İnsan Hastalıklarında Epigenetiğin Rolüne Klinik Bakış
Öz
Anahtar Kelimeler
Kaynakça
- Waddington CH. The epigenotype.1942. Int J Epidemiol. 2012;41(1):10-3.
- Kernohan KD, Cigana Schenkel L, Huang L, et al. Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy. Clin Epigenetics. 2016;5(8):91.
- Hansen RS, Wijmenga C, Luo P, et al. The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome. Proc Natl Acad Sci USA. 1999;96(25):14412-7.
- Ley TJ, Ding L, Walter MJ, et al. DNMT3A mutations in acute myeloid leukemia. N. Engl. J. Med. 2010;363:2424–2433.
- Yamashita Y, Yuan J, Suetake I, et al. Array-based genomic resequencing of human leukemia. Oncogene. 2010;29:3723–3731.
- El-Maarri O, Kareta MS, Mikeska T, et al. A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation. Hum Mol Genet. 2009;18(10):1755-68.
- Kosmider O, Gelsi-Boyer V, Cheok M, et al. TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDSs). Blood. 2009;114:3285–291.
- Grossmann V, Kohlmann A, Eder C, et al. Molecular profiling of chronic myelomonocytic leukemia reveals diverse mutations in >80% of patients with TET2 and EZH2 being of high prognostic relevance. Leukemia. 2011;25:877–9.
Ayrıntılar
Birincil Dil
Türkçe
Konular
Klinik Tıp Bilimleri
Bölüm
Derleme
Yazarlar
Emre Özgür
0000-0002-4995-4759
Türkiye
Hülya Tığlı
*
0000-0001-5997-0122
Türkiye
Hatice Tığlı
0000-0001-9713-4926
Türkiye
Yayımlanma Tarihi
17 Nisan 2020
Gönderilme Tarihi
6 Ocak 2020
Kabul Tarihi
30 Ocak 2020
Yayımlandığı Sayı
Yıl 2020 Sayı: 10
Cited By
Majör Depresif Bozuklukta Gen-Çevre Etkileşimi
Humanistic Perspective
https://doi.org/10.47793/hp.1350943