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FLII
Genes in a Refined Smith-Magenis Syndrome Critical Deletion Interval on Chromosome 17P11.2 and the Syntenic Region of the Mouse
1 Supporting Information for a Microrna Network Regulates
Supplementary Materials
The KMT1A-GATA3-STAT3 Circuit Is a Novel Self-Renewal Signaling of Human Bladder Cancer Stem Cells Zhao Yang1, Luyun He2,3, Kais
Genomic Organization of the Approximately 1.5 Mb Smith
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Downloaded the Amino Acid Sequence and Used PSI-BLAST (Altschul Et Al
FGF6 and FGF9 Regulate UCP1 Expression Independent of Brown Adipogenesis
A High-Throughput Approach to Uncover Novel Roles of APOBEC2, a Functional Orphan of the AID/APOBEC Family
A Novel Locus for Congenital Simple Microphthalmia Family Mapping to 17P12-Q12
Identification of the Flii and Flij Components of the Caulobacter Flagellar Type III Protein Secretion System
Ewing Sarcoma 11;22 Translocation Produces a Chimeric Transcription Factor That Requires the DNA-Binding Domain Encoded by FLII for Transformation WILLIAM A
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Supplementary Table 3. Alternative Exon Usage Following PRMT6 Knockdown in MCF-7 Cells. Table Shows Gene Symbol, NCBI Link
Positive Clear Cell Sarcoma of Soft Tissue Cell Lines Reveals Characteristic Up-Regulation of Potential New Marker Genes Including ERBB3
Detection of Classical 17P11.2 Deletions, an Atypical Deletion and RAI1 Alterations in Patients with Features Suggestive of Smith–Magenis Syndrome
Supplementary Material Peptide-Conjugated Oligonucleotides Evoke Long-Lasting Myotonic Dystrophy Correction in Patient-Derived C
Molecular Cytogenetic Characterization of the Critical Deletion at 17P11.2 in Japanese Patients with Smith-Magenis Syndrome (SMS)
Top View
Downloaded from to Pre-Chilled 1.5 Ml Tubes
DNA Rearrangements on Both Homologues of Chromosome 17 In
Molecular and Mutational Analysis of a Gelsolin-Family Member Encoded by the Flightless I Gene of Drosophila Melanogaster
The Flightless I Protein
View of Parkinson’S Disease
List of 1124 Genes Whose Binding to Eif4e Was Induced by Radiation
Overexpression of Flii During Murine Embryonic Development Increases Symmetrical Division of Epidermal Progenitor Cells
Reticular Basement Membrane Thickness Is Associated With
The Home Stretch, a First Analysis of the Nearly Completed Genome Of
Gelsolin and Related Proteins in Vertebrate Model Organisms
121 RAI1, the Smith–Magenis, and Potocki–Lupski Syndromes
Anti-FLII Antibody (ARG58740)
Differential Genes Gene ID Log2fold Change Pval Padj Gene Title Symbol Cluster-62068.91323 7.9822 6.52E-42 9.39E-37 Ankyrin Repe
Roles of Actin Remodeling Proteins, Gelsolin and Flightless-I in Epidermal Wound Healing
Suppl Table IV
Genomic Structure, Evolution, and Expression of Human FLII, a Gelsolin and Leucine-Rich-Repeat Family Member: Overlap with LLGL Hugh D
Multidisciplinary Roles of LRRFIP1/GCF2 in Human Biological Systems and Diseases
Multi-Species Integrative Biclustering
3.61±0.36 3.47±0.60 3.79±0.71 3.66±0.69 Protein