Non-Viral Episomal Vector Mediates Efficient Gene Transfer of the β-Globin Gene into K562 and Human Haematopoietic Progenitor Cells.

Autor: Lazaris VM; Department of General Biology, Medical School, University of Patras, 26504 Patras, Greece., Simantirakis E; Centre of Basic Research, Biomedical Research Foundation of the Academy of Athens (BRFAA), 11527 Athens, Greece., Stavrou EF; Department of General Biology, Medical School, University of Patras, 26504 Patras, Greece., Verras M; Department of General Biology, Medical School, University of Patras, 26504 Patras, Greece., Sgourou A; Biology Laboratory, School of Science and Technology, Hellenic Open University, 26335 Patras, Greece., Keramida MK; IVF and Andrology Labs, IVF Unit, General University Hospital of Patras, 26504 Patras, Greece., Vassilopoulos G; Centre of Basic Research, Biomedical Research Foundation of the Academy of Athens (BRFAA), 11527 Athens, Greece., Athanassiadou A; Department of General Biology, Medical School, University of Patras, 26504 Patras, Greece.

Publikováno v: Genes [Genes (Basel)] 2023 Sep 08; Vol. 14 (9). Date of Electronic Publication: 2023 Sep 08.

Renal dysgenesis and KAL1 gene defects in patients with sporadic Kallmann syndrome.

Autor: Georgopoulos NA; Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology, University of Patras Medical School, Patras, Greece. neoklisg@hol.gr, Koika V, Galli-Tsinopoulou A, Spiliotis BE, Adonakis G, Keramida MK, Sgourou A, Koufogiannis KD, Papachatzopoulou A, Papavassiliou AG, Kourounis G, Vagenakis GA

Publikováno v: Fertility and sterility [Fertil Steril] 2007 Nov; Vol. 88 (5), pp. 1311-7. Date of Electronic Publication: 2007 Jul 02.

Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report.

Autor: Schierz, Ingrid Anne Mandy¹ (AUTHOR) inschier@tin.it, Giuffrè, Mario¹ (AUTHOR), Cimador, Marcello² (AUTHOR), D'Alessandro, Maria Michela³ (AUTHOR), Serra, Gregorio¹ (AUTHOR), Favata, Federico¹ (AUTHOR), Antona, Vincenzo¹ (AUTHOR), Piro, Ettore¹ (AUTHOR), Corsello, Giovanni¹ (AUTHOR)

Publikováno v: Italian Journal of Pediatrics. 2/3/2022, Vol. 48 Issue 1, p1-7. 7p.

Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life.

Autor: Sarfati, Julie^1,2,3, Bouvattier, Claire^1,2,4, Bry-Gauillard, Hélène^2,3, Cartes, Alejandra^2,3, Bouligand, Jérôme^1,2,5,6, Young, Jacques^1,2,3,5 jacques.young@bct.aphp.fr

Publikováno v: Orphanet Journal of Rare Diseases. Jun2015, Vol. 10 Issue 1, p1-7. 7p.

ERK1/2 signaling is essential for the chemoattraction exerted by human FGF2 and human anosmin-1 on newborn rat and mouse OPCs via FGFR1.

Autor: Murcia‐Belmonte, Verónica, Medina‐Rodríguez, Eva M., Bribián, Ana, Castro, Fernando, Esteban, Pedro F.

Publikováno v: Glia; Mar2014, Vol. 62 Issue 3, p374-386, 13p