about
Functional coherence metrics in protein familiesPCR amplification introduces errors into mononucleotide and dinucleotide repeat sequencesMethods for RNA extraction, cDNA preparation and analysis of CFTR transcripts.Quantification of CFTR transcripts.High-content siRNA screen reveals global ENaC regulators and potential cystic fibrosis therapy targets.GRYFUN: a web application for GO term annotation visualization and analysis in protein sets.Measurements of Functional Responses in Human Primary Lung Cells as a Basis for Personalized Therapy for Cystic Fibrosis.Quantitative methods for the analysis of CFTR transcripts/splicing variants.Extracting microRNA-gene relations from biomedical literature using distant supervision.Annotation extension through protein family annotation coherence metrics.Correction of a Cystic Fibrosis Splicing Mutation by Antisense Oligonucleotides.The replication timing of CFTR and adjacent genes.Transcriptome meta-analysis reveals common differential and global gene expression profiles in cystic fibrosis and other respiratory disorders and identifies CFTR regulators.Comparative ex vivo, in vitro and in silico analyses of a CFTR splicing mutation: Importance of functional studies to establish disease liability of mutations.F508del-CFTR increases intracellular Ca(2+) signaling that causes enhanced calcium-dependent Cl(-) conductance in cystic fibrosis.Generating a Tolerogenic Cell Therapy Knowledge Graph from Literature.Human Epididymis Protein 4: A Novel Serum Inflammatory Biomarker in Cystic Fibrosis.Microarray mRNA Expression Profiling to Study Cystic FibrosisBO-LSTM: classifying relations via long short-term memory networks along biomedical ontologiesExpression and localization of prolactin receptor messenger ribonucleic acid in red deer ovary during the estrous cycle and pregnancyCell type specificity in alternative splicing of the human mismatch repair gene hMSH2Is prolactin a gonadotrophic hormone in red deer (Cervus elaphus)? Pattern of expression of the prolactin receptor gene in the testis and epididymisTMEM16A chloride channel does not drive mucus productionThe effect of premature termination codon mutations on CFTR mRNA abundance in human nasal epithelium and intestinal organoids: a basis for read-through therapies in cystic fibrosis
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description
researcher
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wetenschapper
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հետազոտող
@hy
name
Luka A Clarke
@nl
Luka A Clarke
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Luka A. Clarke
@en
Luka A. Clarke
@es
type
label
Luka A Clarke
@nl
Luka A Clarke
@sl
Luka A. Clarke
@en
Luka A. Clarke
@es
prefLabel
Luka A Clarke
@nl
Luka A Clarke
@sl
Luka A. Clarke
@en
Luka A. Clarke
@es
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P1153
9248448600
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68145066491166590240
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0000-0003-3254-9121