Foetus And NotDavid M. Evans

List of bibliographic references

Number of relevant bibliographic references: 9.

Ident.	Authors (with country if any)	Title
000950	Elizabeth Milne [Australie] ; Kathryn R. Greenop [Australie] ; Catherine Metayer [États-Unis] ; Joachim Schüz [France] ; Eleni Petridou [Grèce] ; Maria S. Pombo-De-Oliveira [Brésil] ; Claire Infante-Rivard [Canada] ; Eve Roman [Royaume-Uni] ; John D. Dockerty [Nouvelle-Zélande] ; Logan G. Spector [États-Unis] ; Sérgio Koifman [Brésil] ; Laurent Orsi [France] ; Jérémie Rudant [France] ; Nick Dessypris [Grèce] ; Jill Simpson [Royaume-Uni] ; Tracy Lightfoot [Royaume-Uni] ; Peter Kaatsch [Allemagne] ; Margarita Baka [Grèce] ; Alessandra Faro [Brésil] ; Bruce K. Armstrong [Australie] ; Jacqueline Clavel [France] ; Patricia A. Buffler [États-Unis]	Fetal growth and childhood acute lymphoblastic leukemia: Findings from the childhood leukemia international consortium
001055	Amy Chui [Australie] ; Charmaine Tay [Australie] ; Melanie Cocquebert [France] ; Penelope Sheehan [Australie] ; Niroshani A. Pathirage [Australie] ; Susan Donath [Australie] ; Thierry Fournier [France] ; Josette Badet [France] ; Daniele Evain-Brion [France] ; Shaun P. Brennecke [Australie] ; Bill Kalionis [Australie] ; Padma Murthi [Australie]	Homeobox gene Distal-Less 3 is a regulator of villous cytotrophoblast differentiation and its expression is increased in human idiopathic foetal growth restriction
001163	J. Demars [Australie, France] ; C. Gicquel [Australie]	Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith-Wiedemann and Silver-Russell syndromes : EPIGENETICS AND MEDICAL GENETICS - UNITED BY PURPOSE
001667	Edwige Roy [France] ; Michele Leduc [France] ; Sarah Guegan [France] ; Latif Rachdi [France] ; Nicolas Kluger [France] ; Raphael Scharfmann [France] ; Selim Aractingi [France] ; Kiarash Khosrotehrani [France, Australie]	Specific maternal microchimeric T cells targeting fetal antigens in β cells predispose to auto-immune diabetes in the child
001872	Denise P. Cavalcanti [Brésil, France] ; Celine Huber [France] ; Kim-Hanh Le Quan Sang [France] ; Geneviève Baujat [France] ; Felicity Collins [Australie] ; Anne-Lise Delezoide [France] ; Nathalie Dagoneau [France] ; Martine Le Merrer [France] ; Jelena Martinovic [France] ; Marcos Fernando S. Mello [Brésil] ; Michel Vekemans [France] ; Arnold Munnich [France] ; Valerie Cormier-Daire [France]	Mutation in IFT80 in a fetus with the phenotype of Verma-Naumoff provides molecular evidence for Jeune-Verma-Naumoff dysplasia spectrum
001B23	J. Demars [Australie] ; Y. Le Bouc [France] ; A. El-Osta [Australie] ; C. Gicquel [Australie]	Epigenetic and Genetic Mechanisms of Abnormal 11p15 Genomic Imprinting in Silver-Russell and Beckwith-Wiedemann Syndromes : Epigeentic Mechanisms and Therapeutic Strategies
002617	Julie Demars [Australie] ; Mansur Ennuri Shmela [Australie] ; Sylvie Rossignol [France] ; Jun Okabe [Australie] ; Irène Netchine [France] ; Salah Azzi [France] ; Sylvie Cabrol [France] ; Cédric Le Caignec [France] ; Albert David [France] ; Yves Le Bouc [France] ; Assam El-Osta [Australie] ; Christine Gicquel [Australie]	Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11 p15 fetal growth disorders
002F41	A.-M. Lepagnol-Bestel [France] ; G. Maussion [France] ; B. Boda [Suisse] ; A. Cardona [France] ; Y. Lwayama [Japon] ; A.-L. Delezoide [France] ; J.-M. Moalic [France] ; D. Muller [Suisse] ; B. Dean [Australie] ; T. Yoshikawa [Japon] ; P. Gorwood [France] ; J. D. Buxbaum [États-Unis] ; N. Ramoz [France] ; M. Simonneau [France]	SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects
004438	G. A. Dekker [Australie, France] ; P. Y. Robillard	Preeclampsia: A couple's disease with maternal and fetal manifestations : Complications in pregnancy. Recent developments in preventive strategies and treatment modalities

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Tue Dec 5 10:43:12 2017. Site generation: Tue Mar 5 14:07:20 2024