Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2

بواسطة Manit Nuinoon, Orapan Thipthara, Suthat Fucharoen
منشور في 2020

Studies of the CETP TaqIB and ApoE Polymorphisms in Southern Thai Subjects with the Metabolic Syndrome

بواسطة Nutjaree Jeenduang, Sureerut Porntadavity, Manit Nuinoon, Dararat Horpet, Nongyao Thepkwan, Pattamawadee Thaworn, Suporn Theanmontri
منشور في 2018

Detection of a known mutation M412T in the LDL receptor in a Chinese Thai FH family

بواسطة Klai Upsorn S. Pongrapeeporn, Manit Nuinoon, Pikun Thepsuriyanont, Bantita Kasemsuk, Patthamawadee Charoensuk, Ruechakorn Chantawee, Uchanee Wongmanee, Wilairat Nuchpramool
منشور في 2018

Promoter polymorphism of TNF-α (Rs1800629) is associated with ischemic stroke susceptibility in a southern Thai population

بواسطة Kornyok Kamdee, Nitirat Panadsako, Onchuma Mueangson, Manit Nuinoon, Penchom Janwan, Wasinee Poonsawat, Pongphan Pongpanitanont, Nakarin Kitkumthorn, Jirapan Thongsroy, Warangkana Chunglok
منشور في 2022

Genetic predictions of life expectancy in southern Thai patients with β⁰-thalassemia/Hb E

بواسطة Manit Nuinoon, Patchara Rattanaporn, Thongchai Benjchareonwong, Anuchit Choowet, Komsai Suwanno, Ngamta Saekoo, Krongjit Lekpetch, Orapan Thipthara, Saovaros Svasti, Suthat Fucharoen
منشور في 2022

Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure

بواسطة Pongsakorn Wangkumhang, Philip James Shaw, Kridsadakorn Chaichoompu, Chumpol Ngamphiw, Anunchai Assawamakin, Manit Nuinoon, Orapan Sripichai, Saovaros Svasti, Suthat Fucharoen, Verayuth Praphanphoj, Sissades Tongsima
منشور في 2018

Validation of the immunochromatographic strip for α-thalassemia screening: A multicenter study

بواسطة Pranee Winichagoon, Pornnapa Kumpan, Paula Holmes, Jill Finlayson, Christopher Newbound, Arnold Kabral, Benjamin Li, Manit Nuinoon, Terry Fawcett, Chatchai Tayapiwatana, Watchara Kasinrerk, Suthat Fucharoen
منشور في 2018

A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin e

بواسطة Manit Nuinoon, Wattanan Makarasara, Taisei Mushiroda, Iswari Setianingsih, Pustika Amalia Wahidiyat, Orapan Sripichai, Natsuhiko Kumasaka, Atsushi Takahashi, Saovaros Svasti, Thongperm Munkongdee, Surakameth Mahasirimongkol, Chayanon Peerapittayamongkol, Vip Viprakasit, Naoyuki Kamatani, Pranee Winichagoon, Michiaki Kubo, Yusuke Nakamura, Suthat Fucharoen
منشور في 2018