Showing 341 - 360 results of 21,761 for search 'Genrō~', query time: 3.01s Refine Results
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    Genetic basis of depressive disorders by Yu. D. Davydova, R. F. Enikeeva, A. V. Kazantseva, R. N. Mustafin, A. R. Romanova, S. B. Malykh, E. K. Khusnutdinov

    Published 2019-07-01
    “…The present review is focused on the studies based on a candidate gene approach, genome-wide association studies (GWAS) and whole exome sequencing (WES), which previously demonstrated associations between gene polymorphisms and DDs. …”
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  6. 346

    Genetic Selection for Gaits in the Horse by Laura Patterson Rosa, Carissa Wickens, Samantha A. Brooks

    Published 2017-07-01
    “…This 4-page fact sheet discusses the connection between locomotion patterns and genetics, DMRT3 and locomotion in the horse, improvement of understanding of the gene function of DMRT3, and current as well as future applications. …”
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    From Genetics to Genomics of Epilepsy by Silvio Garofalo, Marisa Cornacchione, Alfonso Di Costanzo

    Published 2012-01-01
    “…Molecular Karyotype and Next-Generation Sequencing have the potential to identify causative genes or loci also in sporadic or non-familial epilepsy cases and may well represent the transition from a genetic to a genomic approach to epilepsy.…”
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  13. 353

    Structuring the genetic collection of sunflower by V. A. Gavrilova, I. N. Anisimova, N. V. Alpatieva, E. A. Porokhovinova

    Published 2025-01-01
    “…Background. The XRQ sunflower genome has been sequenced but not yet fully annotated, and not all candidate genes for most traits have been identified. …”
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    Genetic Selection for Gaits in the Horse by Laura Patterson Rosa, Carissa Wickens, Samantha A. Brooks

    Published 2017-07-01
    “…This 4-page fact sheet discusses the connection between locomotion patterns and genetics, DMRT3 and locomotion in the horse, improvement of understanding of the gene function of DMRT3, and current as well as future applications. …”
    Get full text
    Article
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    An Update on the Genetics of Usher Syndrome by José M. Millán, Elena Aller, Teresa Jaijo, Fiona Blanco-Kelly, Ascensión Gimenez-Pardo, Carmen Ayuso

    Published 2011-01-01
    “…It is clinically and genetically heterogeneous and is the most common cause underlying deafness and blindness of genetic origin. …”
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