What is she best known for?
The fields of study she is best known for:
- Gene
- DNA
- Transcription factor
Cell biology, Signal transduction, SMAD, Transforming growth factor and Transcription factor are her primary areas of study.
The various areas that Caroline S. Hill examines in her Cell biology study include Cell cycle and Transcription.
Caroline S. Hill has researched Signal transduction in several fields, including TGF beta signaling pathway, ACVR2B, Cancer research and Gene expression.
Her studies deal with areas such as R-SMAD, Response element and MAPK/ERK pathway as well as SMAD.
Her work deals with themes such as SUPERFAMILY, Receptor, Extracellular signal and Signalling, which intersect with Transforming growth factor.
Her research in Transcription factor intersects with topics in Extracellular and Cell membrane.
Her most cited work include:
- SB-431542 Is a Potent and Specific Inhibitor of Transforming Growth Factor-β Superfamily Type I Activin Receptor-Like Kinase (ALK) Receptors ALK4, ALK5, and ALK7 (1378 citations)
- The Rho family GTPases RhoA, Racl , and CDC42Hsregulate transcriptional activation by SRF (1179 citations)
- Transcriptional Regulation by Extracellular Signals: Mechanisms and Specificity (1157 citations)
What are the main themes of her work throughout her whole career to date?
Caroline S. Hill mainly focuses on Cell biology, SMAD, Transforming growth factor, Signal transduction and Molecular biology.
She has included themes like Receptor, Transcription factor and R-SMAD in her Cell biology study.
The study incorporates disciplines such as Epithelial–mesenchymal transition, Xenopus and Peptide sequence in addition to SMAD.
Her Transforming growth factor research includes elements of SUPERFAMILY, Cell culture, Transcription and Signalling.
Her Signal transduction study combines topics from a wide range of disciplines, such as Extracellular, Cancer research and Autocrine signalling.
Her work deals with themes such as DNA, Regulation of gene expression, Bone morphogenetic protein and Mesoderm, which intersect with Molecular biology.
She most often published in these fields:
- Cell biology (64.49%)
- SMAD (33.64%)
- Transforming growth factor (25.23%)
What were the highlights of her more recent work (between 2016-2021)?
- Cell biology (64.49%)
- Transforming growth factor (25.23%)
- Phosphorylation (14.95%)
In recent papers she was focusing on the following fields of study:
Her primary scientific interests are in Cell biology, Transforming growth factor, Phosphorylation, Receptor and SMAD.
She studies Cell biology, focusing on Nodal signaling in particular.
Her Transforming growth factor research incorporates elements of Carcinogenesis, Cancer research, Signal transduction and Downregulation and upregulation.
Her Signal transduction research includes elements of Extracellular, Signalling and In vivo.
Her ACVR1, ACVR2A and Receptor clustering study in the realm of Receptor interacts with subjects such as Fibrodysplasia ossificans progressiva.
Her SMAD study integrates concerns from other disciplines, such as Transcription, Kinase, Cell signaling and Gene isoform.
Between 2016 and 2021, her most popular works were:
- TGF-β uses a novel mode of receptor activation to phosphorylate SMAD1/5 and induce epithelial-to-mesenchymal transition (81 citations)
- Distinct modes of SMAD2 chromatin binding and remodeling shape the transcriptional response to NODAL/Activin signaling. (28 citations)
- Spatial and temporal control of NODAL signaling. (25 citations)
In her most recent research, the most cited papers focused on:
- Gene
- DNA
- Transcription factor
The scientist’s investigation covers issues in Cell biology, Nodal signaling, NODAL, Transforming growth factor and Signal transduction.
She works on Cell biology which deals in particular with Lefty.
Her Lefty research is multidisciplinary, incorporating elements of Signalling and Cell fate determination.
Her Nodal signaling research includes themes of Chromatin, Transcription factor, Chromatin binding and Activin type 2 receptors.
As a part of the same scientific family, Caroline S. Hill mostly works in the field of Epithelial–mesenchymal transition, focusing on Cell and, on occasion, SMAD.
Her Morphogen study combines topics in areas such as Nodal Signaling Ligands, Endoderm, Mesoderm and Fibroblast growth factor.
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