247 related articles for article (PubMed ID: 18809571)
1. Redundant roles of SMAD2 and SMAD3 in ovarian granulosa cells in vivo.
Li Q; Pangas SA; Jorgez CJ; Graff JM; Weinstein M; Matzuk MM
Mol Cell Biol; 2008 Dec; 28(23):7001-11. PubMed ID: 18809571
[TBL] [Abstract][Full Text] [Related]
2. Smad2 and Smad3 are redundantly essential for the TGF-beta-mediated regulation of regulatory T plasticity and Th1 development.
Takimoto T; Wakabayashi Y; Sekiya T; Inoue N; Morita R; Ichiyama K; Takahashi R; Asakawa M; Muto G; Mori T; Hasegawa E; Saika S; Hara T; Nomura M; Yoshimura A
J Immunol; 2010 Jul; 185(2):842-55. PubMed ID: 20548029
[TBL] [Abstract][Full Text] [Related]
3. Oocyte-secreted factor activation of SMAD 2/3 signaling enables initiation of mouse cumulus cell expansion.
Dragovic RA; Ritter LJ; Schulz SJ; Amato F; Thompson JG; Armstrong DT; Gilchrist RB
Biol Reprod; 2007 May; 76(5):848-57. PubMed ID: 17192514
[TBL] [Abstract][Full Text] [Related]
4. Smad2 and Smad3 are redundantly essential for the suppression of iNOS synthesis in macrophages by regulating IRF3 and STAT1 pathways.
Sugiyama Y; Kakoi K; Kimura A; Takada I; Kashiwagi I; Wakabayashi Y; Morita R; Nomura M; Yoshimura A
Int Immunol; 2012 Apr; 24(4):253-65. PubMed ID: 22331441
[TBL] [Abstract][Full Text] [Related]
5. Premature luteinization and cumulus cell defects in ovarian-specific Smad4 knockout mice.
Pangas SA; Li X; Robertson EJ; Matzuk MM
Mol Endocrinol; 2006 Jun; 20(6):1406-22. PubMed ID: 16513794
[TBL] [Abstract][Full Text] [Related]
6. Ephrin-A5 Is Required for Optimal Fertility and a Complete Ovulatory Response to Gonadotropins in the Female Mouse.
Buensuceso AV; Son AI; Zhou R; Paquet M; Withers BM; Deroo BJ
Endocrinology; 2016 Feb; 157(2):942-55. PubMed ID: 26672804
[TBL] [Abstract][Full Text] [Related]
7. Comparative effects of TGF-β2/Smad2 and TGF-β2/Smad3 signaling pathways on proliferation, migration, and extracellular matrix production in a human lens cell line.
Li J; Tang X; Chen X
Exp Eye Res; 2011 Mar; 92(3):173-9. PubMed ID: 21276793
[TBL] [Abstract][Full Text] [Related]
8. Implication of Smad2 and Smad3 in transforming growth factor-β-induced posterior capsular opacification of human lens epithelial cells.
Li H; Yuan X; Li J; Tang X
Curr Eye Res; 2015 Apr; 40(4):386-97. PubMed ID: 24911914
[TBL] [Abstract][Full Text] [Related]
9. Using RNA interference to identify the different roles of SMAD2 and SMAD3 in NIH/3T3 fibroblast cells.
Zheng R; Xiong Q; Zuo B; Jiang S; Li F; Lei M; Deng C; Xiong Y
Cell Biochem Funct; 2008; 26(5):548-56. PubMed ID: 18506886
[TBL] [Abstract][Full Text] [Related]
10. Smad2 and Smad3 have differential sensitivity in relaying TGFβ signaling and inversely regulate early lineage specification.
Liu L; Liu X; Ren X; Tian Y; Chen Z; Xu X; Du Y; Jiang C; Fang Y; Liu Z; Fan B; Zhang Q; Jin G; Yang X; Zhang X
Sci Rep; 2016 Feb; 6():21602. PubMed ID: 26905010
[TBL] [Abstract][Full Text] [Related]
11. Paracrine actions of growth differentiation factor-9 in the mammalian ovary.
Elvin JA; Clark AT; Wang P; Wolfman NM; Matzuk MM
Mol Endocrinol; 1999 Jun; 13(6):1035-48. PubMed ID: 10379900
[TBL] [Abstract][Full Text] [Related]
12. Maternal Smad3 deficiency compromises decidualization in mice.
Zhao KQ; Lin HY; Zhu C; Yang X; Wang H
J Cell Biochem; 2012 Oct; 113(10):3266-75. PubMed ID: 22644778
[TBL] [Abstract][Full Text] [Related]
13. Distinct roles of myofibroblast-specific Smad2 and Smad3 signaling in repair and remodeling of the infarcted heart.
Huang S; Chen B; Su Y; Alex L; Humeres C; Shinde AV; Conway SJ; Frangogiannis NG
J Mol Cell Cardiol; 2019 Jul; 132():84-97. PubMed ID: 31085202
[TBL] [Abstract][Full Text] [Related]
14. Differential activation of noncanonical SMAD2/SMAD3 signaling by bone morphogenetic proteins causes disproportionate induction of hyaluronan production in immortalized human granulosa cells.
Zhang H; Tian S; Klausen C; Zhu H; Liu R; Leung PC
Mol Cell Endocrinol; 2016 Jun; 428():17-27. PubMed ID: 26992562
[TBL] [Abstract][Full Text] [Related]
15. Unique and redundant roles of Smad3 in TGF-beta-mediated regulation of long bone development in organ culture.
Alvarez J; Serra R
Dev Dyn; 2004 Aug; 230(4):685-99. PubMed ID: 15254903
[TBL] [Abstract][Full Text] [Related]
16. The endogenous ratio of Smad2 and Smad3 influences the cytostatic function of Smad3.
Kim SG; Kim HA; Jong HS; Park JH; Kim NK; Hong SH; Kim TY; Bang YJ
Mol Biol Cell; 2005 Oct; 16(10):4672-83. PubMed ID: 16093355
[TBL] [Abstract][Full Text] [Related]
17. Follicle-restricted compartmentalization of transforming growth factor beta superfamily ligands in the feline ovary.
Bristol SK; Woodruff TK
Biol Reprod; 2004 Mar; 70(3):846-59. PubMed ID: 14656728
[TBL] [Abstract][Full Text] [Related]
18. Granulosa cell-expressed BMPR1A and BMPR1B have unique functions in regulating fertility but act redundantly to suppress ovarian tumor development.
Edson MA; Nalam RL; Clementi C; Franco HL; Demayo FJ; Lyons KM; Pangas SA; Matzuk MM
Mol Endocrinol; 2010 Jun; 24(6):1251-66. PubMed ID: 20363875
[TBL] [Abstract][Full Text] [Related]
19. Uterine double-conditional inactivation of
Kriseman M; Monsivais D; Agno J; Masand RP; Creighton CJ; Matzuk MM
Proc Natl Acad Sci U S A; 2019 Feb; 116(9):3873-3882. PubMed ID: 30651315
[TBL] [Abstract][Full Text] [Related]
20. SMAD2 and SMAD3 differentially regulate adiposity and the growth of subcutaneous white adipose tissue.
Kumari R; Irudayam MJ; Al Abdallah Q; Jones TL; Mims TS; Puchowicz MA; Pierre JF; Brown CW
FASEB J; 2021 Dec; 35(12):e22018. PubMed ID: 34731499
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
