[PDF] Top 20 Igf2 imprinting in development and disease
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Igf2 imprinting in development and disease
... of Igf2 has dramatic and apparently dose dependent ...lacking Igf2 expression in endoderm (liver, gut, ...lowered Igf2 expression limited to the fetus (with normal levels in the placenta) has an ... See full document
6
Fatty acid binding proteins in brain development and disease
... brain development awaits more in-depth studies, investigations using animal models have revealed a number of possible functions in neurogenesis, neuronal migration and differentiation, and axis ... See full document
11
Pax2 in development and renal disease
... on development. This effect has serious implications for human disease, since, unlike many disease genes, loss of heterozygosity is not required for phenotypic ... See full document
6
Human brain gangliosides in development, aging and disease
... Int I Dc, BioI 35 2St) 295 (I t)t)1) 289 Human brain gangliosides in development, aging and disease IVICA KRACUN'*, HARALD ROSNER', VALERIJA DRNOVSEK', MARIJA HEFFER LAUC', CEDOMIR COSOVIC' and GORDAN[.] ... See full document
7
PAX genes in development and disease: the role of PAX2 in urogenital tract development
... During development many thousands of genes are expressed to control patterning of the developing ...of development, very rapid cell proliferation and differentiation occurs, but this rapid growth is under ... See full document
10
Epithelial Mesenchymal Transitions in development and disease: old views and new perspectives
... Fig. 1. Snail and the Epithelial-Mesenchymal Transition (EMT) in health and disease. (A,B) The EMT is fundamental for the development of many tissues and organs, including the neural crest and the mesoderm ... See full document
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Hox and Tale transcription factors in heart development and disease
... Machon et al., (2015) showed that the loss of Meis2 function results in OFT defect (Machon et al., 2015). Although cardiac de- fects have also been reported in a neural crest-targeted deletion no OFT defects were ... See full document
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Epigenetics and imprinting in human disease
... Surprisingly, several rare cases of mosaic genome-wide paternal UPD have been reported (Gogiel et al., 2013, Inbar-Feigenberg et al., 2013, Kalish et al., 2013). While no cases of live-born complete UPD cases have been ... See full document
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Congenital imprinting disorders: EUCID.net - a network to decipher their aetiology and to improve the diagnostic and clinical care
... growth, development and ...specific imprinting defects, they have been widely regarded as separate ...congenital imprinting disorders) now aims to promote better clinical care and scientific ... See full document
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Original Article The expression of imprinted genes IGF2 and PHLDA2 in mid-pregnancy have predictive values for the development of pre-eclampsia
... Preeclampsia (PE), identified by the presence of hypertension and proteinuria after 20 weeks of pregnancy [1], is a systemic disease that involved many organs such as the brain, eyes, liver and kidneys [2]. It’s ... See full document
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DNA methylation at the Igf2/H19 imprinting control region is associated with cerebellum mass in outbred mice
... that Igf2 mRNA levels are coordinated with specific growth patterns in the brain ...and development are important as a growing body of work from human and animal studies suggests that the role of the ... See full document
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Imprinting mechanisms
... and Igf2 are not completely demethylated and slightly higher levels of methylation are present in male compared to fe- male PGCs (Tada et ...and Igf2 seemed to be 50% methylated in chimeras, suggest- ing ... See full document
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Genomic imprinting in development, growth, behavior and stem cells
... The identification of the first imprinted genes (Igf2r, Igf2 and H19) in 1991 (Barlow et al., 1991; Bartolomei et al., 1991; DeChiara et al., 1991) sparked initial efforts towards elucidating the mechanisms of ... See full document
9
DNA methylation of the IGF2/H19 imprinting control region and adiposity distribution in young adults
... with IGF2/H19 ICR ...subsequent development of increased obesity and adverse metabolic ...early development [47] a finding supported by experimental evi- dence of altered H19 methylation and ... See full document
11
Overexpression of IGF2 and IGF2 receptor in malignant solitary fibrous tumor with hypoglycemia: a case report
... excessive IGF2 production [4, ...to IGF2 hyper-secretion by pleural SFT is more commonly known as “Doege-Potter syn- drome” [6, ...ligand, IGF2 binds to IGF1 receptor (IGF1R), IGF2 receptor ... See full document
5
Decreased expression of cell proliferation-related genes in clonally derived skin fibroblasts from children with Silver-Russell syndrome is independent of the degree of 11p15 ICR1 hypomethylation
... primers: IGF2 for, 5′-CAGTGAGACCCTGTGCGGCG-′3; IGF2 rev, 5′-TCCCTCTCGGACTTGGCGGG-′3; H19 for, 5′-TGAG CTCTCAGGAGGGAGGATGGT-′3; H19 rev, 5′-TTGTC ACGTCCACCGGACCTG-′3; GAPDH for, 5′-TGCACCA CCAACTGCTTAGC-′3; ... See full document
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Myod and H19 Igf2 locus interactions are required for diaphragm formation in the mouse
... the development of the ...hypaxial development that is compensated by the presence of Myf5, as shown by the lethality of Myod;Myf5 double-knockout mutants (Kablar et ... See full document
9
Severe paraneoplastic hypoglycemia secondary to a gastrointestinal stromal tumour masquerading as a stroke
... an IGF2:IGF1 ratio of R10 as well as low insulin, c-peptide and growth hormone ...auto-paracrine IGF2-mediated increased glucose metabolism may contri- bute in explaining hypoglycaemia in GISTs ... See full document
7
IGF2 ApaI A/G Polymorphism Evaluated in ESRD Individuals as a Biomarker to Identify Patients with New Onset Diabetes Mellitus after Renal Transplant in Asian Indians
... A three step PCR-RFLP method was followed for IGF2 exon 9 ApaI genotyping, which has been published by our group [13]. Specific primers: forward primer: 5’- CTTGGACTTTGAGTCAAATTGG-3’; reverse primer: ... See full document
5
Akt1 and insulin like growth factor 2 (Igf2) regulate placentation and fetal/postnatal development
... pre-weaning development was more severely affected by a deficiency in the Akt1 gene than a deficiency of the Igf2 ...to development of a competent lactating mammary gland (Boxer et ...pre-weaning ... See full document
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