The role and interaction of imprinted genes in human fetal growth

Autor: Moore, GE, Ishida, M, Demetriou, C, Al-Olabi, L, Leon, LJ, Thomas, AC, Abu-Amero, S, Frost, JM, Stafford, JL, Yao, C, Duncan, AJ, Baigel, R, Brimioulle, M, Iglesias-Platas, I, Apostolidou, S, Aggarwal, R, Whittaker, JC, Syngelaki, A, Nicolaides, KH, Regan, L, Monk, D, Stanier, P

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

The Effects of Growth Hormone Treatment Beyond Growth Promotion in Patients with Genetic Syndromes: A Systematic Review of the Literature.

Autor: Kucharska, Anna¹ (AUTHOR) anna.kucharska1@wum.edu.pl, Witkowska-Sędek, Ewelina¹ (AUTHOR) anna.kucharska1@wum.edu.pl, Erazmus, Michał¹ (AUTHOR), Artemniak-Wojtowicz, Dorota¹ (AUTHOR), Krajewska, Maria¹ (AUTHOR), Pyrżak, Beata¹ (AUTHOR)

Publikováno v: International Journal of Molecular Sciences. Sep2024, Vol. 25 Issue 18, p10169. 24p.

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/

Genetic Analyses in Small-for-Gestational-Age Newborns.

Autor: Stalman SE; Department of Pediatrics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.; Department of Genetics and Genomic Medicine, Institute of Child Health, University College London, London, United Kingdom., Solanky N; Department of Genetics and Genomic Medicine, Institute of Child Health, University College London, London, United Kingdom., Ishida M; Department of Genetics and Genomic Medicine, Institute of Child Health, University College London, London, United Kingdom., Alemán-Charlet C; Department of Genetics and Genomic Medicine, Institute of Child Health, University College London, London, United Kingdom., Abu-Amero S; Department of Genetics and Genomic Medicine, Institute of Child Health, University College London, London, United Kingdom., Alders M; Department of Clinical Genetics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands., Alvizi L; Centro de Pesquisas Sobre o Genoma Humano e Células-Tronco, Instituto de Biociências, Universidade de São Paulo, São Paulo, Brazil., Baird W; Department of Genetics and Genomic Medicine, Institute of Child Health, University College London, London, United Kingdom., Demetriou C; Department of Genetics and Genomic Medicine, Institute of Child Health, University College London, London, United Kingdom., Henneman P; Department of Clinical Genetics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands., James C; UCL Cancer Institute, University College London, London, United Kingdom., Knegt LC; Department of Clinical Genetics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands., Leon LJ; Department of Genetics and Genomic Medicine, Institute of Child Health, University College London, London, United Kingdom., Mannens MMAM; Department of Clinical Genetics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands., Mul AN; Department of Clinical Genetics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands., Nibbering NA; Department of Clinical Genetics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands., Peskett E; Department of Genetics and Genomic Medicine, Institute of Child Health, University College London, London, United Kingdom., Rezwan FI; Department of Human Development and Health, Southampton General Hospital, University of Southampton, Southampton, United Kingdom., Ris-Stalpers C; Department of Gynecology and Obstetrics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands., van der Post JAM; Department of Gynecology and Obstetrics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands., Kamp GA; Department of Pediatrics, Tergooi Hospitals, Blaricum, The Netherlands., Plötz FB; Department of Pediatrics, Tergooi Hospitals, Blaricum, The Netherlands., Wit JM; Department of Pediatrics, Leiden University Medical Centre, Leiden, The Netherlands., Stanier P; Department of Genetics and Genomic Medicine, Institute of Child Health, University College London, London, United Kingdom., Moore GE; Department of Genetics and Genomic Medicine, Institute of Child Health, University College London, London, United Kingdom., Hennekam RC; Department of Pediatrics, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.

Publikováno v: The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2018 Mar 01; Vol. 103 (3), pp. 917-925.

Primary Meningeal Melanocytic Tumors of the Central Nervous System: A Review from the Ultra-Rare Brain Tumors Task Force of the European Network for Rare Cancers (EURACAN).

Autor: Pellerino, Alessia¹ (AUTHOR) alessia.pellerino@unito.it, Verdijk, Robert M.^2,3 (AUTHOR) r.verdijk@erasmusmc.nl, Nichelli, Lucia⁴ (AUTHOR) lucia.nichelli@aphp.fr, Andratschke, Nicolaus H.⁵ (AUTHOR) nicolaus.andratschke@usz.ch, Idbaih, Ahmed⁶ (AUTHOR) ahmed.idbaih@aphp.fr, Goldbrunner, Roland⁷ (AUTHOR) roland.goldbrunner@uk-koeln.de

Publikováno v: Cancers. Jul2024, Vol. 16 Issue 14, p2508. 17p.