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

Particulate Adenylate Cyclase Plays a Key Role in Human Sperm Olfactory Receptor-mediated Chemotaxis

Spehr, M., Schwane, K., Riffell, J. A., Barbour, J., Zimmer, R. K., Neuhaus, E. M., & Hatt, H. H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m403913200 · Cited by 156

Ca2+-related changes in the capacitation state of human spermatozoa assessed by a chlortetracycline fluorescence assay

DasGupta, S., Mills, C., & Fraser, L. R. (1993) · Reproduction · doi:10.1530/jrf.0.0990135 · Cited by 155

Nongenomic activation of spermatozoa by steroid hormones: Facts and fictions

Baldi, E., Luconi, M., Muratori, M., Marchiani, S., Tamburrino, L., & Forti, G. (2009) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2009.02.006 · Cited by 153

Inhibition of Ser/Thr Phosphatases Induces Capacitation-associated Signaling in the Presence of Src Kinase Inhibitors

Krapf, D., Arcelay, E., Wertheimer, E. V., Sanjay, A., Pilder, S. H., Salicioni, A. M., & Visconti, P. E. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.085845 · Cited by 153

Sperm Deliver a New Second Messenger

Churchill, G. C., O'Neill, J. S., Masgrau, R., Patel, S., Thomas, J. M., Genazzani, A. A., & Galione, A. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00002-2 · Cited by 153

Molecular determinants of Ca 2+ /calmodulin-dependent regulation of Ca v 2.1 channels

Lee, A., Zhou, H., Scheuer, T., & Catterall, W. A. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2237000100 · Cited by 150

The Fucose Sulfate Polymer of Egg Jelly Binds to Sperm REJ and Is the Inducer of the Sea Urchin Sperm Acrosome Reaction

Vacquier, V. D., & Moy, G. W. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8729 · Cited by 150

Ion channels that control fertility in mammalian spermatozoa

Navarro, B., Kirichok, Y., Chung, J., & Clapham, D. E. (2008) · The International Journal of Developmental Biology · doi:10.1387/ijdb.072554bn · Cited by 148

CatSper-null mutant spermatozoa are unable to ascend beyond the oviductal reservoir

Ho, K., Wolff, C. A., & Suárez, S. S. (2009) · Reproduction Fertility and Development · doi:10.1071/rd08183 · Cited by 148

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

Xia, J., Reigada, D., Mitchell, C. H., & Ren, D. (2007) · Biology of Reproduction · doi:10.1095/biolreprod.107.061358 · Cited by 148

Assessment of the CFTR and ENaC association

Berdiev, B. K., Qadri, Y. J., & Benos, D. J. (2008) · Molecular BioSystems · doi:10.1039/b810471a · Cited by 147

The Inositol 1,4,5-Trisphosphate Receptor (IP 3 R) and Its Regulators: Sometimes Good and Sometimes Bad Teamwork

Choe, C.-U., & Ehrlich, B. E. (2006) · Science s STKE · doi:10.1126/stke.3632006re15 · Cited by 147

Functional and physical coupling of voltage‐sensitive calcium channels with exocytotic proteins: ramifications for the secretion mechanism

Atlas, D. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00347.x · Cited by 145

An endoplasmic reticulum/plasma membrane junction: STIM1/Orai1/TRPCs

Lee, K. P., Yuan, J. P., Hong, J. H., So, I., Worley, P. F., & Muallem, S. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.11.078 · Cited by 145

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

Ino, M., Yoshinaga, T., Wakamori, M., Miyamoto, N., Takahashi, E., Sonoda, J., Kagaya, T., Oki, T., Nagasu, T., Nishizawa, Y., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081089398 · Cited by 144

Thinking about flagellar oscillation

Brokaw, C. J. (2008) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.20313 · Cited by 143

Protein synthesis in sperm: Dialog between mitochondria and cytoplasm

Gur, Y., & Breitbart, H. (2008) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2007.11.015 · Cited by 142

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

Skålhegg, B. S., Huang, Y., Su, T. T., Idzerda, R. L., McKnight, G. S., & Burton, K. A. (2002) · Molecular Endocrinology · doi:10.1210/mend.16.3.0793 · Cited by 140

ZP3-dependent activation of sperm cation channels regulates acrosomal secretion during mammalian fertilization.

Arnoult, C., Zeng, Y., & Florman, H. M. (1996) · The Journal of Cell Biology · doi:10.1083/jcb.134.3.637 · Cited by 139

Drosophila TRP channels

Montell, C. (2005) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-005-1426-2 · Cited by 138

Calcium signaling via two-pore channels: local or global, that is the question

Zhu, M. X., Ma, J., Parrington, J., Calcraft, P. J., Galione, A., & Evans, A. M. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00475.2009 · Cited by 138

Sperm Chemotaxis: Egg Peptides Control Cytosolic Calcium to Regulate Flagellar Responses

Cook, S. P., Brokaw, C. J., MULLER, C. H., & Babcock, D. F. (1994) · Developmental Biology · doi:10.1006/dbio.1994.1229 · Cited by 137

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

Santi, C. M., Darszon, A., & Hernández‐Cruz, A. (1996) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1996.271.5.c1583 · Cited by 137

IRBIT coordinates epithelial fluid and HCO3–secretion by stimulating the transporters pNBC1 and CFTR in the murine pancreatic duct

Yang, D., Shcheynikov, N., Zeng, W., Ohana, E., So, I., Ando, H., Mizutani, A., Mikoshiba, K., & Muallem, S. (2008) · Journal of Clinical Investigation · doi:10.1172/jci36983 · Cited by 136

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

Suárez, S. S., & Osman, R. A. (1987) · Biology of Reproduction · doi:10.1095/biolreprod36.5.1191 · Cited by 136

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

Wang, H., Liu, J., Cho, K., & Ren, D. (2009) · Biology of Reproduction · doi:10.1095/biolreprod.109.077107 · Cited by 135

A preovulatory temperature gradient between the isthmus and ampulla of pig oviducts during the phase of sperm storage

Hunter, R. H. F., & Nichol, R. C. (1986) · Reproduction · doi:10.1530/jrf.0.0770599 · Cited by 133

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

Hernández-González, E. O., Sosnik, J., Edwards, J. L., Acevedo‐Fernández, J. J., Mendoza-Lujambio, I., López‐González, I., Demarco, I. A., Wertheimer, E. V., Darszon, A., & Visconti, P. E. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m508172200 · Cited by 133

Signaling pathways in sperm capacitation and acrosome reaction.

Breitbart, H. (2003) · PubMed · Cited by 133

Multiple proteins present in purified porcine sperm apical plasma membranes interact with the zona pellucida of the oocyte

van Gestel, R. A., Brewis, I. A., Ashton, P. R., et al. (2007) · Molecular Human Reproduction · doi:10.1093/molehr/gam030 · Cited by 131

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

Maas, D. H. A., Storey, B. T., & Mastroianni, L. (1977) · Fertility and Sterility · doi:10.1016/s0015-0282(16)42801-3 · Cited by 130

Rapid PKA‐catalysed phosphorylation of boar sperm proteins induced by the capacitating agent bicarbonate

Harrison, R. A. P. (2004) · Molecular Reproduction and Development · doi:10.1002/mrd.20028 · Cited by 129

STIM and Orai: Dynamic Intermembrane Coupling to Control Cellular Calcium Signals

Deng, X., Wang, Y., Zhou, Y., Soboloff, J., & Gill, D. L. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.r109.018655 · Cited by 128

Calcium Signaling Through CatSper Channels in Mammalian Fertilization

Ren, D., & Xia, J. (2010) · Physiology · doi:10.1152/physiol.00049.2009 · Cited by 126

T-Type Calcium Channel Inhibition Underlies the Analgesic Effects of the Endogenous Lipoamino Acids

Barbara, G., Alloui, A., Nargeot, J., Lory, P., Eschalier, A., Bourinet, E., & Chemin, J. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2919-09.2009 · Cited by 125

Enkurin is a novel calmodulin and TRPC channel binding protein in sperm

Sutton, K. A., Jungnickel, M. K., Wang, Y., Cullen, K. J., Lambert, S., & Florman, H. M. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.07.031 · Cited by 125

An intracellular trafficking pathway in the seminiferous epithelium regulating spermatogenesis: a biochemical and molecular perspective

Cheng, C. Y., & Mruk, D. D. (2009) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409230903061207 · Cited by 125

Ca2+ signalling in the control of motility and guidance in mammalian sperm

Publicover, S. J. (2008) · Frontiers in bioscience · doi:10.2741/3105 · Cited by 125

Polycystin-2 Activation by Inositol 1,4,5-Trisphosphate-induced Ca2+ Release Requires Its Direct Association with the Inositol 1,4,5-Trisphosphate Receptor in a Signaling Microdomain

Sammels, E., Devogelaere, B., Mekahli, D., Bultynck, G., Missiaen, L., Parys, J. B., Cai, Y., Somlo, S., & SMEDT, H. D. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.090662 · Cited by 125

Real-time analysis of the role of Ca2+ in flagellar movement and motility in single sea urchin sperm

Wood, C. D., Nishigaki, T., Furuta, T., Baba, S. A., & Darszon, A. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200411001 · Cited by 125

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

Marquez, B., Ignotz, G. G., & Suárez, S. S. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.11.007 · Cited by 124

Identification of a human homologue of the sea urchin receptor for egg jelly: a polycystic kidney disease-like protein

Hughes, J. R., Ward, C. J., Aspinwall, R., Butler, R., & Harris, P. C. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.3.543 · Cited by 124

The STIM/Orai coupling machinery

Frischauf, I., Schindl, R., Derler, I., Bergsmann, J., Fahrner, M., & Romanin, C. (2008) · Channels · doi:10.4161/chan.2.4.6705 · Cited by 123

Deficiency of SPAG16L Causes Male Infertility Associated with Impaired Sperm Motility1

Zhang, Z., Kostetskii, I., Tang, W., Haig-Ladewig, L. A., Sapiro, R., Wei, Z., Patel, A. M., Bennett, J., Gerton, G. L., Moss, S. B., et al. (2005) · Biology of Reproduction · doi:10.1095/biolreprod.105.049254 · Cited by 122

The acrosomal vesicle of mouse sperm is a calcium store

Herrick, S. B., Schweissinger, D. L., Kim, S., Bayan, K. R., Mann, S., & Cardullo, R. A. (2004) · Journal of Cellular Physiology · doi:10.1002/jcp.20172 · Cited by 120

A K+-selective cGMP-gated ion channel controls chemosensation of sperm

Strünker, T., Weyand, I., Bönigk, W., Van, Q., Loogen, A., Brown, J. E., Kashikar, N. D., Hagen, V., Krause, E., & Kaupp, U. B. (2006) · Nature Cell Biology · doi:10.1038/ncb1473 · Cited by 120

Dissecting ICRAC, a store-operated calcium current

Hogan, P. G., & Rao, A. (2007) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2007.03.009 · Cited by 117

Sperm binding to the zona pellucida is not sufficient to induce acrosome exocytosis

Baibakov, B. A., Gauthier, L., Talbot, P., Rankin, T. L., & Dean, J. (2007) · Development · doi:10.1242/dev.02752 · Cited by 117

SOCIC: The store-operated calcium influx complex

Vaca, L. A. (2010) · Cell Calcium · doi:10.1016/j.ceca.2010.01.002 · Cited by 116

The regulation of spermatozoa by calcium cyclic nucleotides.

Dl, G., & Gs, K. (1980) · PubMed · Cited by 113

Acrosomal exocytosis, a special type of regulated secretion

Mayorga, L. S., Tomes, C. N., & Belmonte, S. A. (2007) · IUBMB Life · doi:10.1080/15216540701222872 · Cited by 111

Physiological volume regulation by spermatozoa

Yeung, C., Barfield, J. P., & Cooper, T. G. (2006) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2005.12.030 · Cited by 111

Sperm-activating peptides in the regulation of ion fluxes, signal transduction and motility

Darszon, A., Guerrero, A., Galindo, B. E., Nishigaki, T., & Wood, C. D. (2008) · The International Journal of Developmental Biology · doi:10.1387/ijdb.072550ad · Cited by 111

Soluble Adenylyl Cyclase Is Localized to Cilia and Contributes to Ciliary Beat Frequency Regulation via Production of cAMP

Schmid, A., Süttő, Z., Nlend, M.-C., Horváth, G., Schmid, N., Buck, J., Levin, L. R., Conner, G. E., Fregien, N. L., & Salathe, M. A. (2007) · The Journal of General Physiology · doi:10.1085/jgp.200709784 · Cited by 110

Sperm Chemotaxis during the Process of Fertilization in the Ascidians Ciona savignyi and Ciona intestinalis

Yoshida, M., Inaba, K., & Morisawa, M. (1993) · Developmental Biology · doi:10.1006/dbio.1993.1152 · Cited by 109

Tuning sperm chemotaxis by calcium burst timing

Guerrero, A., Nishigaki, T., Carneiro, J., Tatsu, Y., Wood, C. D., & Darszon, A. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.04.013 · Cited by 108

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

Cai, X., & Clapham, D. E. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003569 · Cited by 108

Involvement of Cystic Fibrosis Transmembrane Conductance Regulator in Mouse Sperm Capacitation

Hernández-González, E. O., Treviño, C. L., Castellano, L. E., de la Vega‐Beltrán, J. L., Ocampo, A. Y., Wertheimer, E. V., Visconti, P. E., & Darszon, A. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m701603200 · Cited by 108

Mg2+ Homeostasis: The Mg2+nificent TRPM Chanzymes

Montell, C. (2003) · Current Biology · doi:10.1016/j.cub.2003.09.048 · Cited by 107

Two novel 2-aminoethyl diphenylborinate (2-APB) analogues differentially activate and inhibit store-operated Ca2+ entry via STIM proteins

Goto, J.-I., Suzuki, A. Z., Ozaki, S., Matsumoto, N., Nakamura, T., Ebisui, E., Fleig, A., Penner, R., & Mikoshiba, K. (2009) · Cell Calcium · doi:10.1016/j.ceca.2009.10.004 · Cited by 107

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

Carlson, A. E., Hille, B., & Babcock, D. F. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.09.017 · Cited by 106

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

Jin, J., O’Doherty, A., Wang, S., Zheng, H., Sanders, K. M., & Yan, W. (2005) · Biology of Reproduction · doi:10.1095/biolreprod.105.045468 · Cited by 106

How spermatozoa come to be confined to surfaces

Cosson, J., Huitorel, P., & Gagnon, C. (2002) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.10085 · Cited by 105

Fertilization in Mammals

Florman, H. M., & Ducibella, T. (2006) · Elsevier eBooks · doi:10.1016/b978-012515400-0/50007-5 · Cited by 105

Hyperactivation of mammalian sperm.

Suárez, S. S., & Ho, H. (2003) · PubMed · Cited by 104

Epac Activates the Small G Proteins Rap1 and Rab3A to Achieve Exocytosis*

Branham, M., Bustos, M., Blas, G. D. D., Rehmann, H., Zarelli, V. E. P., Treviño, C., Darszon, A., Mayorga, L., & Tomes, C. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.015362 · Cited by 104

Voltage‐dependent modulation of T‐type calcium channels by protein tyrosine phosphorylation

Arnoult, C., Lémos, J. R., & Florman, H. M. (1997) · The EMBO Journal · doi:10.1093/emboj/16.7.1593 · Cited by 103

Progesterone Triggers a Wave of Increased Free Calcium during the Human Sperm Acrosome Reaction

Meizel, S., Turner, K. O., & Nuccitelli, R. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8477 · Cited by 102

Polycystins and renovascular mechanosensory transduction

Patel, A. J., & Honoré, É. (2010) · Nature Reviews Nephrology · doi:10.1038/nrneph.2010.97 · Cited by 101

Transient receptor potential channels and vascular function

Earley, S., & Brayden, J. E. (2010) · Clinical Science · doi:10.1042/cs20090641 · Cited by 100

Cyclic nucleotide‐gated ion channels in sensory transduction

Pifferi, S., Boccaccio, A., & Menini, A. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.03.086 · Cited by 100

Polycystin-1 Activates and Stabilizes the Polycystin-2 Channel

Xu, G. M., González‐Perrett, S., Essafi, M., Timpanaro, G. A., Montalbetti, N., Arnaout, M. A., & Cantiello, H. F. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m209996200 · Cited by 100

The Fallopian tubes in domestic mammals: how vital is their physiological activity?

Hunter, R. H. F. (2005) · annales de biologie animale biochimie biophysique · doi:10.1051/rnd:2005020 · Cited by 99

Two-pore channels: Regulation by NAADP and customized roles in triggering calcium signals

Patel, S., Marchant, J. S., & Brailoiu, E. (2010) · Cell Calcium · doi:10.1016/j.ceca.2010.05.001 · Cited by 98

Speract induces calcium oscillations in the sperm tail

Wood, C. D., Darszon, A., & Whitaker, M. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200212053 · Cited by 98

Ca2+-dependent PKC activation mediates menthol-induced desensitization of transient receptor potential M8

Abe, J., Hosokawa, H., Sawada, Y., Matsumura, K., & Kobayashi, S. (2005) · Neuroscience Letters · doi:10.1016/j.neulet.2005.12.005 · Cited by 97

The “switching on” of mammalian spermatozoa: Molecular events involved in promotion and regulation of capacitation

Fraser, L. R. (2009) · Molecular Reproduction and Development · doi:10.1002/mrd.21124 · Cited by 97

The acid test: the discovery of two-pore channels (TPCs) as NAADP-gated endolysosomal Ca2+ release channels

Galione, A., Evans, A. M., Ma, J., Parrington, J., Arredouani, A., Cheng, X., & Zhu, M. X. (2009) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-009-0682-y · Cited by 97

Activation of a Gi protein in mouse sperm membranes by solubilized proteins of the zona pellucida, the egg's extracellular matrix.

Ward, C. R., Storey, B. T., & Kopf, G. S. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)49678-6 · Cited by 96

In defense of a function for the human epididymis

Wallach, E. E., & Cooper, T. G. (1990) · Fertility and Sterility · doi:10.1016/s0015-0282(16)53988-0 · Cited by 96

Molecular Basis of Sperm Flagellar Axonemes

Inaba, K. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1389.017 · Cited by 93

Calcium channel γ subunits: a functionally diverse protein family

Chen, R., Deng, T.-C., Garcia, T. X., Sellers, Z. M., & Best, P. M. (2007) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-007-0002-0 · Cited by 91

Membrane Potential Regulates Sea Urchin Sperm Adenylylcyclase

Beltrán, C., Zapata, O., & Darszon, A. (1996) · Biochemistry · doi:10.1021/bi952806v · Cited by 90

Antagonism of T-type calcium channels inhibits high-fat diet–induced weight gain in mice

Uebele, V. N., Gotter, A. L., Nuss, C. E., Kraus, R. L., Doran, S. M., Garson, S. L., Reiss, D. R., Li, Y., Barrow, J. C., Reger, T. S., et al. (2009) · Journal of Clinical Investigation · doi:10.1172/jci36954 · Cited by 90

Positive selection on protein-length in the evolution of a primate sperm ion channel

Podlaha, O., & Zhang, J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2033555100 · Cited by 89

Atomic Force Microscopy Reveals the Alternating Subunit Arrangement of the TRPP2-TRPV4 Heterotetramer

Stewart, A. P., Smith, G. D., Sandford, R. N., & Edwardson, J. M. (2010) · Biophysical Journal · doi:10.1016/j.bpj.2010.05.012 · Cited by 89

Molecular Pharmacology of Human Cav3.2 T-Type Ca2+ Channels: Block by Antihypertensives, Antiarrhythmics, and Their Analogs

Perez‐Reyes, E., Deusen, A. L. V., & Vitko, I. (2008) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.108.145672 · Cited by 89

A flagellar K + -dependent Na + /Ca 2+ exchanger keeps Ca 2+ low in sea urchin spermatozoa

Su, Y., & Vacquier, V. D. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.102186699 · Cited by 89

Molecular pathways underlying the modulation of T-type calcium channels by neurotransmitters and hormones

Chemin, J., Traboulsie, A., & Lory, P. (2006) · Cell Calcium · doi:10.1016/j.ceca.2006.04.015 · Cited by 88

A Gradient of 2-Arachidonoylglycerol Regulates Mouse Epididymal Sperm Cell Start-Up1

Cobellis, G., Ricci, G., Cacciola, G., Orlando, P., Petrosino, S., Cascio, M. G., Bisogno, T., PETROCELLIS, L. D., Chioccarelli, T., Altucci, L., et al. (2009) · Biology of Reproduction · doi:10.1095/biolreprod.109.079210 · Cited by 88

suREJ3, a Polycystin-1 Protein, Is Cleaved at the GPS Domain and Localizes to the Acrosomal Region of Sea Urchin Sperm

Mengerink, K. J., Moy, G. W., & Vacquier, V. D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m109673200 · Cited by 87

A Role of the Transient Receptor Potential Domain of Vanilloid Receptor I in Channel Gating

García‐Sanz, N., Valente, P., Gomis, A., Fernández-Carvajal, A. M., Fernandez-Ballester, G. J., Viana, F., Belmonte, C., & Ferrer-Montiel, A. V. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2457-07.2007 · Cited by 87

A guanine nucleotide‐binding regulatory protein in human sperm mediates acrosomal exocytosis induced by the human zona pellucida

Lee, M. A., CHECK, J. H., & Kopf, G. S. (1992) · Molecular Reproduction and Development · doi:10.1002/mrd.1080310114 · Cited by 87

Effects of Native Human Zona Pellucida Glycoproteins 3 and 4 on Acrosome Reaction and Zona Pellucida Binding of Human Spermatozoa

Chiu, P. C. N., Wong, B. S. T., Chung, M., et al. (2008) · Biology of Reproduction · doi:10.1095/biolreprod.108.069344 · Cited by 86

Investigation of the role of SRC in capacitation-associated tyrosine phosphorylation of human spermatozoa

Mitchell, L. A., Nixon, B., Baker, M. A., & Aitken, R. J. (2008) · Molecular Human Reproduction · doi:10.1093/molehr/gan007 · Cited by 86

Activation of Na+/H+ Exchanger NHE3 by Angiotensin II Is Mediated by Inositol 1,4,5-Triphosphate (IP3) Receptor-binding Protein Released with IP3 (IRBIT) and Ca2+/Calmodulin-dependent Protein Kinase II

He, P., Klein, J. D., & Yun, C. C. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.133066 · Cited by 85

Cl− Is Required for HCO3− Entry Necessary for Sperm Capacitation in Guinea Pig: Involvement of a Cl−/HCO3− Exchanger (SLC26A3) and CFTR1

Chen, W. Y., Xu, W., Chen, Z. H., Ni, Y., Yuan, Y. Y., Zhou, S. C., Zhou, W. W., Tsang, L. L., Chung, Y. W., Höglund, P., et al. (2008) · Biology of Reproduction · doi:10.1095/biolreprod.108.068528 · Cited by 85

Evidence for multiple distinctly localized adenylyl cyclase isoforms in mammalian spermatozoa

Baxendale, R. W., & Fraser, L. R. (2003) · Molecular Reproduction and Development · doi:10.1002/mrd.10344 · Cited by 85

A sperm-activating peptide controls a cGMP-signaling pathway in starfish sperm☆

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Store-operated calcium channel regulates the chemotactic behavior of ascidian sperm

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