Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Domenico M. Ranieri"'
Autor:
A Doshi, Sioban SenGupta, Georgia Kakourou, Joyce C. Harper, Domenico M. Ranieri, Suzanne Cawood, Paul Serhal, S. Jaroudi
Publikováno v:
Human Reproduction. 24:2649-2655
background: The early preimplantation embryo relies on mRNA and protein from the oocyte to detect DNA damage and activate DNA repair, cell cycle arrest or apoptosis. Expression of some repair genes has been detected in mammalian oocytes and embryos;
Autor:
Joyce C. Harper, A Doshi, Sioban SenGupta, Paul Serhal, S Dhanjal, Georgia Kakourou, T Mamas, Joy D. A. Delhanty, Karen Fordham, Sarah Gotts, Domenico M. Ranieri
Publikováno v:
Neuromuscular disorders : NMD. 18(2)
Myotonic dystrophy type 1 (DM1) is a dominant multisystemic disorder caused by expansion of a trinucleotide repeat in a non-coding region of DMPK. Prenatal diagnosis (PND) is available; however, the decision to terminate affected pregnancies is diffi
Autor:
HH McGarrigle, Iffat Khadum, Shanthi Muttukrishna, R. Wakim, Domenico M. Ranieri, Paul Serhal
Publikováno v:
BJOG : an international journal of obstetrics and gynaecology. 112(10)
Objective The objective of this study was to evaluate the relationship between anti-mullerian hormone (AMH), inhibin B and antral follicle count (AFC) with ovarian response. Design Retrospective study. Setting Fertility unit. Sample AFC was recorded,
Publikováno v:
Fertility and sterility. 74(6)
Objective: To verify the correlation of basal 17β-E 2 with ovarian response to stimulation and outcome of in vitro fertilization (IVF). Design: Retrospective observational study. Setting: The Assisted Conception Unit, University College London Hospi
Autor:
L. Xanthopoulou, A Doshi, Domenico M. Ranieri, A Mantzouratou, A. Mania, Suzanne Cawood, Joy D. A. Delhanty
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 3, Iss 1, p 2 (2010)
Molecular Cytogenetics, Vol 3, Iss 1, p 2 (2010)
Background Two related family members, a female and a male balanced carrier of an intrachromosomal insertion on chromosome 7 were referred to our centre for preimplantation genetic diagnosis. This presented a rare opportunity to investigate the behav
Publikováno v:
Human Fertility. Jun2010, Vol. 13 Issue 2, p109-111. 3p.