Zobrazeno 1 - 10 of 206 pro vyhledávání: '"Anagnou, NP"'
1
Origin and spread of mitochondrial DNA haplogroup U7
Autor: Sahakyan, H, Kashani, BH, Tamang, R, Kushniarevich, A, Francis, A, Costa, MD, Pathak, AK, Khachatryan, Z, Sharma, I, van Oven, M, Parik, J, Hovhannisyan, H, Metspalu, E, Pennarun, E, Karmin, M, Tamm, E, Tambets, K, Bahmanimehr, A, Reisberg, T, Reidla, M, Achilli, A, Olivieri, A, Gandini, F, Perego, UA, Al-Zahery, N, Houshmand, M, Sanati, MH, Soares, P, Rai, E, Šarac, J, Šarić, T, Sharma, V, Pereira, L, Fernandes, V, Černý, V, Farjadian, S, Singh, DP, Azakli, H, Üstek, D, Ekomasova, NT, Kutuev, I, Litvinov, S, Bermisheva, M, Khusnutdinova, EK, Rai, N, Singh, M, Singh, VK, Reddy, AG, Tolk, HV, Cvjetan, S, Lauc, LB, Rudan, P, Michalodimitrakis, EN, Anagnou, NP, Pappa, KI, Golubenko, MV, Orekhov, V, Borinskaya, SA, Kaldma, K, Schauer, MA, Simionescu, M, Gusar, V, Grechanina, E, Govindaraj, P, Voevoda, M, Damba, L, Sharma, S, Singh, L, Semino, O, Behar, DM, Yepiskoposyan, L, Richards, MB, Metspalu, M, Kivisild, T, Thangaraj, K, Endicott, P, Chaubey, G, Torroni, A, Villems, R
Publikováno v: Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Human mitochondrial DNA haplogroup U is among the initial maternal founders in Southwest Asia and Europe and one that best indicates matrilineal genetic continuity between late Pleistocene huntergatherer groups and present-day populations of Europe.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::295d1d60df4f28f9a1f525eaf5788b88
https://hdl.handle.net/10216/109249
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2
Gestational diabetes exhibits lack of carnitine deficiency despite relatively low carnitine levels and alterations in ketogenesis
Autor: Pappa, KI Anagnou, NP Salamalekis, E Bikouvarakis, S and Maropoulos, G Anogianaki, N Evangeliou, A Koumantakis, E
Objective: Previous studies have underlined the importance of the carnitine shuttle system and its dysfunction both in normal pregnancy and in type 1 and 2 diabetes. The objective of this paper was to delineate more systematically the role of the car
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::546059ecdaec8b4e2f8049b6dae1f3c7
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3092985
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3
Emerging issues of the expression profiling technologies for the study of gynecologic cancer
Autor: Pappa, KI Anagnou, NP
Evaluation of the prognostic parameters of gynecologic cancer has shown their failure for classification according to the clinical behavior or the prediction of its outcome. This weakness has important implications on prognosis and treatment. The inc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::5f34c0a6afcb609caf190b97c6992cbd
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3097140
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4
Structural analysis and expression profile of a novel gene on chromosome 5q23 encoding a Golgi-associated protein with six splice variants, and involved within the 5q deletion of a Ph(-) CML patient
Autor: Kamakari, S Roussou, A Jefferson, A Ragoussis, I and Anagnou, NP
We have identified a novel gene, upstream of the cytokine gene cluster region in 5q23-31, residing within one of the most common deleted segments associated with MDS. The novel gene exhibits significant alternative splicing generating at least six sp
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::a206e0386ad4b14c68018042600edd36
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3093005
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6
An embryonic-specific repressor element located 3 ' to the (A)gamma-globin gene influences transcription of the human beta-globin locus in transgenic mice
Autor: Katsantoni, EZ de Krom, M Kong-a-San, J Imam, AMA and Grosveld, F Anagnou, NP Strouboulis, J
Objective. Persistent expression of the human fetal gamma-globin genes in the adult stage is often associated with naturally occurring deletions in the human beta-globin locus. The mapping of the 5’ breakpoints of these deletions within the (A)gamm
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::6910229dac6f34f45387dd9a185d65b8
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3085304
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8
Persistent gamma-globin expression in adult transgenic mice is mediated by HPFH-2, HPFH-3, and HPFH-6 breakpoint sequences
Autor: Katsantoni, EZ Langeveld, A Wai, AWK Drabek, D Grosveld, F Anagnou, NP Strouboulis, J
Deletions at the 3’ end of the human beta-globin locus are associated with the hereditary persistence of fetal hemoglobin (HPFH) in adults, potentially through the juxtaposition of enhancer elements in the vicinity of the fetal gamma-globin genes.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::72e4e9135dd8b61a4a4b1e482da149a6
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084524
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9
Functional role of the four different types of (AT)(X)T-Y motifs 5 ' to the beta-globin gene and their distribution in the Greek population
Autor: Kalotychou, V Kollia, P Voskaridou, E Patargias, T and Anagnou, NP Loukopoulos, D
The polymorphic sequence (AT)(X)T-Y motif residing 0.5 kb 5’ to the human beta-globin gene has been shown to be a binding site for a putative repressor protein, BP1, in K562 cells. The (AT)(X)T-Y sequence is characterized by variable length and sev
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::c71fb545487a4c8a62a4667beda671dd
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3081126
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10
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Plný text Recenzováno Digitální knihovna AV ČR
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