Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: GLRA1[original query] |
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A mutation (V260M) in the middle of the M2 pore-lining domain of the glycine receptor causes hereditary hyperekplexia. European journal of human genetics : EJHG 2002 1 9 (11): 873-6. del Giudice E M, Coppola G, Bellini G, Cirillo G, Scuccimarra G, Pascotto |
Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay. Brain : a journal of neurology 2013 Oct 136 (Pt 10): 3085-95. Thomas Rhys H, Chung Seo-Kyung, Wood Sian E, Cushion Thomas D, Drew Cheney J G, Hammond Carrie L, Vanbellinghen Jean-Francois, Mullins Jonathan G L, Rees Mark |
Stress-related genes and heroin addiction: a role for a functional FKBP5 haplotype. Psychoneuroendocrinology 2014 Jul 45 67-76. Levran O, Peles E, Randesi M, Li Y, Rotrosen J, Ott J, Adelson M, Kreek M |
Dimensional Traits of Schizotypy Associated With Glycine Receptor GLRA1 Polymorphism: An Exploratory Candidate-Gene Association Study. Journal of personality disorders 2017 Jul 1-12. Vora Anvi K, Fisher Amanda M, New Antonia S, Hazlett Erin A, McNamara Margaret, Yuan Qiaoping, Zhou Zhifeng, Hodgkinson Colin, Goldman David, Siever Larry J, Roussos Panos, Perez-Rodriguez M Merced |
Anxiety and Startle Phenotypes in Glrb Spastic and Glra1 Spasmodic Mouse Mutants. Frontiers in molecular neuroscience 2020 13 152. Schaefer Natascha, Signoret-Genest Jérémy, von Collenberg Cora R, Wachter Britta, Deckert Jürgen, Tovote Philip, Blum Robert, Villmann Carm |
Sex and Menopause Modify the Effect of Single Nucleotide Polymorphism Genotypes on Fibrosis in NAFLD. Hepatology communications 2021 4 5 (4): 598-607. Wegermann Kara, Garrett Melanie E, Zheng Jiayin, Coviello Andrea, Moylan Cynthia A, Abdelmalek Manal F, Chow Shein-Chung, Guy Cynthia D, Diehl Anna Mae, Ashley-Koch Allison, Suzuki Aya |
CYP2A6 and GABRA2 Gene Polymorphisms are Associated With Dexmedetomidine Drug Response. Frontiers in pharmacology 2022 13 943200. Fang Chao, Ouyang Wen, Zeng Youjie, Pei Qi, Xia Yuhao, Luo Siwan, Chen Mingh |
Hereditary Hyperekplexia in Saudi Arabia. Pediatric neurology 2022 7 134 78-82. Aldhilan Amal, Alhakeem Afnan, Al Hajjaj Sumayah, Abukhalid Musaad, Aldhalaan Hisham, Salah Ehab, Saeed Muhammed, Tabassum Sadia, El Khashab Heba Y, Aljabri Mohammed, Ali El-Sayed, Alwadei Ali, Hundallah Khalid, Alghamdi Abdulaziz, Hakami Wejdan, AlShafi Shatha, Alkuraya Fowzan S, Alanazy Naif, Seidahmed Mohammed Zain, Alfadhel Majid, Tabarki Brah |
Dual role of dysfunctional Asc-1 transporter in distinct human pathologies - human startle disease and developmental delay. eNeuro 2023 10 . Paul Drehmann, Sinem Milanos, Natascha Schaefer, Vikram Kasaragod, Sarah Herterich, Ulrike Holzbach-Eberle, Robert J Harvey, Carmen Villma |
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- Page last updated:Apr 22, 2024
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