Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: MPDZ[original query] |
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Sequence variations of the human MPDZ gene and association with alcoholism in subjects with European ancestry. Alcoholism, clinical and experimental research 2009 Apr 33 (4): 712-21. Karpyak Victor M, Kim Jeong-Hyun, Biernacka Joanna M, Wieben Eric D, Mrazek David A, Black John L, Choi Doo-S |
Genetic variability in the NMDA-dependent AMPA trafficking cascade is associated with alcohol dependence. Addiction biology 2012 Jul 17 (4): 798-806. Karpyak Victor M, Geske Jennifer R, Colby Colin L, Mrazek David A, Biernacka Joanna |
Genetic variants associated with development of TMD and its intermediate phenotypes: the genetic architecture of TMD in the OPPERA prospective cohort study. The journal of pain : official journal of the American Pain Society 2013 Dec 14 (12 Suppl): 12 Suppl. Smith SB, Mir E, Bair E, Slade GD, Dubner R, Fillingim RB, Greenspan JD, Ohrbach R, Knott C, Weir B, Maixner W, Diatchenko L |
Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian population. Investigative ophthalmology & visual science 2013 Nov . Sahebjada S, Schache M, Richardson AJ, Macgregor S, Snibson GR, Daniell M, Baird PN |
Synaptic Plasticity and Signal Transduction Gene Polymorphisms and Vulnerability to Drug Addictions in Populations of European or African Ancestry. CNS neuroscience & therapeutics 2015 Sep . Levran Orna, Peles Einat, Randesi Matthew, Correa da Rosa Joel, Ott Jurg, Rotrosen John, Adelson Miriam, Kreek Mary Jean |
Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population. Journal of negative results in biomedicine 2015 14 10. Abu-Amero Khaled K, Helwa Inas, Al-Muammar Abdulrahman, Strickland Shelby, Hauser Michael A, Allingham R Rand, Liu Yut |
Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population. Ophthalmic genetics 2015 Jun 36 (2): 132-6. Hao Xiao-Dan, Chen Peng, Chen Zhao-Li, Li Su-Xia, Wang |
Genetic Characteristics of Polycythemia Vera and Essential Thrombocythemia in Korean Patients. Journal of clinical laboratory analysis 2016 May . Yoo Eun-Hyung, Park Kyung-Jin, Won Hong-Hee, Park Jun-Hee, Park Jong-Ho, Lee Seung-Tae, Kim Hee-Jin, Bang Soo-Mee, Chi Hyun-Sook, Jung Chul Won, Kim Sun-Hee, Yun Hongseok, Sun Choong-Hyun, Park Inho, Lee Seungmook, Lee Clarence, Merriman Barry, Luo Raymond, Tan Eileen Hwee Hong, Park Keun-Joon, Yoo Na-Kyung, Kang Jason J, Kim Jong-W |
Replication of SNP associations with keratoconus in a Czech cohort. PloS one 2017 12 (2): e0172365. Liskova Petra, Dudakova Lubica, Krepelova Anna, Klema Jiri, Hysi Pirro |
A genome-wide significant association on chromosome 2 for footrot resistance/susceptibility in Swiss White Alpine sheep. Animal genetics 2017 10 48 (6): 712-715. Niggeler A, Tetens J, Stäuble A, Steiner A, Drögemüller |
Analysis of multiple genetic loci reveals MPDZ-NF1B rs1324183 as a putative genetic marker for keratoconus. The British journal of ophthalmology 2018 Jul . Wang Yu Meng, Ma Li, Lu Shi Yao, Chan Tommy Chung Yan, Yam Jason C S, Tang Shu Min, Kam Ka Wai, Tam Pancy O S, Tham Clement C, Young Alvin L, Jhanji Vishal, Pang Chi Pui, Chen Li J |
Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent. PloS one 2018 13 (6): e0199178. Lucas Sionne E M, Zhou Tiger, Blackburn Nicholas B, Mills Richard A, Ellis Jonathan, Leo Paul, Souzeau Emmanuelle, Ridge Bronwyn, Charlesworth Jac C, Lindsay Richard, Craig Jamie E, Burdon Kathryn |
Observation of nine previously reported and 10 non-reported SLC4A11 mutations among 20 Iranian CHED probands and identification of an MPDZ mutation as possible cause of CHED and FECD in one family. The British journal of ophthalmology 2019 8 104 (11): 1621-1628. Moazzeni Hamidreza, Javadi Mohammad Ali, Asgari Danial, Khani Marzieh, Emami Mohammad, Moghadam Abolfazl, Panahi-Bazaz Mahmoud-Reza, Hosseini Tehrani Mehdi, Karimian Farid, Hosseini Bagher, Nekuie Moghadam Tayebeh, Hassanpour Hossein, Akbari Mohammad Taghi, Elahi Ela |
Rare single nucleotide variants in COL5A1 promoter do not play a major role in keratoconus susceptibility associated with rs1536482. BMC ophthalmology 2021 Oct 21 (1): 357. Skorodumova Liubov O, Belodedova Alexandra V, Sharova Elena I, Zakharova Elena S, Iulmetova Liliia N, Bikbov Mukharram M, Usubov Emin L, Antonova Olga P, Selezneva Oksana V, Levchenko Anastasia, Fedorenko Olga Yu, Ivanova Svetlana A, Gainetdinov Raul R, Malyugin Boris |
Genomic analysis of paired IDHwt glioblastomas reveals recurrent alterations of MPDZ at relapse after radiotherapy and chemotherapy. Journal of the neurological sciences 2022 3 436 120207. Chanez Brice, Appay Romain, Guille Arnaud, Lagarde Arnaud, Colin Carole, Adelaide José, Denicolai Emilie, Jiguet-Jiglaire Carine, Bequet Céline, Graillon Thomas, Boissonneau Sébastien, Nanni-Metellus Isabelle, Dufour Henry, Figarella-Branger Dominique, Chinot Olivier, Tabouret Emeli |
Evaluating the association between MPDZ-NF1B rs1324183 and keratoconus in an independent northwestern Chinese population. BMC ophthalmology 2022 3 22 (1): 129. Yuan Shiqin, Li Dong, Ma Meijiao, Zhou Lingjie, Ma Zhen, Shi Baoyu, Zhang Shuang, Li Huiping, Sheng Xunlun, Liu Junx |
Novel Mutations Identified in the Chinese Han Population with Keratoconus by Next-Generation Sequencing. Journal of ophthalmology 2022 2 2022 9991910. Chen Binbin, Yu Xiaoning, Zhang Xin, Yang Hao, Cui Yilei, Shentu Xingch |
MPDZ variants associated with epilepsies and/or febrile seizures and the individualized genotype-phenotype correlation. Genes & diseases 2024 1 11 (3): 101032. Junxia Luo, Yun Li, Yong Lv, Xin Li, Bing Qin, Chuanfang Cheng, Xiaorong Liu, Weiping Liao, Jie Wang, Zaifen G |
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- Page last updated:Apr 22, 2024
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