Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yuri K. Moliaka"'
Autor:
Evgeny I Rogaev, Yuri K Moliaka, Boris A Malyarchuk, Fyodor A Kondrashov, Miroslava V Derenko, Ilya Chumakov, Anastasia P Grigorenko
Publikováno v:
PLoS Biology, Vol 4, Iss 3, p e73 (2006)
Phylogenetic relationships between the extinct woolly mammoth (Mammuthus primigenius), and the Asian (Elephas maximus) and African savanna (Loxodonta africana) elephants remain unresolved. Here, we report the sequence of the complete mitochondrial ge
Externí odkaz:
https://doaj.org/article/0ca52670afaf4c6dbdc05c2aedaa7ae2
Autor:
Anastasiya V. Kazantseva, Zhiru Guo, Rena A. Zinchenko, Anna V. Abrukova, Alexander G. Kirillov, Andrey Goltsov, Evgeny I. Rogaev, E. K. Ginter, Yuri K. Moliaka, Anastasia P. Grigorenko, Stephen Lyle
Publikováno v:
Science. 314:982-985
The molecular mechanisms controlling human hair growth and scalp hair loss are poorly understood. By screening about 350,000 individuals in two populations from the Volga-Ural region of Russia, we identified a gene mutation in families who show an in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28a1927b64ada3c17eca96414a10a8d2
https://doi.org/10.1126/science.1133276
https://doi.org/10.1126/science.1133276
Publikováno v:
FEBS Letters. 557:185-192
Presenilins (PS1 and PS2) are supposed to be unusual aspartic proteases and components of the γ-secretase complex regulating cleavage of type I proteins. Multiple mutations in PS1 are a major cause of familial early-onset Alzheimer’s disease (AD).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db0a630b09a64ba47d39578d749819cb
https://doi.org/10.1016/s0014-5793(03)01489-3
https://doi.org/10.1016/s0014-5793(03)01489-3
Autor:
E. L. Rogaev, Lindsay A. Farrer, Nicolas G. Bazan, Michael Nicolaou, Walter J. Lukiw, Yuri K. Moliaka, N. Riazanskaia, Gennady Dvoryanchikov, G. I. Korovaitseva, Anastasia P. Grigorenko
Publikováno v:
Molecular Psychiatry. 7:891-898
We have analyzed the 5'-upstream promoter region of the presenilin 2 gene (PSEN2) for regulatory elements and examined Alzheimer disease (AD) patients and non-demented individuals for polymorphisms in the 5' upstream promoter region of the PSEN2 gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d44976d603e41b980ed33f73146b908e
https://doi.org/10.1038/sj.mp.4001101
https://doi.org/10.1038/sj.mp.4001101
Publikováno v:
Biochemistry (Moscow). 67:826-834
A significant proportion of early onset Alzheimer's disease (AD) is caused by mutations in human genes for amyloid precursor protein (APP), presenilins 1 and 2 (PSEN1,2). AD associated mutations in PSEN1,2 genes alter the γ-secretase cleavage activi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f886d8c51f000ce6f9618c23a68c932
https://doi.org/10.1023/a:1016365227942
https://doi.org/10.1023/a:1016365227942
Autor:
Nikolay P. Bochkov, Gieri Cathomas, Alla P. Chudina, Marina Cella, Luigi Terracciano, Jean-Marie Buerstedde, Tatiana N. Kolesnikova, Yuri K. Moliaka
Publikováno v:
Genes, Chromosomes and Cancer. 20:305-309
Hereditary nonpolyposis colon cancer (HNPCC) is an autosomal dominantly inherited cancer predisposition which is linked to heterozygous mutations in mismatch repair genes. HNPCC tumour cells, in which the remaining wild-type copy of the mismatch repa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7295f2edaa791292268aeba3b1027414
https://doi.org/10.1002/(sici)1098-2264(199711)20:3<305::aid-gcc12>3.0.co
https://doi.org/10.1002/(sici)1098-2264(199711)20:3<305::aid-gcc12>3.0.co
Autor:
Gulnaz Faskhutdinova, Ellen L. W. Kittler, Anastasia P. Grigorenko, Yuri K. Moliaka, Evgeny I. Rogaev
Publikováno v:
Science (New York, N.Y.). 326(5954)
The "royal disease," a blood disorder transmitted from Queen Victoria to European royal families, is a striking example of X-linked recessive inheritance. Although the disease is widely recognized to be a form of the blood clotting disorder hemophili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc62e3f66e9dfee960c5c1ece2e70a9c
https://pubmed.ncbi.nlm.nih.gov/19815722
https://pubmed.ncbi.nlm.nih.gov/19815722
Autor:
Gulnaz Faskhutdinova, Ellen L. W. Kittler, I. Morozova, Anastasia P. Grigorenko, Yuri K. Moliaka, Evgeny I. Rogaev
Publikováno v:
Forensic Science International: Genetics Supplement Series.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::240ca8f3de0f81b40b417d4fecb7703c
https://doi.org/10.1016/j.fsigss.2009.09.003
https://doi.org/10.1016/j.fsigss.2009.09.003
Autor:
Gulnaz Faskhutdinova, Irina Morozova, Curtis Hildebrandt, Andrey Goltsov, Evgeny I. Rogaev, Ellen L. W. Kittler, Arlene Lahti, Anastasia P. Grigorenko, Yuri K. Moliaka
Accurate unambiguous identification of ancient or historical specimens can potentially be achieved by DNA analysis. The controversy surrounding the fate of the last Russian Emperor, Nicholas II, and his family has persisted, in part, because the bodi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e42eafc59dad48bd428f862d900e3a4a
https://europepmc.org/articles/PMC2664067/
https://europepmc.org/articles/PMC2664067/
Autor:
Vera A. Nikishina, Olga V. Plotnikova, Yuri K. Moliaka, Anastasia P. Grigorenko, Egor M. Veselovsky, Evgeny I. Rogaev
Publikováno v:
Alzheimer's & Dementia. 3
not available. PL3-02 CHOLINESTERASES IN NEURODEGENERATION: HAVE WE MISSED SOMETHING? Roger Lane, Novartis Neuroscience Clinical Development and Medical Affairs, East Hanover, NJ, USA. Contact e-mail: roger.lane@novartis.com Background: In addition t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0775ea78ccfac8abd00fa267171a1702
https://doi.org/10.1016/j.jalz.2007.04.023
https://doi.org/10.1016/j.jalz.2007.04.023