MUSTAFA OZEN to Female
This is a "connection" page, showing publications MUSTAFA OZEN has written about Female.
Connection Strength
0.239
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Revealing the functions of novel mutations in RAB3GAP1 in Martsolf and Warburg micro syndromes. Am J Med Genet A. 2019 04; 179(4):579-587.
Score: 0.018
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Identification of microRNA profile specific to cancer stem-like cells directly isolated from human larynx cancer specimens. BMC Cancer. 2016 11 05; 16(1):853.
Score: 0.015
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Identification of miR-139-5p as a saliva biomarker for tongue squamous cell carcinoma: a pilot study. Cell Oncol (Dordr). 2016 Apr; 39(2):187-93.
Score: 0.015
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Revealing the function of a novel splice-site mutation of CHD7 in CHARGE syndrome. Gene. 2016 Feb 01; 576(2 Pt 2):776-81.
Score: 0.014
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The role of miR-145 in stem cell characteristics of human laryngeal squamous cell carcinoma Hep-2 cells. Tumour Biol. 2016 Mar; 37(3):4183-92.
Score: 0.014
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Novel POC1A mutation in primordial dwarfism reveals new insights for centriole biogenesis. Hum Mol Genet. 2015 Oct 01; 24(19):5378-87.
Score: 0.014
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Role of miR-145 in human laryngeal squamous cell carcinoma. Head Neck. 2016 Feb; 38(2):260-6.
Score: 0.014
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MiR-221 as a pre- and postoperative plasma biomarker for larynx cancer patients. Laryngoscope. 2015 Dec; 125(12):E377-81.
Score: 0.014
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Differential expression of hypertension-associated microRNAs in the plasma of patients with white coat hypertension. Medicine (Baltimore). 2015 Apr; 94(13):e693.
Score: 0.014
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Designing a gold nanoparticle-based nanocarrier for microRNA transfection into the prostate and breast cancer cells. J Gene Med. 2014 Nov-Dec; 16(11-12):331-5.
Score: 0.013
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Poikiloderma with neutropenia: genotype-ethnic origin correlation, expanding phenotype and literature review. Am J Med Genet A. 2014 Oct; 164A(10):2535-40.
Score: 0.013
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Characterization of stem-like cells directly isolated from freshly resected laryngeal squamous cell carcinoma specimens. Curr Stem Cell Res Ther. 2014; 9(4):347-53.
Score: 0.013
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A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplication. Gene. 2013 Sep 25; 527(2):675-8.
Score: 0.012
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A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia. Clin Dysmorphol. 2013 Jan; 22(1):33-5.
Score: 0.012
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Identification of a novel mutation in ZAP70 and prenatal diagnosis in a Turkish family with severe combined immunodeficiency disorder. Gene. 2013 Jan 10; 512(2):189-93.
Score: 0.012
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Comparison of microRNA expression levels in patients with schizophrenia before and after electroconvulsive therapy. Psychiatr Genet. 2024 Aug 01; 34(4):79-85.
Score: 0.007
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The altered promoter methylation of oxytocin receptor gene in autism. J Neurogenet. 2016 Sep - Dec; 30(3-4):280-284.
Score: 0.004
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Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease. Neuron. 2015 Nov 04; 88(3):499-513.
Score: 0.004
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Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome. Orphanet J Rare Dis. 2015 Sep 30; 10:128.
Score: 0.004
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Human CLP1 mutations alter tRNA biogenesis, affecting both peripheral and central nervous system function. Cell. 2014 Apr 24; 157(3):636-50.
Score: 0.003
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Circumferential skin folds and multiple anomalies: confirmation of a distinct autosomal recessive Michelin tire baby syndrome. Clin Dysmorphol. 2013 Apr; 22(2):87-90.
Score: 0.003
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Characterization of cancer stem-like cells in chordoma. J Neurosurg. 2012 Apr; 116(4):810-20.
Score: 0.003
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Global gene expression analysis of reactive stroma in prostate cancer. Clin Cancer Res. 2009 Jun 15; 15(12):3979-89.
Score: 0.002
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Fibroblast growth factor 2 promotes tumor progression in an autochthonous mouse model of prostate cancer. Cancer Res. 2003 Sep 15; 63(18):5754-60.
Score: 0.002