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Sequence variations in the FII, FV, F13A1, FGB and PAI-1 genes are associated with differences in myocardial perfusion.
Pharmacogenomics. 2011 Feb;12(2):195-203. doi: 10.2217/pgs.10.180.
Pharmacogenomics. 2011.
PMID: 21332313
The 5' regulatory region of the human fetal globin genes is a gene conversion hotspot.
Kalamaras A, Chassanidis C, Samara M, Chiotoglou I, Vamvakopoulos NK, Papadakis MN, Kollia P, Patrinos GP.
Kalamaras A, et al. Among authors: vamvakopoulos nk.
Hemoglobin. 2008;32(6):572-81. doi: 10.1080/03630260802507824.
Hemoglobin. 2008.
PMID: 19065335
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The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter.
Chassanidis C, Kalamaras A, Phylactides M, Pourfarzad F, Likousi S, Maroulis V, Papadakis MN, Vamvakopoulos NK, Aleporou-Marinou V, Patrinos GP, Kollia P.
Chassanidis C, et al. Among authors: vamvakopoulos nk.
Ann Hematol. 2009 Jun;88(6):549-55. doi: 10.1007/s00277-008-0643-0. Epub 2008 Dec 3.
Ann Hematol. 2009.
PMID: 19050890
Free PMC article.
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Large-scale population genetic analysis for hemoglobinopathies reveals different mutation spectra in central Greece compared to the rest of the country.
Samara M, Chiotoglou I, Kalamaras A, Likousi S, Chassanidis C, Vagena A, Vagenas C, Eftichiadis E, Vamvakopoulos N, Patrinos GP, Kollia P.
Samara M, et al.
Am J Hematol. 2007 Jul;82(7):634-6. doi: 10.1002/ajh.20889.
Am J Hematol. 2007.
PMID: 17301974
Free article.
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Predominantly post-transcriptional regulation of activation molecules in chronic lymphocytic leukemia: the case of transferrin receptors.
Chiotoglou I, Smilevska T, Samara M, Likousi S, Belessi C, Athanasiadou I, Stavroyianni N, Samara S, Laoutaris N, Vamvakopoulos N, Anagnostopoulos A, Fassas A, Stamatopoulos K, Kollia P.
Chiotoglou I, et al.
Blood Cells Mol Dis. 2008 Sep-Oct;41(2):203-9. doi: 10.1016/j.bcmd.2008.05.003. Epub 2008 Jul 14.
Blood Cells Mol Dis. 2008.
PMID: 18621559
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Growth hormone, insulin-like growth factor I, and leptin interaction in human cultured lutein granulosa cells steroidogenesis.
Karamouti M, Kollia P, Kallitsaris A, Vamvakopoulos N, Kollios G, Messinis IE.
Karamouti M, et al.
Fertil Steril. 2008 Oct;90(4 Suppl):1444-50. doi: 10.1016/j.fertnstert.2007.08.076. Epub 2007 Dec 20.
Fertil Steril. 2008.
PMID: 18082739
Free article.
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Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the Agamma -158 C>T mutation in gamma-globin gene transcription.
Kollia P, Kalamaras A, Chassanidis C, Samara M, Vamvakopoulos NK, Radmilovic M, Pavlovic S, Papadakis MN, Patrinos GP.
Kollia P, et al. Among authors: vamvakopoulos nk.
Blood Cells Mol Dis. 2008 Nov-Dec;41(3):263-4. doi: 10.1016/j.bcmd.2008.05.009. Epub 2008 Aug 20.
Blood Cells Mol Dis. 2008.
PMID: 18718799
No abstract available.
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