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Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human

Autor: Monk, M, Sanches, S, Arnaud, Philippe, Apostolidou, A, Hills, H, Abu-Amero, A, Murrell, M., Friess, H., Reik, W., Stanier, P., Constancia, M., Moore, G.E., Monk, D., Sanches, R., Apostolidou, S., Hills, A., Abu-Amero, S., Murrell, A.

Publikováno v: Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2006, 15 (8), pp.1259-1269. ⟨10.1093/hmg/ddl041⟩
Human Molecular Genetics, 2006, 15 (8), pp.1259-1269. ⟨10.1093/hmg/ddl041⟩

International audience; Genomic imprinting is limited to a subset of genes that play critical roles in fetal growth, development and behaviour. One of the most studied imprinted genes encodes insulin-like growth factor 2, and aberrant imprinting and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e00a6585ea5f7df2c97151c9fa78cd0
https://doi.org/10.1093/hmg/ddl041

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The role and interaction of imprinted genes in human fetal growth

Publikováno v: Philosophical Transactions of the Royal Society B: Biological Sciences
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Moore, G E, Ishida, M, Demetriou, C, Al-Olabi, L, Leon, L J, Thomas, A C, Abu-Amero, S, Frost, J M, Stafford, J L, Yao Chaoqun, N V, Duncan, A J, Baigel, R, Brimioulle, M, Iglesias-Platas, I, Apostolidou, S, Aggarwal, R, Whittaker, J C, Syngelaki, A, Nicolaides, K H, Regan, L, Monk, D & Stanier, P 2015, ' The role and interaction of imprinted genes in human fetal growth ', Philosophical Transactions of the Royal Society of London Series B: Biological Sciences, vol. 370, no. 1663, 20140074, pp. 1-12 . https://doi.org/10.1098/rstb.2014.0074
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu

Identifying the genetic input for fetal growth will help to understand common, serious complications of pregnancy such as fetal growth restriction. Genomic imprinting is an epigenetic process that silences one parental allele, resulting in monoalleli

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::70cdf98f47253ce0586e9ecf0766bd07
http://europepmc.org/articles/PMC4305174

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An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands

Autor: Preece, M, Abu-Amero, S, Ali, Z, Abu-Amero, K, Wakeling, E, Stanier, P, Moore, G

Silver-Russell syndrome (SRS) shares common features of intrauterine growth retardation (IUGR) and a number of dysmorphic features including lateral asymmetry in about 50% of subjects. Its genetic aetiology is complex and most probably heterogeneous.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fa18103426f06d618f1fefc5da57047c
https://europepmc.org/articles/PMC1734382/

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An analysis of common isodisomic regions in five mUPD 16 probands

Autor: Abu-Amero, S., Ali, Z., Abu-Amero, K., Stanier, P., Moore, G.

Intrauterine growth retardation (IUGR) with or without additional abnormalities is recognised as a common feature of maternal uniparental disomy for chromosome 16 (mUPD 16) and is usually associated with confined placental mosaicism (CPM). Although i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fef879aa729c10da5d00d43e1082efb3
https://europepmc.org/articles/PMC1734327/

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