نتایج جستجو برای: smads

تعداد نتایج: 965  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
Sayyed K Zaidi Andrew J Sullivan Andre J van Wijnen Janet L Stein Gary S Stein Jane B Lian

Runx factors control lineage commitment and are transcriptional effectors of Smad signaling. Genetic defects in these pathways interfere with normal development. The in situ localization of Runx and Smad proteins must impact the mechanisms by which these proteins function together in gene regulation. We show that the integration of Runx and Smad signals is mediated by in situ interactions at sp...

Journal: :Mechanisms of Development 2003
Yutaka Yoshida Andreas von Bubnoff Naoko Ikematsu Ira L. Blitz Junko K. Tsuzuku Eri H. Yoshida Hisashi Umemori Kohei Miyazono Tadashi Yamamoto Ken W.Y. Cho

Tob inhibits bone morphogenetic protein (BMP) signaling by interacting with receptor-regulated Smads in osteoblasts. Here we provide evidence that Tob also interacts with the inhibitory Smads 6 and 7. A yeast two-hybrid screen identified Smad6 as a protein interacting with Tob. Tob co-localizes with Smad6 at the plasma membrane and enhances the interaction between Smad6 and activated BMP type I...

Journal: :Cell 2000
Yutaka Yoshida Sakae Tanaka Hisashi Umemori Osamu Minowa Michihiko Usui Naoko Ikematsu Eri Hosoda Takeshi Imamura Junko Kuno Teruhito Yamashita Kohei Miyazono Masaki Noda Tetsuo Noda Tadashi Yamamoto

Bone morphogenetic protein (BMP) controls osteoblast proliferation and differentiation through Smad proteins. Here we show that Tob, a member of the emerging family of antiproliferative proteins, is a negative regulator of BMP/Smad signaling in osteoblasts. Mice carrying a targeted deletion of the tob gene have a greater bone mass resulting from increased numbers of osteoblasts. Orthotopic bone...

2017
Seiyu Sugiyama Kenji Yamamoto Tetsuya Matsuda Seiyu Imoto Kenji Sugiyama Tetsuya Yamamoto Tadashi Matsuda

Bone morphogenetic proteins (BMPs) play central roles in differentiation, development, and physiologic tissue remodeling. Recently, we have demonstrated that a protein inhibitor of activated STAT, PIASy suppresses TGF-b signaling by interacting with Sma and MADrelated protein 3 (Smad3). In this study, we examined a PIASy dependent inhibitory effect on BMP signaling. PIASy expression was induced...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Tao Lu Liping Tian Yulong Han Michael Vogelbaum George R Stark

Some tumor cell lines secrete high concentrations of TGFbeta or IL-1. Similarly high concentrations of each of these cytokines cross-activate the other pathway: TGFbeta activates NFkappaB, and IL-1beta activates Smads. The IL-1 signaling components IRAK, MyD88, TRAF6, and TAK1 are all required for cross-activation of NFkappaB by TGFbeta. Knockdown experiments revealed that both TGFbeta receptor...

Journal: :Cold Spring Harbor Perspectives in Biology 2016

2014
Kan Xiao Ze-He Song Le-Fei Jiao Ya-Lu Ke Cai-Hong Hu

Weaning stress caused marked changes in intestinal structure and function. Transforming growth factor-β1 (TGF-β1) and canonical Smads signaling pathway are suspected to play an important regulatory role in post-weaning adaptation of the small intestine. In the present study, the intestinal morphology and permeability, developmental expressions of tight junction proteins and TGF-β1 in the intest...

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