Zobrazeno 1 - 10
of 291
pro vyhledávání: '"Stanier Philip"'
Autor:
Moore Gudrun E, Stanier Philip
Publikováno v:
BMC Medicine, Vol 11, Iss 1, p 30 (2013)
Abstract The relationship between the parental genomes in terms of the future growth and development of their offspring is not critical. For the majority of the genome the tissue-specific gene expression and epigenetic status is shared between the pa
Externí odkaz:
https://doaj.org/article/31a86f3827e64ef8902b05e0225267f0
Autor:
Clark Taane G, Campino Susana, Forrest Matthew S, Sudbery Ian M, Abu-Amero Sayeda, Smits Guillaume, Ritchie Matthew E, Daelemans Caroline, Stanier Philip, Kwiatkowski Dominic, Deloukas Panos, Dermitzakis Emmanouil T, Tavaré Simon, Moore Gudrun E, Dunham Ian
Publikováno v:
BMC Genetics, Vol 11, Iss 1, p 25 (2010)
Abstract Background Imprinted genes show expression from one parental allele only and are important for development and behaviour. This extreme mode of allelic imbalance has been described for approximately 56 human genes. Imprinting status is often
Externí odkaz:
https://doaj.org/article/31251477ad2740b99fb1417b229f8f86
Autor:
Demetriou, Charalambos *, Abu-amero, Sayeda, White, Shawnelle, Peskett, Emma, Markoff, Arseni, Stanier, Philip, Moore, Gudrun E., Regan, Lesley
Publikováno v:
In Reproductive BioMedicine Online November 2015 31(5):681-688
Autor:
Moore, Gudrun E., Ishida, Miho, Demetriou, Charalambos, Al-Olabi, Lara, Leon, Lydia J., Thomas, Anna C., Abu-Amero, Sayeda, Frost, Jennifer M., Stafford, Jaime L., Chaoqun, Yao, Duncan, Andrew J., Baigel, Rachel, Brimioulle, Marina, Iglesias-Platas, Isabel, Apostolidou, Sophia, Aggarwal, Reena, Whittaker, John C., Syngelaki, Argyro, Nicolaides, Kypros H., Regan, Lesley, Monk, David, Stanier, Philip
Publikováno v:
Philosophical Transactions: Biological Sciences, 2015 Mar 01. 370(1663), 1-12.
Externí odkaz:
http://www.jstor.org/stable/24504284
Autor:
Setó-Salvia, Núria, Stanier, Philip
Publikováno v:
In European Journal of Medical Genetics August 2014 57(8):381-393
Autor:
Muggenthaler, Martina M. A., Chowdhury, Biswajit, Hasan, S. Naimul, Cross, Harold E., Mark, Brian, Harlalka, Gaurav V., Patton, Michael A., Ishida, Miho, Behr, Elijah R., Sharma, Sanjay, Zahka, Kenneth, Faqeih, Eissa, Blakley, Brian, Jackson, Mike, Lees, Melissa, Dolinsky, Vernon, Cross, Leroy, Stanier, Philip, Salter, Claire, Baple, Emma L., Alkuraya, Fowzan S., Crosby, Andrew H., Triggs-Raine, Barbara, Chioza, Barry A.
Orofacial clefting is amongst the most common of birth defects, with both genetic and environmental components. Although numerous studies have been undertaken to investigate the complexities of the genetic etiology of this heterogeneous condition, th
Externí odkaz:
http://hdl.handle.net/10150/623116
http://arizona.openrepository.com/arizona/handle/10150/623116
http://arizona.openrepository.com/arizona/handle/10150/623116
Publikováno v:
In Lancet Neurology August 2013 12(8):799-810
Akademický článek
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Akademický článek
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Autor:
De Castro, Sandra C P, Gustavsson, Peter, Marshall, Abigail R, Gordon, William M, Galea, Gabriel, Nikolopoulou, Evanthia, Savery, Dawn, Rolo, Ana, Stanier, Philip, Andersen, Bogi, Copp, Andrew J, Greene, Nicholas D E
Publikováno v:
Human Molecular Genetics
Human molecular genetics, vol 27, iss 24
Human molecular genetics, vol 27, iss 24
The genetic basis of human neural tube defects (NTDs), such as anencephaly and spina bifida (SB), is complex and heterogeneous. Grainyhead-like genes represent candidates for involvement in NTDs based on the presence of SB and exencephaly in mice car