| scholarly article | Q13442814 |
| P50 | author | Pierre Jouannet | Q16027696 |
| P2093 | author name string | M Jeanpierre | |
| C Vasseur | |||
| A Pàldi | |||
| L Cuisset | |||
| A Kerjean | |||
| D Le Tessier | |||
| J M Dupont | |||
| P433 | issue | 14 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | spermatogenesis | Q36961 |
| P304 | page(s) | 2183-7 | |
| P577 | publication date | 2000-09-01 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis | |
| P478 | volume | 9 |
| Q48864404 | A global disorder of imprinting in the human female germ line. |
| Q33719048 | A paternal environmental legacy: evidence for epigenetic inheritance through the male germ line. |
| Q41440845 | Aberrant DNA methylation of imprinted loci in hepatocellular carcinoma and after in vitro exposure to common risk factors |
| Q50645854 | Aberrant DNA methylation of imprinted loci in superovulated oocytes. |
| Q34589530 | Altered of microRNA expression level in oligospermic patients |
| Q28217059 | An imprinted PEG1/MEST antisense expressed predominantly in human testis and in mature spermatozoa |
| Q36643840 | Are cranial germ cell tumours really tumours of germ cells? |
| Q35766037 | Assisted reproduction treatment and epigenetic inheritance. |
| Q33325809 | Association of ATRX with pericentric heterochromatin and the Y chromosome of neonatal mouse spermatogonia |
| Q33948369 | Bisulfite genomic sequencing of microdissected cells |
| Q90043077 | Comparison of perinatal outcomes between spontaneous vs. commissioned cycles in gestational carriers for single and same-sex male intended parents |
| Q39147599 | Comparison of the Clinical Outcomes of Intracytoplasmic Sperm Injection Between Spermatozoa Retrieved From Testicular Biopsy and From Ejaculate in Cryptozoospermia Patients |
| Q34786014 | DNA methylation analysis reveals distinct methylation signatures in pediatric germ cell tumors |
| Q47837042 | DNA methylation imprinting errors in spermatogenic cells from maturation arrest azoospermic patients |
| Q37288310 | DNA methylation in spermatogenesis and male infertility |
| Q39362648 | DNA methylation in spermatozoa as a prospective marker in andrology |
| Q35008254 | DNMT1 and AIM1 Imprinting in human placenta revealed through a genome-wide screen for allele-specific DNA methylation. |
| Q46469894 | De novo methylation in male germ cells of the common marmoset monkey occurs during postnatal development and is maintained in vitro |
| Q50664633 | Dynamic CpG and non-CpG methylation of the Peg1/Mest gene in the mouse oocyte and preimplantation embryo. |
| Q52660446 | Effects of Cadmium Exposure on DNA Methylation at Imprinting Control Regions and Genome-Wide in Mothers and Newborn Children. |
| Q37287350 | Endonuclease-sensitive regions of human spermatozoal chromatin are highly enriched in promoter and CTCF binding sequences |
| Q91844308 | Epigenetic Transgenerational Inheritance |
| Q38554712 | Epigenetic alterations in sperm associated with male infertility |
| Q39351600 | Epigenetic consequences of a changing human diet |
| Q73549548 | Epigenetic detection of human chromosome 14 uniparental disomy |
| Q36830244 | Epigenetic profile of testicular germ cell tumours |
| Q50654192 | Epigenetic status of the H19 locus in human oocytes following in vitro maturation. |
| Q34567418 | Epigenetics and phenotypic variation in mammals. |
| Q37989167 | Epigenetics: a way to understand the origin and biology of testicular germ cell tumors |
| Q82363568 | Erasure of methylation imprint at the promoter and CTCF-binding site upstream of H19 in human testicular germ cell tumors of adolescents indicate their fetal germ cell origin |
| Q61852021 | Estudo do imprinting genómico em espermatozóides de pacientes com oligozoospermia |
| Q51668667 | Evaluation of DNA methylation at imprinted DMRs in the spermatozoa of oligozoospermic men in association with MTHFR C677T genotype. |
| Q33649243 | Fate of induced pluripotent stem cells following transplantation to murine seminiferous tubules |
| Q37056903 | Functional characterization of a testis-specific DNA binding activity at the H19/Igf2 imprinting control region. |
| Q34374761 | Functional neuronal cells generated by human parthenogenetic stem cells |
| Q36251483 | Gametes and embryo epigenetic reprogramming affect developmental outcome: implication for assisted reproductive technologies |
| Q36730925 | Gene-environment interactions and epigenetic basis of human diseases |
| Q35598887 | Genome wide DNA methylation profiles provide clues to the origin and pathogenesis of germ cell tumors |
| Q34691192 | Genome-wide promoter methylation profile of human testis and epididymis: identified from cell-free seminal DNA |
| Q47440233 | Genomic imprinting in disruptive spermatogenesis |
| Q35037387 | Genomic imprinting: could the chromatin structure be the driving force? |
| Q35561940 | Germline and somatic imprinting in the nonhuman primate highlights species differences in oocyte methylation. |
| Q92962893 | High-resolution analysis of germ cells from men with sex chromosomal aneuploidies reveals normal transcriptome but impaired imprinting |
| Q35097679 | Human DAZL, DAZ and BOULE genes modulate primordial germ-cell and haploid gamete formation |
| Q28654301 | Hypothesis: gonadal temperature influences sex-specific imprinting |
| Q80408702 | IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia |
| Q54655211 | IGF2/H19 imprinting analysis of human germ cell tumors (GCTs) using the methylation-sensitive single-nucleotide primer extension method reflects the origin of GCTs in different stages of primordial germ cell development. |
| Q33276952 | Identification and characterization of bovine regulator of telomere length elongation helicase gene (RTEL): molecular cloning, expression distribution, splice variants and DNA methylation profile |
| Q21092496 | Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution |
| Q48110063 | Impairment of sperm DNA methylation in male infertility: a meta-analytic study. |
| Q36917079 | In vitro spermatogenesis as a method to bypass pre-meiotic or post-meiotic barriers blocking the spermatogenetic process: genetic and epigenetic implications in assisted reproductive technology |
| Q64086187 | Increased methylation upstream of the MEG3 promotor is observed in acute myeloid leukemia patients with better overall survival |
| Q34014319 | Inter- and intra-individual variation in allele-specific DNA methylation and gene expression in children conceived using assisted reproductive technology |
| Q36524664 | Intracytoplasmic sperm injection--an assisted reproduction technique that should make us cautious about imprinting deregulation |
| Q49341161 | In Vitro Modeling of Human Germ Cell Development Using Pluripotent Stem Cells. |
| Q37312589 | Isolation and characterization of pluripotent human spermatogonial stem cell-derived cells |
| Q33906102 | Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome. |
| Q50640391 | Methylation analysis of the intergenic differentially methylated region of DLK1-GTL2 in human. |
| Q41856493 | Methylation loss at H19 imprinted gene correlates with methylenetetrahydrofolate reductase gene promoter hypermethylation in semen samples from infertile males |
| Q36853758 | Origins and consequences of DNA damage in male germ cells. |
| Q28392407 | Oxidative DNA damage impairs global sperm DNA methylation in infertile men |
| Q34432589 | Paternal exposure to drugs and environmental chemicals: effects on progeny outcome |
| Q34578946 | Paternal obesity is associated with IGF2 hypomethylation in newborns: results from a Newborn Epigenetics Study (NEST) cohort |
| Q58088530 | Reactive oxygen species-induced alterations in H19-Igf2 methylation patterns, seminal plasma metabolites, and semen quality |
| Q37338436 | Role of ART in imprinting disorders |
| Q42531468 | Routine cryopreservation of spermatozoa is safe--evidence from the DNA methylation pattern of nine spermatozoa genes |
| Q36312101 | Semen samples showing an increased rate of spermatozoa with imprinting errors have a negligible effect in the outcome of assisted reproduction techniques |
| Q37686537 | Significance of microRNA targeted estrogen receptor in male fertility |
| Q34328467 | Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men |
| Q38745063 | Sperm DNA methylation of H19 imprinted gene and male infertility. |
| Q36905922 | Spermatozoal RNA as reservoir, marker and carrier of epigenetic information: implications for cloning |
| Q36927144 | The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region |
| Q28254096 | The implications of heterogeneous DNA methylation for the accurate quantification of methylation |
| Q37401950 | The paternally imprinted DLK1-GTL2 locus is differentially methylated in embryonal and alveolar rhabdomyosarcomas |
| Q36943376 | The stem cell identity of testicular cancer |
| Q47962620 | What the human sperm methylome tells us. |
| Q33309935 | Widespread epigenetic abnormalities suggest a broad DNA methylation erasure defect in abnormal human sperm |
| Q83185162 | [Influence of the male genomic imprinting on the reproduction] |
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