Zobrazeno 1 - 9
of 9
pro vyhledávání: '"E. A. Rogaeva"'
Autor:
A. M. Saunders, E. R. Martin, S. M. Abou-Donia, Lindsay A. Farrer, Y. Song, E. A. Rogaeva, D. Blacker, Ac Bruni, PH St George-Hyslop, S. Sorbi, P. M. Conneally, F. Van Leuven, A D Roses, B. Roberge, J. J. Vance, Rudolph E. Tanzi, A. Orlacchio, M. A. Wilcox, G. W. Small, J. Grubber, J Haines, N. M. Laird, A. Supala, M. A. Pericak Vance, D. M. Hill, G. Yu, M. Nishimura, Y. Pei, L. Serneels, D. Schmechel, A. S. Crystal, W. K. Scott, A. Crane-Gatherum, T. Kawarai, Smita Premkumar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2cbb56070e0787ee05d99ebdc9014b2
http://hdl.handle.net/2108/90074
http://hdl.handle.net/2108/90074
Autor:
M G, Ramirez-Dueñas, E A, Rogaeva, C A, Leal, C, Lin, G A, Ramirez-Casillas, J A, Hernandez-Romo, P H, St George-Hyslop, J M, Cantu
Publikováno v:
Annales de genetique. 41(3)
A search for mutations in exons 6, 7, 9 and 12 of the PS1 gene in four Mexican families with Early-Onset (36-40 years) Alzheimer Disease yielded the discovery in one family of a T--C mismatch in exon 7 which correspond to nucleotide 760 of cDNA, lead
Autor:
Y. Takiyama, S. Igasrashi, E. A. Rogaeva, K. Endo, E. I. Rogaev, H. Tanaka, R. Sherrington, K. Sanpei, Y. Liang, M. Saito, T. Tsuda, H. Takano, M. Ikeda, C. Lin, H. Chi, J. L. Kennedy, A. E. Lang, J. R. Wherrett, M. Segawa, Y. Nomura, T. Yuasa, J. Weissenbach, M. Yoshida, M. Nishizawa, K. K. Kidd, S. Tsuji, P. H. St George-Hyslop
Publikováno v:
Human molecular genetics. 4(7)
The size of the (CAG)n repeat array in the 3' end of the MJD1 gene and the haplotype at a series of microsatellite markers surrounding the MJD1 gene were examined in a large cohort of Japanese and Caucasian subjects affected with Machado-Joseph disea
Publikováno v:
Genetika. 31(4)
We describe a simple method for the identification of pathologically expanded (CCG)n and (CTG)n three nucleotides repeat arrays in the human genome and for the recovery of flanking sequences. We were able to detect the presence of novel high-molecula
Autor:
E I, Rogaev, E A, Rogaeva, E K, Ginter, G I, Korovaĭtseva, L, Farrer, A B, Shlenskiĭ, A N, Prytkov, P, St George-Hyslop, V N, Mordovtsev
Publikováno v:
Genetika. 30(3)
Mapping of the genetic defect causing dominant palmoplantaris hyperkeratosis (PPHK) was continued based on the material of an extended Uzbek pedigree. No linkage between the PPHK gene and hypervariable DNA markers from 8p, 12p, 14q, and 22q were reve
Publikováno v:
Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952). 91(10)
Hybridoma technique was used to obtain a clone producing IgG antibodies. Paired helical neurofilaments isolated from the brain of patients suffering from Alzheimer's disease were used as an antigen during preparation of the clone. Antibodies recogniz
Publikováno v:
Voprosy meditsinskoi khimii. 33(4)
Blood sera from patients with arterial hypertension exhibited more distinct inhibitory effect on purified Na+,K+-ATPase as compared with blood sera of healthy persons. Moreover, the fraction of 12-15 kDa protein components was usually increased in bl
Autor:
A A, Boldyrev, E A, Rogaeva
Publikováno v:
Nauchnye doklady vysshei shkoly. Biologicheskie nauki. (12)
Molecular mechanisms of disturbances in the system responsible for ion transport taking place in the development of the initial hypertension in linear animals have been analysed in this review. On the basis of own and literary data the diagnostic sig
Autor:
E A, Rogaeva, A A, Boldyrev, O D, Lopina, A M, Rubtsov, N V, Perova, N N, Zhigareva, R G, Oganov
Publikováno v:
Biochemistry international. 18(6)
Using multivariate statistical analysis, an attempt has been made to select hypertensive and normotensive sub-groups of subjects on the basis of certain parameters of their blood serum, such as the inhibition of purified Na,K-ATPase by serum and the