D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 78 Citations 23,536 242 World Ranking 2830 National Ranking 181

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • Internal medicine

Hiroshi Sato mostly deals with Molecular biology, Matrix metalloproteinase, Gelatinase A, Cell biology and Biochemistry. Hiroshi Sato has researched Molecular biology in several fields, including Cell culture, Gene expression, Northern blot, C-terminus and Expression vector. The concepts of his Matrix metalloproteinase study are interwoven with issues in Cell, Zymogen, Membrane, Activator and Extracellular matrix.

His study in Gelatinase A is interdisciplinary in nature, drawing from both Concanavalin A, Messenger RNA, Gelatinase and Pathology. His Cell biology research includes themes of Transfection, Cell membrane, Metalloproteinase, Cytotoxic T cell and Lymphokine-activated killer cell. As a part of the same scientific study, Hiroshi Sato usually deals with the Biochemistry, concentrating on Type I collagen and frequently concerns with Bone remodeling, Bone resorption, Osteoclast and Matrix metalloproteinase inhibitor.

His most cited work include:

  • A matrix metalloproteinase expressed on the surface of invasive tumour cells (2326 citations)
  • CD1d-restricted and TCR-mediated activation of valpha14 NKT cells by glycosylceramides. (2191 citations)
  • Membrane Type 1 Matrix Metalloproteinase Digests Interstitial Collagens and Other Extracellular Matrix Macromolecules (815 citations)

What are the main themes of his work throughout his whole career to date?

Hiroshi Sato mainly investigates Molecular biology, Matrix metalloproteinase, Internal medicine, Pathology and Cell culture. His Molecular biology research is multidisciplinary, incorporating elements of Gene expression, Transcription factor, Transfection, Northern blot and Gene. His Matrix metalloproteinase study incorporates themes from Cell and Extracellular matrix, Cell biology.

Hiroshi Sato has included themes like Gastroenterology and Endocrinology in his Internal medicine study. The concepts of his Pathology study are interwoven with issues in Metastasis and In situ hybridization. His Cell culture research includes elements of Virus, Virology and In vitro.

He most often published in these fields:

  • Molecular biology (26.99%)
  • Matrix metalloproteinase (22.84%)
  • Internal medicine (16.61%)

What were the highlights of his more recent work (between 2008-2020)?

  • Internal medicine (16.61%)
  • Gastroenterology (5.54%)
  • Surgery (5.19%)

In recent papers he was focusing on the following fields of study:

Internal medicine, Gastroenterology, Surgery, Cancer research and Pathology are his primary areas of study. His research investigates the link between Internal medicine and topics such as Endocrinology that cross with problems in Cell culture, Signal transduction, Zymography and Proinflammatory cytokine. His Pathology research integrates issues from Stenosis and Primary biliary cirrhosis.

Hiroshi Sato works mostly in the field of Cell growth, limiting it down to topics relating to Glioma and, in certain cases, Molecular biology. His Molecular biology study combines topics in areas such as HEK 293 cells, Akt/PKB signaling pathway and Transfection. His study looks at the intersection of Carcinoma and topics like Metastasis with Matrix metalloproteinase.

Between 2008 and 2020, his most popular works were:

  • A multicenter study on the prevalence of eosinophilic esophagitis and PPI-responsive esophageal eosinophilic infiltration. (55 citations)
  • Cyclooxygenase-2 Is Involved in the Up-Regulation of Matrix Metalloproteinase-9 in Cholangiocarcinoma Induced by Tumor Necrosis Factor-α (54 citations)
  • Aberrant glycogen synthase kinase 3β is involved in pancreatic cancer cell invasion and resistance to therapy. (45 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • Enzyme

His primary areas of investigation include Cancer research, Internal medicine, Gastroenterology, MMP9 and Gene knockdown. His Cancer research study integrates concerns from other disciplines, such as Tumor necrosis factor alpha, Cell growth, Cytokine, Molecular biology and Gene silencing. He interconnects v-Src, Gene expression and Proto-oncogene tyrosine-protein kinase Src in the investigation of issues within Molecular biology.

His MMP9 study is associated with Biochemistry. His research in Transfection focuses on subjects like HT1080, which are connected to Cell biology and Receptor. Hiroshi Sato combines subjects such as microRNA and Matrix metalloproteinase with his study of Small interfering RNA.

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.

Best Publications

CD1d-restricted and TCR-mediated activation of valpha14 NKT cells by glycosylceramides.

Tetsu Kawano;Junqing Cui;Yasuhiko Koezuka;Isao Toura.
Science (1997)

3709 Citations

A matrix metalloproteinase expressed on the surface of invasive tumour cells

Hiroshi Sato;Takahisa Takino;Yasunori Okada;Jian Cao.
Nature (1994)

3200 Citations

Membrane Type 1 Matrix Metalloproteinase Digests Interstitial Collagens and Other Extracellular Matrix Macromolecules

Eiko Ohuchi;Kazushi Imai;Yutaka Fujii;Hiroshi Sato.
Journal of Biological Chemistry (1997)

1147 Citations

Regulatory mechanism of 92 kDa type IV collagenase gene expression which is associated with invasiveness of tumor cells

H Sato;M Seiki.
Oncogene (1993)

874 Citations

Identification of the second membrane-type matrix metalloproteinase (MT-MMP-2) gene from a human placenta cDNA library. MT-MMPs form a unique membrane-type subclass in the MMP family.

Takahisa Takino;Hiroshi Sato;Akira Shinagawa;Motoharu Seiki.
Journal of Biological Chemistry (1995)

708 Citations

Natural killer-like nonspecific tumor cell lysis mediated by specific ligand-activated Vα14 NKT cells

Tetsu Kawano;Junqing Cui;Yasuhiko Koezuka;Isao Toura.
Proceedings of the National Academy of Sciences of the United States of America (1998)

705 Citations

Transmembrane/cytoplasmic domain-mediated membrane type 1-matrix metalloprotease docking to invadopodia is required for cell invasion

Hirokazu Nakahara;Linda Howard;Erik W. Thompson;Hiroshi Sato.
Proceedings of the National Academy of Sciences of the United States of America (1997)

532 Citations

Stimulation of 92-kDa gelatinase B promoter activity by ras is mitogen-activated protein kinase kinase 1-independent and requires multiple transcription factor binding sites including closely spaced PEA3/ets and AP-1 sequences.

Rebecca Gum;Ernst Lengyel;Jose Juarez;Ji Hshiung Chen.
Journal of Biological Chemistry (1996)

527 Citations

Homophilic complex formation of MT1-MMP facilitates proMMP-2 activation on the cell surface and promotes tumor cell invasion.

Yoshifumi Itoh;Akiko Takamura;Noriko Ito;Yoshiro Maru.
The EMBO Journal (2001)

487 Citations

Activation of a recombinant membrane type 1-matrix metalloproteinase (MT1-MMP) by furin and its interaction with tissue inhibitor of metalloproteinases (TIMP)-2

Hiroshi Sato;Takeshi Kinoshita;Takahisa Takino;Kazuo Nakayama.
FEBS Letters (1996)

457 Citations

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