Published in Dev Biol on August 15, 2001
Highly efficient modification of bacterial artificial chromosomes (BACs) using novel shuttle vectors containing the R6Kgamma origin of replication. Genome Res (2002) 3.61
Genome-wide prediction of imprinted murine genes. Genome Res (2005) 2.76
Gene expression in Wilms' tumor mimics the earliest committed stage in the metanephric mesenchymal-epithelial transition. Am J Pathol (2002) 2.17
Identification of novel imprinted genes in a genome-wide screen for maternal methylation. Genome Res (2003) 1.67
The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene. Mol Cell Biol (2004) 1.40
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Transcript- and tissue-specific imprinting of a tumour suppressor gene. Hum Mol Genet (2008) 1.13
Coexpression of neuronatin splice forms promotes medulloblastoma growth. Neuro Oncol (2008) 0.96
Comparative phylogenetic analysis reveals multiple non-imprinted isoforms of opossum Dlk1. Mamm Genome (2006) 0.88
Bio-informatics analysis of a gene co-expression module in adipose tissue containing the diet-responsive gene Nnat. BMC Syst Biol (2010) 0.82
Nuclear Factor I genomic binding associates with chromatin boundaries. BMC Genomics (2013) 0.80
Analysis of imprinted murine Peg3 locus in transgenic mice. Mamm Genome (2004) 0.79
BACs as tools for the study of genomic imprinting. J Biomed Biotechnol (2010) 0.76
Altered neuronatin expression in the rat dorsal root ganglion after sciatic nerve transection. J Biomed Sci (2010) 0.76
Neuronatin is a stress-responsive protein of rod photoreceptors. Neuroscience (2016) 0.75
Differential pre-mRNA splicing regulates Nnat isoforms in the hypothalamus after gastric bypass surgery in mice. PLoS One (2013) 0.75
High neuronatin (NNAT) expression is associated with poor outcome in breast cancer. Virchows Arch (2017) 0.75
The polycomb-group gene Ezh2 is required for early mouse development. Mol Cell Biol (2001) 7.20
How to count ... human genes. Nat Genet (2000) 4.78
A unitary model for involutional osteoporosis: estrogen deficiency causes both type I and type II osteoporosis in postmenopausal women and contributes to bone loss in aging men. J Bone Miner Res (1998) 4.24
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Eomesodermin is required for mouse trophoblast development and mesoderm formation. Nature (2000) 3.53
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The roles of osteoprotegerin and osteoprotegerin ligand in the paracrine regulation of bone resorption. J Bone Miner Res (2000) 3.38
The utility of MRI in suspected MS: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology (2003) 3.21
Parental-origin-specific epigenetic modification of the mouse H19 gene. Nature (1993) 3.11
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Relative contributions of testosterone and estrogen in regulating bone resorption and formation in normal elderly men. J Clin Invest (2000) 2.94
Implications of absolute fracture risk assessment for osteoporosis practice guidelines in the USA. Osteoporos Int (2008) 2.74
Cost-effective osteoporosis treatment thresholds: the United States perspective. Osteoporos Int (2008) 2.72
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Leptin acts on human marrow stromal cells to enhance differentiation to osteoblasts and to inhibit differentiation to adipocytes. Endocrinology (1999) 2.65
Imprinting and the epigenetic asymmetry between parental genomes. Science (2001) 2.56
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Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene. Genes Dev (1992) 2.19
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Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein. Nat Genet (1996) 2.06
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Epidemiology of sarcopenia. J Am Geriatr Soc (2000) 1.97
Two novel missense mutations in g protein-coupled receptor 54 in a patient with hypogonadotropic hypogonadism. J Clin Endocrinol Metab (2004) 1.91
Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q. Genes Cells (2000) 1.90
Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development. Cell (1994) 1.86
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Assessing forearm fracture risk in postmenopausal women. Osteoporos Int (2009) 1.71
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The fragilis interferon-inducible gene family of transmembrane proteins is associated with germ cell specification in mice. BMC Dev Biol (2003) 1.70
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Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization. Nat Genet (1995) 1.67
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MRI characteristics of the MLF in MS patients with chronic internuclear ophthalmoparesis. Neurology (2001) 1.57
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DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1. Mol Cell Biol (2001) 1.55
Genomic imprinting and the differential roles of parental genomes in brain development. Brain Res Dev Brain Res (1996) 1.54
Epigenotype switching of imprintable loci in embryonic germ cells. Dev Genes Evol (1998) 1.44
The expression of osteoprotegerin and RANK ligand and the support of osteoclast formation by stromal-osteoblast lineage cells is developmentally regulated. Endocrinology (2000) 1.43
Imprinting of Igf2 and H19 from a 130 kb YAC transgene. Development (1997) 1.43
Effect of gender on outcomes following renal artery stent placement for renovascular hypertension. Cathet Cardiovasc Diagn (1997) 1.43
A functional analysis of imprinting in parthenogenetic embryonic stem cells. Development (1994) 1.41
Nuclear transplantation in the mouse: heritable differences between parental genomes after activation of the embryonic genome. Cell (1986) 1.40
Leptin reduces ovariectomy-induced bone loss in rats. Endocrinology (2001) 1.40
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Segmental and developmental regulation of a presumptive T-cell oncogene in the central nervous system. Nature (1990) 1.38
Cross-sectional versus longitudinal evaluation of bone loss in men and women. Osteoporos Int (2000) 1.37
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The rise and fall of primary hyperparathyroidism: a population-based study in Rochester, Minnesota, 1965-1992. Ann Intern Med (1997) 1.35
Effects of estrogen therapy on bone marrow adipocytes in postmenopausal osteoporotic women. Osteoporos Int (2008) 1.35
Distant cis-elements regulate imprinted expression of the mouse p57( Kip2) (Cdkn1c) gene: implications for the human disorder, Beckwith--Wiedemann syndrome. Hum Mol Genet (2001) 1.34
The Splotch mutation interferes with muscle development in the limbs. Anat Embryol (Berl) (1993) 1.34
An imprinting element from the mouse H19 locus functions as a silencer in Drosophila. Nat Genet (1997) 1.34
Towards a diagnostic and therapeutic consensus in male osteoporosis. Osteoporos Int (2011) 1.33
Osteoprotegerin production by human osteoblast lineage cells is stimulated by vitamin D, bone morphogenetic protein-2, and cytokines. Biochem Biophys Res Commun (1998) 1.33
Temporal and spatial regulation of H19 imprinting in normal and uniparental mouse embryos. Development (1995) 1.31
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Increased body fat in mice with a targeted mutation of the paternally expressed imprinted gene Peg3. FASEB J (2005) 1.31
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Organization of the Fugu rubripes Hox clusters: evidence for continuing evolution of vertebrate Hox complexes. Nat Genet (1997) 1.28
Open-source work even more vital to genome project than to software. Nature (2000) 1.27
Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2. Dev Biol (1997) 1.27