Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Rustam Mustafin"'
Autor:
Rustam Mustafin
Publikováno v:
Cancer Urology. 18:99-107
The review article analyzes the data accumulated in the literature on the association of Wilms’ tumor with chromosomal syndromes and searches for possible causes of this phenomenon. In 10 % of all cases, nephroblastoma is represented by a hereditar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1896e8a70c9cb7804d6d33be8a913888
https://doi.org/10.17650/1726-9776-2022-18-4-99-107
https://doi.org/10.17650/1726-9776-2022-18-4-99-107
Autor:
Rustam Mustafin
Publikováno v:
Kazan medical journal. 103:986-995
One of the mechanisms for the development of autoimmune diseases is changes in epigenetic regulation, the root causes of which have not yet been established. At the same time, data on the role of transposons as sources of long noncoding ribonucleic a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c80aecfe73ea9bde8f3a178d347d845
https://doi.org/10.17816/kmj104291
https://doi.org/10.17816/kmj104291
Autor:
Rustam Mustafin
Publikováno v:
MD-Onco. 2:59-64
Frequency of atherosclerosis significantly increases with age, same as malignant tumor morbidity. Concurrent pathology (including in the cardiovascular system) affects selection of antitumor treatment limiting use of cardiotoxic (though highly effect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26c33e5e3c860ac0c9b2d770af42eee4
https://doi.org/10.17650/2782-3202-2022-2-3-59-64
https://doi.org/10.17650/2782-3202-2022-2-3-59-64
Autor:
Rustam Mustafin
Publikováno v:
Advances in Molecular Oncology. 9:15-23
Neurofibromatosis type 1 is caused by a germline mutation in the NF1 gene encoding the tumor suppressor neurofibromin. Deficiency of this protein causes hyperactivation of Ras proto-oncogenes. This leads to the development of tumors. Ras proteins und
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40309c8f51ee6a48f3f5d139f955907e
https://doi.org/10.17650/2313-805x-2022-9-3-15-23
https://doi.org/10.17650/2313-805x-2022-9-3-15-23
Autor:
Rustam Mustafin
Publikováno v:
Siberian journal of oncology. 21:98-109
Purpose of the study: Analysis of available data on geno-phenotypic correlations and atypical forms of neurofibromatosis type 1. Material and methods. We searched for relevant sources in the Scopus, Web of Science, PubMed systems, including publicati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::607df2aa1b2f812f8c250b833313ef09
https://doi.org/10.21294/1814-4861-2022-21-4-98-109
https://doi.org/10.21294/1814-4861-2022-21-4-98-109
Autor:
Rustam Mustafin
Publikováno v:
Russian Journal of Pediatric Hematology and Oncology. 9:54-59
Neurofibromatosis type 1 (NF1) is a hereditary tumor syndrome caused by a mutation in tumor suppressor gene NF1. The disease occurs with a frequency of 1:3000 of the population. Typical manifestations of NF1 are multiple cutaneous, subcutaneous and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecd382b70e35e55e8e9bfe6f55a911ec
https://doi.org/10.21682/2311-1267-2022-9-2-54-59
https://doi.org/10.21682/2311-1267-2022-9-2-54-59
Autor:
Rustam Mustafin, Elza Khusnutdinova
Publikováno v:
Morphology. 159:37-46
Recently, a lot of data has been gathered which demonstrates neurogenesis in the brain of adult humans. In genetics, findings have been obtained that not only prove, but also elucidate the molecular mechanisms of neurogenesis. In some publications, h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27c35b53b9840be952e7fe29aa4cec5d
https://doi.org/10.17816/1026-3543-2021-159-2-37-46
https://doi.org/10.17816/1026-3543-2021-159-2-37-46
Autor:
Khusnutdinova, Anastasiya Kazantseva, Yuliya Davydova, Renata Enikeeva, Rustam Mustafin, Sergey Malykh, Marina Lobaskova, Alexander Kanapin, Inga Prokopenko, Elza
Publikováno v:
Genes; Volume 14; Issue 7; Pages: 1355
The risk of depression could be evaluated through its multifactorial nature using the polygenic score (PGS) approach. Assuming a “clinical continuum” hypothesis of mental diseases, a preliminary assessment of individuals with elevated risk for de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::7d695d7d4eb35b66e49752cbb019f2c8
Autor:
Rustam Mustafin
Publikováno v:
Oncohematology. 17:108-113
Antitumor drug treatment of hemoblastoses always takes into account the patient comorbidity. Due to the frequent cardiovascular pathology and atherosclerosis, patients have to take statins along with antitumor treatment. Experimental studies have sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d13e918f245ef9b28eef93194fea1cff
https://doi.org/10.17650/1818-8346-2022-17-3-108-113
https://doi.org/10.17650/1818-8346-2022-17-3-108-113
Autor:
Rustam Mustafin
Publikováno v:
Journal of Modern Oncology. 24:209-215
Neurofibromatosis type 1 (NF1) is an autosomal dominant hereditary tumor syndrome with a prevalence of 1:3000 in human population. About 50% of NF1 cases are sporadic due to newly emerging germline mutations in NF1 gene. Protein product of NF1 is a n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0bc09a5f09b10c57cf6c37360816ba6
https://doi.org/10.26442/18151434.2022.2.201431
https://doi.org/10.26442/18151434.2022.2.201431