Zobrazeno 1 - 8
of 8
pro vyhledávání: '"11"'
Autor:
Thomas Dahse, Donald Peebles, Holm Schneider, M Nivsarkar, David E. Noakes, M Miah, Anna L. David, Simon N. Waddington, Charles Coutelle, Terence Cook, HJ Knapton, Michael Themis, Charles H. Rodeck
Publikováno v:
Human Gene Therapy. 14:353-364
In utero gene therapy may provide treatment of genetic diseases before significant organ damage, allow permanent genetic correction by reaching stem cell populations, and provide immune tolerance against the therapeutic transgenes and vectors. We hav
Autor:
Ardythe L. Morrow, Kristin Collins, Amanda Hodge, Lynette K. Rogers, Michael L. Pennell, Christina J. Valentine, Annette Haban-Bartz, Georgia Morrow
Publikováno v:
Breastfeeding Medicine. 8:86-91
Docosahexaenoic acid (DHA) is a long-chain polyunsaturated fatty acid important for neonatal neurodevelopment and immune homeostasis. Preterm infants fed donor milk from a Midwestern source receive only 20% of the intrauterine accretion of DHA. We te
Autor:
Katerina Kotlabova, R. Vlk, Ilona Hromadnikova, Ladislav Krofta, Jan E. Jirasek, K. Dlouha, Lenka Zejskova, Tereza Jancuskova, Jindrich Doucha
Publikováno v:
DNA and Cell Biology. 29:295-301
This study evaluated quantification of fetal extracellular DNA in maternal plasma for differentiation between cases at risk of onset of placental-insufficiency-related complications and normal pregnancies. Using real-time polymerase chain reaction, f
Autor:
Spiros Gerou, Christina Kolonelou, Magda Pappa, Constantinos Mitropoulos, George Bertolis, Adamantia Papachatzopoulou, Panagiotis G. Menounos, George P. Patrinos
Publikováno v:
Genetic Testing, 11(2), 128-132. Mary Ann Liebert Inc.
Pheromones are water-soluble chemicals that elicit neuroendocrine and physiological changes, while they also provide information about gender within individuals of the same species. VN1R1 is the only functional pheromone receptor in humans. We have u
Autor:
Anna Caciotti, Enrico Zammarchi, Anthi Drousiotou, Theodoros Georgiou, Alessandra d'Azzo, Violetta Anastasiadou, Goula Stylianidou, Yvan Campos, Amelia Morrone
Publikováno v:
Genetic Testing. 9:126-132
GM1 gangliosidosis is a lysosomal storage disorder caused by deficiency of beta-galactosidase. It is mainly characterized by progressive neurodegeneration, and in its most severe infantile form, it leads to death before the age of 4. The GLB1 gene gi
Autor:
Anne G. Rizzo
Publikováno v:
Journal of Laparoendoscopic & Advanced Surgical Techniques. 13:11-15
To describe the long-term consequences of laparoscopic surgery during pregnancy.Laparoscopic surgery is well established in the surgical community. Laparoscopic surgery in the pregnant patient is not yet broadly accepted; concern has been for fetal w
Publikováno v:
Journal of Endourology. 12:15-21
The potential effects of extracorporeal application of shockwaves on an embryo or fetus were explored in an animal model. In experimental Series A, the fetuses of 30 gravid rabbits were exposed to piezoelectrically induced and sonographically guided
Autor:
Bruce C. Trapnell, Susan E. Wert, Jeffrey A. Whitsett, Harriet S. Iwamoto, Martin C. Vincent, Robert P. Baughman
Publikováno v:
Human Gene Therapy. 6:1019-1028
Many human genetic diseases, such as congenital surfactant protein B deficiency, manifest in the perinatal period. Prenatal gene therapy may be necessary to minimize morbidity in these diseases. We hypothesized that bacterial beta-galactosidase (beta