On the public citation graph

Ion channels that control fertility in mammalian spermatozoa

0 signed · 196 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cm.970100309openalex-snapshot

Calcium regulation of flagellar curvature and swimming pattern in triton X‐100–extracted rat sperm

inferredcites →https://doi.org/10.1002/jcp.21075openalex-snapshot

Expression, localization and functions in acrosome reaction and sperm motility of CaV3.1 and CaV3.2 channels in sperm cells: An evaluation from CaV3.1 and CaV3.2 deficient mice

inferredcites →https://doi.org/10.1006/dbio.1995.1304openalex-snapshot

Sperm Membrane Potential: Hyperpolarization during Capacitation Regulates Zona Pellucida-Dependent Acrosomal Secretion

inferredcites →https://doi.org/10.1006/dbio.1999.9428openalex-snapshot

Cholesterol Efflux-Mediated Signal Transduction in Mammalian Sperm: Cholesterol Release Signals an Increase in Protein Tyrosine Phosphorylation during Mouse Sperm Capacitation

inferredcites →https://doi.org/10.1016/j.anireprosci.2004.04.030openalex-snapshot

Bicarbonate and its role in mammalian sperm function

inferredcites →https://doi.org/10.1016/s0015-0282(16)42801-3openalex-snapshot

Hydrogen Ion and Carbon Dioxide Content of the Oviductal Fluid of the Rhesus Monkey (Macaca Mulatta)

inferredcites →https://doi.org/10.1016/s0092-8674(00)00013-1openalex-snapshot

Congenital Deafness and Sinoatrial Node Dysfunction in Mice Lacking Class D L-Type Ca2+ Channels

inferredcites →https://doi.org/10.1016/s0378-4320(03)00134-9openalex-snapshot

Sperm capacitation in the porcine oviduct

inferredcites →https://doi.org/10.1016/s0378-4320(04)00085-5openalex-snapshot

Bicarbonate and its role in mammalian sperm function

inferredcites →https://doi.org/10.1016/s0896-6273(01)00343-9openalex-snapshot

Lack of the Burst Firing of Thalamocortical Relay Neurons and Resistance to Absence Seizures in Mice Lacking α1G T-Type Ca2+ Channels

inferredcites →https://doi.org/10.1038/35098027openalex-snapshot

A sperm ion channel required for sperm motility and male fertility

inferredcites →https://doi.org/10.1038/nature02246openalex-snapshot

The mitochondrial calcium uniporter is a highly selective ion channel

inferredcites →https://doi.org/10.1038/nature04417openalex-snapshot

Whole-cell patch-clamp measurements of spermatozoa reveal an alkaline-activated Ca2+ channel

inferredcites →https://doi.org/10.1038/ncb0307-235openalex-snapshot

[Ca2+]i signalling in sperm — making the most of what you've got

inferredcites →https://doi.org/10.1038/ncb1072openalex-snapshot

A new sperm-specific Na+/H+ Exchanger required for sperm motility and fertility

inferredcites →https://doi.org/10.1038/sj.ejhg.5200991openalex-snapshot

CATSPER2, a human autosomal nonsyndromic male infertility gene

inferredcites →https://doi.org/10.1073/pnas.0400050101openalex-snapshot

Mice deficient for soluble adenylyl cyclase are infertile because of a severe sperm-motility defect

inferredcites →https://doi.org/10.1073/pnas.0407708101openalex-snapshot

Glyceraldehyde 3-phosphate dehydrogenase-S, a sperm-specific glycolytic enzyme, is required for sperm motility and male fertility

inferredcites →https://doi.org/10.1073/pnas.0610286104openalex-snapshot

All four CatSper ion channel proteins are required for male fertility and sperm cell hyperactivated motility

inferredcites →https://doi.org/10.1073/pnas.0611296104openalex-snapshot

A sperm-specific Na + /H + exchanger (sNHE) is critical for expression and in vivo bicarbonate regulation of the soluble adenylyl cyclase (sAC)

inferredcites →https://doi.org/10.1073/pnas.0702018104openalex-snapshot

KSper, a pH-sensitive K + current that controls sperm membrane potential

inferredcites →https://doi.org/10.1073/pnas.081089398openalex-snapshot

Functional disorders of the sympathetic nervous system in mice lacking the α 1B subunit (Ca v 2.2) of N-type calcium channels

inferredcites →https://doi.org/10.1073/pnas.100124197openalex-snapshot

Altered pain responses in mice lacking α 1E subunit of the voltage-dependent Ca 2+ channel

inferredcites →https://doi.org/10.1073/pnas.1635054100openalex-snapshot

A multitude of genes expressed solely in meiotic or postmeiotic spermatogenic cells offers a myriad of contraceptive targets

inferredcites →https://doi.org/10.1073/pnas.2136654100openalex-snapshot

Hyperactivated sperm motility driven by CatSper2 is required for fertilization

inferredcites →https://doi.org/10.1073/pnas.221454998openalex-snapshot

A voltage-gated ion channel expressed specifically in spermatozoa

inferredcites →https://doi.org/10.1073/pnas.2536658100openalex-snapshot

CatSper1 required for evoked Ca 2+ entry and control of flagellar function in sperm

inferredcites →https://doi.org/10.1073/pnas.96.12.6757openalex-snapshot

Control of the low voltage-activated calcium channel of mouse sperm by egg ZP3 and by membrane hyperpolarization during capacitation

inferredcites →https://doi.org/10.1073/pnas.96.13.7553openalex-snapshot

Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3

inferredcites →https://doi.org/10.1073/pnas.96.26.15245openalex-snapshot

Ablation of P/Q-type Ca 2+ channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the α 1A -subunit

inferredcites →https://doi.org/10.1074/jbc.273.6.3509openalex-snapshot

Slo3, a Novel pH-sensitive K+ Channel from Mammalian Spermatocytes

inferredcites →https://doi.org/10.1074/jbc.m006467200openalex-snapshot

Functional Embryonic Cardiomyocytes after Disruption of the L-type α1C (Ca 1.2) Calcium Channel Gene in the Mouse

inferredcites →https://doi.org/10.1074/jbc.m501430200openalex-snapshot

Identical Phenotypes of CatSper1 and CatSper2 Null Sperm

inferredcites →https://doi.org/10.1074/jbc.m508172200openalex-snapshot

Sodium and Epithelial Sodium Channels Participate in the Regulation of the Capacitation-associated Hyperpolarization in Mouse Sperm

inferredcites →https://doi.org/10.1074/jbc.m701083200openalex-snapshot

CatSperβ, a Novel Transmembrane Protein in the CatSper Channel Complex

inferredcites →https://doi.org/10.1093/molehr/gam009openalex-snapshot

Expression of CatSper family transcripts in the mouse testis during post-natal development and human ejaculated spermatozoa: relationship to sperm motility

inferredcites →https://doi.org/10.1095/biolreprod.105.045468openalex-snapshot

Catsper3 and Catsper4 Encode Two Cation Channel-Like Proteins Exclusively Expressed in the Testis

inferredcites →https://doi.org/10.1095/biolreprod.107.060186openalex-snapshot

Catsper3 and Catsper4 Are Essential for Sperm Hyperactivated Motility and Male Fertility in the Mouse1

inferredcites →https://doi.org/10.1095/biolreprod.107.061358openalex-snapshot

CATSPER Channel-Mediated Ca2+ Entry into Mouse Sperm Triggers a Tail-to-Head Propagation1

inferredcites →https://doi.org/10.1095/biolreprod61.1.76openalex-snapshot

Roles of Bicarbonate, cAMP, and Protein Tyrosine Phosphorylation on Capacitation and the Spontaneous Acrosome Reaction of Hamster Sperm1

inferredcites →https://doi.org/10.1111/j.1469-7793.2000.00037.xopenalex-snapshot

Mitochondria as all‐round players of the calcium game

inferredcites →https://doi.org/10.1126/science.1069259openalex-snapshot

Loss of Sex Discrimination and Male-Male Aggression in Mice Deficient for TRP2

inferredcites →https://doi.org/10.1126/science.1089268openalex-snapshot

Abnormal Coronary Function in Mice Deficient in α 1H T-type Ca 2+ Channels

inferredcites →https://doi.org/10.1126/science.289.5479.625openalex-snapshot

Soluble Adenylyl Cyclase as an Evolutionarily Conserved Bicarbonate Sensor

inferredcites →https://doi.org/10.1152/ajpcell.1996.271.5.c1583openalex-snapshot

A dihydropyridine-sensitive T-type Ca2+ current is the main Ca2+ current carrier in mouse primary spermatocytes

inferredcites →https://doi.org/10.1186/1477-7827-1-53openalex-snapshot

Identification of human and mouse CatSper3 and CatSper4 genes: Characterisation of a common interaction domain and evidence for expression in testis

inferredcites →https://doi.org/10.1242/dev.121.4.1129openalex-snapshot

Capacitation of mouse spermatozoa: I. Correlation between the capacitation state and protein tyrosine phosphorylation

inferredcites →https://doi.org/10.1242/dev.121.4.1139openalex-snapshot

Capacitation of mouse spermatozoa: II. Protein tyrosine phosphorylation and capacitation are regulated by a cAMP-dependent pathway

inferredcites →https://doi.org/10.1387/ijdb.072296emopenalex-snapshot

The role of ion fluxes in polarized cell growth and morphogenesis: the pollen tube as an experimental paradigm

inferredcites →https://doi.org/10.1387/ijdb.072344mkopenalex-snapshot

Shaping the mammalian auditory sensory organ by the planar cell polarity pathway

inferredcites →https://doi.org/10.1387/ijdb.072523dsopenalex-snapshot

Regionalized calcium signaling in zebrafish fertilization

inferredcites →https://doi.org/10.1387/ijdb.11206329openalex-snapshot

Tissue-specific distribution and variation of the channel-forming protein ductin during development of Drosophila melanogaster

inferredcites →https://doi.org/10.1387/ijdb.14584779openalex-snapshot

Ca2+ released via IP3 receptors is required for furrow deepening during cytokinesis in zebrafish embryos

inferredcites →https://doi.org/10.1530/rep.0.1220519openalex-snapshot

Hyperactivation of mammalian spermatozoa: function and regulation

inferredcites →https://doi.org/10.1530/rep.1.00612openalex-snapshot

Sperm channel diversity and functional multiplicity

inferredcites →https://doi.org/10.7326/0003-4819-109-2-176_1openalex-snapshot

The Physiology of Reproduction

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3188435openalex-extracted

Asymmetrically Positioned Flagellar Control Units Regulate Human Sperm Rotation

inferred← citeshttps://doi.org/10.1002/9780470015902.a0025310openalex-snapshot

Autosomal Mutations and Spermatogenic Failure

inferred← citeshttps://doi.org/10.1002/cphy.c110056openalex-snapshot

Roles of Ion Transport in Control of Cell Motility

inferred← citeshttps://doi.org/10.1002/j.2040-4603.2013.tb00481.xopenalex-snapshot

Roles of Ion Transport in Control of Cell Motility

inferred← citeshttps://doi.org/10.1002/jcp.22493openalex-snapshot

TRPM8 in mouse sperm detects temperature changes and may influence the acrosome reaction

inferred← citeshttps://doi.org/10.1002/mrd.22454openalex-snapshot

Role of human Na,K‐ATPase alpha 4 in sperm function, derived from studies in transgenic mice

inferred← citeshttps://doi.org/10.1002/mrd.22639openalex-snapshot

CABCOCO1, a novel coiled‐coil protein With calcium‐binding activity, is localized in the sperm flagellum

inferred← citeshttps://doi.org/10.1002/vms3.70459openalex-snapshot

Presence and Location of CatSper 1–4, Opioid (μ, δ and κ) and CD44 Receptors in Spermatozoa from Aoudad, Iberian Ibex and Mouflon

inferred← citeshttps://doi.org/10.1007/s00424-014-1478-2openalex-snapshot

T-type Ca2+ channels in spermatogenic cells and sperm

inferred← citeshttps://doi.org/10.1007/s10815-023-02810-2openalex-snapshot

Advances in the study of genetic factors and clinical interventions for fertilization failure

inferred← citeshttps://doi.org/10.1007/s10867-023-09645-zopenalex-snapshot

Ion currents through the voltage sensor domain of distinct families of proteins

inferred← citeshttps://doi.org/10.1016/b978-0-12-397944-5.00004-3openalex-snapshot

Sperm Patch-Clamp

inferred← citeshttps://doi.org/10.1016/b978-0-12-397945-2.00003-2openalex-snapshot

Methods for Analysis of Calcium/Calmodulin Signaling in Cilia and Flagella

inferred← citeshttps://doi.org/10.1016/b978-0-12-802002-9.00009-1openalex-snapshot

The Role of Sperm Ion Channels in Reproduction

inferred← citeshttps://doi.org/10.1016/j.anireprosci.2022.107052openalex-snapshot

Introduction to the pathways involved in the activation and regulation of sperm motility: A review of the relevance of ion channels

inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.02.042openalex-snapshot

pH-dependent Ca+2 oscillations prevent untimely acrosome reaction in human sperm

inferred← citeshttps://doi.org/10.1016/j.ceca.2014.10.009openalex-snapshot

Flagellar ion channels of sperm: similarities and differences between species

inferred← citeshttps://doi.org/10.1016/j.ceca.2016.03.011openalex-snapshot

Cd2+ sensitivity and permeability of a low voltage-activated Ca2+ channel with CatSper-like selectivity filter

inferred← citeshttps://doi.org/10.1016/j.cell.2009.12.053openalex-snapshot

Acid Extrusion from Human Spermatozoa Is Mediated by Flagellar Voltage-Gated Proton Channel

inferred← citeshttps://doi.org/10.1016/j.celrep.2018.08.016openalex-snapshot

Asymmetrically Positioned Flagellar Control Units Regulate Human Sperm Rotation

inferred← citeshttps://doi.org/10.1016/j.contraception.2010.03.017openalex-snapshot

New frontiers in nonhormonal male contraception

inferred← citeshttps://doi.org/10.1016/j.csbj.2014.09.002openalex-snapshot

The biological networks in studying cell signal transduction complexity: The examples of sperm capacitation and of endocannabinoid system

inferred← citeshttps://doi.org/10.1016/j.envpol.2021.118739openalex-snapshot

TET1 mediated male reproductive toxicity induced by Bisphenol A through Catsper-Ca2+ signaling pathway

inferred← citeshttps://doi.org/10.1016/j.fertnstert.2009.07.1671openalex-snapshot

The transcriptome of spermatozoa used in homologous intrauterine insemination varies considerably between samples that achieve pregnancy and those that do not

inferred← citeshttps://doi.org/10.1016/j.jbc.2022.101868openalex-snapshot

A genetically targeted sensor reveals spatial and temporal dynamics of acrosomal calcium and sperm acrosome exocytosis

inferred← citeshttps://doi.org/10.1016/j.jep.2019.112321openalex-snapshot

Influence of Echeveria gibbiflora DC aqueous crude extract on mouse sperm energy metabolism and calcium-dependent channels

inferred← citeshttps://doi.org/10.1016/j.mce.2020.110951openalex-snapshot

CatSper: The complex main gate of calcium entry in mammalian spermatozoa

inferred← citeshttps://doi.org/10.1016/j.rbmo.2014.09.014openalex-snapshot

CatSper channel, sperm function and male fertility

inferred← citeshttps://doi.org/10.1016/j.repbio.2018.01.005openalex-snapshot

Intramembranal disulfide cross-linking elucidates the super-quaternary structure of mammalian CatSpers

inferred← citeshttps://doi.org/10.1016/j.tcb.2016.10.002openalex-snapshot

Signaling in Sperm: More Different than Similar

inferred← citeshttps://doi.org/10.1016/j.theriogenology.2015.09.013openalex-snapshot

A phosphodiesterase type-5 inhibitor, sildenafil, induces sperm capacitation and penetration into porcine oocytes in a chemically defined medium

inferred← citeshttps://doi.org/10.1016/j.theriogenology.2016.12.010openalex-snapshot

Functional and molecular characterization of voltage gated sodium channel Na v 1.8 in bull spermatozoa

inferred← citeshttps://doi.org/10.1016/j.theriogenology.2017.11.024openalex-snapshot

Modulation of voltage-gated sodium channels induces capacitation in bull spermatozoa through phosphorylation of tyrosine containing proteins

inferred← citeshttps://doi.org/10.1016/j.theriogenology.2018.03.030openalex-snapshot

Molecular characterization of voltage-gated potassium channel (Kv) and its importance in functional dynamics in bull spermatozoa

inferred← citeshttps://doi.org/10.1016/j.theriogenology.2019.01.029openalex-snapshot

Molecular and functional insights into Transient Receptor Potential Vanilloid 1 (TRPV1) in bull spermatozoa

inferred← citeshttps://doi.org/10.1016/j.toxrep.2019.08.004openalex-snapshot

Influence of cryopreservation on the CATSPER2 and TEKT2 expression levels and protein levels in human spermatozoa

inferred← citeshttps://doi.org/10.1016/j.yexmp.2020.104528openalex-snapshot

Investigating the regulatory function of the ANO1-AS2 on the ANO1 gene in infertile men with asthenozoospermia and terato-asthenozoospermia

inferred← citeshttps://doi.org/10.1016/s0091-679x(08)92011-2openalex-snapshot

Calcium Regulation of Ciliary Motility

inferred← citeshttps://doi.org/10.1016/s0246-0335(12)50151-1openalex-snapshot

Fécondation dans l’espèce humaine

inferred← citeshttps://doi.org/10.1016/s0246-0335(20)42828-5openalex-snapshot

10.1016/s0246-0335(20)42828-5

inferred← citeshttps://doi.org/10.1021/acs.jmedchem.7b00925openalex-snapshot

Design, Synthesis, and in Vitro and in Vivo Evaluation of Ouabain Analogues as Potent and Selective Na,K-ATPase α4 Isoform Inhibitors for Male Contraception

inferred← citeshttps://doi.org/10.1038/aja.2010.69openalex-snapshot

Ion channels, phosphorylation and mammalian sperm capacitation

inferred← citeshttps://doi.org/10.1038/ejhg.2010.108openalex-snapshot

Genetic male infertility and mutation of CATSPER ion channels

inferred← citeshttps://doi.org/10.1038/emboj.2012.30openalex-snapshot

The CatSper channel: a polymodal chemosensor in human sperm

inferred← citeshttps://doi.org/10.1055/a-1553-3265openalex-snapshot

Astaxanthin Induces the Expression of CatSper1 Gene and Protects Sperms in Toxicity Induced by Cadmium in Mice

inferred← citeshttps://doi.org/10.1073/pnas.1100240108openalex-snapshot

Deletion of the Slo3 gene abolishes alkalization-activated K + current in mouse spermatozoa

inferred← citeshttps://doi.org/10.1073/pnas.1111695108openalex-snapshot

ATP-activated P2X2 current in mouse spermatozoa

inferred← citeshttps://doi.org/10.1073/pnas.1216588110openalex-snapshot

Disruption of the principal, progesterone-activated sperm Ca 2+ channel in a CatSper2-deficient infertile patient

inferred← citeshttps://doi.org/10.1073/pnas.1423869112openalex-snapshot

SLO3 auxiliary subunit LRRC52 controls gating of sperm KSPER currents and is critical for normal fertility

inferred← citeshttps://doi.org/10.1073/pnas.2109993118openalex-snapshot

Molecular mechanisms of sperm motility are conserved in an early-branching metazoan

inferred← citeshttps://doi.org/10.1074/jbc.m109.100156openalex-snapshot

Phosphatidylinositol 4,5-Bisphosphate Activates Slo3 Currents and Its Hydrolysis Underlies the Epidermal Growth Factor-induced Current Inhibition

inferred← citeshttps://doi.org/10.1074/jbc.m110.211524openalex-snapshot

Chemosensory Ca2+ Dynamics Correlate with Diverse Behavioral Phenotypes in Human Sperm

inferred← citeshttps://doi.org/10.1080/15569543.2020.1868007openalex-snapshot

Down-regulation of CatSper 1 and CatSper 2 genes by methamphetamine

inferred← citeshttps://doi.org/10.1080/19396368.2022.2122761openalex-snapshot

Participation of signaling proteins in sperm hyperactivation

inferred← citeshttps://doi.org/10.1085/jgp.201311011openalex-snapshot

Simultaneous knockout ofSlo3andCatSper1abolishes all alkalization- and voltage-activated current in mouse spermatozoa

inferred← citeshttps://doi.org/10.1093/biolre/ioaa093openalex-snapshot

The Na+ and K+ transport system of sperm (ATP1A4) is essential for male fertility and an attractive target for male contraception†

inferred← citeshttps://doi.org/10.1093/biolre/ioae183openalex-snapshot

Oxidation of thiol groups in membrane proteins inhibits the fertilization ability and motility of sperm by suppressing calcium influx

inferred← citeshttps://doi.org/10.1093/biolre/ioaf268openalex-snapshot

Thermal modulation of CatSper activity regulates hyperactivated motility in human sperm

inferred← citeshttps://doi.org/10.1093/biolre/ioy197openalex-snapshot

Faster and more efficient swimming: energy consumption of murine spermatozoa under sperm competition†

inferred← citeshttps://doi.org/10.1093/function/zqaf016openalex-snapshot

Role of Pannexin 1, P2X7, and CFTR in ATP Release and Autocrine Signaling by Principal Cells of the Epididymis

inferred← citeshttps://doi.org/10.1093/humupd/dmab029openalex-snapshot

Contribution of epididymal epithelial cell functions to sperm epigenetic changes and the health of progeny

inferred← citeshttps://doi.org/10.1093/molehr/gaae007openalex-snapshot

Differential role of bovine serum albumin and HCO3− in the regulation of GSK3 alpha during mouse sperm capacitation

inferred← citeshttps://doi.org/10.1093/molehr/gar044openalex-snapshot

Rediscovering sperm ion channels with the patch-clamp technique

inferred← citeshttps://doi.org/10.1095/biolreprod.109.083113openalex-snapshot

Rethinking the Relationship Between Hyperactivation and Chemotaxis in Mammalian Sperm1

inferred← citeshttps://doi.org/10.1095/biolreprod.110.089789openalex-snapshot

Two Distinct Ca2+ Signaling Pathways Modulate Sperm Flagellar Beating Patterns in Mice1

inferred← citeshttps://doi.org/10.1095/biolreprod.111.096578openalex-snapshot

Unexpected Flagellar Movement Patterns and Epithelial Binding Behavior of Mouse Sperm in the Oviduct1

inferred← citeshttps://doi.org/10.1096/fj.202002773rropenalex-snapshot

Cdc42 localized in the CatSper signaling complex regulates cAMP‐dependent pathways in mouse sperm

inferred← citeshttps://doi.org/10.1101/2020.08.24.264739openalex-snapshot

Cdc42 activity is essential for the interplay between cAMP/PKA pathway and CatSper function

inferred← citeshttps://doi.org/10.1101/2022.11.16.516775openalex-snapshot

New insights into CFTR modulation in reproduction: testicular microenvironment imbalance leads to over-activated caspase signalling in spermatogenesis and adversely affects fertility

inferred← citeshttps://doi.org/10.1101/2024.10.08.617222openalex-snapshot

Within-ejaculate sperm selection in humans acts against molecular signatures of age-related disease

inferred← citeshttps://doi.org/10.1101/2025.02.14.638303openalex-snapshot

The sperm specific Na + ,K + -ATPase α4 shows a highly structured and dynamic distribution at the sperm flagellum

inferred← citeshttps://doi.org/10.1101/757880openalex-snapshot

OR1D2 receptor mediates bourgeonal-induced human CatSper activation in a G-protein dependent manner

inferred← citeshttps://doi.org/10.1111/andr.12632openalex-snapshot

Epithelial dynamics in the epididymis: role in the maturation, protection, and storage of spermatozoa

inferred← citeshttps://doi.org/10.1111/andr.13820openalex-snapshot

Regulation of NHE3 subcellular localization in epididymal principal cells: pH, cyclic adenosine 3,5 monophosphate (cAMP), and adenosine signaling

inferred← citeshttps://doi.org/10.1111/andr.70294openalex-snapshot

A Scalable Flow Cytometry Assay to Evaluate CatSper‐mediated Ca 2+ Influx Triggered by High‐K + /High‐pH Stimulation in Mouse Sperm

inferred← citeshttps://doi.org/10.1111/are.14435openalex-snapshot

Characterization and expression of SLO1 potassium channels during spermatogenesis inEriocheir sinensis

inferred← citeshttps://doi.org/10.1111/j.1439-0531.2012.02046.xopenalex-snapshot

The Membrane of the Mammalian Spermatozoa: Much More Than an Inert Envelope

inferred← citeshttps://doi.org/10.1113/jphysiol.2010.194142openalex-snapshot

The role of Hv1 and CatSper channels in sperm activation

inferred← citeshttps://doi.org/10.1124/mol.120.119982openalex-snapshot

Interaction of MDIMP with the Voltage-Gated Calcium Channels

inferred← citeshttps://doi.org/10.1126/scisignal.2001791openalex-snapshot

Male Fertility Depends on Ca 2+ Absorption by TRPV6 in Epididymal Epithelia

inferred← citeshttps://doi.org/10.1146/annurev-physiol-020911-153258openalex-snapshot

The Control of Male Fertility by Spermatozoan Ion Channels

inferred← citeshttps://doi.org/10.1152/physiol.00049.2009openalex-snapshot

Calcium Signaling Through CatSper Channels in Mammalian Fertilization

inferred← citeshttps://doi.org/10.1152/physrev.00028.2010openalex-snapshot

Calcium Channels in the Development, Maturation, and Function of Spermatozoa

inferred← citeshttps://doi.org/10.1172/jci173564openalex-snapshot

Human fertilization in vivo and in vitro requires the CatSper channel to initiate sperm hyperactivation

inferred← citeshttps://doi.org/10.1186/1471-2148-14-106openalex-snapshot

Structural evolution of CatSper1 in rodents is influenced by sperm competition, with effects on sperm swimming velocity

inferred← citeshttps://doi.org/10.1186/s12958-017-0281-2openalex-snapshot

The Catsper channel and its roles in male fertility: a systematic review

inferred← citeshttps://doi.org/10.1186/s13023-025-04002-wopenalex-snapshot

Determination of carriers of deafness-infertility syndrome in Peru

inferred← citeshttps://doi.org/10.1210/en.2016-1473openalex-snapshot

Chemical UV Filters Mimic the Effect of Progesterone on Ca2+ Signaling in Human Sperm Cells

inferred← citeshttps://doi.org/10.1242/jcs.058263openalex-snapshot

CaMKIIα interacts with multi-PDZ domain protein MUPP1 in spermatozoa and prevents spontaneous acrosomal exocytosis

inferred← citeshttps://doi.org/10.1371/journal.pbio.3003776openalex-snapshot

A histidine-mediated supramolecular mechanism links temperature and pH activation of the sperm channel CatSper

inferred← citeshttps://doi.org/10.1371/journal.pone.0003569openalex-snapshot

Evolutionary Genomics Reveals Lineage-Specific Gene Loss and Rapid Evolution of a Sperm-Specific Ion Channel Complex: CatSpers and CatSperβ

inferred← citeshttps://doi.org/10.1371/journal.pone.0006844openalex-snapshot

Pharmacological Targeting of Native CatSper Channels Reveals a Required Role in Maintenance of Sperm Hyperactivation

inferred← citeshttps://doi.org/10.1371/journal.pone.0020031openalex-snapshot

Drosophila Sperm Swim Backwards in the Female Reproductive Tract and Are Activated via TRPP2 Ion Channels

inferred← citeshttps://doi.org/10.1371/journal.pone.0091302openalex-snapshot

Proteins Involved in Motility and Sperm-Egg Interaction Evolve More Rapidly in Mouse Spermatozoa

inferred← citeshttps://doi.org/10.1371/journal.pone.0127480openalex-snapshot

TMEM203 Is a Novel Regulator of Intracellular Calcium Homeostasis and Is Required for Spermatogenesis

inferred← citeshttps://doi.org/10.1371/journal.pone.0232536openalex-snapshot

Stromal cell-derived factor 1 regulates in vitro sperm migration towards the cumulus-oocyte complex in cattle

inferred← citeshttps://doi.org/10.1387/ijdb.150202etopenalex-snapshot

Ion currents involved in gamete physiology

inferred← citeshttps://doi.org/10.15252/embj.201489376openalex-snapshot

The CatSper channel controls chemosensation in sea urchin sperm

inferred← citeshttps://doi.org/10.15252/embj.2019102363openalex-snapshot

Rotational motion and rheotaxis of human sperm do not require functional CatSper channels and transmembrane Ca2+ signaling

inferred← citeshttps://doi.org/10.15252/embj.2019102723openalex-snapshot

Absolute proteomic quantification reveals design principles of sperm flagellar chemosensation

inferred← citeshttps://doi.org/10.1530/rep-09-0134openalex-snapshot

Ca2+-stores in sperm: their identities and functions

inferred← citeshttps://doi.org/10.1530/rep-17-0664openalex-snapshot

Influence of antifertility agents Dutasteride and Nifedipine on CatSper gene level in epididymis during sperm maturation in BALB/c mice

inferred← citeshttps://doi.org/10.1530/rep-18-0541openalex-snapshot

Update on mammalian sperm capacitation: how much does the horse differ from other species?

inferred← citeshttps://doi.org/10.1530/rep-25-0114openalex-snapshot

Na+,K+-ATPase α isoforms in sperm show a highly structured and distinct pattern of distribution

inferred← citeshttps://doi.org/10.2164/jandrol.111.012971openalex-snapshot

Establishment of Cell-Cell Cross Talk in the Epididymis: Control of Luminal Acidification

inferred← citeshttps://doi.org/10.2164/jandrol.111.015552openalex-snapshot

Ion Channels in Sperm Physiology and Male Fertility and Infertility

inferred← citeshttps://doi.org/10.22201/fesz.23958723e.2024.685openalex-snapshot

Canal catiónico específico del espermatozoide: CatSper

inferred← citeshttps://doi.org/10.24275/uami.7p88cg523openalex-snapshot

Efecto del ácido perfluorooctanoico sobre el flujo del Ca2+ intracelular durante la capacitación in vitro de espermatozoides de cerdo doméstico

inferred← citeshttps://doi.org/10.24275/uami.m613mx73ropenalex-snapshot

Caracterización de la capacitación espermática en el murciélago Corynorhinus Mexicanus

inferred← citeshttps://doi.org/10.3109/19396360903497217openalex-snapshot

Tetraethylammonium-Sensitive K+Current in the Bovine Spermatozoa and its Blocking by the Venom of the ChileanLatrodectus mactans

inferred← citeshttps://doi.org/10.3384/diss.diva-131862openalex-snapshot

Sperm Membrane Channels, Receptors and Kinematics : Using boar spermatozoa for drug toxicity screening

inferred← citeshttps://doi.org/10.3389/fcell.2018.00072openalex-snapshot

Molecular Basis of Human Sperm Capacitation

inferred← citeshttps://doi.org/10.3389/fcell.2019.00366openalex-snapshot

Quantitative Intracellular pH Determinations in Single Live Mammalian Spermatozoa Using the Ratiometric Dye SNARF-5F

inferred← citeshttps://doi.org/10.3389/fcell.2022.827454openalex-snapshot

The Importance of Gene Duplication and Domain Repeat Expansion for the Function and Evolution of Fertilization Proteins

inferred← citeshttps://doi.org/10.3389/fcell.2022.911056openalex-snapshot

Genetic Ablation of Na,K-ATPase α4 Results in Sperm Energetic Defects

inferred← citeshttps://doi.org/10.3389/fcell.2022.935667openalex-snapshot

Saccharides Influence Sperm Quality and Expressions of Motility and Fertilization-Associated Genes in Cryopreserved Sperm of Pacific Abalone, Haliotis discus hannai

inferred← citeshttps://doi.org/10.3389/fcell.2023.1010306openalex-snapshot

High-throughput screening method for discovering CatSper inhibitors using membrane depolarization caused by external calcium chelation and fluorescent cell barcoding

inferred← citeshttps://doi.org/10.3389/fmars.2021.652390openalex-snapshot

Effects of Cryopreservation on Gene Expression and Post Thaw Sperm Quality of Pacific Abalone, Haliotis discus hannai

inferred← citeshttps://doi.org/10.3389/fvets.2026.1830161openalex-snapshot

The impact of supplementation with calcium and naloxone to TRIS and Lepus extenders on the quality of refrigerated rabbit semen

inferred← citeshttps://doi.org/10.3390/ani14020319openalex-snapshot

Astaxanthin Improved the Quality of Hu Ram Semen by Increasing the Antioxidant Capacity and Mitochondrial Potential and Mitigating Free Radicals-Induced Oxidative Damage

inferred← citeshttps://doi.org/10.3390/biom12111685openalex-snapshot

Electrophysiology and Fluorescence Spectroscopy Approaches for Evaluating Gamete and Embryo Functionality in Animals and Humans

inferred← citeshttps://doi.org/10.3390/biomedicines11092519openalex-snapshot

Signaling Roleplay between Ion Channels during Mammalian Sperm Capacitation

inferred← citeshttps://doi.org/10.3390/ijms21051840openalex-snapshot

Does the Pre-Ovulatory Pig Oviduct Rule Sperm Capacitation In Vivo Mediating Transcriptomics of Catsper Channels?

inferred← citeshttps://doi.org/10.3390/ijms22063259openalex-snapshot

Structure and Function of Ion Channels Regulating Sperm Motility—An Overview

inferred← citeshttps://doi.org/10.3390/ijms241813750openalex-snapshot

The Cation/Calcium Channel of Sperm (CatSper): A Common Role Played Despite Inter-Species Variation?

inferred← citeshttps://doi.org/10.3390/ijms26083750openalex-snapshot

TMEM16A Maintains Acrosomal Integrity Through ERK1/2, RhoA, and Actin Cytoskeleton During Capacitation

inferred← citeshttps://doi.org/10.3791/62049openalex-snapshot

Recording Electrical Currents across the Plasma Membrane of Mammalian Sperm Cells

inferred← citeshttps://doi.org/10.3791/62049-vopenalex-snapshot

Recording Electrical Currents across the Plasma Membrane of Mammalian Sperm Cells

inferred← citeshttps://doi.org/10.4018/978-1-5225-1043-7.ch001openalex-snapshot

Ion Channels, Nanomechanics, and Nanomedicine

inferred← citeshttps://doi.org/10.4067/s0717-95022011000300012openalex-snapshot

Molecular Characterization, Electrophysiological and Contraceptive Effect of Chilean Latrodectus Venom

inferred← citeshttps://doi.org/10.4103/1008-682x.129129openalex-snapshot

Panax ginseng induces the expression of CatSper genes and sperm hyperactivation

inferred← citeshttps://doi.org/10.4161/chan.4.1.10481openalex-snapshot

Block of mouse Slo1 and Slo3 K+channels by CTX, IbTX, TEA, 4-AP and quinidine

inferred← citeshttps://doi.org/10.5528/wjtm.v5.i1.26openalex-snapshot

New insights in sperm biology: How benchside results in the search for molecular markers may help understand male infertility

inferred← citeshttps://doi.org/10.5534/wjmh.230118openalex-snapshot

Advances in Male Contraception: When Will the Novel Male Contraception be Available?

inferred← citeshttps://doi.org/10.6116/kjh.2012.27.2.47openalex-snapshot

Effects of Ginseng Radix on sperm count and CatSper3, 4 proteins expression in Male Mice

inferred← citeshttps://doi.org/10.64898/2026.01.05.697741openalex-snapshot

A high-throughput flow cytometry assay to evaluate CatSper-mediated Ca 2+ influx triggered by high-K + /high-pH stimulation in mouse sperm

inferred← citeshttps://doi.org/10.70675/1c589256zd211z4434z87aazbd40d27c1f4dopenalex-snapshot

Recherche et développement de biomolécules permettant l’amélioration des biotechnologies de la reproduction chez le bovin.

inferred← citeshttps://doi.org/10.70675/e047992czce5dz469cza329zbd3a0c87f3c4openalex-snapshot

Polluants environnementaux, stress oxydant : impacts spermatiques structurels, fonctionnels et épigénétiques en modèle murin

inferred← citeshttps://doi.org/10.7554/elife.35853openalex-snapshot

TRPV4 is the temperature-sensitive ion channel of human sperm

inferred← citeshttps://doi.org/10.7717/peerj.18429openalex-snapshot

The regulation role of calcium channels in mammalian sperm function: a narrative review with a focus on humans and mice

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.