What is he best known for?
The fields of study he is best known for:
J. Justin McCormick spends much of his time researching Molecular biology, Xeroderma pigmentosum, Nucleotide excision repair, Cell culture and DNA repair.
His Molecular biology study combines topics from a wide range of disciplines, such as Genetics, Biochemistry, DNA, Gene and DNA replication.
His research in Xeroderma pigmentosum intersects with topics in Mutation, Cytotoxic T cell, DNA excision and Carcinogen.
His Cell culture research is multidisciplinary, incorporating perspectives in Ploidy, Cell, Fibrosarcoma and Oncogene.
His work is dedicated to discovering how DNA repair, DNA damage are connected with Gene mutation and other disciplines.
His Fibroblast study incorporates themes from Malignant transformation and Cancer research.
His most cited work include:
- Frequency of ultraviolet light-induced mutations is higher in xeroderma pigmentosum variant cells than in normal human cells (297 citations)
- Hydrogen ion buffers for biological research (278 citations)
- Overview of matrix metalloproteinase expression in cultured human cells. (226 citations)
What are the main themes of his work throughout his whole career to date?
J. Justin McCormick mainly investigates Molecular biology, DNA, Cell culture, Biochemistry and Nucleotide excision repair.
His Molecular biology research is multidisciplinary, incorporating elements of Mutation, Genetics, Gene, Transfection and Fibroblast.
His Fibroblast research integrates issues from Malignant transformation and Transformation.
He has included themes like Cell and Fibrosarcoma in his Cell culture study.
His Nucleotide excision repair research incorporates themes from Xeroderma pigmentosum and DNA synthesis.
His study focuses on the intersection of Xeroderma pigmentosum and fields such as Cytotoxic T cell with connections in the field of Cytotoxicity.
He most often published in these fields:
- Molecular biology (59.28%)
- DNA (26.95%)
- Cell culture (25.75%)
What were the highlights of his more recent work (between 2004-2020)?
- Molecular biology (59.28%)
- Cell biology (10.18%)
- Cancer research (10.78%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Molecular biology, Cell biology, Cancer research, Malignant transformation and Cell culture.
His Molecular biology research is multidisciplinary, relying on both Genetics, DNA, DNA polymerase, Reporter gene and Cell cycle.
DNA is a subfield of Biochemistry that J. Justin McCormick studies.
His research on Malignant transformation also deals with topics like
- Fibroblast, which have a strong connection to Oncogene, Cell, Transformation, Cdc42 GTP-Binding Protein and Mutant,
- Transcription factor which intersects with area such as Hypoxia-inducible factors, Regulation of gene expression and Sp1 transcription factor.
His research in Cell culture focuses on subjects like Fibrosarcoma, which are connected to MAPK/ERK pathway and Receptor.
J. Justin McCormick regularly ties together related areas like Nucleotide excision repair in his Xeroderma pigmentosum studies.
Between 2004 and 2020, his most popular works were:
- Down-regulation of overexpressed Sp1 protein in human fibrosarcoma cell lines inhibits tumor formation (110 citations)
- Evidence that in Xeroderma Pigmentosum Variant Cells, which Lack DNA Polymerase η, DNA Polymerase ι Causes the Very High Frequency and Unique Spectrum of UV-Induced Mutations (96 citations)
- The Biphasic Role of the Hypoxia-Inducible Factor Prolyl-4-Hydroxylase, PHD2, in Modulating Tumor-Forming Potential (52 citations)
In his most recent research, the most cited papers focused on:
The scientist’s investigation covers issues in Molecular biology, Cancer research, Cell culture, Cell and Mutation.
J. Justin McCormick combines Molecular biology and DNA Polymerase Iota in his studies.
His Cancer research research includes elements of Ovarian tumor, Ovarian cancer, Distribution and In vivo.
His study in Cell culture is interdisciplinary in nature, drawing from both Fibrosarcoma and Oncogene.
His work focuses on many connections between Cell and other disciplines, such as Mutagenesis, that overlap with his field of interest in Fibroblast.
His studies deal with areas such as Cell cycle, Protein subunit and DNA, DNA polymerase as well as Mutation.
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