Whole-Exome Sequencing in Koreans Identifies PAX4 R192H Variant as Susceptibility Locus for Type 2 Diabetes

被引：0
|
作者：
Kwak, Soo Heon
Lee, Seungbok
Kim, Hyun-Jin
Ahn, Chang Ho
Kim, Min Kyeong
Roh, Eun
Ku, Eu Jeong
Jung, Kyongyeun
Lee, Dong Hwa
Koo, Bokyung
Jung, Hye Seung
Moon, Min Kyong
Cho, Young Min
Lim, Soo
Kim, Kyunga
Kim, Jong-Il
Jang, Hak C.
Park, Kyong Soo
机构：
来源：
DIABETES | 2014年 / 63卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
1607-P
引用
收藏
页码：A419 / A419
页数：1
相关论文
共 50 条
  • [1] Association of PAX4 gene R192H polymorphisms in Chinese Han type 2 diabetes
    Leng, Fei
    Ling, Yan
    Aji, Gulibositan
    Li, Fang
    Chen, Jiachao
    Luo, Yu
    Zhang, Jing
    Hu, Ke
    Cheng, Ziyun
    Lu, Zhiqiang
    INTERNATIONAL JOURNAL OF DIABETES IN DEVELOPING COUNTRIES, 2018, 38 (04) : 397 - 402
  • [2] Association of PAX4 gene R192H polymorphisms in Chinese Han type 2 diabetes
    Fei Leng
    Yan Ling
    Gulibositan Aji
    Fang Li
    Jiachao Chen
    Yu Luo
    Jing Zhang
    Ke Hu
    Ziyun Cheng
    Zhiqiang Lu
    International Journal of Diabetes in Developing Countries, 2018, 38 : 397 - 402
  • [3] PAX4 R192H and P321H polymorphisms in type 2 diabetes and their functional defects
    Sujjitjoon, Jatuporn
    Kooptiwut, Suwattanee
    Chongjaroen, Nalinee
    Semprasert, Namoiy
    Hanchang, Wanthanee
    Chanprasert, Kanjana
    Tangjittipokin, Watip
    Yenchitsomanus, Pa-thai
    Plengvidhya, Nattachet
    JOURNAL OF HUMAN GENETICS, 2016, 61 (11) : 943 - 949
  • [4] PAX4 R192H is associated with younger onset of Type 2 diabetes in East Asians in Singapore
    Ang, Su Fen
    Tan, Clara S. H.
    Wang, Ling
    Dorajoo, Rajkumar
    Fong, Jessie C. W.
    Kon, Winston Y. C.
    Lian, Joyce X.
    Ang, Keven
    Rahim, Jamaliah Bte
    Jeevith, Babitha
    Lee, Simon B. M.
    Tang, Wern Ee
    Subramanium, Tavintharan
    Sum, Chee Fang
    Liu, Jian Jun
    Lim, Su Chi
    JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2019, 33 (01) : 53 - 58
  • [5] PAX4 R192H and P321H polymorphisms in type 2 diabetes and their functional defects
    Jatuporn Sujjitjoon
    Suwattanee Kooptiwut
    Nalinee Chongjaroen
    Namoiy Semprasert
    Wanthanee Hanchang
    Kanjana Chanprasert
    Watip Tangjittipokin
    Pa-thai Yenchitsomanus
    Nattachet Plengvidhya
    Journal of Human Genetics, 2016, 61 : 943 - 949
  • [6] Whole-Exome Sequencing in a Family with Highly Aggregated Type 2 Diabetes Identifies a Candidate Susceptibility Variant
    Tanaka, Daisuke
    Nagashima, Kazuaki
    Harashima, Shinichi
    Inagaki, Nobuya
    DIABETES, 2014, 63 : A417 - A417
  • [7] 一MODY家系PAX4基因R192H变异的分析
    冷斐
    古丽波斯坦
    陆志强
    中华内分泌代谢杂志, 2017, 33 (12) : 1068 - 1070
  • [8] Ethnic-Specific Type 2 Diabetes Risk Factor PAX4 R192H Is Associated with Attention-Specific Cognitive Impairment in Chinese with Type 2 Diabetes
    Ang, Su Fen
    Low, Serena
    Ng, Tze Pin
    Tan, Clara S. H.
    Ang, Keven
    Lim, Ziliang
    Tang, Wern Ee
    Subramaniam, Tavintharan
    Sum, Chee Fang
    Lim, Su Chi
    JOURNAL OF ALZHEIMERS DISEASE, 2022, 88 (01) : 241 - 249
  • [9] Defective PAX4 R192H transcriptional repressor activities associated with maturity onset diabetes of the young and early onset-age of type 2 diabetes
    Kooptiwut, Suwattanee
    Plengvidhya, Nattachet
    Chukijrungroat, Titikan
    Sujjitjoon, Jatuporn
    Semprasert, Namoiy
    Furuta, Hiroto
    Yenchitsomanus, Pa-thai
    JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2012, 26 (04) : 343 - 347
  • [10] Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene
    Bansal, Vikas
    Winkelmann, Bernhard R.
    Dietrich, Johannes W.
    Boehm, Bernhard O.
    FRONTIERS IN ENDOCRINOLOGY, 2024, 15
12345