Published in Hum Mol Genet on July 17, 2007
A tripartite paternally methylated region within the Gpr1-Zdbf2 imprinted domain on mouse chromosome 1 identified by meDIP-on-chip. Nucleic Acids Res (2010) 1.83
Imprinting disorders and assisted reproductive technology. Fertil Steril (2009) 1.73
Association of assisted reproductive technology (ART) treatment and parental infertility diagnosis with autism in ART-conceived children. Hum Reprod (2014) 1.73
Epigenetic disruption of the PIWI pathway in human spermatogenic disorders. PLoS One (2012) 1.64
The use of genomics, proteomics, and metabolomics in identifying biomarkers of male infertility. Fertil Steril (2013) 1.49
Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men. Eur J Hum Genet (2010) 1.48
Environmental epigenetics: prospects for studying epigenetic mediation of exposure-response relationships. Hum Genet (2012) 1.47
DNA methylation errors at imprinted loci after assisted conception originate in the parental sperm. Eur J Hum Genet (2009) 1.36
Epigenetics and its role in male infertility. J Assist Reprod Genet (2012) 1.27
Oxidative DNA damage impairs global sperm DNA methylation in infertile men. J Assist Reprod Genet (2009) 1.25
Genome-wide analysis identifies changes in histone retention and epigenetic modifications at developmental and imprinted gene loci in the sperm of infertile men. Hum Reprod (2011) 1.18
Novel insights into DNA methylation features in spermatozoa: stability and peculiarities. PLoS One (2012) 1.16
Integrative DNA methylation and gene expression analyses identify DNA packaging and epigenetic regulatory genes associated with low motility sperm. PLoS One (2011) 1.13
Incorrect DNA methylation of the DAZL promoter CpG island associates with defective human sperm. Hum Reprod (2010) 1.12
Assisted reproduction treatment and epigenetic inheritance. Hum Reprod Update (2012) 1.11
Low frequency of imprinting defects in ICSI children born small for gestational age. Eur J Hum Genet (2008) 1.05
Idiopathic male infertility is strongly associated with aberrant promoter methylation of methylenetetrahydrofolate reductase (MTHFR). PLoS One (2010) 1.04
Specific changes in the expression of imprinted genes in prostate cancer--implications for cancer progression and epigenetic regulation. Asian J Androl (2012) 0.95
Environmentally induced epigenetic transgenerational inheritance of male infertility. Curr Opin Genet Dev (2014) 0.95
Novel insights into the genetic and epigenetic paternal contribution to the human embryo. Clinics (Sao Paulo) (2013) 0.95
Methylation of AR locus does not always reflect X chromosome inactivation state. Blood (2012) 0.93
Bringing epigenetics into the diagnostics of the andrology laboratory: challenges and perspectives. Asian J Androl (2014) 0.88
Epigenetic regulation of the RHOX homeobox gene cluster and its association with human male infertility. Hum Mol Genet (2013) 0.87
Stability of genomic imprinting in human induced pluripotent stem cells. BMC Genet (2013) 0.85
Restoring fertility in sterile childhood cancer survivors by autotransplanting spermatogonial stem cells: are we there yet? Biomed Res Int (2013) 0.85
Association of the MTHFR A1298C variant with unexplained severe male infertility. PLoS One (2012) 0.85
Imprinting methylation errors in ART. Reprod Med Biol (2014) 0.84
Routine cryopreservation of spermatozoa is safe--evidence from the DNA methylation pattern of nine spermatozoa genes. J Assist Reprod Genet (2012) 0.84
Seminal biomarkers for the evaluation of male infertility. Asian J Androl (2016) 0.84
Different sperm sources and parameters can influence intracytoplasmic sperm injection outcomes before embryo implantation. J Zhejiang Univ Sci B (2012) 0.84
MTHFR 677C>T polymorphism increases the male infertility risk: a meta-analysis involving 26 studies. PLoS One (2015) 0.83
Analysis of the methylation pattern of six gene promoters in sperm of men with abnormal protamination. Asian J Androl (2011) 0.83
Genes and Conditions Controlling Mammalian Pre- and Post-implantation Embryo Development. Curr Genomics (2015) 0.83
Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime health. Clin Epigenetics (2015) 0.83
Significant impact of the MTHFR polymorphisms and haplotypes on male infertility risk. PLoS One (2013) 0.82
Variable imprinting of the MEST gene in human preimplantation embryos. Eur J Hum Genet (2012) 0.82
Sperm transcriptome profiling in oligozoospermia. J Assist Reprod Genet (2011) 0.82
The paternally imprinted DLK1-GTL2 locus is differentially methylated in embryonal and alveolar rhabdomyosarcomas. Int J Oncol (2013) 0.82
Semen samples showing an increased rate of spermatozoa with imprinting errors have a negligible effect in the outcome of assisted reproduction techniques. Epigenetics (2012) 0.82
The current status of biomarkers for predicting toxicity. Expert Opin Drug Metab Toxicol (2013) 0.81
DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins. Eur J Pediatr (2009) 0.80
Biomarkers of chemotherapy-induced testicular damage. Fertil Steril (2013) 0.80
Lack of association of MTHFR rs1801133 polymorphism and CTCFL mutations with sperm methylation errors in infertile patients. J Assist Reprod Genet (2013) 0.80
A clinical appraisal of the genetic basis in unexplained male infertility. J Hum Reprod Sci (2013) 0.80
Effects of increased paternal age on sperm quality, reproductive outcome and associated epigenetic risks to offspring. Reprod Biol Endocrinol (2015) 0.80
Direct but no transgenerational effects of decitabine and vorinostat on male fertility. PLoS One (2015) 0.77
Identification and characterization of methylation-dependent/independent DNA regulatory elements in the human SLC9B1 gene. Gene (2015) 0.77
Male Pronuclear Formation using Dog Sperm Derived from Ectopic Testicular Xenografts, Testis, and Epididymis. Avicenna J Med Biotechnol (2014) 0.76
A multi-faceted approach to understanding male infertility: gene mutations, molecular defects and assisted reproductive techniques (ART). J Assist Reprod Genet (2014) 0.76
Quality evaluation of IVM embryo and imprinting genes of IVM babies. J Assist Reprod Genet (2013) 0.76
Normal epigenetic inheritance in mice conceived by in vitro fertilization and embryo transfer. J Zhejiang Univ Sci B (2011) 0.76
Repeated assessment by high-throughput assay demonstrates that sperm DNA methylation levels are highly reproducible. Fertil Steril (2011) 0.76
High-throughput detection of aberrant imprint methylation in the ovarian cancer by the bisulphite PCR-Luminex method. BMC Med Genomics (2012) 0.76
Methylation loss at H19 imprinted gene correlates with methylenetetrahydrofolate reductase gene promoter hypermethylation in semen samples from infertile males. Epigenetics (2013) 0.76
Assisted Reproductive Technologies (ART) with baboons generate live offspring: a nonhuman primate model for ART and reproductive sciences. Reprod Sci (2010) 0.76
Haploinsufficiency of the paternal-effect gene Dnmt3L results in transient DNA hypomethylation in progenitor cells of the male germline. Hum Reprod (2012) 0.75
Effect of temozolomide on male gametes: an epigenetic risk to the offspring? J Assist Reprod Genet (2013) 0.75
H19 gene methylation status is associated with male infertility. Exp Ther Med (2016) 0.75
Rapid method for the isolation of mammalian sperm DNA. Biotechniques (2015) 0.75
Genetic and Epigenetic Changes After Spermatogonial Stem Cell Culture and Transplantation. EJIFCC (2014) 0.75
Genome-Scale Assessment of Age-Related DNA Methylation Changes in Mouse Spermatozoa. PLoS One (2016) 0.75
The role of epigenetics in idiopathic male infertility. J Assist Reprod Genet (2016) 0.75
Factors associated with aberrant imprint methylation and oligozoospermia. Sci Rep (2017) 0.75
From the Cover: Sperm Molecular Biomarkers Are Sensitive Indicators of Testicular Injury following Subchronic Model Toxicant Exposure. Toxicol Sci (2016) 0.75
Epigenetic Alterations in Density Selected Human Spermatozoa for Assisted Reproduction. PLoS One (2015) 0.75
Endogenous siRNAs from naturally formed dsRNAs regulate transcripts in mouse oocytes. Nature (2008) 10.11
Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting. Nature (2004) 7.42
Size-selective loosening of the blood-brain barrier in claudin-5-deficient mice. J Cell Biol (2003) 5.74
DNA methylation of retrotransposon genes is regulated by Piwi family members MILI and MIWI2 in murine fetal testes. Genes Dev (2008) 5.58
Identification and characterization of two novel classes of small RNAs in the mouse germline: retrotransposon-derived siRNAs in oocytes and germline small RNAs in testes. Genes Dev (2006) 4.97
ZO-1 and ZO-2 independently determine where claudins are polymerized in tight-junction strand formation. Cell (2006) 4.61
Targets and dynamics of promoter DNA methylation during early mouse development. Nat Genet (2010) 4.27
CLASP1 and CLASP2 bind to EB1 and regulate microtubule plus-end dynamics at the cell cortex. J Cell Biol (2005) 3.54
Role of the Dnmt3 family in de novo methylation of imprinted and repetitive sequences during male germ cell development in the mouse. Hum Mol Genet (2007) 3.27
Tricellulin constitutes a novel barrier at tricellular contacts of epithelial cells. J Cell Biol (2005) 3.05
Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development. Genes Dev (2008) 2.99
The TDRD9-MIWI2 complex is essential for piRNA-mediated retrotransposon silencing in the mouse male germline. Dev Cell (2009) 2.96
Dynamic stage-specific changes in imprinted differentially methylated regions during early mammalian development and prevalence of non-CpG methylation in oocytes. Development (2011) 2.28
Role for piRNAs and noncoding RNA in de novo DNA methylation of the imprinted mouse Rasgrf1 locus. Science (2011) 2.17
Synergistic function of DNA methyltransferases Dnmt3a and Dnmt3b in the methylation of Oct4 and Nanog. Mol Cell Biol (2007) 2.15
Unregulated expression of the imprinted genes H19 and Igf2r in mouse uniparental fetuses. J Biol Chem (2002) 2.01
Tsix silences Xist through modification of chromatin structure. Dev Cell (2005) 1.97
Multi-PDZ domain protein 1 (MUPP1) is concentrated at tight junctions through its possible interaction with claudin-1 and junctional adhesion molecule. J Biol Chem (2001) 1.96
External antigen uptake by Langerhans cells with reorganization of epidermal tight junction barriers. J Exp Med (2009) 1.95
MITOPLD is a mitochondrial protein essential for nuage formation and piRNA biogenesis in the mouse germline. Dev Cell (2011) 1.94
Establishment and characterization of cultured epithelial cells lacking expression of ZO-1. J Biol Chem (2004) 1.94
Changes in microRNA expression levels correlate with clinicopathological features and prognoses in endometrial serous adenocarcinomas. Cancer Sci (2009) 1.85
MVH in piRNA processing and gene silencing of retrotransposons. Genes Dev (2010) 1.84
A tripartite paternally methylated region within the Gpr1-Zdbf2 imprinted domain on mouse chromosome 1 identified by meDIP-on-chip. Nucleic Acids Res (2010) 1.83
High concentrations of HGF inhibit skeletal muscle satellite cell proliferation in vitro by inducing expression of myostatin: a possible mechanism for reestablishing satellite cell quiescence in vivo. Am J Physiol Cell Physiol (2009) 1.82
Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution. PLoS Genet (2007) 1.79
Tight junctions in Schwann cells of peripheral myelinated axons: a lesson from claudin-19-deficient mice. J Cell Biol (2005) 1.69
Multicenter phase II study of fertility-sparing treatment with medroxyprogesterone acetate for endometrial carcinoma and atypical hyperplasia in young women. J Clin Oncol (2007) 1.66
Sentinel lymph node detection in patients with endometrial cancer. Gynecol Oncol (2004) 1.64
Genetic significance of skewed X-chromosome inactivation in premature ovarian failure. Am J Med Genet A (2004) 1.63
Mouse oocyte methylomes at base resolution reveal genome-wide accumulation of non-CpG methylation and role of DNA methyltransferases. PLoS Genet (2013) 1.57
Tight junction-associated MARVEL proteins marveld3, tricellulin, and occludin have distinct but overlapping functions. Mol Biol Cell (2010) 1.51
De novo DNA methylation independent establishment of maternal imprint on X chromosome in mouse oocytes. Genesis (2008) 1.51
Crucial role of antisense transcription across the Xist promoter in Tsix-mediated Xist chromatin modification. Development (2007) 1.50
Compartmentalization established by claudin-11-based tight junctions in stria vascularis is required for hearing through generation of endocochlear potential. J Cell Sci (2004) 1.50
Claudin-2-deficient mice are defective in the leaky and cation-selective paracellular permeability properties of renal proximal tubules. Proc Natl Acad Sci U S A (2010) 1.49
Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia. J Cell Biol (2004) 1.47
LSR defines cell corners for tricellular tight junction formation in epithelial cells. J Cell Sci (2011) 1.47
Vitamin E as a treatment for ulcerative dermatitis in C57BL/6 mice and strains with a C57BL/6 background. Contemp Top Lab Anim Sci (2005) 1.46
Inhibition of estrogen actions in human gynecological malignancies: new aspects of endocrine therapy for endometrial cancer and ovarian cancer. Mol Cell Endocrinol (2010) 1.45
Outcomes of fertility-sparing surgery for stage I epithelial ovarian cancer: a proposal for patient selection. J Clin Oncol (2010) 1.43
Characterization of side-population cells in human normal endometrium. Hum Reprod (2007) 1.42
Successful conservative treatment of a cesarean scar pregnancy with uterine artery embolization. Tohoku J Exp Med (2005) 1.41
Prostaglandin E2 via steroidogenic factor-1 coordinately regulates transcription of steroidogenic genes necessary for estrogen synthesis in endometriosis. J Clin Endocrinol Metab (2008) 1.41
A novel culture system for mouse spermatid maturation which produces elongating spermatids capable of inducing calcium oscillation during fertilization and embryonic development. J Assist Reprod Genet (2010) 1.40
Loss of occludin affects tricellular localization of tricellulin. Mol Biol Cell (2008) 1.40
Re-investigation and RNA sequencing-based identification of genes with placenta-specific imprinted expression. Hum Mol Genet (2011) 1.39
De novo DNA methylation is dispensable for the initiation and propagation of X chromosome inactivation. Development (2004) 1.39
An atomic model of Zfp57 recognition of CpG methylation within a specific DNA sequence. Genes Dev (2012) 1.38
DNA methylation errors at imprinted loci after assisted conception originate in the parental sperm. Eur J Hum Genet (2009) 1.36
A proximal conserved repeat in the Xist gene is essential as a genomic element for X-inactivation in mouse. Development (2008) 1.35
Genomic imprinting in mammals: its life cycle, molecular mechanisms and reprogramming. Cell Res (2011) 1.33
Small RNA class transition from siRNA/piRNA to miRNA during pre-implantation mouse development. Nucleic Acids Res (2010) 1.27
Megaintestine in claudin-15-deficient mice. Gastroenterology (2007) 1.25
Stochastic imprinting in the progeny of Dnmt3L-/- females. Hum Mol Genet (2006) 1.24
Developing 100 ps-resolved X-ray structural analysis capabilities on beamline NW14A at the Photon Factory Advanced Ring. J Synchrotron Radiat (2007) 1.22
Meiotic and epigenetic aberrations in Dnmt3L-deficient male germ cells. Mol Reprod Dev (2006) 1.21
Interaction of alpha1-adrenoceptor subtypes with different G proteins induces opposite effects on cardiac L-type Ca2+ channel. Circ Res (2008) 1.21
Biological roles of estrogen and progesterone in human endometrial carcinoma--new developments in potential endocrine therapy for endometrial cancer. Endocr J (2007) 1.20
JACOP, a novel plaque protein localizing at the apical junctional complex with sequence similarity to cingulin. J Biol Chem (2004) 1.20
Conditional knockdown of Nanog induces apoptotic cell death in mouse migrating primordial germ cells. Development (2009) 1.20
Isolation, characterization, and in vitro and in vivo differentiation of putative thecal stem cells. Proc Natl Acad Sci U S A (2007) 1.19
Parvovirus B19 and the pathogenesis of anaemia. Rev Med Virol (2003) 1.18
Three novel DNMT3B mutations in Japanese patients with ICF syndrome. Am J Med Genet (2002) 1.18
The E3 ubiquitin ligase LNX1p80 promotes the removal of claudins from tight junctions in MDCK cells. J Cell Sci (2009) 1.17
Molecular dissection of premalignant colorectal lesions reveals early onset of the CpG island methylator phenotype. Am J Pathol (2012) 1.17
Decreased expression of 14-3-3 sigma is associated with advanced disease in human epithelial ovarian cancer: its correlation with aberrant DNA methylation. Clin Cancer Res (2004) 1.16
Endometrioid uterine cancer: histopathological risk factors of local and distant recurrence. Gynecol Oncol (2008) 1.15
Epigenetic silencing of the imprinted gene ZAC by DNA methylation is an early event in the progression of human ovarian cancer. Int J Cancer (2005) 1.15
Genetic evidence for Dnmt3a-dependent imprinting during oocyte growth obtained by conditional knockout with Zp3-Cre and complete exclusion of Dnmt3b by chimera formation. Genes Cells (2010) 1.14
Electron tomography of cryofixed, isometrically contracting insect flight muscle reveals novel actin-myosin interactions. PLoS One (2010) 1.13
Novel conserved elements upstream of the H19 gene are transcribed and act as mesodermal enhancers. Development (2002) 1.13
Lysyl 5-hydroxylation, a novel histone modification, by Jumonji domain containing 6 (JMJD6). J Biol Chem (2013) 1.12
Clinical experience with combination paclitaxel and carboplatin therapy for advanced or recurrent carcinosarcoma of the uterus. Gynecol Oncol (2004) 1.12
Identification of the mouse paternally expressed imprinted gene Zdbf2 on chromosome 1 and its imprinted human homolog ZDBF2 on chromosome 2. Genomics (2009) 1.11
Identification of FOXC1 as a TGF-beta1 responsive gene and its involvement in negative regulation of cell growth. Genomics (2002) 1.10
Loss of the maternal imprint in Dnmt3Lmat-/- mice leads to a differentiation defect in the extraembryonic tissue. Dev Biol (2006) 1.10
Decrease and senescence of endothelial progenitor cells in patients with preeclampsia. J Clin Endocrinol Metab (2005) 1.10
Microarray analysis of promoter methylation in lung cancers. J Hum Genet (2006) 1.09
Evidence-based guidelines for treatment of cervical cancer in Japan: Japan Society of Gynecologic Oncology (JSGO) 2007 edition. Int J Clin Oncol (2010) 1.09
alpha1-adrenoceptor stimulation potentiates L-type Ca2+ current through Ca2+/calmodulin-dependent PK II (CaMKII) activation in rat ventricular myocytes. Proc Natl Acad Sci U S A (2005) 1.09
The Tohoku Medical Megabank Project: Design and Mission. J Epidemiol (2016) 1.08
Accumulation and loss of asymmetric non-CpG methylation during male germ-cell development. Nucleic Acids Res (2012) 1.05
Mutations in DNA methyltransferase DNMT3B in ICF syndrome affect its regulation by DNMT3L. Hum Mol Genet (2006) 1.05
Mammalian CLASPs are required for mitotic spindle organization and kinetochore alignment. Genes Cells (2006) 1.05
Down-regulation of cIAP2 enhances 5-FU sensitivity through the apoptotic pathway in human colon cancer cells. Cancer Sci (2009) 1.04
Expression of vasohibin as a novel endothelium-derived angiogenesis inhibitor in endometrial cancer. Cancer Sci (2008) 1.04