scholarly article | Q13442814 |
P356 | DOI | 10.1074/JBC.M609132200 |
P698 | PubMed publication ID | 17289678 |
P50 | author | Randall S. Prather | Q48812359 |
Alexander Th Wu | Q63229815 | ||
P2093 | author name string | Gaurishankar Manandhar | |
Peter Sutovsky | |||
Wei Xu | |||
Richard Oko | |||
Young-Joo Yi | |||
Kwang-Wook Park | |||
Mika Katayama | |||
Billy N Day | |||
Yan Wei Xi | |||
P2860 | cites work | Interactions of sperm perinuclear theca with the oocyte: implications for oocyte activation, anti-polyspermy defense, and assisted reproduction | Q23919483 |
Yes-associated protein and p53-binding protein-2 interact through their WW and SH3 domains | Q24291010 | ||
The interaction of dystrophin with beta-dystroglycan is regulated by tyrosine phosphorylation | Q24291543 | ||
Characterization of the WW domain of human yes-associated protein and its polyproline-containing ligands | Q24313075 | ||
The WW domain of Yes-associated protein binds a proline-rich ligand that differs from the consensus established for Src homology 3-binding modules | Q24323939 | ||
A WW domain-containing yes-associated protein (YAP) is a novel transcriptional co-activator | Q24534123 | ||
A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity | Q24564608 | ||
Structure of a WW domain containing fragment of dystrophin in complex with beta-dystroglycan | Q27626122 | ||
WW and SH3 domains, two different scaffolds to recognize proline-rich ligands | Q28209648 | ||
The WW domain of neural protein FE65 interacts with proline-rich motifs in Mena, the mammalian homolog of Drosophila enabled | Q28257310 | ||
Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome | Q28288744 | ||
Characterization of a novel protein-binding module--the WW domain | Q28295526 | ||
The importance of being proline: the interaction of proline-rich motifs in signaling proteins with their cognate domains | Q29618469 | ||
On-stage selection of single round spermatids using a vital, mitochondrion-specific fluorescent probe MitoTracker(TM) and high resolution differential interference contrast microscopy | Q30763498 | ||
NeW wrinkles for an old domain | Q34132908 | ||
Tr-kit-induced resumption of the cell cycle in mouse eggs requires activation of a Src-like kinase | Q34150271 | ||
WW domain binding protein-2, an E6-associated protein interacting protein, acts as a coactivator of estrogen and progesterone receptors | Q34537904 | ||
Egg activation at fertilization: where it all begins | Q34615390 | ||
The molecular foundations of the maternal to zygotic transition in the preimplantation embryo | Q34806720 | ||
Cdc42 activation couples spindle positioning to first polar body formation in oocyte maturation. | Q35230006 | ||
The cytosolic sperm factor that triggers Ca2+ oscillations and egg activation in mammals is a novel phospholipase C: PLCzeta. | Q35719009 | ||
Calcium at fertilization and in early development | Q35822230 | ||
Functional, biochemical, and chromatographic characterization of the complete [Ca2+]i oscillation-inducing activity of porcine sperm | Q42482615 | ||
Molecular nature of calicin, a major basic protein of the mammalian sperm head cytoskeleton. | Q42680634 | ||
Sperm phospholipase Czeta from humans and cynomolgus monkeys triggers Ca2+ oscillations, activation and development of mouse oocytes | Q44205140 | ||
Fertilization and subsequent development in vitro of pig oocytes inseminated in a modified tris-buffered medium with frozen-thawed ejaculated spermatozoa | Q44868775 | ||
Novel aspect of perinuclear theca assembly revealed by immunolocalization of non-nuclear somatic histones during bovine spermiogenesis | Q47365301 | ||
Are Src family kinases involved in cell cycle resumption in rat eggs? | Q47869641 | ||
Novel actin-related proteins Arp-T1 and Arp-T2 as components of the cytoskeletal calyx of the mammalian sperm head | Q48282131 | ||
A novel trans-complementation assay suggests full mammalian oocyte activation is coordinately initiated by multiple, submembrane sperm components | Q48923611 | ||
Analysis of mouse oocyte activation suggests the involvement of sperm perinuclear material | Q48939401 | ||
The removal of the sperm perinuclear theca and its association with the bovine oocyte surface during fertilization | Q48954230 | ||
Activation of mouse oocytes requires multiple sperm factors but not sperm PLCgamma1. | Q50723559 | ||
Repetitive calcium transients and the role of calcium in exocytosis and cell cycle activation in the mouse egg | Q67721277 | ||
Distribution and possible role of perinuclear theca proteins during bovine spermiogenesis | Q71010692 | ||
Protein composition of the perinuclear theca of bull spermatozoa | Q72046091 | ||
Characterization of boar sperm cytoskeletal cylicin II as an actin-binding protein | Q73148490 | ||
Actin-binding properties and colocalization with actin during spermiogenesis of mammalian sperm calicin | Q73221260 | ||
Somatic histones are components of the perinuclear theca in bovine spermatozoa | Q73459062 | ||
P433 | issue | 16 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | perinuclear theca | Q21122951 |
WBP2 N-terminal like | Q21122954 | ||
WW domain binding | Q21831245 | ||
WBP2 N-terminal like | Q21992810 | ||
P304 | page(s) | 12164-12175 | |
P577 | publication date | 2007-02-08 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | PAWP, a sperm-specific WW domain-binding protein, promotes meiotic resumption and pronuclear development during fertilization | |
P478 | volume | 282 |
Q33710470 | "This is where it all started" - the pivotal role of PLCζ within the sophisticated process of mammalian reproduction: a systemic review |
Q38785469 | Antigen unmasking enhances visualization efficacy of the oocyte activation factor, phospholipase C zeta, in mammalian sperm. |
Q38948842 | Biochemical alterations in the oocyte in support of early embryonic development. |
Q45406028 | Calcium influx and sperm-evoked calcium responses during oocyte maturation and egg activation |
Q38125408 | Comparative biology of sperm factors and fertilization-induced calcium signals across the animal kingdom |
Q38017958 | Delivering value from sperm proteomics for fertility. |
Q46298639 | Detection of Regional Variation in Selection Intensity within Protein-Coding Genes Using DNA Sequence Polymorphism and Divergence |
Q36805175 | Diagnosis of genetic defects through parallel assessment of PLCζ and CAPZA3 in infertile men with history of failed oocyte activation |
Q39038802 | Egg Activation at Fertilization |
Q35811147 | Elevated Expression of the Testis-specific Gene WBP2NL in Breast Cancer |
Q34539672 | Evaluation of PLCζ and PAWP Expression in Globozoospermic Individuals |
Q39038023 | Expression analysis of PAWP during mouse embryonic stem cell-based spermatogenesis in vitro |
Q48553014 | Expression profile of PLCζ, PAWP, and TR-KIT in association with fertilization potential, embryo development, and pregnancy outcomes in globozoospermic candidates for intra-cytoplasmic sperm injection and artificial oocyte activation. |
Q36332055 | Fourteen babies born after round spermatid injection into human oocytes |
Q99712195 | From Sperm Motility to Sperm-Borne microRNA Signatures: New Approaches to Predict Male Fertility Potential |
Q48575344 | Functional disparity between human PAWP and PLCζ in the generation of Ca2+ oscillations for oocyte activation |
Q64121072 | Genetic Variation in Pan Species Is Shaped by Demographic History and Harbors Lineage-Specific Functions |
Q35685874 | Genome Wide Distributions and Functional Characterization of Copy Number Variations between Chinese and Western Pigs |
Q28116434 | Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP |
Q36938264 | Human sperm devoid of PLC, zeta 1 fail to induce Ca(2+) release and are unable to initiate the first step of embryo development |
Q48620824 | Incubation of sperm heads impairs fertilization and early embryo development following intracytoplasmic sperm injection (ICSI) by decreasing oocyte activation in mice |
Q35604397 | Is PAWP the "real" sperm factor? |
Q64101741 | Mechanisms of tethering and cargo transfer during epididymosome-sperm interactions |
Q26750781 | Molecular triggers of egg activation at fertilization in mammals |
Q35819818 | Negative biomarker based male fertility evaluation: Sperm phenotypes associated with molecular-level anomalies. |
Q44765540 | Novel animal pole-enriched maternal mRNAs are preferentially expressed in neural ectoderm |
Q38502046 | Novel signalling mechanism and clinical applications of sperm-specific PLCζ. |
Q39155622 | Oocyte Activation and Fertilisation: Crucial Contributors from the Sperm and Oocyte |
Q36086851 | Oocyte activation and phospholipase C zeta (PLCζ): diagnostic and therapeutic implications for assisted reproductive technology |
Q38582312 | Oocyte activation deficiency: a role for an oocyte contribution? |
Q33614538 | Oocyte activation, phospholipase C zeta and human infertility |
Q37732273 | Oolemma receptors and oocyte activation |
Q27024569 | PLCζ or PAWP: revisiting the putative mammalian sperm factor that triggers egg activation and embryogenesis |
Q90705572 | Phospholipase Cζ (PLCζ) versus postacrosomal sheath WW domain-binding protein (PAWP): Which molecule will survive as a sperm factor? |
Q43181878 | Preservation of sperm within the mouse cauda epididymidis in salt or sugars at room temperature |
Q36415409 | Protein-tyrosine kinase signaling in the biological functions associated with sperm |
Q33327478 | RAB2A: a major subacrosomal protein of bovine spermatozoa implicated in acrosomal biogenesis |
Q35604405 | Re: Is PAWP the 'real' sperm factor? |
Q37378245 | Relationship between Potential Sperm Factors Involved in Oocyte Activation and Sperm DNA Fragmentation with Intra-Cytoplasmic Sperm Injection Clinical Outcomes |
Q52730590 | Review: Sperm-oocyte interactions and their implications for bull fertility, with emphasis on the ubiquitin-proteasome system. |
Q48162485 | Revolutionizing male fertility factor research in mice by using the genome editing tool CRISPR/Cas9. |
Q36427058 | Signal transduction in mammalian oocytes during fertilization |
Q38544251 | Sperm Factors and Oocyte Activation: Current Controversies and Considerations |
Q38155316 | Sperm PLCζ: from structure to Ca2+ oscillations, egg activation and therapeutic potential. |
Q38701090 | Sperm contributions to oocyte activation: more that meets the eye |
Q48569378 | Sperm postacrosomal WW domain-binding protein is not required for mouse egg activation |
Q35673842 | Sperm-borne microRNA-34c is required for the first cleavage division in mouse |
Q47550282 | Sperm-borne phospholipase C zeta-1 ensures monospermic fertilization in mice. |
Q48507390 | Sperm-derived factors enhance the in vitro developmental potential of haploid parthenotes |
Q34230268 | Sperm-specific post-acrosomal WW-domain binding protein (PAWP) does not cause Ca2+ release in mouse oocytes. |
Q37956573 | Starting a new life: sperm PLC-zeta mobilizes the Ca2+ signal that induces egg activation and embryo development: an essential phospholipase C with implications for male infertility. |
Q58585851 | The Eggstraordinary Story of How Life Begins |
Q38938421 | The Evaluation of WBP2NL-Related Genes Expression in Breast Cancer |
Q38010640 | The composition, protein genesis and significance of the inner acrosomal membrane of eutherian sperm |
Q47647186 | The developmental origin and compartmentalization of glutathione-s-transferase omega 2 isoforms in the perinuclear theca of eutherian spermatozoa. |
Q64956074 | The perforatorium and postacrosomal sheath of rat spermatozoa share common developmental origins and protein constituents†. |
Q48773093 | The postacrosomal assembly of sperm head protein, PAWP, is independent of acrosome formation and dependent on microtubular manchette transport. |
Q34201037 | The testicular and epididymal expression profile of PLCζ in mouse and human does not support its role as a sperm-borne oocyte activating factor |
Q48786341 | Ubiquitin C-terminal hydrolase-activity is involved in sperm acrosomal function and anti-polyspermy defense during porcine fertilization. |
Q90237461 | WBP2 shares a common location in mouse spermatozoa with WBP2NL/PAWP and like its descendent is a candidate mouse oocyte-activating factor |
Q48522670 | WBP2NL/PAWP mRNA and protein expression in sperm cells are not related to semen parameters, fertilization rate, or reproductive outcome |
Q39445786 | WW domain-binding protein 2: an adaptor protein closely linked to the development of breast cancer |
Q50433464 | Wbp2nl has a developmental role in establishing neural and non-neural ectodermal fates. |
Q53158570 | [Assisted oocyte activation: a new tool for severe male factor infertility treatment]. |
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