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- Güncel gönderiler
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Güncel Gönderiler: Tıbbi Biyoloji Anabilim Dalı
Toplam kayıt 29, listelenen: 1-20
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(2021)Facioscapulohumeral Muscular Dystrophy (FSHD) is in the top three list of all dystrophies with an approximate 1:8000 incidence. It is not a life-threatening disease; however, the progression of the disease extends over ...
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(2022)Sargassurn vulgare was sampled by free dives in Iskenderun Bay, Hatay, Turkey, in September 2018. Sargassum vulgare is a material with high economic value because it has compounds that can be used in medical applications ...
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(2021)The outbreak of COVID-19 caused by SARS-CoV-2 has promptly spread worldwide. This study aimed to predict mature miRNA sequences in the SARS-CoV-2 genome, their effects on protein-protein interactions in the affected cells, ...
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(2019)The common cause of hereditary mental retardation is Fragile X Syndrome (FXS). This disease occurs when the trinucleotiderepeat number (CGG)n in the promoter region of the Fragile X mental retardation 1 (FMR1) gene located ...
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(2020)This study aimed to determine candidate miRNAs that could help to evaluate whether patients with hypopharyngeal squamous cell carcinoma (HSCC) would benefit from docetaxel, cisplatin, and 5-fluorouracil (TPF) induction ...
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(Galenos, 2020)Objective: This study investigates the role of ATG16L1 rs2241880, ATG10 rs1864183 and ATG5 rs2245214 gene polymorphisms, which are involved in autophagosome formation, in the susceptibility to postmenopausal osteoporosis ...
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(De Gruyter, 2019)Objectives: Since studies regarding the effect of polysomy 17 (P17) in breast cancer cases with some specific clinical findings are few in number and are in small sample sizes, meta-analysis was implemented to exhibit the ...
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(Morion LLC, 2015)Aim: The expression differences of SCN8A (which encodes type VIII alpha subunit of voltage gated sodium channel) and NDUFC2 (which encodes C2 subunit of Complex I enzyme in oxidative phosphorylation) genes were evaluated ...
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(SPRINGERONE NEW YORK PLAZA, SUITE 4600 , NEW YORK, NY 10004, UNITED STATES, 2021)
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(FRONTIERS IN BIOSCIENCE INC16471 SCIENTIFIC WAY, IRVINE, CA 92618, 2021-01-01)Chronic Myeloid Leukemia (CML) is a myeloproliferative neoplasm characterized by presence of the BCR-ABL fusion gene which encodes the constitutively active BCR-ABL chimeric protein. Imatinib is first FDA approved first-line ...
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(MARY ANN LIEBERT, INC140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801, 2020)Schizophrenia (SZ) is a disease that causes mental disability and affects 1% of the total population in the world. Our aim was to identify new molecular targets that would help to diagnose and treat these patients. The ...
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(GENERAL PHYSIOL AND BIOPHYSICSINST OF MOLEC PHYSIOL GENETICS SLOVAK ACAD OF SCI VLARSKA 5, 83334 BRATISLAVA, SLOVAKIA, 2020-01-01)Lung cancer (LC) is the prominent cause of cancer-related death worldwide, and non-small cell lung cancer (NSCLC) represents approximately 85% of all diagnosed LC cases. It is stated that LC and chronic obstructive pulmonary ...
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(PORTLAND PRESS LTD5TH FLR, 90 HIGH HOLBORN, LONDON WC1V 6LJ, ENGLAND, 2019)MicroRNAs (miRNAs) have been proven to play a crucial role in postmenopausal osteoporosis (PMO), and studies on their diagnostic value have been increasing. In our study, we aim to identify the key miRNAs in the PMO that ...
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(SOC BRASIL GENETICARUA CAP ADELMIO NORBET DA SILVA, 736, ALTO DA BOA VISTA, 14025-670 RIBEIRAO, 2019)Lung cancer is the leading cause of cancer-related death, and NSCLC constitutes nearly 85%-90% of all cases. The IRS proteins function as adaptors and transmit signals from multiple receptors. Upon binding of insulin to ...
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(GAZI UNIV, FAC MEDGAZI UNIV, FAC MED, ANKARA, 06500, TURKEY, 2019)Aim: Ulcerative Colitis (UC) of which the etiopathogenesis is not yet fully elucidated is a disease that comes out as a result of an exaggerated immune response against environmental factors in genetically susceptible ...
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(DE GRUYTER POLAND SP ZOOBOGUMILA ZUGA 32A STR., 01-811 WARSAW, POLAND, 2018)Placental mesenchymal dysplasia is an increasingly recognizable abnormality. Early cases have been confused with partial hydatidiform mole. Placental mesenchymal dysplasia is probably under-diagnosed because of being an ...
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(ELSEVIER SCIENCE BVPO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS, 2017)Abstract Although the carriers with apparently balanced structural rearrangements have usually normal phenotype, phenotypical abnormalities can be seen in approximately 6% de novo cases. A number of different mechanisms ...
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(2017)Objective:The reports about Factor V (FV) Leiden, Factor II (FII) G20210A and Methylenetetrahydrofolate reductase (MTHFR) C677T gene mutations of parents and fetal viability are frequently encountered in the literature, ...
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(SAGE PUBLICATIONS LTD, 1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND, 2016)Long non-coding RNAs (lncRNAs) are found to play crucial roles in several biological processes and have been associated with many complex human diseases including cancers. Several lines of evidences indicate that lncRNAs ...
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(SPRINGER INDIA, 7TH FLOOR, VIJAYA BUILDING, 17, BARAKHAMBA ROAD, NEW DELHI, 110 001, INDIA, 2016)Childhood acute lymphoblastic leukemia (ALL) is the most common type of childhood leukemia. Specifically, ALL is a malignant disorder of the lymphoid progenitor cells, with a peak incidence among children aged 2-5 years. ...
Toplam kayıt 29, listelenen: 1-20
Diğer Bağlantılar
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Gazimuhtar Paşa Bulvarı
No:36
27090
Şehitkamil / GAZİANTEP
