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Displaying 20 of 262 results for "FMN1"
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  1. Biochemische Studien am limb deformity-Protein der Vertebralen Figshare

    ID: doi:10.6084/M9.FIGSHARE.963595.V1

    Release Date: 01-18-2016

    Description:

  2. Biochemische Studien am limb deformity-Protein der Vertebraten Figshare

    ID: doi:10.6084/M9.FIGSHARE.963595.V2

    Release Date: 01-18-2016

    Description:

  3. Biochemische Studien am limb deformity-Protein der Vertebraten Figshare

    ID: doi:10.6084/M9.FIGSHARE.963595

    Release Date: 07-04-2014

    Description:

  4. Comparative gene expression profile of Ngn3-overexpressing cultured hippocampal neurons vs the corresponding control populations ArrayExpress

    ID: E-GEOD-26911

    Description: lated with cytoskeleton dynamics. One of then was Fmn1 whose protein is associated with actin and microtubule cytoskeleton. Overexpression of the isoform Fmn1-Ib in cultured hippocampal neurons induced an increase in the number of primary dendrites and in the number of glutamatergic synaptic inputs without affecting GABAergic synapses resulting in a modification in the balance between excitation and inhibition. The same changes were provoked by overexpression of Ngn3. In addition downregulation of Fmn1 by the use of Fmn1-siRNAs impaired such morphological and synaptic changes i...

  5. Comparative gene expression profile of Ngn3-overexpressing cultured hippocampal neurons vs the corresponding control populations OmicsDI

    ID: E-GEOD-26911

    Date Released: 01-27-2011

    Description: lated with cytoskeleton dynamics. One of then was Fmn1 whose protein is associated with actin and microtubule cytoskeleton. Overexpression of the isoform Fmn1-Ib in cultured hippocampal neurons induced an increase in the number of primary dendrites and in the number of glutamatergic synaptic inputs without affecting GABAergic synapses resulting in a modification in the balance between excitation and inhibition. The same changes were provoked by overexpression of Ngn3. In addition downregulation of Fmn1 by the use of Fmn1-siRNAs impaired such morphological and synaptic changes i...

  6. Comparative gene expression profile of Ngn3-overexpressing cultured hippocampal neurons vs the corresponding control populations BioProject

    ID: PRJNA136173

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: lated with cytoskeleton dynamics. One of then was Fmn1 whose protein is associated with actin and microtubule cytoskeleton. Overexpression of the isoform Fmn1-Ib in cultured hippocampal neurons induced an increase in the number of primary dendrites and in the number of glutamatergic synaptic inputs without affecting GABAergic synapses resulting in a modification in the balance between excitation and inhibition. The same changes were provoked by overexpression of Ngn3. In addition downregulation of Fmn1 by the use of Fmn1-siRNAs impaired such morphological and synaptic changes i...
  7. Crystal structure of the formin homology 2 domain of FMNL3 bound to actin PDB

    ID: PDB:4EAH

    Description: Actin, alpha skeletal muscle, Formin-like protein 3

  8. Crystal structure of the autoinhibitory switch in Formin mDia1; the DID/DAD complex PDB

    ID: PDB:2F31

    Description: Diaphanous protein homolog 1

  9. Capra hircus : Genetic analysis of inherited coat color and morphological traits in Swiss goat breeds BioProject

    ID: PRJNA310684

    Keywords: genome sequencing

    Access Type: download

    dataset.description: throat of goats we found an association with the FMN1/GREM1 region on chromosome 10. Furthermore we identified that the brown coat color of Coppernecked goats is associated with a non-synonymous variant at the TYRP1 locus on chromosome 8. The breed specific depigmentation phenotype of Boer goats was shown to be associated with a 1 Mb duplication...
  10. CRYSTAL STRUCTURES OF A FORMIN HOMOLOGY-2 DOMAIN REVEAL A TETHERED-DIMER ARCHITECTURE PDB

    ID: PDB:1UX4

    Description: BNI1 PROTEIN

  11. Solution NMR structure of the N-terminal GTPase-like domain of dictyostelium discoideum Fomin C PDB

    ID: PDB:2L1A

    Description: Formin-C

  12. Bni1p Formin Homology 2 Domain complexed with ATP-actin PDB

    ID: PDB:1Y64

    Description: Actin, alpha skeletal muscle, BNI1 protein

  13. Autoinhibited Formin mDia1 Structure PDB

    ID: PDB:3OBV

    Description: Protein diaphanous homolog 1, Protein diaphanous homolog 1

  14. CRYSTAL STRUCTURE OF THE DIMERIC REGULATORY DOMAIN OF MOUSE DIAPHANEOUS-RELATED FORMIN (DRF), MDIA1 PDB

    ID: PDB:2BNX

    Description: DIAPHANOUS PROTEIN HOMOLOG 1

  15. CRYSTAL STRUCTURES OF A FORMIN HOMOLOGY-2 DOMAIN REVEAL A FLEXIBLY TETHERED DIMER ARCHITECTURE PDB

    ID: PDB:1UX5

    Description: BNI1 PROTEIN

  16. FBP28WW2 domain in complex with the PPLIPPPP peptide PDB

    ID: PDB:2JUP

    Description: Transcription elongation regulator 1, Formin-1

  17. FBP28WW2 domain in complex with a PPPLIPPPP peptide PDB

    ID: PDB:2RM0

    Description: Transcription elongation regulator 1, Formin-1

  18. FBP28WW2 domain in complex with PTPPPLPP peptide PDB

    ID: PDB:2RLY

    Description: Transcription elongation regulator 1, Formin-1

  19. Transcription profiling by array of human NSCLC U1810 residual clones 9 days after a one-hour pulse treatment with cisplatin ArrayExpress

    ID: E-GEOD-48244

    Description: y (XRCC2) and cell-cell/ cell-matrix interaction (FMN1 and LGALS9) were among the top deregulated genes by microarray and were subsequently validated by q-RT-PCR. We focused on DKK1, which was previously reported to be overexpressed in NSCLC. IPA network analysis revealed coordinate up-regulation of several DKK1 transcriptional regulators (TCF4, EZH2, DNAJB6 and HDAC2) in cisplatin-surviving clones. Knockdown of DKK1 by siRNA sensitized untreated NSCLC cells to cisplatin, illustrating a putative role of DKK1 in intrinsic platinum resistance. Conclusions: Gene expression analysis identified DKK1 as a putative cisplatin resistance marker and a potential novel therapeutic target to overcome platinum resistance in NSCLC. U1810 cells were sparsely seeded for clonogenic survival assay in three separate experiments (replicate 1-3), left untreated or treated with cisplatin for

  20. Genome-wide profiling of p63 binding sites identifies genes and regulatory elements for p63-related disorders ArrayExpress

    ID: E-GEOD-17611

    Description: identified a novel de novo microdeletion causing limb defects (SHFM1) that includes a p63 binding site functioning as a cis-regulatory element to control expression of the distally located DLX5/DLX6 genes essential for limb development. Our data demonstrate that target genes and regulatory elements detected in this study can serve as powerful tools to identify causative mutations of unresolved ectodermal disord...


Displaying 20 of 262 results for "FMN1"