Wissenschaftliche Arbeiten

Dr. Öğr. Üyesi Gökçe Güllü Amuran

23 Publikationen. Neben jeder Publikation steht die Quelle der Angabe.

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  1. NOS1AP: a potential subtype-specific dual role as a tumor suppressor and oncogene in breast cancer subtypes

    Molecular Biology Reports, 2026

    DOI 10.1007/s11033-025-11178-8 PMID 41128806 1 Zitation (Europe PMC) Quelle: ORCID

  2. A rapid LNA-PCR assay from blood lysate without DNA purification for the diagnosis of homozygous SMN1 deletion in spinal muscular atrophy

    Scientific Reports, 2026

    DOI 10.1038/s41598-026-69572-6 Frei zugänglicher VolltextQuelle: ORCID

  3. Locked nucleic acid (LNA) based PCR approach for the diagnosis and screening of spinal muscular atrophy

    Indian Journal of Medical Research, 2026

    DOI 10.25259/ijmr_2408_2025 PMID 41949145 Frei zugänglicher VolltextQuelle: ORCID

  4. IP47-13 UCIPREDICT: LIQUID BIOPSY-BASED PREDICTION OF IMMUNOTHERAPY RESPONSE IN UROTHELIAL CARCINOMA — INTERIM MULTICENTER RESULTS

    The Journal of Urology, 2026

    DOI 10.1097/01.ju.0001191556.17107.c7.13 Quelle: OpenAlex

  5. Apocynin exhibits an ameliorative effect on endothelial dysfunction/ atherosclerosis-related factors in high-fat diet-induced obesity in rats

    Marmara medical journal, 2024

    DOI 10.5472/marumj.1479796 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  6. Neoadjuvant Chemotherapy Shortens the cfDNA Telomere Length in Breast Cancer Patients

    International Journal of Breast Cancer, 2024

    DOI 10.1155/2024/6117394 PMID 39574517 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  7. A simple and cost-effective real-time PCR method using diluted and heat-treated whole blood lysate

    Scientific Reports, 2024

    DOI 10.1038/s41598-024-78802-8 PMID 39516287 5 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  8. Correlation between plasma ccfDNA, mtDNA changes, CTCs, and epithelialmesenchymal transition in breast cancer patients undergoing NACT

    Turkish Journal of Medical Sciences, 2024

    DOI 10.55730/1300-0144.5834 PMID 39295614 4 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  9. Methodological Study on the Evaluation of the Performance of Archived RNA Samples in Terms of Gene Expression Analyzes,Arşivlenmiş RNA Örneklerinin Gen Ekspresyon Analizleri Açısından Performansının Değerlendirilmesi Üzerine Metodolojik Çalışma

    Turkiye Klinikleri Journal of Medical Sciences, 2023

    DOI 10.5336/medsci.2022-91563 Frei zugänglicher VolltextQuelle: ORCID

  10. Comment for the "EpCAM-based Flow Cytometric Detection of Circulating Tumor Cells in Gallbladder Carcinoma Cases".

    Asian Pacific journal of cancer prevention : APJCP, 2020

    DOI 10.31557/apjcp.2020.21.8.2179 PMID 32856840 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  11. Response Assessment With Molecular Characterization of Circulating Tumor Cells and Plasma MicroRNA Profiling in Patients With Locally Advanced Breast Cancer During Neoadjuvant Chemotherapy

    Clinical Breast Cancer, 2020

    DOI 10.1016/j.clbc.2020.02.006 PMID 32201164 9 Zitationen (Europe PMC) Quelle: ORCID

  12. Next-Generation Sequencing Identifies BRCA1 and/or BRCA2 Mutations in Women at High Hereditary Risk for Breast Cancer with Shorter Telomere Length

    OMICS: A Journal of Integrative Biology, 2020

    DOI 10.1089/omi.2019.0103 PMID 31851867 6 Zitationen (Europe PMC) Quelle: ORCID

  13. Comment on “Bladder Cancer–Specific Nuclear Matrix Proteins-4 May Be a Potential Biomarker for Non-Muscle-Invasive Bladder Cancer Detection”

    Disease Markers, 2019

    DOI 10.1155/2019/6432596 PMID 31871501 Frei zugänglicher VolltextQuelle: ORCID

  14. Urinary micro-RNA expressions and protein concentrations may differentiate bladder cancer patients from healthy controls.

    International urology and nephrology, 2019

    DOI 10.1007/s11255-019-02328-6 PMID 31679136 26 Zitationen (Europe PMC) Quelle: ORCID

  15. New Insights in Bladder Cancer Diagnosis: Urinary miRNAs and Proteins.

    Medical sciences (Basel, Switzerland), 2018

    DOI 10.3390/medsci6040113 PMID 30544619 16 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  16. Exploring the role of miRNAs in the diagnosis of MODY3

    Turkish journal of medical sciences, 2018

    DOI 10.3906/sag-1711-98 PMID 29916222 5 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  17. Comparison of telomere length and insulin-like growth factor-binding protein 7 promoter methylation between breast cancer tissues and adjacent normal tissues in Turkish women

    Journal of Clinical Laboratory Analysis, 2017

    DOI 10.1002/jcla.22083 PMID 27775181 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  18. Kanserde Genetik Üstü (Epigenetik) Mekanizmalar

    2017

    Quelle: OpenAlex

  19. Correlation between the DNA methylation and gene expression of IGFBP5 in breast cancer.

    Breast disease, 2016

    DOI 10.3233/bd-160234 PMID 27612043 10 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  20. Clinical significance of miR-140-5p and miR-193b expression in patients with breast cancer and relationship to IGFBP5

    Genetics and Molecular Biology, 2015

    DOI 10.1590/s1415-475738120140167 PMID 25983620 21 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  21. Identification of Differentially Expressed IGFBP5-Related Genes in Breast Cancer Tumor Tissues Using cDNA Microarray Experiments

    Genes, 2015

    DOI 10.3390/genes6041201 PMID 26569312 22 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  22. Detection of PIK3CA Gene Mutations with HRM Analysis and Association with IGFBP-5 Expression Levels in Breast Cancer

    Asian Pacific Journal of Cancer Prevention, 2014

    DOI 10.7314/apjcp.2014.15.21.9327 PMID 25422220 9 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  23. Functional roles and clinical values of insulin-like growth factor-binding protein-5 in different types of cancers

    Chinese Journal of Cancer, 2012

    DOI 10.5732/cjc.011.10405 PMID 22313597 53 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID