about
Human CCS gene: genomic organization and exclusion as a candidate for amyotrophic lateral sclerosis (ALS).Antagonism of microRNA-122 in mice by systemically administered LNA-antimiR leads to up-regulation of a large set of predicted target mRNAs in the liverSimulation based virtual learning environment in medical genetics counseling: an example of bridging the gap between theory and practice in medical education.Genomic profiling of microRNAs in bladder cancer: miR-129 is associated with poor outcome and promotes cell death in vitroAltered MicroRNA expression confined to specific epithelial cell subpopulations in breast cancerSequence and expression analysis of gaps in human chromosome 20Single-molecule denaturation mapping of DNA in nanofluidic channels.Detection of illegitimate rearrangement within the immunoglobulin locus on 14q32.3 in B-cell malignancies using end-sequenced probes.Not para-, not peri-, but centric inversion of chromosome 12.Sequencing and mapping of the porcine CCS gene.Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.Epigenetic remodelling and dysregulation of DLGAP4 is linked with early-onset cerebellar ataxiaIsolation of the human beaded-filament structural protein 1 gene (BFSP1) and assignment to chromosome 20p11.23-p12.1.Diagnostic and prognostic microRNAs in stage II colon cancer.Fluorescence-based codetection with protein markers reveals distinct cellular compartments for altered MicroRNA expression in solid tumors.Olfactomedin 4 defines a subset of human neutrophils.miR-200b mediates post-transcriptional repression of ZFHX1B.Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies.MicroRNA expression in the adult mouse central nervous system.Loss of microRNA cluster miR-29a/b-1 in sporadic Alzheimer's disease correlates with increased BACE1/beta-secretase expression.Breakpoints around the HOXD cluster result in various limb malformations.The utility of LNA in microRNA-based cancer diagnostics and therapeutics.MicroRNAs, epigenetics and disease.Advanced microtechnologies for detection of chromosome abnormalities by fluorescent in situ hybridization.MicroRNAs in the hypothalamus.Locked nucleic acid-based in situ hybridisation reveals miR-7a as a hypothalamus-enriched microRNA with a distinct expression pattern.LNA-modified oligonucleotides are highly efficient as FISH probes.FISHing with locked nucleic acids (LNA): evaluation of different LNA/DNA mixmers.Associating transcription factors and conserved RNA structures with gene regulation in the human brain.RUNX2 analysis of Danish cleidocranial dysplasia families.The DLGAP family: neuronal expression, function and role in brain disorders.Aberrant expression of miR-218 and miR-204 in human mesial temporal lobe epilepsy and hippocampal sclerosis-convergence on axonal guidance.An association study between the norepinephrine transporter gene and depression.Detection of microRNAs in frozen tissue sections by fluorescence in situ hybridization using locked nucleic acid probes and tyramide signal amplification.Enrichment of megabase-sized DNA molecules for single-molecule optical mapping and next-generation sequencing.Genetic ablation of Dicer in adult forebrain neurons results in abnormal tau hyperphosphorylation and neurodegeneration.Deficiency of the miR-29a/b-1 cluster leads to ataxic features and cerebellar alterations in mice.Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort.Centrifugally driven microfluidic disc for detection of chromosomal translocations.Cell-specific detection of microRNA expression during cardiomyogenesis by combined in situ hybridization and immunohistochemistry.
P50
Q21283799-572F5494-9626-47C5-A1A8-C3B411C331AAQ24649633-D5EE958E-62E9-4043-B4DC-C0F86D9ED4C0Q27308756-BC474FA4-73DA-4031-8CB7-1EF80AAD0A0BQ28247046-02578373-EF0A-4557-8DFD-9A1E65D00A50Q28261558-7E60D328-FBDA-4EE6-8E80-3F96EF28282DQ28728564-529971BE-15EB-4425-8182-8FA7E015114CQ30496076-70DDE457-B220-450F-AB6F-6174F4DE49AEQ30727143-F631B334-C53E-484F-9CF8-E6F6FCE205E3Q33681161-5FDE8E16-5CE6-49EA-92C6-CE6872E28911Q34334702-1E4680A4-B54A-4779-94DE-4C44D1436F88Q34356769-EBC836A4-508E-4145-977D-E2F78918DA0FQ34463195-A51EAE1D-4D1D-463E-9B1F-7EC66F253200Q34476904-6163C095-1388-49C7-A6B2-DCEB0458B0B2Q34803800-346C43F7-7E85-4E47-BEBE-2C91957B5E46Q35588532-714506B4-BE52-429A-9A01-E0C114DD1DD8Q35787343-7F793394-38D6-4327-9730-487EF70CBD74Q35902048-BA686E8E-1379-482E-AE1E-759F14CEA7CBQ36096140-A5E86770-D7A0-4AB2-85DD-D0C4EB17BF13Q36470289-4B171669-B7BB-4002-8936-6E9B3FC7323AQ36609033-6DDF256D-DF33-4936-B1CC-026848588520Q36930275-536404A7-CB6C-4FE0-9802-CF7C451B4CA1Q37092847-14A090D6-9161-4EC4-A3DC-8CE4CFD23D3BQ37785997-8EBAC940-3636-476F-8303-3793D8204141Q37973579-EF3B70A5-23B4-4BD2-9D6A-907EB1ADA551Q38147881-B51ADEB9-D9B6-41FA-9501-160FD2A2B9A1Q38323747-E62CDDA5-903C-4470-8F5C-B6320A0BB080Q38337876-15393457-8219-4EC2-A338-5FAC32617634Q38351049-142E1234-BAF1-42AA-82CA-49FF0B610BF5Q38673142-1888F2D5-FD13-4666-8852-99C863699B76Q39862347-BD036D24-5063-4A2F-BD0D-8C0F0EB64F31Q41611100-DDB42EA5-FEB3-4DDC-AC16-5AE7EFC77C3DQ42775825-93528EA8-EE05-4305-BF70-4F79ADEA343DQ45891980-41307227-0DA7-4055-831D-E00AF1EA6AE3Q46941943-F0676FED-AF1E-4AC7-9E90-832E0E182893Q47118042-A065793F-5818-41AA-8435-A0E0AA66E59AQ48112220-AEA5123C-31AD-42C6-8F24-0CF049253214Q48485360-AB5C3561-53EF-4AF8-895E-4AE700A0781FQ50560937-2B4FF1CF-9590-4F8B-8FD8-5DD43E46AC98Q51537736-2F2A4BDC-57A8-42A7-85A7-A64D7A007F5AQ51865105-33C0D6E8-7F63-45E1-A730-12ADDA9A9017
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Asli Silahtaroglu
@ast
Asli Silahtaroglu
@en
Asli Silahtaroglu
@es
Asli Silahtaroglu
@nl
type
label
Asli Silahtaroglu
@ast
Asli Silahtaroglu
@en
Asli Silahtaroglu
@es
Asli Silahtaroglu
@nl
prefLabel
Asli Silahtaroglu
@ast
Asli Silahtaroglu
@en
Asli Silahtaroglu
@es
Asli Silahtaroglu
@nl
P106
P21
P31
P496
0000-0001-6181-2705