Zobrazeno 1 - 4
of 4
pro vyhledávání: '"George S Razmakhaev"'
Autor:
Anna V. Kudryavtseva, Dmitry V. Kalinin, Vladislav S. Pavlov, Maria V. Savvateeva, Maria S. Fedorova, Elena A. Pudova, Anastasiya A. Kobelyatskaya, Alexander L. Golovyuk, Zulfiya G. Guvatova, George S. Razmakhaev, Tatiana B. Demidova, Sergey A. Simanovsky, Elena N. Slavnova, Andrey А. Poloznikov, Andrey P. Polyakov, Nataliya V. Melnikova, Alexey A. Dmitriev, George S. Krasnov, Anastasiya V. Snezhkina
Publikováno v:
BMC Medical Genomics, Vol 13, Iss S8, Pp 1-11 (2020)
Abstract Background Vagal paragangliomas (VPGLs) belong to a group of rare head and neck neuroendocrine tumors. VPGLs arise from the vagus nerve and are less common than carotid paragangliomas. Both diagnostics and therapy of the tumors raise signifi
Externí odkaz:
https://doaj.org/article/d3d667cb88dc4d0782b8c0c21e300aac
Autor:
Anastasiya V. Snezhkina, Maria S. Fedorova, Vladislav S. Pavlov, Dmitry V. Kalinin, Alexander L. Golovyuk, Elena A. Pudova, Zulfiya G. Guvatova, Nataliya V. Melnikova, Alexey A. Dmitriev, George S. Razmakhaev, Andrey A. Poloznikov, Galina S. Alekseeva, Andrey D. Kaprin, George S. Krasnov, Anna V. Kudryavtseva
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Head and neck paragangliomas (HNPGLs) are rare neuroendocrine tumors that have a high degree of heritability and are predominantly associated with mutations in ten genes, such as SDHx, SDHAF2, VHL, RET, NF1, TMEM127, MAX, FH, MEN2, and SLC25A11. Eluc
Externí odkaz:
https://doaj.org/article/0984d7b56b80408e99976452d1ef8d8b
Autor:
Elena A. Pudova, George S. Krasnov, Zulfiya G Guvatova, Maria S. Fedorova, Anastasiya V. Snezhkina, Vladislav S Pavlov, Alexander L. Golovyuk, Anna V. Kudryavtseva, Alexey A. Dmitriev, Andrey Kaprin, Andrey A. Poloznikov, Galina S Alekseeva, George S Razmakhaev, Dmitry V. Kalinin, Nataliya V. Melnikova
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Frontiers in Genetics
Frontiers in Genetics
Head and neck paragangliomas (HNPGLs) are rare neuroendocrine tumors that have a high degree of heritability and are predominantly associated with mutations in ten genes, such as SDHx, SDHAF2, VHL, RET, NF1, TMEM127, MAX, FH, MEN2, and SLC25A11. Eluc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bcae8806191a9da58de558a8920baed
https://www.frontiersin.org/articles/10.3389/fgene.2020.614908/full
https://www.frontiersin.org/articles/10.3389/fgene.2020.614908/full
Autor:
Alexander L. Golovyuk, Andrey P. Polyakov, Elena N. Slavnova, Maria V Savvateeva, Anna V. Kudryavtseva, Vladislav S Pavlov, George S Razmakhaev, Sergey A. Simanovsky, Andrey А Poloznikov, Alexey A. Dmitriev, Elena A. Pudova, George S. Krasnov, Nataliya V. Melnikova, Anastasiya A. Kobelyatskaya, Maria S. Fedorova, Dmitry V. Kalinin, Zulfiya G Guvatova, Anastasiya V. Snezhkina, T. B. Demidova
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 13, Iss S8, Pp 1-11 (2020)
BMC Medical Genomics, Vol 13, Iss S8, Pp 1-11 (2020)
Background Vagal paragangliomas (VPGLs) belong to a group of rare head and neck neuroendocrine tumors. VPGLs arise from the vagus nerve and are less common than carotid paragangliomas. Both diagnostics and therapy of the tumors raise significant chal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42b991ecc3da0344804f4b43789b6ad3
http://europepmc.org/articles/PMC7500026
http://europepmc.org/articles/PMC7500026