The scientist’s investigation covers issues in Signal transduction, Cell biology, SMAD, Transforming growth factor beta and Molecular biology. His Signal transduction research is multidisciplinary, incorporating perspectives in Receptor, Receptor complex, Cellular differentiation and R-SMAD. Xin-Hua Feng has researched Cell biology in several fields, including Genetics, Autocrine signalling and SOCS2.
His SMAD research incorporates elements of Transcription, Kinase and Ectopic expression. His Transforming growth factor beta study combines topics in areas such as Cancer research, Immunology, DNA-binding protein, TGF beta signaling pathway and Phosphorylation. He combines subjects such as Peptide sequence, Transcription factor, Protein kinase domain and Mitogen-activated protein kinase kinase with his study of Molecular biology.
His primary areas of investigation include Cell biology, Signal transduction, Phosphorylation, SMAD and Cancer research. His work carried out in the field of Cell biology brings together such families of science as Genetics, Ubiquitin and Cellular differentiation. His Signal transduction research is multidisciplinary, relying on both Molecular biology, Receptor and Ubiquitin ligase.
His studies deal with areas such as BMPR2 and Kinase as well as Phosphorylation. His SMAD study incorporates themes from Growth factor receptor, Transcription factor and Transcription. The Transforming growth factor beta study combines topics in areas such as R-SMAD and DNA-binding protein.
His scientific interests lie mostly in Cell biology, Phosphorylation, Signal transduction, Cancer research and Transforming growth factor. His Cell biology study focuses mostly on SMAD, Transforming growth factor beta, Kinase, Cell signaling and TANK-binding kinase 1. His SMAD study improves the overall literature in Genetics.
Xin-Hua Feng interconnects Tyrosine and Function in the investigation of issues within Phosphorylation. His research in Signal transduction intersects with topics in Molecular biology, Ubiquitin and R-SMAD. His work deals with themes such as Suppressor and Receptor, which intersect with Transforming growth factor.
Xin-Hua Feng mainly focuses on Cell biology, Signal transduction, Cancer research, SMAD and Transforming growth factor beta. The various areas that Xin-Hua Feng examines in his Cell biology study include Innate immune system and Immunity. The concepts of his Signal transduction study are interwoven with issues in Protein kinase domain, Ubiquitin and Immunology.
The study incorporates disciplines such as Carcinogenesis, Transcription factor, STAT3, Gene silencing and Immunotherapy in addition to Cancer research. His Transforming growth factor beta research is multidisciplinary, incorporating elements of Acetylation, Cell morphology, Tubulin, Microtubule and Cytoskeleton. His research integrates issues of Receptor, Gene expression and Transforming growth factor in his study of Phosphorylation.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
SPECIFICITY AND VERSATILITY IN TGF-β SIGNALING THROUGH SMADS
Xin-Hua Feng;Rik Derynck.
Annual Review of Cell and Developmental Biology (2005)
Smads: transcriptional activators of TGF-beta responses.
Rik Derynck;Ying Zhang;Xin-Hua Feng.
Molecular Antagonism and Plasticity of Regulatory and Inflammatory T Cell Programs
Xuexian O. Yang;Roza Nurieva;Gustavo J. Martinez;Hong Soon Kang.
Receptor-associated Mad homologues synergize as effectors of the TGF-β response
Ying Zhang;Xin-Hua Feng;Rui-Yun Wu;Rik Derynck.
Smad3 and Smad4 cooperate with c-Jun/c-Fos to mediate TGF-beta-induced transcription.
Ying Zhang;Xin-Hua Feng;Rik Derynck.
TGF-beta receptor signaling.
Rik Derynck;Xin-Hua Feng.
Biochimica et Biophysica Acta (1997)
The tumor suppressor Smad4/DPC4 and transcriptional adaptor CBP/p300 are coactivators for Smad3 in TGF-β-induced transcriptional activation
Xin-Hua Feng;Ying Zhang;Rui-Yun Wu;Rik Derynck.
Genes & Development (1998)
Smurf2 Is a Ubiquitin E3 Ligase Mediating Proteasome-dependent Degradation of Smad2 in Transforming Growth Factor-β Signaling
Xia Lin;Min Liang;Xin-Hua Feng.
Journal of Biological Chemistry (2000)
PPM1A Functions as a Smad Phosphatase to Terminate TGFβ Signaling
Xia Lin;Xueyan Duan;Yao Yun Liang;Ying Su.
Smad2, Smad3 and Smad4 cooperate with Sp1 to induce p15Ink4B transcription in response to TGF‐β
Xin‐Hua Feng;Xin‐Hua Feng;Xia Lin;Rik Derynck.
The EMBO Journal (2000)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: