What is he best known for?
The fields of study he is best known for:
His primary scientific interests are in Molecular biology, Transcription factor, Cell biology, Cell cycle and Genetics.
His work deals with themes such as Gene expression, Enhancer, Chromatin, Gene and Gene product, which intersect with Molecular biology.
His research integrates issues of Internal medicine, Insulin and Endocrinology in his study of Gene expression.
His Transcription factor research is multidisciplinary, relying on both Regulation of gene expression and Phosphorylation.
The Cell biology study combines topics in areas such as Cell, Homologous recombination, Hepatocyte nuclear factors, Hepatocyte and Morphogenesis.
His Cell cycle study combines topics from a wide range of disciplines, such as Transcription, Cell growth and c-jun.
His most cited work include:
- A c-jun dominant negative mutant protects sympathetic neurons against programmed cell death (778 citations)
- Two distinct enhancers with different cell specificities coexist in the regulatory region of polyoma (578 citations)
- A human homologue of Saccharomyces cerevisiae SNF2/SWI2 and Drosophila brm genes potentiates transcriptional activation by the glucocorticoid receptor. (537 citations)
What are the main themes of his work throughout his whole career to date?
Moshe Yaniv mainly focuses on Molecular biology, Transcription factor, Cell biology, Transcription and Genetics.
His Molecular biology research is multidisciplinary, incorporating perspectives in Chromatin, Gene, DNA, Promoter and Enhancer.
His biological study spans a wide range of topics, including Regulation of gene expression and Binding site.
His studies deal with areas such as Cell cycle and Transactivation as well as Cell biology.
His work in Cell cycle covers topics such as Cell growth which are related to areas like Fibroblast and Cell culture.
His work deals with themes such as CAAT box, RNA polymerase II, Mutant and Cellular differentiation, which intersect with Transcription.
He most often published in these fields:
- Molecular biology (57.62%)
- Transcription factor (25.71%)
- Cell biology (23.33%)
What were the highlights of his more recent work (between 2000-2016)?
- Molecular biology (57.62%)
- Transcription factor (25.71%)
- Cell biology (23.33%)
In recent papers he was focusing on the following fields of study:
Molecular biology, Transcription factor, Cell biology, Genetics and Chromatin are his primary areas of study.
His Molecular biology research is multidisciplinary, relying on both Cell growth, Chromatin immunoprecipitation, Regulation of gene expression, Nuclear protein and Transcription.
The various areas that Moshe Yaniv examines in his Transcription factor study include Promoter and Keratinocyte.
His Cell biology research includes elements of Cell cycle, Histone H2A, Histone methyltransferase and Histone code.
His study in the field of Gene, Epigenetics and Function is also linked to topics like Faith and Temperature sensitive.
His Chromatin research incorporates elements of Epigenomics and DNA methylation.
Between 2000 and 2016, his most popular works were:
- CARD4/Nod1 mediates NF‐κB and JNK activation by invasive Shigella flexneri (534 citations)
- JunD Reduces Tumor Angiogenesis by Protecting Cells from Oxidative Stress (471 citations)
- The human SWI/SNF subunit Brm is a regulator of alternative splicing (392 citations)
In his most recent research, the most cited papers focused on:
His primary scientific interests are in Cell biology, Molecular biology, Transcription factor, Genetics and Transcription factor complex.
The study incorporates disciplines such as Regulation of gene expression, Histone H3, Histone octamer and Heterochromatin protein 1 in addition to Cell biology.
His work carried out in the field of Molecular biology brings together such families of science as Retinoblastoma, Chromatin structure remodeling complex and Haploinsufficiency.
Moshe Yaniv has researched Transcription factor in several fields, including Cell and Cell cycle.
His study in Transcription factor complex is interdisciplinary in nature, drawing from both Tumor suppressor gene, Cell culture, Cyclin D1 and Cell growth.
The concepts of his DNA-binding protein study are interwoven with issues in Histone acetyltransferase activity, Histone acetyltransferase and Transcription.
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