L38 von Anagnou, N

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Serotonin Transporter and G Protein Beta 3 Subunit Gene Polymorphisms in Greeks with Irritable Bowel Syndrome von Markoutsaki, T., Karantanos, T., Gazouli, M., Anagnou, N. P., Ladas, S. D., Karamanolis, D. G.

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AF-MSCs fate can be regulated by culture conditions von Zagoura, D S, Trohatou, O, Bitsika, V, Makridakis, M, Pappa, K I, Vlahou, A, Roubelakis, M G, Anagnou, N P

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Y chromosomal haplogroup J as a signature of the post-neolithic colonization of Europe von Di Giacomo, F, Luca, F, Popa, L O, Akar, N, Anagnou, N, Banyko, J, Brdicka, R, Barbujani, G, Papola, F, Ciavarella, G, Cucci, F, Di Stasi, L, Gavrila, L, Kerimova, M G, Kovatchev, D, Kozlov, A I, Loutradis, A, Mandarino, V, Mammi', C, Michalodimitrakis, E N, Paoli, G, Pappa, K I, Pedicini, G, Terrenato, L, Tofanelli, S, Malaspina, P, Novelletto, A

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Thiopurine S-methyltransferase genotype and the use of thiopurines in paediatric inflammatory bowel disease Greek patients von Gazouli, M., Pachoula, I., Panayotou, I., Mantzaris, G., Syriopoulou, V. P., Goutas, N., Vlachodimitropoulos, D., Anagnou, N. P., Roma-Giannikou, E.

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Use of the hereditary persistence of fetal hemoglobin 2 enhancer to increase the expression of oncoretrovirus vectors for human gamma-globin von Fragkos, M, Anagnou, N P, Tubb, J, Emery, D W

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Clinal patterns of human Y chromosomal diversity in continental Italy and Greece are dominated by drift and founder effects von Di Giacomo, F., Luca, F., Anagnou, N., Ciavarella, G., Corbo, R.M., Cresta, M., Cucci, F., Di Stasi, L., Agostiano, V., Giparaki, M., Loutradis, A., Mammi’, C., Michalodimitrakis, E.N., Papola, F., Pedicini, G., Plata, E., Terrenato, L., Tofanelli, S., Malaspina, P., Novelletto, A.

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Mimiviruses: Giant viruses with novel and intriguing features (Review) von Kalafati, Eleni, Papanikolaou, Eleni, Marinos, Evangelos, Anagnou, Nicholas P, Pappa, Kalliopi I

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Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3' end... von KOSTEAS, T, PALENA, A, ANAGNOU, N. P

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PII: S0165-0378(09)00297-6 von Anagnou, N.

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Acute myeloid/NK precursor cell leukemia with trisomy 4 and a novel point mutation in the extracellular domain of the G-CSF receptor in a patient with chronic idiopathic neutropeni... von Papadaki, H A, Kosteas, T, Gemetzi, C, Damianaki, A, Anagnou, N P, Eliopoulos, G D

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HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server von Hardison, Ross C., Chui, David H.K., Giardine, Belinda, Riemer, Cathy, Patrinos, George P., Anagnou, Nicholas, Miller, Webb, Wajcman, Henri

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P228 Thiopurine methyltransferase genotype and thiopurine S-methyltransferase activity in Greek children with inflammatory bowel disease von Gazouli, M., Pachoula, I., Panayotou, I., Chouliaras, G., Anagnou, N., Roma, E.

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A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area von MALASPINA, P., TSOPANOMICHALOU, M., DUMAN, T., STEFAN, M., SILVESTRI, A., RINALDI, B., GARCIA, O., GIPARAKI, M., PLATA, E., KOZLOV, A. I., BARBUJANI, G., VERNESI, C., PAPOLA, F., CIAVARELLA, G., KOVATCHEV, D., KERIMOVA, M. G., ANAGNOU, N., GAVRILA, L., VENEZIANO, L., AKAR, N., LOUTRADIS, A., MICHALODIMITRAKIS, E. N., TERRENATO, L., NOVELLETTO, A.

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A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area von MALASPINA, P., TSOPANOMICHALOU, M., DUMAN, T., STEFAN, M., SILVESTRI, A., RINALDI, B., GARCIA, O., GIPARAKI, M., PLATA, E., KOZLOV, A. I., BARBUJANI, G., VERNESI, C., PAPOLA, F., CIAVARELLA, G., KOVATCHEV, D., KERIMOVA, M. G., ANAGNOU, N., GAVRILA, L., VENEZIANO, L., AKAR, N., LOUTRADIS, A., MICHALODIMITRAKIS, E. N., TERRENATO, L., NOVELLETTO, A.

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Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies von Patrinos, George P., Giardine, Belinda, Riemer, Cathy, Miller, Webb, Chui, David H. K., Anagnou, Nicholas P., Wajcman, Henri, Hardison, Ross C.

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Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulations von Ciminelli, B M, Pompei, F, Malaspina, P, Hammer, M, Persichetti, F, Pignatti, P F, Palena, A, Anagnou, N, Guanti, G, Jodice, C

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Advances in Thalassemia Research von Nienhuis, Arthur W., Anagnou, Nicholas P., Ley, Timothy J.

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RNA Processing Errors in Patients with β -thalassemia von Ley, Timothy J., Anagnou, Nicholas P., Pepe, Guglielmina, Nienhuis, Arthur W.

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P225 - Association between NOD2, ATG16L1 And IL23R gene polymorphisms and childhood-onset of Crohn's disease: results from a case control study among Greek cases von Gazouli, M., Pachoula, I., Panayotou, I., Mantzaris, G.J., Franke, A., Chroussos, G., Schreiber, S., Anagnou, N., Roma-Giannikou, E.

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