| Multiple genes in the Pate5-13 genomic region contribute to ADAM3 processingdagger. | Multiple genes in the Pate5-13 genomic region contribute to ADAM3 processing†.
Noda T, Shinohara H, Kobayashi S, Taira A, Oura S, Tahara D, Tokuyasu M, Araki K, Ikawa M., | 04/29/2024 |
| Dissecting the PRSS37 interactome and potential mechanisms leading to ADAM3 loss in PRSS37-null sperm. | Dissecting the PRSS37 interactome and potential mechanisms leading to ADAM3 loss in PRSS37-null sperm.
Xiong W, Shen C, Li C, Zhang X, Ge H, Tang L, Shen Y, Lu S, Zhang H, Han M, Zhang A, Wang J, Wu Y, Fei J, Wang Z. | 09/4/2021 |
| co-expression of sperm membrane proteins CMTM2A and CMTM2B is required for male fertility and affects the localization of the sperm membrane protein ADAM3 in regulating sperm fertilizing ability. | Co-expression of sperm membrane proteins CMTM2A and CMTM2B is essential for ADAM3 localization and male fertility in mice.
Fujihara Y, Oji A, Kojima-Kita K, Larasati T, Ikawa M., Free PMC Article | 10/19/2019 |
| Protein disulfide isomerase homolog PDILT is required for quality control of sperm membrane protein ADAM3 and male infertility | Protein disulfide isomerase homolog PDILT is required for quality control of sperm membrane protein ADAM3 and male fertility [corrected].
Tokuhiro K, Ikawa M, Benham AM, Okabe M., Free PMC Article | 05/5/2012 |
| Lack of tyrosylprotein sulfotransferase-2 activity results in altered sperm-egg interactions and loss of ADAM3 and ADAM6 in epididymal sperm. | Lack of tyrosylprotein sulfotransferase-2 activity results in altered sperm-egg interactions and loss of ADAM3 and ADAM6 in epididymal sperm.
Marcello MR, Jia W, Leary JA, Moore KL, Evans JP., Free PMC Article | 07/2/2011 |
| we report that Adam2 and Adam3 knockout sperm have severely impaired sperm aggregation and that this defect is not restored over time during in vitro cultivation. | Impaired sperm aggregation in Adam2 and Adam3 null mice.
Han C, Kwon JT, Park I, Lee B, Jin S, Choi H, Cho C. | 06/14/2010 |
| The Adam3-disrupted sperm were unable to migrate into the oviduct after coitus. | Disruption of ADAM3 impairs the migration of sperm into oviduct in mouse.
Yamaguchi R, Muro Y, Isotani A, Tokuhiro K, Takumi K, Adham I, Ikawa M, Okabe M. | 01/21/2010 |
| Results suggest that association with ADAM2 is a key element for stability of ADAM3 in epididymal sperm, and the presence of the ADAM2-ADAM3 complex in sperm also suggests a potential role of ADAM2 with ADAM3 in sperm binding to the egg zona pellucida. | Identification of an ADAM2-ADAM3 complex on the surface of mouse testicular germ cells and cauda epididymal sperm.
Nishimura H, Myles DG, Primakoff P. | 01/21/2010 |
| ADAM3 expression is regulated by ADAM1a/ADAM2 Fertilin complex on the cell surface of mouse sperm | Possible function of the ADAM1a/ADAM2 Fertilin complex in the appearance of ADAM3 on the sperm surface.
Nishimura H, Kim E, Nakanishi T, Baba T. | 01/21/2010 |
| the mature form of ADAM3 is involved in the binding of sperm to the egg zona pellucida, not in the membrane fusion between sperm and egg. | Synthesis, processing, and subcellular localization of mouse ADAM3 during spermatogenesis and epididymal sperm transport.
Kim E, Nishimura H, Iwase S, Yamagata K, Kashiwabara S, Baba T. | 01/21/2010 |
| Angiotensin-converting enzyme is involved in distributing ADAM3 to a location where it can participate in sperm-zona pellucida binding. | Aberrant distribution of ADAM3 in sperm from both angiotensin-converting enzyme (Ace)- and calmegin (Clgn)-deficient mice.
Yamaguchi R, Yamagata K, Ikawa M, Moss SB, Okabe M. | 01/21/2010 |