Clinical significance of NCOA5 gene rs2903908 polymorphism in Behçet's disease.

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A novel tumor suppressor gene NCOA5 is correlated with progression in papillary thyroid carcinoma.

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Clinical significance of NCOA5 gene rs2903908 polymorphism in Behçet's disease.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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Clinical significance of NCOA5 gene rs2903908 polymorphism in Behçet's disease.

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Clinical significance of NCOA5 gene rs2903908 polymorphism in Behçet's disease.

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Clinical significance of NCOA5 gene rs2903908 polymorphism in Behçet's disease.

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Clinical significance of NCOA5 gene rs2903908 polymorphism in Behçet's disease.

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Ahmet Inanir

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Aydin Rustemoglu

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Duygu Ekinci

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Esra Erkol Inal

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Nevin Karakus

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Omer Ates

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Serbulent Yigit

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Ulker Gul

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P2860

NCOA5 haploinsufficiency results in glucose intolerance and subsequent hepatocellular carcinoma

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Differential recruitment of coregulators to the RORA promoter adds another layer of complexity to gene (dys) regulation by sex hormones in autism.

NCOA5, a molecular link between type 2 diabetes and liver cancer.

Analysis of candidate genes on chromosome 20q12-13.1 reveals evidence for BMI mediated association of PREX1 with type 2 diabetes in European Americans.

Study of association of CD40-CD154 gene polymorphisms with disease susceptibility and cardiovascular risk in Spanish rheumatoid arthritis patients.

Gene expression profiles in human autoimmune disease.

Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling Study

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609-617

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scholarly article

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10.17179/EXCLI2017-189

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2017-05-04T00:00:00Z

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28694762

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Behcet's disease

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5491927

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Clinical significance of NCOA5 gene rs2903908 polymorphism in Behçet's disease.

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P2860

P2860

Clinical significance of NCOA5 gene rs2903908 polymorphism in Behçet's disease.

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P1476

P2093

P2860

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P356

P478

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P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P698

P921

P932