₁Shinobu Tamura

Summary for 2004 [at-glance overview of Shinobu Tamura work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Shinobu Tamura. According to available data, in 2004 Shinobu Tamura published at least 1 articles. This work was completed in collaboration with several authors including Miyajima, Atsushi and Senba, Emiko. There is no information about the funding or the grants awarded to support this work.

Analysis of the article abstracts and the titles suggests that Shinobu Tamura professional interests are focused around "dorsal root ganglia", "nociceptive neurons dorsal" and "oncostatin nociceptive neurons". These might also be referred to as "osm-deficient mice", "osmr-positive neurons" or "dorsal root". Statistical analysis shows that Shinobu Tamura's writing is likely to contains terms "neurons", "drgs", "osmr-positive", "osm-deficient", "mice" and "dorsal".

The majority of Shinobu Tamura articles are affiliated with Department of Anatomy and Neurobiology, Wakayama Medical University, Wakayama, 641-8509 Japan. Luckily, one email address is on file.

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Alternative names (1) [other authors with names similar to Shinobu Tamura]

₁₆₈Tamura, S

Year 2004 Charts [Shinobu Tamura frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of Shinobu Tamura publication and funding history for the range of years]

Emails (1) [email addresses extracted from Shinobu Tamura affiliations]

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Shinobu Tamura Coauthors (4) [all coauthors with the number of joint publications]

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Affiliations (1) [condensed summary of the Shinobu Tamura affiliations, the leading number and the color conveys importance]

₁Department of Anatomy and Neurobiology, Wakayama Medical University, Wakayama, 641-8509 Japan.

Key Opinion Leader In [Shinobu Tamura is considered a key opinion leader in any keyword where the rank of 5 is achieved, the leading number before the keyword shows the author's rank as compared to all other authors]

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Keywords (24) [keywords assigned to Shinobu Tamura articles by PubMed, the leading number and the color conveys importance]

₁Receptors, Drug | ₁Antigens, Differentiation | ₁Peptides | ₁Receptors, Oncostatin M | ₁Neurons | ₁Mice | ₁Pain | ₁Pain Measurement | ₁Animals | ₁Male | ₁Oncostatin M | ₁Cell Size | ₁Behavior, Animal | ₁Ganglia, Spinal | ₁Mice, Inbred C57BL | ₁Mice, Knockout | ₁RNA, Messenger | ₁Cell Count | ₁In Situ Hybridization | ₁Receptors, Purinergic P2 | ₁Fluorescent Antibody Technique | ₁Receptors, Cytokine | ₁Gene Targeting | ₁Gene Expression Regulation, Developmental

Shinobu Tamura Unique Vocabulary (96) [single words, word pairs and phrases obtained by analysis of abstracts and titles, the leading number and the color conveys importance; Shinobu Tamura might be a good expert witness on these terms]

₉neurons | ₅drgs | ₃osmr-positive | ₃osm-deficient | ₃mice | ₃dorsal | ₃ganglia | ₃oncostatin | ₃osm | ₃essential | ₃nociceptive | ₃root | ₂significantly | ₂adult | ₂receptor | ₂development | ₂reduced | ₂function | ₂vr1 | ₂decreased | ₁nucleus | ₁p14 | ₁situ | ₁interleukin-6 | ₁addition | ₁visceral | ₁vanilloid | ₁thus | ₁member | ₁reached | ₁hybridization | ₁investigated
₃osm-deficient mice | ₃osmr-positive neurons | ₃dorsal root | ₃nociceptive neurons | ₃root ganglia | ₃neurons drgs | ₂drgs osm-deficient | ₂function oncostatin | ₂neurons dorsal | ₂oncostatin nociceptive | ₂essential function | ₁p2x3 osmr-triple | ₁development subtype | ₁interleukin-6 family | ₁adult trigeminal | ₁thermal mechanical | ₁role development | ₁osm member | ₁hybridization revealed | ₁reduced noxious | ₁mice essential | ₁murine osm | ₁positive neurons | ₁previously murine | ₁significantly reduced | ₁models acute | ₁plays essential | ₁reduced number | ₁osm receptor | ₁thus | ₁thus osm | ₁drgs began
₃dorsal root ganglia | ₂nociceptive neurons dorsal | ₂oncostatin nociceptive neurons | ₂essential function oncostatin | ₂neurons dorsal root | ₂drgs osm-deficient mice | ₂osmr-positive neurons drgs | ₂function oncostatin nociceptive | ₁began appear postnatal | ₁addition osmr-positive neurons | ₁neurons drgs osm-deficient | ₁investigated development osmr-positive | ₁thus | ₁oncostatin osm member | ₁thus osm | ₁ganglia drgs perineonatal | ₁mechanical chemical visceral | ₁neurons decreased resulting | ₁osm member interleukin-6 | ₁thus osm plays | ₁osm-deficient mice essential | ₁subtype nociceptive neurons | ₁models acute thermal | ₁neurons drgs essential | ₁neurons adult trigeminal | ₁reported previously murine | ₁study investigated development | ₁member interleukin-6 family | ₁root ganglia osm-deficient | ₁present study investigated | ₁cytokines reported previously | ₁osm-deficient mice displayed

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