1 mES cells (129 S7/SvEvBrd, male) as reference. For Ts8-JM8 and Ts12-JM8 ES cells, we usedJM8A3 mES cells (C57BL/6N, male) as reference. The copy number variants of all the cell lines were analyzed by Nim...
  7. Mutation screening of the LRIT3, CABP4, and GPR179 genes in Chinese patients with Schubert-Bornschein congenital stationary night blindness Figshare

    ID: doi:10.6084/M9.FIGSHARE.3490619

    Release Date: 07-18-2016

    Description: previous study, in which we screened the NYX, CACNA1F, GRM6, and TRPM1 genes for mutations but identified none. The other two patients were newly recruited and had not been screened for mutations in these genes. Genomic DNA and clinical data were collected from the eight recruited families. Variants of the LRIT3, CABP4, and GPR179 genes were identified by Sanger sequencing. All of the identified variants were also assessed in 192 control individuals. Results: In this study, a novel compound heterozygous mutation, c.[1A>G]; [608G>T] (p.[0?]; p.[W203L]), was identified in the LRIT3 gene of a proband. These two mutation...

  8. Mutation screening of the LRIT3, CABP4, and GPR179 genes in Chinese patients with Schubert-Bornschein congenital stationary night blindness Figshare

    ID: doi:10.6084/M9.FIGSHARE.3490619.V1

    Release Date: 07-18-2016

    Description: previous study, in which we screened the NYX, CACNA1F, GRM6, and TRPM1 genes for mutations but identified none. The other two patients were newly recruited and had not been screened for mutations in these genes. Genomic DNA and clinical data were collected from the eight recruited families. Variants of the LRIT3, CABP4, and GPR179 genes were identified by Sanger sequencing. All of the identified variants were also assessed in 192 control individuals. Results: In this study, a novel compound heterozygous mutation, c.[1A>G]; [608G>T] (p.[0?]; p.[W203L]), was identified in the LRIT3 gene of a proband. These two mutation...

  9. Functional and Mechanistic Studies of XPC DNA-Repair Complex as Transcriptional Coactivator in Embryonic Stem Cells OmicsDI

    ID: E-GEOD-64040

    Date Released: 04-27-2015

    Description: urine ESCs by mapping regions bound by its RAD23B subunit in wild type and Xpc-/- ESCs, and analyzing transcriptional profiles of SCC-depleted ESCs. RAD23B ChIP-seq in wild type murine ESCs was performed in two replicates; normal IgG were used as controls. RAD23B ChIP-seq in Xpc-/- mESCs was compared to normal IgG. Antibodies to immunoprecipita...


Displaying 9 of 9 results for "CACNA1F"