Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Alexander, Poliakov"'
Autor:
V.G. Pshennikova, Olga L. Posukh, Gabriel Minarik, Nikolay A. Barashkov, Elza Khusnutdinova, Ludevit Kadasi, Aisen V. Solovyev, Alexander Poliakov, Mait Metspalu, Alena Kushniarevich, M. R. Lalayants, Fedor M. Teryutin, E. A. Bliznetz, Marita S. Bady-Khoo, T. G. Markova, Ene Metspalu, Sardana A. Fedorova
Publikováno v:
Human Genetics. 141:697-707
Mutations in the GJB2 gene are known to be a major cause of autosomal recessive deafness 1A (OMIM 220290). The most common pathogenic variants of the GJB2 gene have a high ethno-geographic specificity in their distribution, being attributed to a foun
Autor:
Aisen V Solovyev, Alena Kushniarevich, Elena Bliznetz, Marita Bady-Khoo, Maria R Lalayants, Tatiana G Markova, Gabriel Minárik, L'udevít Kádasi, Ene Metspalu, Vera G Pshennikova, Fedor M Teryutin, Anatoly N Alekseev, Elza K Khusnutdinova, Alexander Poliakov, Mait Мetspalu, Olga L Posukh, Nikolay A Barashkov, Sardana A Fedorova
The mutations in the GJB2 gene are known to be a major cause of autosomal recessive deafness 1A (OMIM 220290). The most common pathogenic variants of the GJB2 gene have high ethno-geographic specificity in their distribution that being attributed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a1dcbfd6f9ec92417babfcf62bd10b3
https://doi.org/10.21203/rs.3.rs-670020/v1
https://doi.org/10.21203/rs.3.rs-670020/v1
Autor:
Aisen V, Solovyev, Alena, Kushniarevich, Elena, Bliznetz, Marita, Bady-Khoo, Maria R, Lalayants, Tatiana G, Markova, Gabriel, Minárik, L'udevít, Kádasi, Ene, Metspalu, Vera G, Pshennikova, Fedor M, Teryutin, Elza K, Khusnutdinova, Alexander, Poliakov, Mait, Metspalu, Olga L, Posukh, Nikolay A, Barashkov, Sardana A, Fedorova
Publikováno v:
Human genetics. 141(3-4)
Mutations in the GJB2 gene are known to be a major cause of autosomal recessive deafness 1A (OMIM 220290). The most common pathogenic variants of the GJB2 gene have a high ethno-geographic specificity in their distribution, being attributed to a foun
Autor:
Inna Dubchak, Sandhya Balasubramanian, Sheng Wang, Meydan Cem, Dinanath Sulakhe, Alexander Poliakov, Daniela Börnigen, Bingqing Xie, Andrew Taylor, Jianzhu Ma, Alex R Paciorkowski, Ghayda M Mirzaa, Paul Dave, Gady Agam, Jinbo Xu, Lihadh Al-Gazali, Christopher E Mason, M Elizabeth Ross, Natalia Maltsev, T Conrad Gilliam
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e114903 (2014)
An essential step in the discovery of molecular mechanisms contributing to disease phenotypes and efficient experimental planning is the development of weighted hypotheses that estimate the functional effects of sequence variants discovered by high-t
Externí odkaz:
https://doaj.org/article/7a98642da2014259af2beccf0a35c397
Autor:
Alexander Poliakov
Publikováno v:
Journal of Robotics and Mechanical Engineering Research. 1:17-27
In recent years, the increasing use acquires mechatronic devices to implement complex laws of motion of the executive bodies of the machinery. In this regard, there was a need for modification of the classical approaches to the mechanisms synthesis a
Autor:
Min Li, Miaolin Chen, Kevin Palis, Rod A. Wing, Dario Copetti, Jinyuan Lu, Hei Leung, Jeffrey Detras, Xianchang He, Zhiqiang Hu, Yanhong Li, Zhen Yue, Jayson Talag, Jiayang Li, John Robert Mendoza, Jiabao Xu, Locedie Mansueto, Wensheng Wang, Victor Jun Ulat, Tianqing Zheng, Ye Yin, Ma. Elizabeth B. Naredo, Kenneth L. McNally, Nickolai Alexandrov, Jauhar Ali, Alexander Poliakov, Fei Shen, Roven Rommel Fuentes, Xiaodong Fang, Rui Li, Xiuqin Zhao, Jue Ruan, Yongming Gao, Yue Zhao, Zhikang Li, Chaochun Wei, Dmytro Chebotarov, Jing Li, Jianlong Xu, Jia Ben, Hong Yu, Dave Kudrna, Millicent D. Sanciangco, Hongliang Zhang, Shuaishuai Tai, Xueqiang Wang, Yongchao Niu, Wushu Hu, Fan Zhang, Chunchao Wang, Binying Fu, Zhichao Wu, Xinyuan Zhang, Inna Dubchak, Jianxin Shi, Qiang Gao, Xiao Cui, Frances Nikki Borja, Zhaotong Dong, Jianwei Zhang, Chen Sun, Ruaraidh Sackville Hamilton, Miao Wang, Jinjie Li, Jean-Christophe Glaszmann, Seunghee Lee, Dabing Zhang, Gengyun Zhang, Zichao Li, Ramil Mauleon, Yongli Zhou
Publikováno v:
Nature
Here we analyse genetic variation, population structure and diversity among 3,010 diverse Asian cultivated rice (Oryza sativa L.) genomes from the 3,000 Rice Genomes Project. Our results are consistent with the five major groups previously recognized
Publikováno v:
Proceedings of the 26th International DAAAM Symposium 2016
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc5989974ccd3a889648738085cb88cb
https://doi.org/10.2507/26th.daaam.proceedings.047
https://doi.org/10.2507/26th.daaam.proceedings.047
Publikováno v:
Gene. 481:1-6
It was proposed that if some mRNA characteristics resulted in a low efficiency of termination signal, an additional closely located stop codon (tandem stop codons) could be used to prevent the harmful readthrough. However, the role of tandem terminat
Publikováno v:
Genome Research. 19:682-689
Multiple sequence alignments have become one of the most commonly used resources in genomics research. Most algorithms for multiple alignment of whole genomes rely either on a reference genome, against which all of the other sequences are laid out, o
Publikováno v:
Nucleic Acids Research
Brudno, Michael; Poliakov, Alexander; Minovitsky, Simon; Ratnere, Igor; & Dubchak, Inna. (2008). Multiple Whole Genome Alignments and Novel Biomedical Applications at the VISTA Portal. Lawrence Berkeley National Laboratory. Lawrence Berkeley National Laboratory: Lawrence Berkeley National Laboratory. Retrieved from: http://www.escholarship.org/uc/item/5326x08w
Brudno, Michael; Poliakov, Alexander; Minovitsky, Simon; Ratnere, Igor; & Dubchak, Inna. (2008). Multiple Whole Genome Alignments and Novel Biomedical Applications at the VISTA Portal. Lawrence Berkeley National Laboratory. Lawrence Berkeley National Laboratory: Lawrence Berkeley National Laboratory. Retrieved from: http://www.escholarship.org/uc/item/5326x08w
The VISTA portal for comparative genomics is designed to give biomedical scientists a unified set of tools to lead them from the raw DNA sequences through the alignment and annotation to the visualization of the results. The VISTA portal also hosts a