Ş. Güran

发表

Zinc increases nestin but not vimentin gene expression in mouse mesenchymal stem cells

Ş. Güran, Z. D. Çoban, M. P. Elçi, 2018 .

Rheumatic and Autoimmune Diseases May Have a Role in Disease Progression of Myelodysplastic Syndrome

Y. Terzi, D. Torun, C. Beyan, 2012 .

Sorefenib inhibits the expressions of heat shock protein70 gene on multiple myeloma (RPMI-8226) and plasma cell leukemia (ARH-77) cell lines

H. Kayir, Ş. Güran, Z. D. Çoban, 2017 .

Prenatal diagnosis history of a Li-Fraumeni syndrome family.

Ş. Güran, Y. Tunca, 2005, Cancer genetics and cytogenetics.

The Cytogenetic Results of The Cases Who Had Chronic Myeloproliferative Disorders Except Chronic Myeloid Leukemia

C. Beyan, A. Ural, Ş. Güran, 2005 .

Folic acid and zinc inhibit angiogenesis in chicken chorioallontoic membrane model via angiogenic factor genes

Ş. Güran, Z. D. Çoban, O. Fermanlı, 2018 .

Genomic Large Rearrangement Screening of BRCA1 and BRCA2 Genes in High-Risk Turkish Breast/Ovarian Cancer Patients by Using Multiplex Ligation-Dependent Probe Amplification Assay

G. Lüleci, M. Şımşek, Ş. Güran, 2011, Cancer investigation.

Germline mutations of BRCA1 and BRCA2 genes in Turkish breast, ovarian, and prostate cancer patients.

M. Baykara, G. Lüleci, M. Şımşek, 2010, Cancer genetics and cytogenetics.

Monosodium glutamate below the neurotoxic doses has no cytotoxic effect on mouse mesenchymal stem cells

Ş. Güran, Z. D. Çoban, E. Altaylı, 2017 .

Cumulation of TP53 mutations and p16INK4A/p15INK4B homozygous deletions in human papilloma virus type 16 positive scrotal cancer.

Ş. Güran, I. Pak, 1999, Cancer genetics and cytogenetics.

Trisomy 8 finding treatment of imatinib mesylate in chronic myeloid leukemia cases.

Ş. Güran, Y. Tunca, 2005, Experimental hematology.

P53, p15INK4B, p16INK4A and p57KIP2 mutations during the progression of chronic myeloid leukemia.

C. Beyan, Ş. Güran, A. Yalçın, 1998, Haematologia.

Dextrose solution used for prolotherapy decreases cell viability and increases gene expressions of angiogenic and apopitotic factors

N. Karaağaç, Ş. Güran, Z. D. Çoban, 2018 .

Unilateral tubal ectopic twin pregnancy.

Ş. Güran, S. Kozan, M. Dede, 2008, Taiwanese journal of obstetrics & gynecology.

p53 and p16INK4A Mutations during the progression of glomus tumor

E. Tali, Ş. Güran, 1999, Pathology & Oncology Research.

First report of almond leaf scorch in Turkey.

G. Martelli, Ş. Güran, B. K. Çağlar, 2005 .

Importance of Myc‐related microRNAs in induced pluripotency

Ş. Güran, E. Çağlayan, 2015, Cell biology international.

Low Zip 4 gene expression levels in RPMI - 8226 and ARH - 77 cell lines support the possible role of zip 4 transporter protein in plasma cell tumorogenesis

D. Torun, A. Ural, Ş. Güran, 2013 .

Synchronous double malignancies of renal cell carcinoma and acute myeloid leukemia: An unreported co‐existence

C. Beyan, Ş. Güran, A. Ifran, 2005, American journal of hematology.

ANTI-ANGIOGENIC ROLE OF ANKAFERD ON CHICK CHORIOALLONTOIC MEMBRANE MODEL

Ş. Güran, Z. D. Çoban, F. Avcu, 2015 .

A case of neurofibromatosis and breast cancer: loss of heterozygosity of NF1 in breast cancer.

Ş. Güran, M. Safali, 2005, Cancer genetics and cytogenetics.

Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family.

Ş. Güran, Y. Tunca, N. Imirzalioğlu, 1999, Cancer genetics and cytogenetics.

Familial multiple myeloma associated with disorders of chronic inflammation: first report from Turkey.

A. Ozet, Ş. Güran, M. Beksaç, 2008, Clinical lymphoma & myeloma.

Methylation of SOCS3 in Myeloproliferative Neoplasms and Secondary Erythrocytosis/Thrombocythemia

D. Torun, C. Beyan, Ş. Güran, 2013, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Methylation of SOCS 3 in Myeloproliferative Neoplasms and Secondary Erythrocytosis / Thrombocythemia Miyeloproliferatif Neoplazmlar ve Sekonder Eritrositoz / Trombositemide SOCS 3 Metilasyonu

D. Torun, C. Beyan, Ş. Güran, 2013 .

The Results of Analyses for Common MEFV Gene Mutation in 110 Patients in Whom was Considered FMF and Their Correlation with Clinical Findings

A. Uygun, A. Tüzün, A. Dursun, 2004 .

A Case with Neurosensorial Hearing Loss and Anodonty Findings: Is This a Variant of Otodental Syndrome?

D. Torun, Ş. Güran, M. Bahçe, 2010 .

Effect of progesterone hormon on cell viability and stem cell activation in dental pulp cells

Ş. Güran, D. Aksoy, Z. Çoban, 2016 .

LITHIUM HAS NEUROPROTECTIVE EFFECT ON NEUROBLASTOMA CELL LINE IN LOW DOSAGES

Ş. Güran, H. Gündeşli, Z. Çoban, 2023, Cumhuriyet Medical Journal.

Persistent mullerian duct syndrome with transverse testicular ectopia

Ş. Güran, T. Kanmaz, M. Kaya, 2007, International Urology and Nephrology.

Joubert syndrome with oculomotor apraxia: a case report

R. Rosti, D. Torun, Ş. Güran, 2010 .

A case with oto-spondylo-mega-epiphyseal-dysplasia (OSMED): the clinical recognition and differential diagnosis.

R. Rosti, D. Torun, H. Sanal, 2011, Turkish Journal of Pediatrics.

Hereditary breast cancer syndromes in a Turkish population. Results of molecular germline analysis.

J. Gille, A. Ozet, Ş. Güran, 2005, Cancer genetics and cytogenetics.

Specific Polymorphisms of IL-1? Genes (-511, +3953) and Their Probable Effects on IL-1? Production in Idiopatic Hypogonadotropic Hypogonadism

M. Kutlu, E. Bolu, D. Gül, 2010 .

Molecular view to the effect of centaury oil on wound healing

Ş. Güran, E. Altaylı, Z. Çoban, 2016 .

Familial multiple myeloma associated with disorders of chronic inflammation: first report from Turkey.

A. Ozet, Ş. Güran, M. Beksaç, 2008, Clinical lymphoma & myeloma.