Mosaic loss of the Y chromosome in human neurodegenerative and oncological diseases.

Autor: Kuznetsova IL; Vavilov Institute of General Genetics, Russian Academy of Sciences, Department of Genomics and Human Genetics, Moscow, Russia Sirius University of Science and Technology, Scientific Center for Genetics and Life Sciences, Sochi, Russia., Uralsky LI; Vavilov Institute of General Genetics, Russian Academy of Sciences, Department of Genomics and Human Genetics, Moscow, Russia Sirius University of Science and Technology, Scientific Center for Genetics and Life Sciences, Sochi, Russia., Tyazhelova TV; Vavilov Institute of General Genetics, Russian Academy of Sciences, Department of Genomics and Human Genetics, Moscow, Russia., Andreeva TV; Vavilov Institute of General Genetics, Russian Academy of Sciences, Department of Genomics and Human Genetics, Moscow, Russia Sirius University of Science and Technology, Scientific Center for Genetics and Life Sciences, Sochi, Russia Lomonosov Moscow State University, Center for Genetics and Genetic Technologies, Faculty of Biology, Moscow, Russia., Rogaev EI; Vavilov Institute of General Genetics, Russian Academy of Sciences, Department of Genomics and Human Genetics, Moscow, Russia Sirius University of Science and Technology, Scientific Center for Genetics and Life Sciences, Sochi, Russia Lomonosov Moscow State University, Center for Genetics and Genetic Technologies, Faculty of Biology, Moscow, Russia.

Publikováno v: Vavilovskii zhurnal genetiki i selektsii [Vavilovskii Zhurnal Genet Selektsii] 2023 Sep; Vol. 27 (5), pp. 502-511.

Identification of mutant gene for Black crystal coat and non-allelic gene interactions in Neogale vison.

Autor: Manakhov AD; Department of Genetics, Centre for Genetics and Life Science, Sirius University of Science and Technology, 354340, Sochi, Russia.; Laboratory of Evolutionary Genomics, Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, 119333, Moscow, Russia.; Centre for Genetics and Genetic Technologies, Faculty of Biology, Lomonosov Moscow State University, 119192, Moscow, Russia., Mintseva MY; Laboratory of Evolutionary Genomics, Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, 119333, Moscow, Russia., Uralsky LI; Department of Genetics, Centre for Genetics and Life Science, Sirius University of Science and Technology, 354340, Sochi, Russia.; Laboratory of Evolutionary Genomics, Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, 119333, Moscow, Russia., Andreeva TV; Laboratory of Evolutionary Genomics, Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, 119333, Moscow, Russia.; Centre for Genetics and Genetic Technologies, Faculty of Biology, Lomonosov Moscow State University, 119192, Moscow, Russia., Trapezov OV; Department of Animals and Human Genetics, Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 630090, Novosibirsk, Russia.; Novosibirsk State University, 630090, Novosibirsk, Russia., Rogaev EI; Department of Genetics, Centre for Genetics and Life Science, Sirius University of Science and Technology, 354340, Sochi, Russia. rogaev@vigg.ru.; Laboratory of Evolutionary Genomics, Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, 119333, Moscow, Russia. rogaev@vigg.ru.; Centre for Genetics and Genetic Technologies, Faculty of Biology, Lomonosov Moscow State University, 119192, Moscow, Russia. rogaev@vigg.ru.; Department of Psychiatry, UMass Chan Medical School, Worcester, MA, 01604, USA. rogaev@vigg.ru.

Publikováno v: Scientific reports [Sci Rep] 2022 Jun 21; Vol. 12 (1), pp. 10483. Date of Electronic Publication: 2022 Jun 21.

Genome analysis of American minks reveals link of mutations in Ras-related protein-38 gene to Moyle brown coat phenotype.

Autor: Manakhov AD; Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia, 119333.; Center for Genetics and Genetic Technologies, Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia, 119192.; Sirius University of Science and Technology, Sochi, Russia, 354340., Mintseva MY; Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia, 119333.; Center for Genetics and Genetic Technologies, Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia, 119192., Andreev IA; Center for Genetics and Genetic Technologies, Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia, 119192., Uralsky LI; Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia, 119333., Andreeva TV; Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia, 119333.; Center for Genetics and Genetic Technologies, Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia, 119192., Trapezov OV; Department of Animals and Human Genetics, Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia, 630090.; Novosibirsk State University, Novosibirsk, Russia, 630090., Rogaev EI; Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia, 119333. rogaev@vigg.ru.; Center for Genetics and Genetic Technologies, Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia, 119192. rogaev@vigg.ru.; Sirius University of Science and Technology, Sochi, Russia, 354340. rogaev@vigg.ru.; Department of Psychiatry, University of Massachusetts Medical School, Worcester, MA, 01604, USA. rogaev@vigg.ru.

Publikováno v: Scientific reports [Sci Rep] 2020 Sep 28; Vol. 10 (1), pp. 15876. Date of Electronic Publication: 2020 Sep 28.

Annotation of suprachromosomal families reveals uncommon types of alpha satellite organization in pericentromeric regions of hg38 human genome assembly.

Autor: Shepelev VA; Institute of Molecular Genetics, Russian Academy of Sciences, Kurchatov sq. 2, Moscow 123182, Russia ; Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow 119991, Russia ; Center for Brain Neurobiology and Neurogenetics, Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia., Uralsky LI; Institute of Molecular Genetics, Russian Academy of Sciences, Kurchatov sq. 2, Moscow 123182, Russia ; Center for Brain Neurobiology and Neurogenetics, Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia., Alexandrov AA; Institute of Molecular Genetics, Russian Academy of Sciences, Kurchatov sq. 2, Moscow 123182, Russia., Yurov YB; Research Center of Mental Health, Russian Academy of Medical Sciences, Zagorodnoe sh. 2, Moscow 113152, Russia., Rogaev EI; Department of Genomics and Human Genetics, Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow 119991, Russia ; Center for Brain Neurobiology and Neurogenetics, Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia ; Department of Psychiatry, Brudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, MA 01604, USA ; Faculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow 119234, Russia., Alexandrov IA; Research Center of Mental Health, Russian Academy of Medical Sciences, Zagorodnoe sh. 2, Moscow 113152, Russia.

Publikováno v: Genomics data [Genom Data] 2015 Sep 01; Vol. 5, pp. 139-146.