about
Association between gene expression profile and tumor invasion in oral squamous cell carcinomaProfiling and functional analyses of microRNAs and their target gene products in human uterine leiomyomas.A lactotransferrin single nucleotide polymorphism demonstrates biological activity that can reduce susceptibility to cariesImmunological characterization and transcription profiling of peripheral blood (PB) monocytes in children with autism spectrum disorders (ASD) and specific polysaccharide antibody deficiency (SPAD): case studyEvolution of genetic techniques: past, present, and beyond.Laboratory genetic testing in clinical practice 2014.A multicenter, cross-platform clinical validation study of cancer cytogenomic arrays.Laboratory Genetic Testing in Clinical Practice 2016.Laboratory genetic testing in clinical practice.AKT, EGFR, C-ErbB-2, and C-kit expression in uterine carcinosarcoma.Polymorphisms of glutathione S-transferase genes (GSTM1, GSTP1 and GSTT1) and bladder cancer susceptibility in the Turkish population.Molecular and immunohistochemical evidence for the origin of uterine leiomyosarcomas from associated leiomyoma and symplastic leiomyoma-like areas.Children with autism spectrum disorders (ASD) who exhibit chronic gastrointestinal (GI) symptoms and marked fluctuation of behavioral symptoms exhibit distinct innate immune abnormalities and transcriptional profiles of peripheral blood (PB) monocytGenome profiling of chondrosarcoma using oligonucleotide array-based comparative genomic hybridization.Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity.An oligonucleotide based array-CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation.Expression profiling reveals MSX1 and EphB2 expression correlates with the invasion capacity of Wilms tumors.Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization.Copy number variations in three children with sudden infant death.P53 codon 72 polymorphism in bladder cancer--no evidence of association with increased risk or invasivenessArvanil and anandamide up-regulate CD36 expression in human peripheral blood mononuclear cellsMonozygous twins with a microdeletion syndrome involving BTK, DDP1, and two other genes; evidence of intact dendritic cell development and TLR responsesExclusion of APC and VHL gene deletions by array-based comparative hybridization in two patients with microscopically visible chromosomal aberrationsTerminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocationArray comparative genomic hybridization analysis of adult acute leukemia patientsMatricellular protein CCN1 (CYR61) expression is associated with high-grade ductal carcinoma in situChromosomal microarrays: influential players in the diagnosis of developmental disordersClinical utility of DNA testingResearch Highlights: Copy-number variation in patients with developmental delay and autistic spectrum disorders underscored by targeted exonic array CGH
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description
researcher
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wetenschapper
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հետազոտող
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name
Gokce A. Toruner
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Gokce A. Toruner
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Gokce A. Toruner
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Gokce A. Toruner
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Gokce A. Toruner
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type
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Gokce A. Toruner
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Gokce A. Toruner
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Gokce A. Toruner
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Gokce A. Toruner
@nl
Gokce A. Toruner
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prefLabel
Gokce A. Toruner
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Gokce A. Toruner
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Gokce A. Toruner
@es
Gokce A. Toruner
@nl
Gokce A. Toruner
@sl
P106
P1153
6506458937
P31
P496
0000-0002-5305-6337