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Public Health Genomics and Precision Health Knowledge Base (v10.0)
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Human Genome Epidemiology Literature Finder|Home|PHGKB
Human Genome Epidemiology Literature Finder
Last data update: Jan 25, 2025
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Diabetes Mellitus and PTX3[original query]
APO A2 -265T/C Polymorphism Is Associated with Increased Inflammatory Responses in Patients with Type 2 Diabetes Mellitus.
Diabetes & metabolism journal 2016 Jun 40 (3): 222-9.
Koohdani Fariba, Sadrzadeh-Yeganeh Haleh, Djalali Mahmoud, Eshraghian Mohammadreza, Zamani Elham, Sotoudeh Gity, Mansournia Mohammad Ali, Keramat Lal
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Interaction between CETP polymorphism and dietary insulin index and load in relation to cardiovascular risk factors in diabetic adults.
Scientific reports 2021 Aug 11 (1): 15906.
Abaj Faezeh, Rafiee Masoumeh, Koohdani Fari
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Interaction between Apo A-II -265T > C polymorphism and dietary total antioxidant capacity on some oxidative stress and inflammatory markers in patients with type 2 diabetes mellitus.
The British journal of nutrition 2021 Aug 1-41.
Jafari Azad Banafsheh, Yaseri Mehdi, Daneshzad Elnaz, Koohdani Fari
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Interaction between the dietary indices and PPAR-? Pro12Ala gene variants on cardiovascular risk factors in patients with type 2 diabetes mellitus.
International journal of clinical practice 2021 4 75 (8): e14307.
Abaj Faezeh, Sotoudeh Gity, Karimi Elmira, Rafiee Masoumeh, Koohdani Fari
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A personalised diet study: The interaction between ApoA2 -265T > C polymorphism and dietary inflammatory index on oxidative and inflammatory markers and lipid profile in patients with type 2 diabetes mellitus: A cross-sectional study.
International journal of clinical practice 2021 Mar e14178.
Karimi Elmira, Tondkar Pourya, Sotoudeh Gity, Qorbani Mostafa, Rafiee Masoumeh, Koohdani Fari
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Dietary acid load modifies the effects of ApoA2-265?T?>?C polymorphism on lipid profile and serum leptin and ghrelin levels among type 2 diabetic patients.
BMC endocrine disorders 2022 7 22 (1): 190.
Abaj Faezeh, Esmaeily Zahra, Naeini Zeinab, Rafiee Masoumeh, Koohdani Fari
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Page last reviewed:
Feb 1, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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