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The obstructive interval predicts pregnancy rates in post-vasectomy patients undergoing ICSI with surgical sperm retrieval
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MicroRNAs Absent in Caput Sperm Are Required for Normal Embryonic Development
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Caput Epididymidal Mouse Sperm Support Full Development
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Evaluation of the morphokinetic parameters and development of pre-implantation embryos obtained by testicular, epididymal and ejaculate spermatozoa using time-lapse imaging system
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Judit Castillo et al.
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Small RNAs Are Trafficked from the Epididymis to Developing Mammalian Sperm
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MYC and DNMT3A-mediated DNA methylation represses microRNA-200b in triple negative breast cancer
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Testicular Spermatozoa Are of Better Quality Than Epididymal Spermatozoa in Patients With Obstructive Azoospermia
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The Rodent-Specific MicroRNA Cluster within the Sfmbt2 Gene Is Imprinted and Essential for Placental Development
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Biogenesis and function of tRNA fragments during sperm maturation and fertilization in mammals
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The MicroRNA Signature of Mouse Spermatozoa Is Substantially Modified During Epididymal Maturation
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BIOLOGY OF REPRODUCTION (2015)
Live birth rates after MESA or TESE in men with obstructive azoospermia: is there a difference?
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HUMAN REPRODUCTION (2015)
Transgenerational epigenetic programming via sperm microRNA recapitulates effects of paternal stress
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
The role, mechanism and potentially novel biomarker of microRNA-17-92 cluster in macrosomia
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RNA-mediated paternal heredity of diet-induced obesity and metabolic disorders
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Obstructive Azoospermia
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Epididymosomes Convey Different Repertoires of MicroRNAs Throughout the Bovine Epididymis
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The imprinted polycomb group gene Sfmbt2 is required for trophoblast maintenance and placenta development
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DEVELOPMENT (2013)
microRNA signature is altered in both human epididymis and seminal microvesicles following vasectomy
Clemence Belleannee et al.
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Peter A. Jones
NATURE REVIEWS GENETICS (2012)
Sperm-borne microRNA-34c is required for the first cleavage division in mouse
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans
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Targeted deletion reveals essential and overlapping functions of the miR-17∼92 family of miRNA clusters
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