Cell biology, Internal medicine, Myocyte, Endoplasmic reticulum and Skeletal muscle are her primary areas of study. Miyuki Nishi performs integrative study on Cell biology and CXCL2. Her biological study deals with issues like Endocrinology, which deal with fields such as Hyperalgesia, Nociceptin receptor, Receptor and Neuroscience.
Miyuki Nishi combines subjects such as Depolarization and Intracellular with her study of Endoplasmic reticulum. Her Skeletal muscle study which covers Ryanodine receptor that intersects with Homeostasis, Cardiac muscle, Signal transduction and In vivo. Her Junctional membrane complex research is multidisciplinary, incorporating perspectives in Cytoplasm, Ion channel, Muscle contraction and T-tubule.
Her main research concerns Cell biology, Endoplasmic reticulum, Skeletal muscle, Internal medicine and Endocrinology. Her work investigates the relationship between Cell biology and topics such as Knockout mouse that intersect with problems in Nociceptin receptor. The Endoplasmic reticulum study combines topics in areas such as Biophysics and Anatomy.
She has researched Skeletal muscle in several fields, including Signal transduction, Sarcomere, Depolarization and Muscle contraction. Her Endocrinology research includes elements of Triad and Voltage-dependent calcium channel. Her biological study spans a wide range of topics, including Cytoplasm, Mutant and Cell type.
Her primary areas of investigation include Cell biology, Endoplasmic reticulum, Skeletal muscle, Knockout mouse and Ryanodine receptor. Her research in Cell biology is mostly focused on Intracellular. In the field of Endoplasmic reticulum, her study on Unfolded protein response overlaps with subjects such as MBOAT.
The concepts of her Skeletal muscle study are interwoven with issues in Myocyte and Biochemistry. She works in the field of Myocyte, namely T-tubule. The various areas that Miyuki Nishi examines in her Ryanodine receptor study include Endocrinology and Muscle contraction.
Miyuki Nishi mainly focuses on Cell biology, Endoplasmic reticulum, Knockout mouse, Lung injury and Lung. Cell biology is closely attributed to Transient receptor potential channel in her study. Her Endoplasmic reticulum research incorporates themes from Membrane, Intracellular, Cell–cell interaction and Skeletal muscle.
Her Skeletal muscle research incorporates elements of Calcium-activated potassium channel, Vesicle, Sarcoplasm, Ion channel and Analytical chemistry. Miyuki Nishi has researched Knockout mouse in several fields, including Synaptic plasticity, Startle response, Neuroscience, Open field and Regulation of gene expression. In her research, Myocyte is intimately related to Ryanodine receptor, which falls under the overarching field of T-tubule.
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Junctophilins: a novel family of junctional membrane complex proteins.
Hiroshi Takeshima;Hiroshi Takeshima;Shinji Komazaki;Miyuki Nishi;Miyuki Nishi;Masamitsu Iino.
Molecular Cell (2000)
cDNA cloning and regional distribution of a novel member of the opioid receptor family
Kazuhiko Fukuda;Shigehisa Kato;Kenjiro Mori;Miyuki Nishi.
FEBS Letters (1994)
TRPM2-mediated Ca2+influx induces chemokine production in monocytes that aggravates inflammatory neutrophil infiltration.
Shinichiro Yamamoto;Shunichi Shimizu;Shigeki Kiyonaka;Nobuaki Takahashi.
Nature Medicine (2008)
Excitation-contraction uncoupling and muscular degeneration in mice lacking functional skeletal muscle ryanodine-receptor gene
Hiroshi Takeshima;Masamitsu lino;Hiroaki Takekura;Miyuki Nishi.
Nature (1994)
Facilitation of long-term potentiation and memory in mice lacking nociceptin receptors
Toshiya Manabe;Yukihiro Noda;Takayoshi Mamiya;Hiroyuki Katagiri.
Nature (1998)
Unrestrained nociceptive response and disregulation of hearing ability in mice lacking the nociceptin/orphaninFQ receptor
Miyuki Nishi;Takeshi Houtani;Yukihiro Noda;Takayoshi Mamiya.
The EMBO Journal (1997)
Primary structures and expression from cDNAs of rat opioid receptor δ-and μ-subtypes
Kazuhiko Fukuda;Shigehisa Kato;Kenjiro Mori;Miyuki Nishi.
FEBS Letters (1993)
MG53 nucleates assembly of cell membrane repair machinery
Chuanxi Cai;Haruko Masumiya;Noah Weisleder;Noriyuki Matsuda.
Nature Cell Biology (2009)
The POU domain transcription factor Brn-2 is required for the determination of specific neuronal lineages in the hypothalamus of the mouse.
S Nakai;H Kawano;T Yudate;M Nishi.
Genes & Development (1995)
Brn-1 and Brn-2 share crucial roles in the production and positioning of mouse neocortical neurons.
Yoshinobu Sugitani;Shigeyasu Nakai;Osamu Minowa;Miyuki Nishi.
Genes & Development (2002)
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