AbstractIt is known that a characteristic of the mammalian preimplantation-embryo-specific cell cycle is the substantially shortened G1-phase, although the regulation mechanisms of the unique cell cycle remain unclear. In the present study, we first examined the presence of retinoblastoma (RB) tumor suppressor gene product throughout mouse preimplantation embryo development and found that the RB expression was down-regulated between the four-cell and morula stages. Furthermore, the overexpression of RB protein in the mouse embryos during this phase inhibited their development significantly. These results suggest that the absence of RB protein contributes to the preimplantation-embryo-specific cell cycle
The product of the retinoblastoma tumor suppressor gene (Rb) can control cell proliferation and prom...
The retinoblastoma (RB) family of proteins are found in organisms as distantly related as humans, pl...
Loss of G1/S control is a hallmark of cancer, and is often caused by inactivation of the retinoblast...
AbstractIt is known that a characteristic of the mammalian preimplantation-embryo-specific cell cycl...
AbstractIt is clear that G1–S phase control is exerted after the mouse embryo implants into the uter...
Fibroblasts prepared from retinoblastoma (Rb) gene-negative mouse embryos exhibit a shorter G1 phase...
During mouse germ cell development, the first sign of sex differentiation occurs when XY germ cells ...
AbstractThe retinoblastoma protein (pRb) is a central regulator of the cell cycle, controlling passa...
AbstractThe preimplantation development of the mammalian embryo encompasses a series of critical eve...
The retinoblastoma protein (pRB) is best known for regulating cell proliferation through E2F transcr...
AbstractThe tumor suppressor RB regulates diverse cellular processes such as G1/S transition, cell d...
AbstractTranscription of endogenous genes in preimplantation 1- and 2-cell mouse embryos was determi...
AbstractThe retinoblastoma gene, RB-1, was the first identified tumor suppressor. Rb−/− mice die in ...
Mutations in the Retinoblastoma (RB) tumor suppressor gene or disruptions in the RB-E2F signaling pa...
During oogenesis, mammalian oocytes accumulate maternal mRNAs that support the embryo until embryoni...
The product of the retinoblastoma tumor suppressor gene (Rb) can control cell proliferation and prom...
The retinoblastoma (RB) family of proteins are found in organisms as distantly related as humans, pl...
Loss of G1/S control is a hallmark of cancer, and is often caused by inactivation of the retinoblast...
AbstractIt is known that a characteristic of the mammalian preimplantation-embryo-specific cell cycl...
AbstractIt is clear that G1–S phase control is exerted after the mouse embryo implants into the uter...
Fibroblasts prepared from retinoblastoma (Rb) gene-negative mouse embryos exhibit a shorter G1 phase...
During mouse germ cell development, the first sign of sex differentiation occurs when XY germ cells ...
AbstractThe retinoblastoma protein (pRb) is a central regulator of the cell cycle, controlling passa...
AbstractThe preimplantation development of the mammalian embryo encompasses a series of critical eve...
The retinoblastoma protein (pRB) is best known for regulating cell proliferation through E2F transcr...
AbstractThe tumor suppressor RB regulates diverse cellular processes such as G1/S transition, cell d...
AbstractTranscription of endogenous genes in preimplantation 1- and 2-cell mouse embryos was determi...
AbstractThe retinoblastoma gene, RB-1, was the first identified tumor suppressor. Rb−/− mice die in ...
Mutations in the Retinoblastoma (RB) tumor suppressor gene or disruptions in the RB-E2F signaling pa...
During oogenesis, mammalian oocytes accumulate maternal mRNAs that support the embryo until embryoni...
The product of the retinoblastoma tumor suppressor gene (Rb) can control cell proliferation and prom...
The retinoblastoma (RB) family of proteins are found in organisms as distantly related as humans, pl...
Loss of G1/S control is a hallmark of cancer, and is often caused by inactivation of the retinoblast...