نتائج البحث

No association of Catechol-O-Methyltransferase (COMT) Gene Haplotypes in Patients with Schizophrenia in a Turkish Sample.

• Authors : Altinyazar, Vesile¹ ; Gunderici, Azad²; Tinaz, Ekrem³

• Source: Klinik Psikofarmakoloji Bulteni. 2015, Vol. 25 Issue 2, p129-135. 7p.

تفاصيل العنوان

Investigation of Catechol-O-methyltransferase (COMT) gene Val158Met polymorphism in ovarian cancer.

• Authors : Abaoğlu, İpek Yağmur¹; Yılmaz, Seda Güleç²; Akdeniz, Fatma Tuba²

• Source: Journal of the Turkish-German Gynecological Association. Mar2021, Vol. 22 Issue 1, p42-46. 5p.

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Polymorphism of catechol- o-methyltransferase and uterine leiomyoma.

• Authors : Ates, Omer¹ ; Demirturk, Fazli²; Toprak, Muhammet²

Subjects: *UTERINE fibroids; *CATECHOL-O-methyltransferase; *POLYMERASE chain reactionTURKEY

• Source: Molecular & Cellular Biochemistry. Apr2013, Vol. 375 Issue 1/2, p179-183. 5p.

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Clinical symptoms in fibromyalgia are associated to catechol -O-methyltransferase ( COMT) gene Val158Met polymorphism.

• Authors : Inanir, Ahmet¹ (AUTHOR); Karakus, Nevin² (AUTHOR) ; Ates, Omer² (AUTHOR)

• Source: Xenobiotica. Oct2014, Vol. 44 Issue 10, p952-956. 5p.

تفاصيل العنوان

Catechol-O-methyltransferase (COMT) genetic polymorphism in a Turkish population.

• Authors : Kocabaş NA; Department of Toxicology, Faculty of Pharmacy, Gazi University, Hipodrom-Ankara, Turkey. ; Karakaya AE

Subjects: Polymorphism, Genetic*; Catechol O-Methyltransferase/Catechol O-Methyltransferase/Catechol O-Methyltransferase/*genetics; Adult

• Source: Archives of toxicology [Arch Toxicol] 2001 Sep; Vol. 75 (7), pp. 407-9.Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0417615 Publication Model: Print Cited Medium: Print ISSN: 0340-5761 (Print)

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