Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 75 checked references that resolve
resolves10.1002/mrd.1051Nuclear fragmentation characterises paraspermiogenesis in <i>Tubifex tubifex</i> (Annelida, Oligochaeta)
resolves10.1038/215862a0Correlation between Sperm “Redundancy” and Chiasma Frequency
resolves10.1530/jrf.0.0390297SPERMATOZOA: THE PROBABLE SELECTION OF A SMALL POPULATION BY THE GENITAL TRACT OF THE FEMALE RABBIT
resolves10.1093/molehr/3.1.61Size differences between human X and Y spermatozoa and prefertilization diagnosis
resolves10.1054/tice.2001.0215Binucleate and biflagellate spermatozoa in Tricholepidion gertschi Wygodzynsky (Insecta, Zygentoma)
resolves10.1016/0889-1605(88)90035-3Structure and function of the metachronal wave in Tubifex tubifex spermatozeugmata (Annelida, Oligochaeta)
resolves10.1530/jrf.0.0620337Fertilization following mixed insemination with 'cervix-selected' and 'unselected' spermatozoa in the rabbit
resolves10.1530/jrf.0.0700075Fertilizing rabbit spermatozoa are not selected as a special population by the female tract
resolves10.1530/REP-06-0292A molecular analysis of the population of mRNA in bovine spermatozoa
resolves10.1101/gad.367606Mammalian sperm translate nuclear-encoded proteins by mitochondrial-type ribosomes
resolves10.1023/A:1016142902511Obstructive Role of the Dimorphic Sperm in a Non-copulatory Marine Sculpin, Hemilepidotus gilberti, to Prevent Other Males' Eusperm from Fertilization
resolves10.1023/A:1020507120692Dimorphic Sperm Influence Semen Distribution in a Non-copulatory Sculpin Hemilepidotus Gilberti
resolves10.1006/dbio.1995.1252Postmeiotic Transcription of X and Y Chromosomal Genes during Spermatogenesis in the Mouse
resolves10.1530/rep.1.00134Concepts in sperm heterogeneity, sperm selection and sperm competition as biological foundations for laboratory tests of semen quality
resolves10.1098/rspb.1994.0067Sib competition and sperm competitiveness: an answer to ‘Why so many sperms?’ and the recombination/sperm number correlation
resolves10.1095/biolreprod52.4.947Sperm Pairing in the Opossum Increases the Efficiency of Sperm Movement in a Viscous Environment1
resolves10.1098/rspb.1999.0929No evidence for killer sperm or other selective interactions between human spermatozoa in ejaculates of different males<i>in vitro</i>
resolves10.1007/s003359900342Mapping of a haploid transcribed and translated sperm-specific gene to the mouse X Chromosome
resolves10.1530/rep.0.1210267Characterization of northern pintail (Anas acuta) ejaculate and the effect of sperm preservation on fertility
resolves10.1038/313143a0Transmission distortion of t-haplotypes is due to interactions between meiotic partners
resolves10.1086/284200Eunuchs: The Role of Apyrene Sperm in Lepidoptera?
resolves10.1002/ar.1092360307Why do spermatozoa of American marsupials form pairs? A clue from the analysis of sperm‐pairing in the epididymis of the grey short‐tailed opossum, <i>Monodelphis domestica</i>
resolves10.1002/j.1939-4640.2001.tb02194.xMorphologically Distinct Sperm Subpopulations Defined by Fourier Shape Descriptors in Fresh Ejaculates Correlate With Variation in Boar Semen Quality Following Cryopreservation
resolves10.1093/genetics/93.3.587SPORE KILLER, A CHROMOSOMAL FACTOR IN NEUROSPORA THAT KILLS MEIOTIC PRODUCTS NOT CONTAINING IT
resolves10.1093/biolreprod/63.2.469Spermatid-Specific Expression of the Novel X-Linked Gene Product SPAN-X Localized to the Nucleus of Human Spermatozoa1
resolves10.1086/285171Sex-Ratio Distortion Caused by Meiotic Drive in Mosquitoes
resolves10.1007/BF00126980The genetic basis of resistance and sensitivity to the meiotic drive gene D in the mosquito Aedes aegypti L.
resolves10.1002/jez.1400850106The function of the apyrene spermatozoa of Goniobasis laqueata (say) I. The behavior of the apyrene and eupyrene spermatozoa under natural and artificial conditions
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