نتائج البحث

MEFV mutation frequencies in a Turkish cohort with low prevalence of familial Mediterranean fever

• Authors : Çakır N; Department of Internal Medicine, Faculty of Medicine, Istanbul Medeniyet University, İstanbul, Turkey; Azaklı H

Subjects: Familial Mediterranean Fever/Familial Mediterranean Fever/Familial Mediterranean Fever/*genetics ; Mutation/Mutation/Mutation/*genetics ; Pyrin/Pyrin/Pyrin/*genetics

• Source: Turkish journal of medical sciences [Turk J Med Sci] 2021 Aug 30; Vol. 51 (4), pp. 1702-1705. Date of Electronic Publication: 2021 Aug 30.Publisher: Scientific and Technical Research Council of Turkey Country of Publication: Turkey NLM ID:

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The distribution of MEFV mutations in Turkish FMF patients: multicenter study representing results of Anatolia

• Authors : Yaşar Bilge Ş; Sarı İ; Solmaz D

Subjects: Genetics, Population*/Genetics, Population*/Genetics, Population*/statistics & numerical data; Cytoskeletal Proteins/Cytoskeletal Proteins/Cytoskeletal Proteins/*genetics ; Familial Mediterranean Fever/Familial Mediterranean Fever/Familial Mediterranean Fever/*genetics

• Source: Turkish journal of medical sciences [Turk J Med Sci] 2019 Apr 18; Vol. 49 (2), pp. 472-477. Date of Electronic Publication: 2019 Apr 18.Publisher: Scientific and Technical Research Council of Turkey Country of Publication: Turkey NLM ID:

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Molecular survey of pfmdr-1, pfcrt, and pfk13 gene mutations among patients returning from Plasmodium falciparum endemic areas to Turkey.

• Authors : Avcı, Kübra Dilan^1,2 (AUTHOR); Karakuş, Mehmet³ (AUTHOR) ; Kart Yaşar, Kadriye¹ (AUTHOR)

• Source: Malaria Journal. 9/27/2024, Vol. 23 Issue 1, p1-9. 9p.

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Genetic characterisation of 13 rapidly mutating Y-STR loci in 100 father and son pairs from South and East Turkey.

• Authors : Ay M; a Department of Forensic Medicine , Institute of Health Science, University of Cukurova , Adana , Turkey.; Serin A

Subjects: Mutation*; Chromosomes, Human, Y/Chromosomes, Human, Y/Chromosomes, Human, Y/*genetics ; Microsatellite Repeats/Microsatellite Repeats/Microsatellite Repeats/*genetics

• Source: Annals of human biology [Ann Hum Biol] 2018 Sep - Dec; Vol. 45 (6-8), pp. 506-515. Date of Electronic Publication: 2019 Feb 20.Publisher: Taylor & Francis Country of Publication: England NLM ID: 0404024 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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The Epidermal Growth Factor, Anaplastic Lymphoma Kinase, and ROS Proto-oncogene 1 Mutation Profile of Non-Small Cell Lung Carcinomas in the Turkish Population: A Single-Center Analysis.

• Authors : Gün, Eylül¹ ; Çakır, İzzetiye Ebru²; Ersöz, Hasan³

• Source: Thoracic Research & Practice. May2024, Vol. 25 Issue 3, p102-109. 8p.

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PTPN22 1858C>T polymorphism distribution in Europe and association with rheumatoid arthritis: case-control study and meta-analysis.

• Authors : Totaro MC; Division of Rheumatology, Catholic University of the Sacred Heart, Rome, Italy.; Tolusso B

Subjects: Polymorphism, Single Nucleotide*; Arthritis, Rheumatoid/Arthritis, Rheumatoid/Arthritis, Rheumatoid/*genetics ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics

• Source: PloS one [PLoS One] 2011; Vol. 6 (9), pp. e24292. Date of Electronic Publication: 2011 Sep 16.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet

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Prevalence of Epidermal Growth Factor Receptor Mutations in Patients with Non-Small Cell Lung Cancer in Turkish Population.

• Authors : Tezel, Gaye Güler¹ ; Şener, Ebru^1,2; Aydın, Çisel¹

• Source: Balkan Medical Journal. Nov2017, Vol. 34 Issue 6, p567-571. 5p.

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Diyarbakır bölgesinde malign melanom hastalarının BRAF mutasyonu analizi.

• Authors : İbiloğlu, İbrahim¹ ; Alabalık, Ulaş¹; Keleş, Ayşe Nur¹

• Source: Cukurova Medical Journal / Çukurova Üniversitesi Tip Fakültesi Dergisi. 2020, Vol. 45 Issue 4, p1384-1392. 9p.

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Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency.

• Authors : Bulut, Fatma Derya¹ ; Dilek, Semine Özdemir²; Kotan, Damla²

• Source: Journal of Clinical Research in Pediatric Endocrinology. Sep2020, Vol. 12 Issue 3, p261-268. 8p.

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Molecular Testing for Thalassemia: Mutation Detection According to Referral Reasons and Demographic Data.

• Authors : Altıner, Şule¹ ; Karabulut, Halil Gürhan¹; Ekinci, Sadiye¹

• Source: Erciyes Medical Journal / Erciyes Tip Dergisi. 2021, Vol. 43 Issue 5, p449-451. 3p.

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