يعرض 1 - 10 نتائج من 20 نتيجة بحث عن '"Timur Tuncali"', وقت الاستعلام: 0.93s تنقيح النتائج
  1. 1
    ROHMM—A flexible hidden Markov model framework to detect runs of homozygosity from genotyping data

    المؤلفون: TIMUR TUNCALI, Gökalp Çelik

    المصدر: Human Mutation. 43:158-168

    مصطلحات موضوعية: Consanguinity, Genotype, Homozygote, Genetics, High-Throughput Nucleotide Sequencing, Humans, Polymorphism, Single Nucleotide, Algorithms, Genetics (clinical)

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b05e7ec7139f61b0a2b545e876ec2a0
    https://doi.org/10.1002/humu.24316

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  2. 2
    Genotype Phenotype Correlation of A Case Having Chromosome 3 Imbalance

    المؤلفون: Şule Altıner, Ezgi Gökpınar İli, Timur Tuncali, Ahmet Cevdet Ceylan, Elifcan Taşdelen

    المصدر: Journal of Ankara University Faculty of Medicine. 74:365-369

    مصطلحات موضوعية: Genetics, Correlation, Chromosome 3, Biology, Genotype phenotype

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::4e4e598fefddd10f6e41d4e74c80f135
    https://doi.org/10.4274/atfm.galenos.2021.66376

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  3. 3
    Right Anterior Theta Hypersynchrony as a Quantitative Measure Associated with Autistic Traits and K-Cl Cotransporter KCC2 Polymorphism

    المؤلفون: Canan Kalaycıoğlu, Timur Tuncali, Simge Aykan, Meghan H. Puglia, Kevin A. Pelphrey, Erhan Nalçaci

    المصدر: Journal of Autism and Developmental Disorders. 52:61-72

    مصطلحات موضوعية: medicine.medical_specialty, Autism Spectrum Disorder, Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Quantitative trait locus, 03 medical and health sciences, 0302 clinical medicine, Polymorphism (computer science), Internal medicine, Developmental and Educational Psychology, medicine, Humans, Solute Carrier Family 12, Member 2, 0501 psychology and cognitive sciences, Autistic Disorder, Symporters, 05 social sciences, Electroencephalography, medicine.disease, Quantitative measure, Autistic traits, Endocrinology, Autism, Psychology, Cotransporter, 030217 neurology & neurosurgery, Right anterior, 050104 developmental & child psychology

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e22123ca3efed19f0f90813c4a2c5d68
    https://doi.org/10.1007/s10803-021-04924-x

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  4. 4
    Coexistence of Ovarian Granulose Cell Tumor, Congenital Adrenal Hyperplasia, and Triple Translocation: Is a Consequence or Coincidence?

    المؤلفون: Sami Akbulut, Timur Tuncali, Nilgun Sogutcu, Şenay Durmaz Ceylan

    المساهمون: Kırıkkale Üniversitesi, KKÜ

    المصدر: Journal of Gastrointestinal Cancer. 52:508-514

    مصطلحات موضوعية: Pathology, medicine.medical_specialty, Abdominal pain, Granulose cell tumor, medicine.medical_treatment, Chromosomal translocation, Physical examination, Translocation, Genetic, 03 medical and health sciences, 0302 clinical medicine, Cytochrome P450 Family 21, Hyperpigmentation, Ambiguous genitalia, Humans, Medicine, Congenital adrenal hyperplasia, Simple virilizing type, Granulosa Cell Tumor, Triple translocations, Adrenal Hyperplasia, Congenital, medicine.diagnostic_test, business.industry, Gastroenterology, Middle Aged, medicine.disease, Radiation therapy, Oncology, 030220 oncology & carcinogenesis, Mutation, Immunohistochemistry, Female, 030211 gastroenterology & hepatology, Steroid 21-Hydroxylase, medicine.symptom, Restriction fragment length polymorphism, business

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::150bdb317cc2f7a4408128e686dc7e30
    https://doi.org/10.1007/s12029-020-00408-w

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  5. 5
    P-045: Immunoglobulin V(D) J Recombination, Protein Ubiquitination, Cell Adhesion and Sonic Hedgehog Gene Variants are detected among familial Multiple Myeloma subjects following whole exome sequencing

    المؤلفون: Meral Beksac, Sevgi Kalayoglu Besisik, Timur Tuncali, Erman Akkus, Ali Ünal, Aysegul Turcan, Emel Gürkan, Deniz Sargin, Yildiz Aydin, Siret Ratip, Ayse Salihoglu

    المصدر: Clinical Lymphoma Myeloma and Leukemia. 21:S63

    مصطلحات موضوعية: Genetics, Cancer Research, education.field_of_study, business.industry, Population, Hematology, medicine.disease, Protein ubiquitination, Familial adenomatous polyposis, Immunoglobulin V(D)J recombination, Germline mutation, Oncology, CDKN2A, Medicine, Missense mutation, business, education, Exome sequencing

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b04a189910aab82a4e8189f7d81a5611
    https://doi.org/10.1016/s2152-2650(21)02179-0

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  6. 6
    Comparative Analysis and Validation of CIBMTR Early Relapse Risk Score with ISS and R-ISS: Single Center Experience from Ankara University

    المؤلفون: Sinem Civriz Bozdag, Timur Tuncali, Muhit Ozcan, Osman Ilhan, Selami Kocak Toprak, Meltem Kurt Yuksel, Guldane Cengiz Seval, Gunhan Gurman, Meral Beksac, Pervin Topcuoglu, Onder Arslan, Taner Demirer

    المصدر: Transplantation and Cellular Therapy. 27:S401

    مصطلحات موضوعية: Transplantation, medicine.medical_specialty, Framingham Risk Score, business.industry, Internal medicine, Molecular Medicine, Immunology and Allergy, Medicine, Early Relapse, Cell Biology, Hematology, business, Single Center

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::dc324cf00e30878ac2ddb9c00b39eb8f
    https://doi.org/10.1016/s2666-6367(21)00516-9

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  7. 7
    Oesophageal achalasia misdiagnosed as uncontrolled asthma

    المؤلفون: İlker Ökten, Murat Özkan, Zeynep Misirligil, Cabir Yüksel, Ömür Aydın, Timur Tuncali, Akin Kaya

    المصدر: Tuberkuloz ve Toraks. 61:147-151

    مصطلحات موضوعية: Male, Pulmonary and Respiratory Medicine, Spirometry, medicine.medical_specialty, Adolescent, Achalasia, Critical Care and Intensive Care Medicine, digestive system, Diagnosis, Differential, otorhinolaryngologic diseases, medicine, Humans, Chest surgery, Diagnostic Errors, Respiratory Sounds, Asthma, Heller myotomy, medicine.diagnostic_test, business.industry, medicine.disease, Dilatation, digestive system diseases, respiratory tract diseases, Surgery, Uncontrolled asthma, Esophageal Achalasia, Dyspnea, Cough, Male patient, Differential diagnosis, business

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30e3b9840c1c759c79155ebab545072e
    https://doi.org/10.5578/tt.5778

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  8. 8
    An Evaluation of the Phenotypic Features of Fanconi Anemia Together with DEB/MMC Positivity in 199 Turkish Patients

    المؤلفون: Halil Gürhan Karabulut, Hatice Ilgin-Ruhi, Ajlan Tükün, Nüket Yürür-Kutlay, Timur Tuncali

    المصدر: Turkiye Klinikleri Journal of Medical Sciences. 33:1-8

    مصطلحات موضوعية: Fanconi anemia, business.industry, Turkish, Immunology, medicine, language, General Medicine, medicine.disease, business, Phenotype, language.human_language

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::70b8f7a719e56c6ee0bba1ec595c4968
    https://doi.org/10.5336/medsci.2011-26589

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  9. 9
    Lack of the Association of the PTPN22 C1858T Gene Polymorphism With Susceptibility to Familial Mediterranean Fever

    المؤلفون: Murat Turgay, Orhan Küçükşahin, Emre Kulahcioglu, Şükran Erten, Ali Şahin, Alexis K. Okoh, Zeynep Şeker, Aşkın Ateş, Timur Tuncali, Gülay Kinikli

    المساهمون: Sivas Cumhuriyet Üniversitesi, [Kucuksahin, Orhan -- Kinikli, Gulay -- Turgay, Murat -- Ates, Askin] Ankara Univ, Fac Med, Dept Internal Med, Div Rheumatol, TR-06100 Ankara, Turkey -- [Seker, Zeynep -- Okoh, Alexis K. -- Kulahcioglu, Emre] Ankara Univ, Fac Med, Dept Internal Med, TR-06100 Ankara, Turkey -- [Tuncali, Timur] Ankara Univ, Fac Med, Dept Med Genet, TR-06100 Ankara, Turkey -- [Sahin, Ali] Cumhuriyet Univ, Fac Med, Dept Rheumatol, Sivas, Turkey -- [Erten, Sukran] Yildirim Beyazit Univ, Ataturk Training & Res Hosp, Dept Rheumatol, Ankara, Turkey

    مصطلحات موضوعية: Turkish population, medicine.medical_specialty, Pathology, Familial Mediterranean fever, Single-nucleotide polymorphism, Gene mutation, Gastroenterology, Article, PTPN22, 03 medical and health sciences, 0302 clinical medicine, Rheumatology, single nucleotide polymorphism, Internal medicine, Genotype, medicine, Family history, 030203 arthritis & rheumatology, protein tyrosine phosphatase non-receptor type 22, business.industry, medicine.disease, Gene polymorphism, business, Romatoloji, 030215 immunology

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eae900969117b9a42d1b9eeb2b30023b
    https://hdl.handle.net/20.500.12418/3982

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  10. 10
    Association of methylenetetrahydrofolate reductase C677T-A1298C polymorphisms with risk for esophageal adenocarcinoma, Barrett's esophagus, and reflux esophagitis

    المؤلفون: N. Alkış, Timur Tuncali, S. Coban, O. Yüksel, Halil Gürhan Karabulut, Necati Örmeci, B. Aktas, F. Ekiz, Ajlan Tükün

    المصدر: Diseases of the Esophagus. 25:437-441

    مصطلحات موضوعية: medicine.medical_specialty, Pathology, biology, business.industry, Gastroenterology, Case-control study, General Medicine, Esophageal cancer, medicine.disease, digestive system diseases, medicine.anatomical_structure, Methylenetetrahydrofolate reductase, Internal medicine, Barrett's esophagus, medicine, biology.protein, Adenocarcinoma, Reflux esophagitis, Esophagus, business, Esophagitis

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7b7570a324f39947a0af361407daf569
    https://doi.org/10.1111/j.1442-2050.2011.01262.x

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