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UMMET ABUR
UMMET ABUR
Tıbbi Genetik Yardımcı Doçent Doktor Ondokuz Mayıs Üniversitesi Tıp Fakültesi
在 omu.edu.tr 的电子邮件经过验证
标题
引用次数
引用次数
年份
Could familial Mediterranean fever gene mutations be related to PFAPA syndrome?
MH Celiksoy, G Ogur, E Yaman, U Abur, S Fazla, R Sancak, A Yildiran
Pediatric Allergy and Immunology 27 (1), 78-82, 2016
442016
Chromosomal and Y‐chromosome microdeletion analysis in 1,300 infertile males and the fertility outcome of patients with AZFc microdeletions
U Abur, S Gunes, R Ascı, E Altundag, OS Akar, B Ayas, ...
Andrologia 51 (11), e13402, 2019
422019
Which ischemic stroke subtype is associated with hyperhomocysteinemia?
L Gungor, M Polat, MB Ozberk, B Avci, U Abur
Journal of Stroke and Cerebrovascular Diseases 27 (7), 1921-1929, 2018
362018
Semiquantitative promoter methylation of MLH1 and MSH2 genes and their impact on sperm DNA fragmentation and chromatin condensation in infertile men
N Hekim, S Gunes, R Asci, R Henkel, U Abur
Andrologia 53 (1), e13827, 2021
152021
Tr-KIT/c-KIT ratio in renal cell carcinoma
S Ergün, DU Altay, S Güneş, R Büyükalpelli, SC Karahan, L Tomak, ...
Molecular Biology Reports 46 (5), 5287-5294, 2019
92019
Multiscale analysis of SRY‐positive 46, XX testicular disorder of sex development: Presentation of nine cases
OS Akar, S Gunes, U Abur, E Altundag, R Asci, OE Onat, T Ozcelik, ...
Andrologia 52 (11), e13739, 2020
82020
Genetic burden and outcome of cystic hygromas detected antenatally: results of 93 pregnancies from a single center in the northern region of Turkey
HS Aymelek, G Oğur, M Tosun, Ü Abur, E Altundağ, H Çelik, E Kurtoğlu, ...
Journal of medical ultrasound 27 (4), 181-186, 2019
52019
Impact of fluorescent in situ hybridization aberrations and CLLU1 expression on the prognosis of chronic lymphocytic leukemia: presentation of 156 patients from Turkey
Ü Abur, G Oğur, ÖS Akar, E Altundağ, HS Aymelek, D Özatlı, M Turgut
Turkish Journal of Hematology 35 (1), 61, 2018
42018
Vesicourethral reflux‐induced renal failure in a patient with ICF syndrome due to a novel DNMT3B mutation
S Kutluğ, G Ogur, A Yilmaz, PE Thijssen, U Abur, A Yildiran
American Journal of Medical Genetics Part A 170 (12), 3253-3257, 2016
42016
Endocrine, sexual and reproductive functions in patients with Klinefelter syndrome compared to non‐obstructive azoospermic patients
F Kocamanoglu, B Ayas, MS Bolat, U Abur, R Bolat, R Asci
International Journal of Clinical Practice 75 (8), e14294, 2021
32021
Sitokalasin-B ile bloklanan hücrelerde yaşa bağlı mikronükleus oranları
YB Kutbay
Ondokuz Mayıs Üniversitesi, Tıp Fakultesi, 2001
32001
Genetic testing can change diagnosis and treatment in children with congenital hypothyroidism
C Kara, J Mammadova, Ü Abur, C Gumuskaptan, Eİ Güllü, A Dağdemir, ...
European Thyroid Journal 12 (3), 2023
22023
The interrelationship between fyn and Mir-128/193a-5p/494 in imatinib resistance in prostate cancer
S Ergün, O Akgün, NT Hekim, S Aslan, F Ari, S Güneş, Ü Abur
Anti-Cancer Agents in Medicinal Chemistry (Formerly Current Medicinal …, 2023
22023
Clinical, cytogenomic, and molecular characterization of isodicentric y-chromosome and prediction of testicular sperm retrieval outcomes in azoospermic and severe …
U Abur, S Gunes, N Hekim, OS Akar, E Altundag, R Asci
Journal of Assisted Reproduction and Genetics 39 (12), 2799-2810, 2022
22022
Evaluation of the promoter methylation status of hypoxia factor 3A and interleukin-6 genes and expression levels of mir-130b and mir-146b in childhood obesity
E Tekcan, N Kara, HM Aydın, Ü Abur, M Abbaszadeh
Revista da Associação Médica Brasileira 68, 1276-1281, 2022
12022
A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation
U Abur, A Atmaca, H Scott, L Gagliardi, E Altundağ, OS Akar, İK Bayrak, ...
Journal of clinical research in pediatric endocrinology 9, 2-2, 2017
12017
CGG Repeat Profile and Clinical Characteristics of Fragile X Full Mutant, Premutant and Gray Zone Patients.
HU Kına, E Altundağ, A Yılmaz, U Abur
Gazi Medical Journal 35, 2024
2024
Evaluation of Germline CHEK2 Variants and Challenges in Genetic Counseling.
ÖS Akar, G Demirağ, AK Polat, İ Yalçın, M Kefeli, B Yılmaz, S Çalışkan, ...
Gazi Medical Journal 35, 2024
2024
MVK, NLRP3, TNFRSF1A and MEFV gene mutation distributions in childhood autoinflammatory diseases: Experiences in North Anatolia
E Altundağ, Ü Abur, ÖS Akar, A Yıldıran, MH Çeliksoy, AGA Paul, ...
Journal of Experimental and Clinical Medicine 40 (4), 681-686, 2023
2023
Correction to: Clinical, cytogenomic, and molecular characterization of isodicentric Y‑chromosome and prediction of testicular sperm retrieval outcomes in azoospermic and …
U Abur, S Gunes, N Hekim, OS Akar, E Altundag, R Asci
Journal of Assisted Reproduction and Genetics 39 (11), 2685, 2022
2022
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