Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and PDYN[original query] |
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| Candidate genes for temporal lobe epilepsy: a replication study. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2008 Dec 29 (6): 397-403. Salzmann Annick, Perroud Nader, Crespel Arielle, Lambercy Carmen, Malafosse Ala |
| Analysis of the prodynorphin promoter polymorphism in atopic dermatitis and disease-related pruritus. Clinical and experimental dermatology 2009 Aug 34 (6): 728-30. Greisenegger E K, Zimprich A, Zimprich F, Stingl G, Kopp |
| Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement. American journal of human genetics 2011 Jul 89 (1): 121-30. Kobayashi Hatasu, Abe Koji, Matsuura Tohru, Ikeda Yoshio, Hitomi Toshiaki, Akechi Yuji, Habu Toshiyuki, Liu Wanyang, Okuda Hiroko, Koizumi Ak |
| Genetic association analyses and meta-analysis of Dynorphin-Kappa Opioid system potential functional variants with heroin dependence. Neuroscience letters 2018 Aug 685 75-82. Yuanyuan Ji, Rui Su, Hua Tang, Jingjing Cui, Cuola Deji, Yuhui Shi, Shuguang W |
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