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au.\*:("KOLLIA, Panagoula")

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Growth hormone, insulin-like growth factor I, and leptin interaction in human cultured lutein granulosa cells steroidogenesisKARAMOULI, Maria; KOLLIA, Panagoula; KALLITSARIS, Athanasios et al.Fertility and sterility. 2008, Vol 90, pp 1444-1450, issn 0015-0282, 7 p., SUP2Article

Valproic acid, trichostatin and their combination with hemin preferentially enhance γ-globin gene expression in human erythroid liquid culturesPOLITOU, Marianna; KOLLIA, Panagoula; AKEL, Salem et al.Haematologica (Roma). 2001, Vol 86, Num 7, pp 700-705, issn 0390-6078Article

Aγ-haplotypes : A new group of genetic markers for thalassemic mutations inside the 5' regulatory region of the human Aγ-globin genePATRINOS, George P; KOLLIA, Panagoula; PAPAPANAGIOTOU, Elisavet et al.American journal of hematology. 2001, Vol 66, Num 2, pp 99-104, issn 0361-8609Article

Increased γ-globin gene expression in β-thalassemia intermedia patients correlates with a mutation in 3'HS1PAPACHATZOPOULOU, Adamantia; KAIMAKIS, Polynikis; POURFARZAD, Farzin et al.American journal of hematology. 2007, Vol 82, Num 11, pp 1005-1009, issn 0361-8609, 5 p.Article

Evidence for the molecular heterogeneity of sickle cell anemia chromosomes bearing the βs/benin haplotypePATRINOS, George P; SAMPERI, Piera; LO NIGRO, Luca et al.American journal of hematology. 2005, Vol 80, Num 1, pp 79-80, issn 0361-8609, 2 p.Article

A Novel de Novo Mutation Within EFNB1 Gene in a Young Girl With Craniofrontonasal SyndromeAPOSTOLOPOULOU, Despina; STRATOUDAKIS, Alexander; HATZAKI, Angeliki et al.The Cleft palate-craniofacial journal. 2012, Vol 49, Num 1, pp 109-113, issn 1055-6656, 5 p.Article

Severe osteoporosis and mutation in NOTCH2 gene in a woman with Hajdu-Cheney syndromeSTATHOPOULOS, Ioannis P; TROVAS, George; LAMPROPOULOU-ADAMIDOU, Kalliopi et al.Bone (New York, NY). 2013, Vol 52, Num 1, pp 366-371, issn 8756-3282, 6 p.Article

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachGIARDINE, Belinda; BORG, Joseph; COSTA, Flavia C et al.Nature genetics. 2011, Vol 43, Num 4, pp 295-301, issn 1061-4036, 7 p.Article

Large-scale population genetic analysis for hemoglobinopathies reveals different mutation spectra in central greece compared to the rest of the countrySAMARA, Maria; CHIOTOGLOU, Ioanna; KOLLIA, Panagoula et al.American journal of hematology. 2007, Vol 82, Num 7, pp 634-636, issn 0361-8609, 3 p.Article

Assessment of Gene-by-Sex Interaction Effect on Bone Mineral DensityLIU, Ching-Ti; ESTRADA, Karol; YANHUA ZHOU et al.Journal of bone and mineral research (Print). 2012, Vol 27, Num 10, pp 2051-2064, issn 0884-0431, 14 p.Article

Immunoglobulin genes in multiple myeloma : expressed and non-expressed repertoires, heavy and light chain pairings and somatic mutation patterns in a series of 101 casesHADZIDIMITRIOU, Anastasia; STAMATOPOULOS, Kostas; FASSAS, Athanasios et al.Haematologica (Roma). 2006, Vol 91, Num 6, pp 781-787, issn 0390-6078, 7 p.Article

Molecular evidence for transferrin receptor 2 expression in all FAB subtypes of acute myeloid leukemiaKOLLIA, Panagoula; SAMARA, Maria; FASSAS, Athanasios et al.Leukemia research. 2003, Vol 27, Num 12, pp 1101-1103, issn 0145-2126, 3 p.Article

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