D-Index & Metrics Best Publications

Hitoshi Arita

Shionogi (Japan)
Japan

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 Citations Publications World Ranking National Ranking

Biology and Biochemistry D-index 45 Citations 7,933 130 World Ranking 15701 National Ranking 1138

Overview

What is he best known for?

The fields of study Hitoshi Arita is best known for:

Gene
Enzyme
Amino acid

Hitoshi Arita performs multidisciplinary study in Biochemistry and Cell in his work. He integrates Cell biology and Molecular biology in his research. Hitoshi Arita performs integrative Molecular biology and Gene research in his work. In his works, he conducts interdisciplinary research on Gene and Genetics. He performs multidisciplinary study in Genetics and Cell biology in his work. Receptor is closely attributed to Receptor tyrosine kinase in his study. He undertakes multidisciplinary investigations into Receptor tyrosine kinase and Tyrosine kinase in his work. In his work, he performs multidisciplinary research in Tyrosine kinase and GAS6. His GAS6 study often links to related topics such as Receptor.

His most cited work include:

Identification of the Product of Growth Arrest-specific Gene 6 as a Common Ligand for Axl, Sky, and Mer Receptor Tyrosine Kinases (449 citations)
Inflammatory factors stimulate expression of group II phospholipase A2 in rat cultured astrocytes. Two distinct pathways of the gene expression (228 citations)
Cell Adhesion to Phosphatidylserine Mediated by a Product of Growth Arrest-specific Gene 6 (227 citations)

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

Hitoshi Arita undertakes multidisciplinary studies into Biochemistry and Organic chemistry in his work. In his works, he undertakes multidisciplinary study on Organic chemistry and Biochemistry. His research on Receptor often connects related areas such as Antagonist. His study ties his expertise on Internal medicine together with the subject of Antagonist. Hitoshi Arita combines topics linked to Thromboxane with his work on Internal medicine. His multidisciplinary approach integrates Thromboxane and Platelet in his work. His multidisciplinary approach integrates Platelet and Thromboxane A2 in his work. Thromboxane A2 connects with themes related to Receptor in his study. Enzyme is often connected to Phospholipase A in his work.

Hitoshi Arita most often published in these fields:

Biochemistry (85.56%)
Receptor (50.00%)
Enzyme (46.67%)

What were the highlights of his more recent work (between 2001-2021)?

Biochemistry (54.55%)
Enzyme (54.55%)
Phospholipase A2 (45.45%)

In recent works Hitoshi Arita was focusing on the following fields of study:

His Biochemistry study frequently draws connections between adjacent fields such as Endogeny. His study connects Biochemistry and Endogeny. While working in this field, Hitoshi Arita studies both Enzyme and Molecular biology. Hitoshi Arita performs multidisciplinary study in Molecular biology and Enzyme in his work. He conducts interdisciplinary study in the fields of Phospholipase A2 and Phospholipase A through his research. Hitoshi Arita conducts interdisciplinary study in the fields of Phospholipase A and Phospholipase A2 through his research. Hitoshi Arita frequently studies issues relating to Osteoporosis and Internal medicine. He integrates Osteoporosis with Osteoarthritis in his research. He incorporates Surgery and Arthroplasty in his studies.

Between 2001 and 2021, his most popular works were:

Potent Modification of Low Density Lipoprotein by Group X Secretory Phospholipase A2 Is Linked to Macrophage Foam Cell Formation (142 citations)
Phospholipase A2 receptor: a regulator of biological functions of secretory phospholipase A2 (115 citations)
Presence of the M-type sPLA₂receptor on neutrophils and its role in elastase release and adhesion (71 citations)

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

Enzyme
Inflammation
Phospholipase A2

Hitoshi Arita merges Biochemistry with Receptor in his research. Receptor and Lipid signaling are commonly linked in his work. Enzyme and Molecular biology are two areas of study in which he engages in interdisciplinary work. Hitoshi Arita performs integrative study on Molecular biology and Biochemistry. Cell biology is frequently linked to Mediator in his study. His research combines Cell biology and Mediator. He brings together Phospholipase A2 and Lipid signaling to produce work in his papers. Hitoshi Arita performs multidisciplinary study in the fields of Endogeny and Enzyme via his papers. His work on Macrophage expands to the thematically related In vitro.

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

Identification of the Product of Growth Arrest-specific Gene 6 as a Common Ligand for Axl, Sky, and Mer Receptor Tyrosine Kinases

Kyoko Nagata;Kazumasa Ohashi;Toru Nakano;Hitoshi Arita.
Journal of Biological Chemistry (1996)

564 Citations

INFLAMMATORY FACTORS STIMULATE EXPRESSION OF GROUP II PHOSPHOLIPASE A2 IN RAT CULTURED ASTROCYTES : TWO DISTINCT PATHWAYS OF THE GENE EXPRESSION

Shogo Oka;Hitoshi Arita.
Journal of Biological Chemistry (1991)

349 Citations

Vascular Smooth Muscle Cell-derived, Gla-containing Growth-potentiating Factor for Ca2+-mobilizing Growth Factors (∗)

Toru Nakano;Ken-ichi Higashino;Norihisa Kikuchi;Junji Kishino.
Journal of Biological Chemistry (1995)

281 Citations

Cell adhesion to phosphatidylserine mediated by a product of growth arrest-specific gene 6.

Toru Nakano;Yoshikazu Ishimoto;Junji Kishino;Masato Umeda.
Journal of Biological Chemistry (1997)

276 Citations

Glucocorticoids suppress group II phospholipase A2 production by blocking mRNA synthesis and post-transcriptional expression.

T Nakano;O Ohara;H Teraoka;H Arita.
Journal of Biological Chemistry (1990)

275 Citations

Molecular Cloning of Pancreatic Group I Phospholipase A2 Receptor

Jun Ishizaki;Kohji Hanasaki;Ken-ichi Higashino;Junji Kishino.
Journal of Biological Chemistry (1994)

266 Citations

Potent modification of low density lipoprotein by group X secretory phospholipase A2 is linked to macrophage foam cell formation

Kohji Hanasaki;Katsutoshi Yamada;Shigenori Yamamoto;Yoshikazu Ishimoto.
Journal of Biological Chemistry (2002)

263 Citations

Group II phospholipase A2 mRNA synthesis is stimulated by two distinct mechanisms in rat vascular smooth muscle cells.

Tohru Nakano;Osamu Ohara;Hiroshi Teraoka;Hitoshi Arita.
FEBS Letters (1990)

258 Citations

Purified Group X Secretory Phospholipase A2 Induced Prominent Release of Arachidonic Acid from Human Myeloid Leukemia Cells

Kohji Hanasaki;Takashi Ono;Akihiko Saiga;Yasuhide Morioka.
Journal of Biological Chemistry (1999)

242 Citations

Different Functional Aspects of the Group II Subfamily (Types IIA and V) and Type X Secretory Phospholipase A2s in Regulating Arachidonic Acid Release and Prostaglandin Generation IMPLICATIONS OF CYCLOOXYGENASE-2 INDUCTION AND PHOSPHOLIPID SCRAMBLASE-MEDIATED CELLULAR MEMBRANE PERTURBATION

Makoto Murakami;Terumi Kambe;Satoko Shimbara;Ken Ichi Higashino.
Journal of Biological Chemistry (1999)

238 Citations

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