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

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What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1098-2795(199601)43:1<82::aid-mrd11>3.0.co;2-6openalex-snapshot

Properties and localization of a tyrosine phosphorylated form of hexokinase in mouse sperm

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/mrd.10017openalex-snapshot

Quantitative analysis of flagellar movement in hyperactivated and acrosome‐reacted golden hamster spermatozoa

inferredcites →https://doi.org/10.1002/mrd.1120050404openalex-snapshot

Requirement of extracellular calcium ions for various stages of fertilization and fertilization‐related phenomena in the hamster

inferredcites →https://doi.org/10.1006/dbio.1998.9172openalex-snapshot

Discrete Regional Distributions Suggest Diverse Functional Roles of Calcium Channel α1 Subunits in Sperm

inferredcites →https://doi.org/10.1016/s0014-5793(99)01518-5openalex-snapshot

Voltage‐dependent Ca2+ channel subunit expression and immunolocalization in mouse spermatogenic cells and sperm

inferredcites →https://doi.org/10.1016/s0021-9258(18)34229-7openalex-snapshot

A requirement of bicarbonate for Ca2+-induced elevations of cyclic AMP in guinea pig spermatozoa.

inferredcites →https://doi.org/10.1016/s0026-895x(25)09802-5openalex-snapshot

Membrane-permeant derivatives of cyclic AMP optimized for high potency, prolonged activity, or rapid reversibility.

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

A sperm ion channel required for sperm motility and male fertility

inferredcites →https://doi.org/10.1038/35098164openalex-snapshot

Swimming with sperm

inferredcites →https://doi.org/10.1038/35098167openalex-snapshot

100 and 50 years ago

inferredcites →https://doi.org/10.1046/j.1439-0531.2003.00400.xopenalex-snapshot

Cyclic AMP Signalling During Mammalian Sperm Capacitation – Still Largely Terra Incognita

inferredcites →https://doi.org/10.1073/pnas.1831008100openalex-snapshot

Calcium regulation of the soluble adenylyl cyclase expressed in mammalian spermatozoa

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/10.1074/jbc.m002068200openalex-snapshot

CaV2.2 and CaV2.3 (N- and R-type) Ca2+ Channels in Depolarization-evoked Entry of Ca2+ into Mouse Sperm

inferredcites →https://doi.org/10.1074/jbc.m011698200openalex-snapshot

Identification and Functional Analysis of Splice Variants of the Germ Cell Soluble Adenylyl Cyclase

inferredcites →https://doi.org/10.1083/jcb.142.2.473openalex-snapshot

Cyclic Nucleotide-gated Channels on the Flagellum Control Ca2+ Entry into Sperm

inferredcites →https://doi.org/10.1083/jcb.82.2.401openalex-snapshot

Calcium-induced asymmetrical beating of triton-demembranated sea urchin sperm flagella.

inferredcites →https://doi.org/10.1083/jcb.86.2.446openalex-snapshot

Calcium control of waveform in isolated flagellar axonemes of chlamydomonas

inferredcites →https://doi.org/10.1085/jgp.200308839openalex-snapshot

Calcium Clearance Mechanisms of Mouse Sperm

inferredcites →https://doi.org/10.1091/mbc.e02-04-0185openalex-snapshot

Regulation of Flagellar Dynein by Calcium and a Role for an Axonemal Calmodulin and Calmodulin-dependent Kinase

inferredcites →https://doi.org/10.1093/biolreprod/22.5.1083openalex-snapshot

Motility of Rabbit Spermatozoa in the Secretions of the Oviduct

inferredcites →https://doi.org/10.1093/humrep/14.4.873openalex-snapshot

Voltage-operated Ca2+ channels and the acrosome reaction: which channels are present and what do they do?

inferredcites →https://doi.org/10.1095/biolreprod22.4.759openalex-snapshot

Movement Characteristics of Hamster Spermatozoa Within the Oviduct1

inferredcites →https://doi.org/10.1095/biolreprod36.5.1191openalex-snapshot

Initiation of Hyperactivated Flagellar Bending in Mouse Sperm within the Female Reproductive Tract1

inferredcites →https://doi.org/10.1115/1.1451234openalex-snapshot

Mechanics of Motor Proteins and the Cytoskeleton

inferredcites →https://doi.org/10.1126/science.176.4034.523openalex-snapshot

Reactivated Triton-Extracted Models of Paramecium : Modification of Ciliary Movement by Calcium Ions

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

Soluble Adenylyl Cyclase as an Evolutionarily Conserved Bicarbonate Sensor

inferredcites →https://doi.org/10.1186/1477-7827-1-53openalex-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/10.1210/mend.16.3.0793openalex-snapshot

Mutation of the Cα Subunit of PKA Leads to Growth Retardation and Sperm Dysfunction

inferredcites →https://doi.org/10.1242/dev.00353openalex-snapshot

Bicarbonate actions on flagellar and Ca2+-channel responses:initial events in sperm activation

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/10.7326/0003-4819-109-2-176_1openalex-snapshot

The Physiology of Reproduction

What points at this work

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

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Flagellar hyperactivation of bull and boar spermatozoa

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Viscous Loading Regulates the Flagellar Energetics of Human and Bull Sperm

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Family Planning: Today and in the Future

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CatSper in Male Infertility

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Cl− Channels and Transporters in Sperm Physiology

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Modulation of Sperm Motility and Function Prior to Fertilization

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The Sperm

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Levels of Tektin 2 and CatSper 2 in normozoospermic and oligoasthenozoospermic men and its association with motility, fertilization rate, embryo quality and pregnancy rate

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Analysis of the correlation of CATSPER single nucleotide polymorphisms (SNPs) with idiopathic asthenospermia

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Perfect date—the review of current research into molecular bases of mammalian fertilization

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

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inferred← citeshttps://doi.org/10.1007/s11010-022-04469-2openalex-snapshot

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inferred← citeshttps://doi.org/10.1007/s11538-010-9516-5openalex-snapshot

A Model of CatSper Channel Mediated Calcium Dynamics in Mammalian Spermatozoa

inferred← citeshttps://doi.org/10.1007/s12403-023-00621-5openalex-snapshot

Transient Decrease in Sperm Motility after Plateletpheresis

inferred← citeshttps://doi.org/10.1007/s43032-023-01397-4openalex-snapshot

The Detection of CatSper1 and CatSper3 Expression in Men with Normozoospermia and Asthenoteratozoospermia and Its Association with Sperm Parameters, Fertilization Rate, Embryo Quality

inferred← citeshttps://doi.org/10.1016/b978-0-12-374145-5.00117-0openalex-snapshot

Intracellular Calcium Signaling

inferred← citeshttps://doi.org/10.1016/b978-0-12-397175-3.00003-xopenalex-snapshot

The Spermatozoon

inferred← citeshttps://doi.org/10.1016/b978-0-12-397175-3.00004-1openalex-snapshot

Fertilization in Mammals

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/b978-0-12-416024-8.00014-3openalex-snapshot

K+ and Cl− Channels and Transporters in Sperm Function

inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64465-3openalex-snapshot

Mechanisms Involved in Mammalian Gamete Interaction

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/b978-0-443-21477-6.00439-9openalex-snapshot

Mechanisms Involved in Mammalian Gamete Interaction

inferred← citeshttps://doi.org/10.1016/b978-012515400-0/50006-3openalex-snapshot

The Spermatozoon

inferred← citeshttps://doi.org/10.1016/b978-012515400-0/50007-5openalex-snapshot

Fertilization in Mammals

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Gamete and Zygote Transport

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Male Contraception

inferred← citeshttps://doi.org/10.1016/j.ajhg.2009.03.004openalex-snapshot

Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein

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Human CATSPER1 Promoter Is Regulated by CREB1 and CREMτ Transcriptional Factors In Vitro

inferred← citeshttps://doi.org/10.1016/j.bbadis.2012.07.006openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.02.095openalex-snapshot

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

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

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Asymmetrically Positioned Flagellar Control Units Regulate Human Sperm Rotation

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Differential expression patterns of selective energy metabolism associated genes in fresh and freeze-thawed bubaline spermatozoa at uniform durations of in vitro capacitation

inferred← citeshttps://doi.org/10.1016/j.febslet.2010.02.005openalex-snapshot

The SLO3 sperm‐specific potassium channel plays a vital role in male fertility

inferred← citeshttps://doi.org/10.1016/j.febslet.2013.05.068openalex-snapshot

The anti‐inflammatory drug celecoxib inhibits t‐type Ca 2+ currents in spermatogenic cells yet it elicits the acrosome reaction in mature sperm

inferred← citeshttps://doi.org/10.1016/j.febslet.2013.07.056openalex-snapshot

Attenuation of fibroblast growth factor signaling by poly‐ N ‐acetyllactosamine type glycans

inferred← citeshttps://doi.org/10.1016/j.febslet.2014.07.024openalex-snapshot

The transcription factors Sox5 and Sox9 regulate Catsper1 gene expression

inferred← citeshttps://doi.org/10.1016/j.fertnstert.2008.07.1751openalex-snapshot

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Down-regulation of CatSper1 channel in epididymal spermatozoa contributes to the pathogenesis of asthenozoospermia, whereas up-regulation of the channel by Sheng-Jing-San treatment improves the sperm motility of asthenozoospermia in rats

inferred← citeshttps://doi.org/10.1016/j.gene.2014.03.055openalex-snapshot

Chromosome microarray analysis: a case report of infertile brothers with CATSPER gene deletion

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The steroid hormone dydrogesterone inhibits myometrial contraction independently of the progesterone/progesterone receptor pathway

inferred← citeshttps://doi.org/10.1016/j.mce.2005.12.031openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.mce.2005.12.035openalex-snapshot

Odorant receptors and olfactory-like signaling mechanisms in mammalian sperm

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The role of Mitogen activated protein kinase (MAPK) in sperm functions

inferred← citeshttps://doi.org/10.1016/j.mce.2014.04.011openalex-snapshot

Aquaporin-11 control of testicular fertility markers in Syrian hamsters

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.nutres.2008.11.007openalex-snapshot

Zinc levels in seminal plasma are associated with sperm quality in fertile and infertile men

inferred← citeshttps://doi.org/10.1016/j.psj.2024.103664openalex-snapshot

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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.theriogenology.2007.05.048openalex-snapshot

Calcium and other ion dynamics during gamete maturation and fertilization

inferred← citeshttps://doi.org/10.1016/j.theriogenology.2008.10.003openalex-snapshot

Changes in calmodulin immunocytochemical localization associated with capacitation and acrosomal exocytosis of ram spermatozoa

inferred← citeshttps://doi.org/10.1016/j.theriogenology.2023.10.030openalex-snapshot

Dietary supplementation with barley sprouts and d-aspartic acid improves reproductive hormone concentrations, testicular histology, antioxidant status, and mRNA expressions of apoptosis-related genes in aged broiler breeder roosters

inferred← citeshttps://doi.org/10.1016/j.tibs.2019.08.001openalex-snapshot

Tiny Dancer: EFCAB9 Triggers Sperm Hyperactivation via CatSper

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.ydbio.2004.06.025openalex-snapshot

Multi-state, 4-aminopyridine-sensitive ion channels in human spermatozoa

inferred← citeshttps://doi.org/10.1016/j.ydbio.2005.06.002openalex-snapshot

The mouse t complex distorter/sterility candidate, Dnahc8, expresses a γ-type axonemal dynein heavy chain isoform confined to the principal piece of the sperm tail

inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.05.038openalex-snapshot

Soluble adenylyl cyclase (sAC) is indispensable for sperm function and fertilization

inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.11.007openalex-snapshot

Contributions of extracellular and intracellular Ca2+ to regulation of sperm motility: Release of intracellular stores can hyperactivate CatSper1 and CatSper2 null sperm

inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.09.017openalex-snapshot

External Ca2+ acts upstream of adenylyl cyclase SACY in the bicarbonate signaled activation of sperm motility

inferred← citeshttps://doi.org/10.1016/s0014-5793(04)00257-1openalex-snapshot

Expression and differential cell distribution of low‐threshold Ca2+ channels in mammalian male germ cells and sperm

inferred← citeshttps://doi.org/10.1016/s0074-7696(05)43002-8openalex-snapshot

Calcium Channels and Ca2+ Fluctuations in Sperm Physiology

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

Calcium Regulation of Ciliary Motility

inferred← citeshttps://doi.org/10.1016/s1166-7087(07)92254-xopenalex-snapshot

Contraceptions masculines non déférentielles : revue de la littérature

inferred← citeshttps://doi.org/10.1016/s1671-2927(11)60197-1openalex-snapshot

Delivery of CatSper2 siRNA into Rat Sperms by Electroporation Repressed Ca2+ Influx During Sperm Hyperactivation

inferred← citeshttps://doi.org/10.1017/9781316411124.010openalex-snapshot

Regulation of Sperm Behaviour

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

Ion channels, phosphorylation and mammalian sperm capacitation

inferred← citeshttps://doi.org/10.1038/aja.2011.118openalex-snapshot

Regulation of fertilization in male rats by CatSper2 knockdown

inferred← citeshttps://doi.org/10.1038/cddis.2016.344openalex-snapshot

The control of male fertility by spermatid-specific factors: searching for contraceptive targets from spermatozoon’s head to tail

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/nature04417openalex-snapshot

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

inferred← citeshttps://doi.org/10.1038/nature09767openalex-snapshot

Progesterone activates the principal Ca2+ channel of human sperm

inferred← citeshttps://doi.org/10.1038/ncb0307-235openalex-snapshot

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

inferred← citeshttps://doi.org/10.1038/ncomms1153openalex-snapshot

A novel gene required for male fertility and functional CATSPER channel formation in spermatozoa

inferred← citeshttps://doi.org/10.1038/nm.f.1895openalex-snapshot

The biology of infertility: research advances and clinical challenges

inferred← citeshttps://doi.org/10.1038/s10038-026-01485-8openalex-snapshot

The importance of integrating genetic testing into reproductive medicine: a retrospective observational study investigating the monogenic causes of human infertility in couples considering ICSI

inferred← citeshttps://doi.org/10.1038/s41467-022-31050-8openalex-snapshot

3D structure and in situ arrangements of CatSper channel in the sperm flagellum

inferred← citeshttps://doi.org/10.1038/s41467-025-58824-0openalex-snapshot

The essential calcium channel of sperm CatSper is temperature-gated

inferred← citeshttps://doi.org/10.1038/s41467-025-65952-0openalex-snapshot

ARMH2 is a cytosolic component of CatSper crucial for sperm function

inferred← citeshttps://doi.org/10.1038/s41467-026-70143-6openalex-snapshot

Sperm hyperactivation drives a circling-and-wandering swimming behavior

inferred← citeshttps://doi.org/10.1038/s41477-026-02334-4openalex-snapshot

Ancient peptide–redox signalling underlies sperm motility in Marchantia

inferred← citeshttps://doi.org/10.1038/s41585-020-00390-9openalex-snapshot

Sperm ion channels and transporters in male fertility and infertility

inferred← citeshttps://doi.org/10.1038/s41586-023-06518-2openalex-snapshot

Structure and electromechanical coupling of a voltage-gated Na+/H+ exchanger

inferred← citeshttps://doi.org/10.1038/s41598-018-35719-3openalex-snapshot

Impaired male fertility and abnormal epididymal epithelium differentiation in mice lacking CRISP1 and CRISP4

inferred← citeshttps://doi.org/10.1038/s41598-022-10390-xopenalex-snapshot

Hyperactivation is sufficient to release porcine sperm from immobilized oviduct glycans

inferred← citeshttps://doi.org/10.1038/sc.2008.81openalex-snapshot

CatSper genes expression, semen characteristics and histology of testes in the contusive spinal cord-injured mice model

inferred← citeshttps://doi.org/10.1038/sj.ijir.3901307openalex-snapshot

Phosphodiesterase 11 (PDE11) regulation of spermatozoa physiology

inferred← citeshttps://doi.org/10.1071/rd25040openalex-snapshot

Investigation of endocannabinoid 2-AG and its hydrolases for regulation on sperm motility and acrosome reaction in Kunming mice

inferred← citeshttps://doi.org/10.1073/pnas.0405580101openalex-snapshot

Sperm-specific protein kinase A catalytic subunit Cα 2 orchestrates cAMP signaling for male fertility

inferred← citeshttps://doi.org/10.1073/pnas.0610286104openalex-snapshot

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

inferred← citeshttps://doi.org/10.1073/pnas.0610909104openalex-snapshot

Wrath of the wraiths of CatSper3 and CatSper4

inferred← citeshttps://doi.org/10.1073/pnas.0810971105openalex-snapshot

Tissue-specific PKA inhibition using a chemical genetic approach and its application to studies on sperm capacitation

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.1111104108openalex-snapshot

LRRC52 (leucine-rich-repeat-containing protein 52), a testis-specific auxiliary subunit of the alkalization-activated Slo3 channel

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.1515159112openalex-snapshot

Bimodal rheotactic behavior reflects flagellar beat asymmetry in human sperm cells

inferred← citeshttps://doi.org/10.1073/pnas.1621279114openalex-snapshot

TCTE1 is a conserved component of the dynein regulatory complex and is required for motility and metabolism in mouse spermatozoa

inferred← citeshttps://doi.org/10.1073/pnas.1700367114openalex-snapshot

Regulation of the sperm calcium channel CatSper by endogenous steroids and plant triterpenoids

inferred← citeshttps://doi.org/10.1073/pnas.2136654100openalex-snapshot

Hyperactivated sperm motility driven by CatSper2 is required for fertilization

inferred← citeshttps://doi.org/10.1073/pnas.2510754123openalex-snapshot

Molecular basis of the higher-order assembly of CatSper

inferred← citeshttps://doi.org/10.1074/jbc.m110.156075openalex-snapshot

Testicular Expression of Adora3i2 in Adora3 Knockout Mice Reveals a Role of Mouse A3Ri2 and Human A3Ri3 Adenosine Receptors in Sperm*

inferred← citeshttps://doi.org/10.1074/jbc.m112.439356openalex-snapshot

Ca2+ Signals Generated by CatSper and Ca2+ Stores Regulate Different Behaviors in Human Sperm*

inferred← citeshttps://doi.org/10.1074/jbc.m114.607556openalex-snapshot

SLO3 K+ Channels Control Calcium Entry through CATSPER Channels in Sperm

inferred← citeshttps://doi.org/10.1074/jbc.m401194200openalex-snapshot

Stimulation of Human Spermatozoa with Progesterone Gradients to Simulate Approach to the Oocyte

inferred← citeshttps://doi.org/10.1074/jbc.m406489200openalex-snapshot

Male Mice That Do Not Express Group VIA Phospholipase A2 Produce Spermatozoa with Impaired Motility and Have Greatly Reduced Fertility

inferred← citeshttps://doi.org/10.1074/jbc.m501430200openalex-snapshot

Identical Phenotypes of CatSper1 and CatSper2 Null Sperm

inferred← citeshttps://doi.org/10.1074/jbc.m511288200openalex-snapshot

Association of Catsper1 or -2 with Cav3.3 Leads to Suppression of T-type Calcium Channel Activity

inferred← citeshttps://doi.org/10.1074/jbc.m701083200openalex-snapshot

CatSperβ, a Novel Transmembrane Protein in the CatSper Channel Complex

inferred← citeshttps://doi.org/10.1074/jbc.ra117.001566openalex-snapshot

CatSper channels are regulated by protein kinase A

inferred← citeshttps://doi.org/10.1074/jbc.ra120.013218openalex-snapshot

The Ca2+ channel CatSper is not activated by cAMP/PKA signaling but directly affected by chemicals used to probe the action of cAMP and PKA

inferred← citeshttps://doi.org/10.1080/01485010701329386openalex-snapshot

Current Concepts of Molecular Events During Bovine and Porcine Spermatozoa Capacitation

inferred← citeshttps://doi.org/10.1080/10495398.2017.1294597openalex-snapshot

Expression Profiling and Identification of Novel SNPs in CatSper2 Gene and Their Influence on Sperm Motility Parameters in Bovines

inferred← citeshttps://doi.org/10.1080/19336950.2018.1476791openalex-snapshot

Conservation of the Ca 2+ -permeability through the voltage sensor domain of mammalian CatSper subunit

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/10.1085/jgp.201912433openalex-snapshot

Paul F. Cranefield Award to Anne E. Carlson

inferred← citeshttps://doi.org/10.1089/ars.2021.0241openalex-snapshot

Exploring the Role of Oxidative Stress in Sperm Motility: A Proteomic Network Approach

inferred← citeshttps://doi.org/10.1093/biolre/ioad067openalex-snapshot

Sialylation: fate decision of mammalian sperm development, fertilization, and male fertility

inferred← citeshttps://doi.org/10.1093/biolre/iox082openalex-snapshot

Genomic identification, expression profiling, and functional characterization of CatSper channels in the bovine†

inferred← citeshttps://doi.org/10.1093/biolre/ioy048openalex-snapshot

Influence of the genetic background on the reproductive phenotype of mice lacking Cysteine-Rich Secretory Protein 1 (CRISP1)†

inferred← citeshttps://doi.org/10.1093/biolre/ioy105openalex-snapshot

The flagellar protein Enkurin is required for mouse sperm motility and for transport through the female reproductive tract†

inferred← citeshttps://doi.org/10.1093/biolre/ioz103openalex-snapshot

CRISPR/Cas9-mediated genome editing reveals 30 testis-enriched genes dispensable for male fertility in mice†

inferred← citeshttps://doi.org/10.1093/evolut/qpad188openalex-snapshot

Convergent rates of protein evolution identify novel targets of sexual selection in primates

inferred← citeshttps://doi.org/10.1093/humrep/deaf132openalex-snapshot

Bacterial vaginosis toxins impair sperm capacitation and fertilization

inferred← citeshttps://doi.org/10.1093/humrep/dei158openalex-snapshot

Reassessing the role of progesterone in fertilization—compartmentalized calcium signalling in human spermatozoa?

inferred← citeshttps://doi.org/10.1093/humrep/des467openalex-snapshot

The clinical significance of calcium-signalling pathways mediating human sperm hyperactivation

inferred← citeshttps://doi.org/10.1093/humrep/det372openalex-snapshot

p,p′-DDE activates CatSper and compromises human sperm function at environmentally relevant concentrations

inferred← citeshttps://doi.org/10.1093/humrep/deu075openalex-snapshot

Role of zinc trafficking in male fertility: from germ to sperm

inferred← citeshttps://doi.org/10.1093/humrep/dev103openalex-snapshot

Quantification of CatSper1 expression in human spermatozoa and relation to functional parameters

inferred← citeshttps://doi.org/10.1093/humrep/dev243openalex-snapshot

Specific loss of CatSper function is sufficient to compromise fertilizing capacity of human spermatozoa

inferred← citeshttps://doi.org/10.1093/humrep/dex055openalex-snapshot

Drug discovery for male subfertility using high-throughput screening: a new approach to an unsolved problem

inferred← citeshttps://doi.org/10.1093/humrep/dey280openalex-snapshot

Effects of pH manipulation, CatSper stimulation and Ca2+-store mobilization on [Ca2+]i and behaviour of human sperm

inferred← citeshttps://doi.org/10.1093/humupd/dmad008openalex-snapshot

Advances in non-hormonal male contraception targeting sperm motility

inferred← citeshttps://doi.org/10.1093/humupd/dmi047openalex-snapshot

Sperm transport in the female reproductive tract

inferred← citeshttps://doi.org/10.1093/humupd/dmi050openalex-snapshot

Calcium signalling in human spermatozoa: a specialized ‘toolkit’ of channels, transporters and stores

inferred← citeshttps://doi.org/10.1093/humupd/dmp032openalex-snapshot

Phenotyping male infertility in the mouse: how to get the most out of a 'non-performer'

inferred← citeshttps://doi.org/10.1093/humupd/dms027openalex-snapshot

Regulation of male fertility by CFTR and implications in male infertility

inferred← citeshttps://doi.org/10.1093/humupd/dmz032openalex-snapshot

Human sperm ion channel (dys)function: implications for fertilization

inferred← citeshttps://doi.org/10.1093/imammb/dqy015openalex-snapshot

Emergent three-dimensional sperm motility: coupling calcium dynamics and preferred curvature in a Kirchhoff rod model

inferred← citeshttps://doi.org/10.1093/molbev/msi178openalex-snapshot

Positive Selection for Indel Substitutions in the Rodent Sperm Protein Catsper1

inferred← citeshttps://doi.org/10.1093/molehr/gaab066openalex-snapshot

Dissecting EPPIN protease inhibitor domains in sperm motility and fertilizing ability: repercussions for male contraceptive development

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1093/molehr/gar040openalex-snapshot

Mathematical modeling of calcium signaling during sperm hyperactivation

inferred← citeshttps://doi.org/10.1093/molehr/gar041openalex-snapshot

Sperm chemotaxis and regulation of flagellar movement by Ca2+

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

Rediscovering sperm ion channels with the patch-clamp technique

inferred← citeshttps://doi.org/10.1093/molehr/gar048openalex-snapshot

Sperm motility: things are moving in the lab!

inferred← citeshttps://doi.org/10.1093/molehr/gat003openalex-snapshot

Molecular cloning and analysis of the Catsper1 gene promoter

inferred← citeshttps://doi.org/10.1093/molehr/gav019openalex-snapshot

Cell-penetrating peptides, targeting the regulation of store-operated channels, slow decay of the progesterone-induced [Ca2+]isignal in human sperm

inferred← citeshttps://doi.org/10.1093/molehr/gaw005openalex-snapshot

Fertilization defects in sperm fromCysteine-rich secretory protein 2(Crisp2) knockout mice: implications for fertility disorders

inferred← citeshttps://doi.org/10.1093/molehr/gaz034openalex-snapshot

Continuous behavioural ‘switching’ in human spermatozoa and its regulation by Ca2+-mobilising stimuli

inferred← citeshttps://doi.org/10.1095/biolreprod.103.026476openalex-snapshot

Different Signaling Pathways in Bovine Sperm Regulate Capacitation and Hyperactivation1

inferred← citeshttps://doi.org/10.1095/biolreprod.105.040733openalex-snapshot

Calcium/Calmodulin and Calmodulin Kinase II Stimulate Hyperactivation in Demembranated Bovine Sperm1

inferred← citeshttps://doi.org/10.1095/biolreprod.105.045468openalex-snapshot

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

inferred← citeshttps://doi.org/10.1095/biolreprod.105.047837openalex-snapshot

Signaling Pathways for Modulation of Mouse Sperm Motility by Adenosine and Catecholamine Agonists1

inferred← citeshttps://doi.org/10.1095/biolreprod.106.055038openalex-snapshot

Bovine Sperm Hyperactivation Is Promoted by Alkaline-Stimulated Ca2+ Influx1

inferred← citeshttps://doi.org/10.1095/biolreprod.107.060186openalex-snapshot

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

inferred← citeshttps://doi.org/10.1095/biolreprod.107.061358openalex-snapshot

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

inferred← citeshttps://doi.org/10.1095/biolreprod.108.074039openalex-snapshot

Egg Coat Proteins Activate Calcium Entry into Mouse Sperm via CATSPER Channels1

inferred← citeshttps://doi.org/10.1095/biolreprod.109.077107openalex-snapshot

A Novel, Single, Transmembrane Protein CATSPERG Is Associated with CATSPER1 Channel Protein1

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