Published in Am J Med Genet on December 04, 1998
Genomic imprinting mechanisms in mammals. Mutat Res (2008) 2.28
Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer. Hum Mol Genet (2008) 1.47
Environmental exposures and gene regulation in disease etiology. Environ Health Perspect (2007) 1.44
Long noncoding RNAs: a potential novel class of cancer biomarkers. Front Genet (2015) 1.17
IGF-II promoter methylation and ovarian cancer prognosis. J Cancer Res Clin Oncol (2007) 0.87
Targeting the insulin-like growth factor pathway in hepatocellular carcinoma. World J Hepatol (2014) 0.87
The long noncoding RNA H19 promotes cell proliferation via E2F-1 in pancreatic ductal adenocarcinoma. Cancer Biol Ther (2016) 0.86
Genetic variation in insulin-like growth factor 2 may play a role in ovarian cancer risk. Hum Mol Genet (2011) 0.85
The Role of Long Non-Coding RNAs in Ovarian Cancer. Iran Biomed J (2016) 0.84
Loss of imprinting and marked gene elevation are 2 forms of aberrant IGF2 expression in colorectal cancer. Int J Cancer (2010) 0.83
IGF-II promoter specific methylation and expression in epithelial ovarian cancer and their associations with disease characteristics. Oncol Rep (2011) 0.79
Development of targeted therapy for a broad spectrum of solid tumors mediated by a double promoter plasmid expressing diphtheria toxin under the control of IGF2-P4 and IGF2-P3 regulatory sequences. Int J Clin Exp Med (2013) 0.76
The Interplay of LncRNA-H19 and Its Binding Partners in Physiological Process and Gastric Carcinogenesis. Int J Mol Sci (2017) 0.75
Prospective trial of supranormal values of survivors as therapeutic goals in high-risk surgical patients. Chest (1988) 6.29
Rapid, efficient detection and drug susceptibility testing of Mycobacterium tuberculosis in sputum by microscopic observation of broth cultures. The Tuberculosis Working Group in Peru. J Clin Microbiol (2000) 5.01
Kabuki make-up syndrome: a syndrome of mental retardation, unusual facies, large and protruding ears, and postnatal growth deficiency. J Pediatr (1981) 3.55
ASC, a novel 22-kDa protein, aggregates during apoptosis of human promyelocytic leukemia HL-60 cells. J Biol Chem (1999) 3.25
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome. Nat Genet (1996) 2.89
Mosaic and polymorphic imprinting of the WT1 gene in humans. Nat Genet (1994) 2.35
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis. Hum Mol Genet (1992) 2.35
Adenovirus-mediated heme oxygenase-1 gene transfer inhibits the development of atherosclerosis in apolipoprotein E-deficient mice. Circulation (2001) 2.32
Abnormal neuronal migration, deranged cerebral cortical organization, and diffuse white matter astrocytosis of human fetal brain: a major effect of methylmercury poisoning in utero. J Neuropathol Exp Neurol (1979) 2.21
Protease nexin-II, a potent antichymotrypsin, shows identity to amyloid beta-protein precursor. Nature (1989) 2.17
LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids. Hum Mol Genet (1999) 2.16
Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease. Nat Genet (2000) 2.02
Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a. Hum Mol Genet (2003) 1.92
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III. Am J Hum Genet (2000) 1.80
Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome. Hum Genet (1989) 1.72
Banding analysis of abnormal karyotypes in spontaneous abortion. Am J Hum Genet (1973) 1.71
Anatomic and chromosomal anomalies in 639 spontaneous abortuses. Hum Genet (1980) 1.68
Involvement of claudin-1 in the beta-catenin/Tcf signaling pathway and its frequent upregulation in human colorectal cancers. Oncol Res (2001) 1.66
Isolation and characterization of mutations in the human holocarboxylase synthetase cDNA. Nat Genet (1994) 1.53
A potential role for skeletal muscle caveolin-1 as an insulin sensitivity modulator in ageing-dependent non-obese type 2 diabetes: studies in a new mouse model. Diabetologia (2008) 1.52
A new study of bacterial motion: superconducting quantum interference device microscopy of magnetotactic bacteria. Biophys J (1999) 1.51
47,XX,UPD(7)mat,+r(7)pat/46,XX,UPD(7)mat mosaicism in a girl with Silver-Russell syndrome (SRS): possible exclusion of the putative SRS gene from a 7p13-q11 region. J Med Genet (1999) 1.50
DNA deletion and its parental origin in Angelman syndrome patients. Am J Med Genet (1991) 1.49
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients. Hum Mol Genet (1993) 1.49
Diagnostic hand anomalies in Smith-Magenis syndrome: four new patients with del (17)(p11.2p11.2) Am J Med Genet (1991) 1.48
High prevalence of current asthma and active smoking effect among the elderly. Clin Exp Allergy (2002) 1.45
Peritoneal inclusion cysts and their relationship to the ovaries: evaluation with sonography. Radiology (1997) 1.43
Structural and functional roles of asparagine 175 in the cysteine protease papain. J Biol Chem (1995) 1.40
Induction of plasma protein secretion in a newly established human hepatoma cell line. Mol Cell Biol (1983) 1.39
Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1. Am J Hum Genet (1999) 1.39
Polymorphic and tissue-specific imprinting of the human Wilms tumor gene, WT1. Jpn J Hum Genet (1997) 1.37
Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit gene. Lancet (1992) 1.37
A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family. J Med Genet (2004) 1.37
Origin of triploidy and tetraploidy in man: 11 cases with chromosomes markers. Cytogenet Cell Genet (1977) 1.36
The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity. Am J Med Genet (1986) 1.31
Expression of heme oxygenase-1 in atherosclerotic lesions. Am J Pathol (1998) 1.28
Glial fibrillary acidic protein in radial glia of early human fetal cerebrum: a light and electron microscopic immunoperoxidase study. J Neuropathol Exp Neurol (1986) 1.28
Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus. Hum Mol Genet (1996) 1.27
Isolation and characterization of a novel gene deleted in DiGeorge syndrome. Hum Mol Genet (1995) 1.26
Genetic structure of pig breeds from Korea and China using microsatellite loci analysis. J Anim Sci (2005) 1.26
Terminology and classification of congenital vascular malformations. Phlebology (2007) 1.25
Bipolar clavicular injury. Med J Malaysia (2003) 1.24
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse. Hum Genet (2003) 1.23
Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors. Hum Mol Genet (1996) 1.21
Use of psoralen as extinguisher of contaminated DNA in PCR. Nucleic Acids Res (1990) 1.21
Oxidative stress in neurotoxic effects of methylmercury poisoning. Neurotoxicology (1996) 1.21
Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation. Hum Genet (1985) 1.19
An angiogenin-binding protein from endothelial cells. Proc Natl Acad Sci U S A (1991) 1.19
Immunofluorescence staining of astrocytes in vitro using antiserum to glial fibrillary acidic protein. Brain Res (1975) 1.17
Molecular cloning of a human protein that binds to the retinoblastoma protein and chromosomal mapping. Genomics (1995) 1.16
Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients. Am J Med Genet (1991) 1.15
Radial glia in the human fetal cerebrum: a combined Golgi, immunofluorescent and electron microscopic study. Brain Res (1978) 1.15
Cortical dysplasia associated with massive ectopia of neurons and glial cells within the subarachnoid space. Acta Neuropathol (1987) 1.15
A stable acentric marker chromosome: possible existence of an intercalary ancient centromere at distal 8p. Am J Hum Genet (1994) 1.15
Cause of sudden, unexpected death of Prader-Willi syndrome patients with or without growth hormone treatment. Am J Med Genet A (2005) 1.14
Altered antigenicity of 'a' determinant variants of hepatitis B virus. J Gen Virol (1997) 1.13
Cloning of the peroxiredoxin gene family in rats and characterization of the fourth member. FEBS Lett (1999) 1.13
Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome. Clin Dysmorphol (1993) 1.09
Blood rheology: effect of fibrinogen deduced by addition. Circ Res (1966) 1.09
The origin of mosaic Down syndrome: four cases with chromosome markers. Am J Hum Genet (1984) 1.08
Accuracy of capnography in nonintubated surgical patients. Chest (1992) 1.08
Molecular characterization of NSD1, a human homologue of the mouse Nsd1 gene. Gene (2001) 1.08
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation. Am J Med Genet (1997) 1.07
Detection of cell free placental DNA in maternal plasma: direct evidence from three cases of confined placental mosaicism. J Med Genet (2004) 1.06
A 1.2-megabase BAC/PAC contig spanning the 14q13 breakpoint of t(2; 14) in a mirror-image polydactyly patient. Genomics (1997) 1.06
Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3). Am J Med Genet (1989) 1.05
New p57KIP2 mutations in Beckwith-Wiedemann syndrome. Hum Genet (1997) 1.05
Ring chromosome 11 [46,XX,r(11) (p15q25)] associated with clinical features of the 11q- syndrome. Ann Genet (1981) 1.04
Identification of proacrosin binding protein sp32 precursor as a human cancer/testis antigen. Proc Natl Acad Sci U S A (2001) 1.04
Non-traumatic ischaemic myelopathy: a review of 25 cases. Paraplegia (1988) 1.04
Airway-obstructing supraglottic edema following anesthesia with the head positioned in forced flexion. Anesthesiology (1981) 1.03
Expression of glial fibrillary acidic protein in immature oligodendroglia. Science (1984) 1.01
Active transposition in zebrafish. Proc Natl Acad Sci U S A (1996) 1.01
EC syndrome in a girl with paracentric inversion (7)(q22.1;q36.3). Clin Dysmorphol (1993) 1.01
Possible narrowed assignment of the loci of monosomy 21-associated microcephaly and intrauterine growth retardation to a 1.2-Mb segment at 21q22.2. Am J Hum Genet (1997) 1.00
Sotos syndrome and haploinsufficiency of NSD1: clinical features of intragenic mutations and submicroscopic deletions. J Med Genet (2003) 1.00
The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting. Hum Genet (1993) 1.00
A system for ubiquitous health monitoring in the bedroom via a Bluetooth network and wireless LAN. Conf Proc IEEE Eng Med Biol Soc (2004) 0.99
Domain-specific mutations of a transforming growth factor (TGF)-beta 1 latency-associated peptide cause Camurati-Engelmann disease because of the formation of a constitutively active form of TGF-beta 1. J Biol Chem (2001) 0.98
Penta X syndrome: a case report with review of the literature. Am J Med Genet (1991) 0.97
No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients. Am J Med Genet (2001) 0.97
cDNA cloning and chromosomal mapping of human N-acetylglucosaminyltransferase V+. Biochem Biophys Res Commun (1994) 0.96
Chylous ascites in acute pancreatitis during pregnancy: case report. Chang Gung Med J (2001) 0.96
cDNA sequence and chromosomal localization of a novel human protein, RBQ-1 (RBBP6), that binds to the retinoblastoma gene product. Genomics (1995) 0.95
Combined Goltz and Aicardi syndromes in a terminal Xp deletion: are they a contiguous gene syndrome? Am J Med Genet (1992) 0.95
The Sugio-Kajii syndrome, proposed tricho-rhino-phalangeal syndrome type III. Am J Med Genet (1986) 0.95
Cloning and characterization of the inversion breakpoint at chromosome 2q35 in a patient with Waardenburg syndrome type I. Hum Mol Genet (1992) 0.94
Association of melanocortin 4 receptor (MC4R) and high mobility group AT-hook 1 (HMGA1) polymorphisms with pig growth and fat deposition traits. Anim Genet (2006) 0.94
Selective transcriptional regulations in the human liver cell by hepatitis B viral X protein. Biochem Biophys Res Commun (2000) 0.93
Origin of acrocentric trisomies in spontaneous abortuses. Hum Genet (1977) 0.93
Identification of a marker chromosome as inv dup(15) by molecular analysis. Clin Genet (1991) 0.93
Paternal expression of WT1 in human fibroblasts and lymphocytes. Hum Mol Genet (1997) 0.93
An autosomal dominant posterior polar cataract locus maps to human chromosome 20p12-q12. Eur J Hum Genet (2000) 0.93
Methylmercury poisoning of the developing nervous system: I. Pattern of neuronal migration in the cerebral cortex. Neurotoxicology (1986) 0.92
Sequential Q- and Acridine orange-marker technique. Humangenetik (1975) 0.92
The demonstration of glial fibrillary acidic protein in the cerebrum of the human fetus by indirect immunofluorescence. Brain Res (1976) 0.92
A case of neonatal McCune-Albright syndrome with Cushing syndrome and hyperthyroidism. Acta Paediatr Scand (1991) 0.91
Population variation in the dinucleotide repeat polymorphism at the D8S360 locus. Hum Mol Genet (1993) 0.91
Three new cases of spondylocarpotarsal synostosis syndrome: clinical and radiographic studies. Am J Med Genet (1998) 0.91
The novel gene, gamma2-COP (COPG2), in the 7q32 imprinted domain escapes genomic imprinting. Genomics (2000) 0.91