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المؤلفون: Neslihan Bascil Tutuncu, Hpb Cebi, Fatma Belgin Ataç, T Tutuncu, Nazli Gulsoy Kirnap, Hasibe Verdi, Yaprak Yılmaz Yalçın, Asli Nar
المصدر: Balkan Journal of Medical Genetics, Vol 24, Iss 1, Pp 73-80 (2021)
مصطلحات موضوعية: 0301 basic medicine, Thyroid nodules, medicine.medical_specialty, endocrine system, endocrine system diseases, Single-nucleotide polymorphism, thyroid cancer genetics, QH426-470, Gastroenterology, Thyroiditis, Thyroid carcinoma, 03 medical and health sciences, 0302 clinical medicine, environmental factors, Internal medicine, Genotype, medicine, xrcc1 gene, Genetics, differentiated thyroid carcinomas (dtc), Thyroid cancer, arg280his, Genetics (clinical), business.industry, Thyroid, medicine.disease, Genotype frequency, 030104 developmental biology, medicine.anatomical_structure, 030220 oncology & carcinogenesis, business
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المؤلفون: F. Belgin Ataç, Sibel Tulgar Kinik, Ayşe Canan Yazıcı-Güvercin, Hasibe Verdi, Neslihan Bascil Tutuncu, H Pınar Baysan-Çebi, Beril Aydin, Yaprak Yılmaz Yalçın
المصدر: The Turkish Journal of Pediatrics. 62:921
مصطلحات موضوعية: Adult, Pediatric Obesity, medicine.medical_specialty, medicine.medical_treatment, Ion Channels, Mitochondrial Proteins, Exon, Internal medicine, Genotype, medicine, Humans, Uncoupling Protein 3, Uncoupling protein, Uncoupling Protein 2, Allele, Child, Gene, Uncoupling Protein 1, UCP3, Polymorphism, Genetic, business.industry, Insulin, medicine.disease, Obesity, Endocrinology, Pediatrics, Perinatology and Child Health, Female, Mitochondrial Uncoupling Proteins, business
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المؤلفون: Hasibe Verdi, Aylin Tarcan, Namik Ozbek, Ayşe Ecevit, N Mutlu Karakaş, Yaprak Yılmaz Yalçın, Ali Haberal, M Ağah Tekindal, Fatma Belgin Ataç, Beril Özdemir
مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Neonatal intensive care unit, Infant, Newborn, Diseases, 03 medical and health sciences, 0302 clinical medicine, Pregnancy, Polymorphism (computer science), Genotype, medicine, Humans, Polymorphism, Genetic, 030219 obstetrics & reproductive medicine, Interleukin-6, Obstetrics, business.industry, Infant, Newborn, Case-control study, Obstetrics and Gynecology, medicine.disease, 030104 developmental biology, Premature birth, Case-Control Studies, Pediatrics, Perinatology and Child Health, Premature Birth, Term Birth, Female, Gene polymorphism, business, Infant, Premature
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9ceb82e455074a5a492dc8434eeb5c5
https://avesis.gazi.edu.tr/publication/details/9997ed84-a9ee-491d-b419-a2f3a4855eaf/oai -
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المؤلفون: Hasibe Verdi, Nursel Muratoglu Sahin, F. Belgin Ataç, Yaprak Yılmaz Yalçın, Sibel Tulgar Kinik, Ayse Canan Yazici
المصدر: Journal of Clinical Research in Pediatric Endocrinology
مصطلحات موضوعية: Blood Glucose, Male, obesity, medicine.medical_specialty, Adolescent, Endocrinology, Diabetes and Metabolism, oral glucose tolerance test, Childhood obesity, Body Mass Index, Endocrinology, children, Internal medicine, Humans, Insulin, Medicine, Child, Receptor, Gene, Plasma glucose, Polymorphism, Genetic, Waist-Hip Ratio, business.industry, Post challenge, Glucose Tolerance Test, Prognosis, medicine.disease, Lipids, β3-adrenergic receptor gene polymorphism, Case-Control Studies, Receptors, Adrenergic, beta-3, beta 3-adrenergic receptor gene polymorphism, Pediatrics, Perinatology and Child Health, Original Article, Female, Insulin Resistance, business, Follow-Up Studies
وصف الملف: application/pdf
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المؤلفون: Hasibe Verdi, Belgin Atac, Neslihan Bascil Tutuncu, Nazli Gulsoy Kirnap, Yaprak Yılmaz Yalçın, Asli Nar
المصدر: Endocrine Abstracts.
مصطلحات موضوعية: Genetics, Loss of heterozygosity, Genotype, Genetic predisposition, Cancer research, medicine, Biology, medicine.disease, Thyroid cancer, XRCC1 Gene
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::569e320877921645c4fe07e2c1912028
https://doi.org/10.1530/endoabs.49.ep1431 -
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المؤلفون: Semra Saygı, Fatma Belgin Atac, Füsun Alehan, Yaprak Yılmaz Yalçın, Ilknur Erol, Gözde Kubat
المصدر: Journal of child neurology. 30(12)
مصطلحات موضوعية: Male, Migraine without Aura, medicine.medical_specialty, Adolescent, Genotype, Genotyping Techniques, Migraine with Aura, SOD2, Biology, Polymorphism, Single Nucleotide, Superoxide dismutase, Superoxide Dismutase-1, Gene Frequency, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Migraine treatment, Allele frequency, Genetics, Superoxide Dismutase, medicine.disease, Catalase, Migraine with aura, Endocrinology, Migraine, Pediatrics, Perinatology and Child Health, biology.protein, Female, Neurology (clinical), Gene polymorphism, medicine.symptom
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::833e9cf6745a234e01daebbc6f466ee3
https://pubmed.ncbi.nlm.nih.gov/25818327 -
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المؤلفون: Semra Saygı, Yaprak Yılmaz Yalçın, Ilknur Erol, Fatma Belgin Atac, Gözde Kubat, Füsun Alehan
المصدر: Journal of child neurology. 30(1)
مصطلحات موضوعية: Pediatric migraine, Male, medicine.medical_specialty, Pediatrics, Adolescent, Genotype, Aura, Migraine Disorders, Gastroenterology, Pathogenesis, Transforming Growth Factor beta1, Gene Frequency, Internal medicine, Medicine, Humans, Genetic Predisposition to Disease, Child, Allele frequency, Genotyping, Polymorphism, Genetic, business.industry, medicine.disease, Migraine, Pediatrics, Perinatology and Child Health, Female, Neurology (clinical), business, Transforming growth factor
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd668a4bbdc3dd52e9f836eaa9d80d67
https://pubmed.ncbi.nlm.nih.gov/24619148