scholarly article | Q13442814 |
P2093 | author name string | D G Myles | |
P Primakoff | |||
R Yuan | |||
P2860 | cites work | A metalloprotease-disintegrin participating in myoblast fusion | Q24311766 |
MDC9, a widely expressed cellular disintegrin containing cytoplasmic SH3 ligand domains | Q24316013 | ||
Solution Structure of Kistrin, a Potent Platelet Aggregation Inhibitor and GP IIb-IIIa Antagonist | Q27651187 | ||
A potential fusion peptide and an integrin ligand domain in a protein active in sperm-egg fusion | Q28291941 | ||
ADAM, a widely distributed and developmentally regulated gene family encoding membrane proteins with a disintegrin and metalloprotease domain | Q28301451 | ||
Traffic signals for lymphocyte recirculation and leukocyte emigration: the multistep paradigm | Q29547181 | ||
Identification of a binding site in the disintegrin domain of fertilin required for sperm-egg fusion | Q30454027 | ||
Mouse egg integrin alpha 6 beta 1 functions as a sperm receptor. | Q30464273 | ||
Proton NMR assignments and secondary structure of the snake venom protein echistatin | Q31036520 | ||
Molecular cloning of the human fertilin beta subunit | Q34388408 | ||
Proteolytic processing of a protein involved in sperm-egg fusion correlates with acquisition of fertilization competence | Q36223191 | ||
Evidence that proteolysis of the surface is an initial step in the mechanism of formation of sperm cell surface domains | Q36223973 | ||
Identification and purification of a sperm surface protein with a potential role in sperm-egg membrane fusion | Q36225276 | ||
The precursor region of a protein active in sperm-egg fusion contains a metalloprotease and a disintegrin domain: structural, functional, and evolutionary implications | Q36673157 | ||
Chromosomal assignment of four testis-expressed mouse genes from a new family of transmembrane proteins (ADAMs) involved in cell-cell adhesion and fusion | Q36817288 | ||
ADM-1, a protein with metalloprotease- and disintegrin-like domains, is expressed in syncytial organs, sperm, and sheath cells of sensory organs in Caenorhabditis elegans | Q37383656 | ||
The disulfide bridge pattern of snake venom disintegrins, flavoridin and echistatin | Q45166473 | ||
Chromosomal assignment of three novel mouse genes expressed in testicular cells | Q46431621 | ||
Mouse sperm-egg plasma membrane interactions: analysis of roles of egg integrins and the mouse sperm homologue of PH-30 (fertilin) β | Q46575601 | ||
Construction of synthetic immunogen: use of new T-helper epitope on malaria circumsporozoite protein | Q47645821 | ||
KUZ, a conserved metalloprotease-disintegrin protein with two roles in Drosophila neurogenesis | Q48060932 | ||
Immobilized Arg-Gly-Asp (RGD) peptides of varying lengths as structural probes of the platelet glycoprotein IIb/IIIa receptor | Q50132660 | ||
Structural and functional relationships between mouse and hamster zona pellucida glycoproteins. | Q52242485 | ||
Repetitive calcium transients and the role of calcium in exocytosis and cell cycle activation in the mouse egg | Q67721277 | ||
Three-dimensional structure of echistatin, the smallest active RGD protein | Q67919161 | ||
Ultrastructural observations on binding and membrane fusion between human sperm and zona pellucida-free hamster oocytes | Q70285519 | ||
Susceptibility to infection and altered hematopoiesis in mice deficient in both P- and E-selectins | Q70993034 | ||
Culture of mouse ova | Q71065322 | ||
Mechanics of in vitro fertilization in the hamster | Q71327016 | ||
Delayed Translation and Posttranslational Processing of Cyritestin, an Integral Transmembrane Protein of the Mouse Acrosome | Q71815496 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 105-112 | |
P577 | publication date | 1997-04-01 | |
P1433 | published in | Journal of Cell Biology | Q1524550 |
P1476 | title | A role for the disintegrin domain of cyritestin, a sperm surface protein belonging to the ADAM family, in mouse sperm-egg plasma membrane adhesion and fusion | |
P478 | volume | 137 |
Q28200043 | A profile of fertilization in mammals |
Q24548850 | ADAM 23/MDC3, a human disintegrin that promotes cell adhesion via interaction with the alphavbeta3 integrin through an RGD-independent mechanism |
Q40500199 | ADAM disintegrin-like domain recognition by the lymphocyte integrins alpha4beta1 and alpha4beta7. |
Q28198038 | ADAM family proteins in the immune system |
Q49525170 | ADAM proteases involved in inflammation are differentially altered in patients with gastritis or ulcer |
Q38691335 | Acrosome markers of human sperm |
Q41682027 | Activation of follicle cell surface phospholipase by tyrosine kinase dependent pathway is an essential event in Ascidian fertilization |
Q33692956 | Adamalysins. A family of metzincins including TNF-alpha converting enzyme (TACE). |
Q42818195 | An ADAM family member with expression in thymic epithelial cells and related tissues |
Q48365931 | Analysis of fertilin alpha (ADAM1)-mediated sperm-egg cell adhesion during fertilization and identification of an adhesion-mediating sequence in the disintegrin-like domain. |
Q30881761 | Analysis of the role of egg integrins in sperm-egg binding and fusion |
Q43925792 | Analysis of the roles of RGD-binding integrins, alpha(4)/alpha(9) integrins, alpha(6) integrins, and CD9 in the interaction of the fertilin beta (ADAM2) disintegrin domain with the mouse egg membrane |
Q35743279 | Approaches to enhance the efficacy of DNA vaccines |
Q37195063 | Beta1 integrin is an adhesion protein for sperm binding to eggs |
Q38417572 | Bovine sperm plasma membrane proteomics through biotinylation and subcellular enrichment |
Q36747539 | Cell-cell membrane fusion during mammalian fertilization |
Q32125976 | Characterisation of two highly conserved but non-allelic cellular disintegrins from rabbit testis. |
Q43261450 | Characterization of a novel cell-surface protein expressed on human sperm |
Q59287181 | Characterization of fertilinβ-disintegrin binding specificity in sperm–egg adhesion |
Q28579867 | Chronological gene expression of ADAMs during testicular development: prespermatogonia (gonocytes) express fertilin beta (ADAM2) |
Q24532037 | Cloning and characterization of ADAM28: evidence for autocatalytic pro-domain removal and for cell surface localization of mature ADAM28 |
Q28261454 | Cloning and initial characterization of mouse meltrin beta and analysis of the expression of four metalloprotease-disintegrins in bone cells |
Q59287168 | Comparison of Fertilinβ-Peptide-Substituted Polymers and Liposomes as Inhibitors of In Vitro Fertilization |
Q55262668 | Critical role of exosomes in sperm-egg fusion and virus-induced cell-cell fusion. |
Q46646799 | Cyclic FEE peptide increases human gamete fusion and potentiates its RGD-induced inhibition. |
Q42048950 | Cysteine-rich domain of human ADAM 12 (meltrin alpha) supports tumor cell adhesion |
Q40652765 | Differential localization of ADAM1a and ADAM1b in the endoplasmic reticulum of testicular germ cells and on the surface of epididymal sperm |
Q33763806 | Direct Binding of the Ligand PSG17 to CD9 Requires a CD9 Site Essential for Sperm-Egg Fusion |
Q34076820 | Dynamics of the mammalian sperm plasma membrane in the process of fertilization |
Q30435566 | Equatorial segment protein (ESP) is a human alloantigen involved in sperm-egg binding and fusion |
Q30442078 | Evidence that distinct states of the integrin alpha6beta1 interact with laminin and an ADAM. |
Q34196614 | Expression, immunolocalization and processing of fertilins ADAM-1 and ADAM-2 in the boar (Sus domesticus) spermatozoa during epididymal maturation |
Q28207538 | Fertilin beta and other ADAMs as integrin ligands: insights into cell adhesion and fertilization |
Q33954767 | Fertilization signalling and protein-tyrosine kinases |
Q40297361 | Fusogenic potential of sperm membrane lipids: nature's wisdom to accomplish targeted gene delivery |
Q42137547 | Human cyritestin genes (CYRN1 and CYRN2) are non-functional |
Q42694215 | Identification and characterization of ADAM32 with testis-predominant gene expression. |
Q22010229 | Identification of four novel ADAMs with potential roles in spermatogenesis and fertilization |
Q31117178 | Identification of the 48-kDa G11 protein from guinea pig testes as sperad |
Q26866008 | Immunocontraceptives: new approaches to fertility control |
Q33198406 | In vitro elucidation of substrate specificity and bioassay of proprotein convertase 4 using intramolecularly quenched fluorogenic peptides. |
Q36994938 | Increased expression of ADAM33 protein in asthmatic patients as compared to non-asthmatic controls |
Q22010715 | Interaction of the metalloprotease disintegrins MDC9 and MDC15 with two SH3 domain-containing proteins, endophilin I and SH3PX1 |
Q48020611 | Intracellular maturation of the mouse metalloprotease disintegrin MDC15. |
Q35896523 | Involvement of the prostate and testis expression (PATE)-like proteins in sperm-oocyte interaction |
Q28145371 | MDC-L, a novel metalloprotease disintegrin cysteine-rich protein family member expressed by human lymphocytes |
Q78167016 | Mammalian fertilization: molecular aspects of gamete adhesion, exocytosis, and fusion |
Q34487656 | Mediation of sperm-egg fusion: evidence that mouse egg alpha6beta1 integrin is the receptor for sperm fertilinbeta |
Q28248448 | Metalloprotease-disintegrins: links to cell adhesion and cleavage of TNF alpha and Notch |
Q24321609 | Metalloproteinase-like, disintegrin-like, cysteine-rich proteins MDC2 and MDC3: novel human cellular disintegrins highly expressed in the brain |
Q34072571 | Molecular and cellular mechanisms of sperm-oocyte interactions opinions relative to in vitro fertilization (IVF). |
Q42679268 | Molecular cloning and characterization of Izumo1 gene from sheep and cashmere goat reveal alternative splicing. |
Q48301776 | Molecular cloning and expression analysis of a novel member of the Disintegrin and Metalloprotease-Domain (ADAM) family |
Q45126624 | Molecular cloning, characterization of porcine IZUMO1, an IgSF family member. |
Q28212343 | Molecular mechanisms involved in mammalian gamete fusion |
Q33738495 | Molecules on the sperm's route to fertilization |
Q34360669 | Molecules that function in the steps of fertilization |
Q34666699 | Multivalent fertilinbeta oligopeptides: the dependence of fertilization inhibition on length and density |
Q33902527 | Multivariate analysis of male reproductive function in Inpp5b-/- mice reveals heterogeneity in defects in fertility, sperm-egg membrane interaction and proteolytic cleavage of sperm ADAMs. |
Q28510333 | None of the integrins known to be present on the mouse egg or to be ADAM receptors are essential for sperm-egg binding and fusion |
Q28284321 | Oocyte CD9 is enriched on the microvillar membrane and required for normal microvillar shape and distribution |
Q24300857 | Oocyte specific oolemmal SAS1B involved in sperm binding through intra-acrosomal SLLP1 during fertilization |
Q37732273 | Oolemma receptors and oocyte activation |
Q33798201 | Paternal contributions to the mammalian zygote: fertilization after sperm-egg fusion |
Q59287174 | Peptides corresponding to the epidermal growth factor-like domain of mouse fertilin: Synthesis and biological activity |
Q37343735 | Polymeric ADAM protein mimics interrogate mammalian sperm-egg binding. |
Q28592718 | Possible function of the ADAM1a/ADAM2 Fertilin complex in the appearance of ADAM3 on the sperm surface |
Q37358452 | Proprotein convertase subtilisin/kexin type 4 in mammalian fertility: a review. |
Q28508065 | Protein disulfide isomerase homolog PDILT is required for quality control of sperm membrane protein ADAM3 and male fertility [corrected]. |
Q30311864 | Role of multiple beta1 integrins in cell adhesion to the disintegrin domains of ADAMs 2 and 3. |
Q24675158 | Role of the integrin-associated protein CD9 in binding between sperm ADAM 2 and the egg integrin alpha6beta1: implications for murine fertilization |
Q30409231 | SAS1B protein [ovastacin] shows temporal and spatial restriction to oocytes in several eutherian orders and initiates translation at the primary to secondary follicle transition |
Q30305569 | Sequence-specific interaction between the disintegrin domain of mouse ADAM 2 (fertilin beta) and murine eggs. Role of the alpha(6) integrin subunit |
Q30307197 | Sequence-specific interaction between the disintegrin domain of mouse ADAM 3 and murine eggs: role of beta1 integrin-associated proteins CD9, CD81, and CD98. |
Q52115392 | SpADAM, a sea urchin ADAM, has conserved structure and expression. |
Q24805371 | Sperm specific proteins-potential candidate molecules for fertility control |
Q33712218 | Structure-function analysis of the ADAM family of disintegrin-like and metalloproteinase-containing proteins (review). |
Q34296287 | Testicular and epididymal ADAMs: expression and function during fertilization |
Q33826746 | The ADAM gene family: surface proteins with adhesion and protease activity |
Q28593547 | The ADAM1a and ADAM1b genes, instead of the ADAM1 (fertilin alpha) gene, are localized on mouse chromosome 5 |
Q41812554 | The gene for the human tMDC I sperm surface protein is non-functional: implications for its proposed role in mammalian sperm-egg recognition. |
Q34120904 | The glycoprotein B disintegrin-like domain binds beta 1 integrin to mediate cytomegalovirus entry |
Q37084769 | The mechanism of sperm–egg interaction and the involvement of IZUMO1 in fusion |
Q33678482 | The potential use of sperm antigens as targets for immunocontraception; past, present and future. |
Q34136288 | The role of ADAM 15 in glomerular mesangial cell migration |
Q28240480 | The splicing and fate of ADAM33 transcripts in primary human airways fibroblasts |
Q42994231 | Transcripts encoding the sperm surface protein tMDC II are non-functional in the human |
Q28506225 | Transgenic mice with inactive alleles for procollagen N-proteinase (ADAMTS-2) develop fragile skin and male sterility |
Q35623183 | Unresolved issues in mammalian fertilization |
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