R. Minakami

发表

Catalytic residues of group VIB calcium-independent phospholipase A2 (iPLA2gamma).

H. Sumimoto, Haruki Tanaka, R. Minakami, 2004, Biochemical and biophysical research communications.

A variant of metabotropic glutamate receptor subtype 5: an evolutionally conserved insertion with no termination codon.

H. Sugiyama, R. Minakami, F. Katsuki, 1993, Biochemical and biophysical research communications.

The insert region of the Rac GTPases is dispensable for activation of superoxide-producing NADPH oxidases.

H. Sumimoto, R. Minakami, K. Miyano, 2009, The Biochemical journal.

Visualization of phagosomal hydrogen peroxide production by a novel fluorescent probe that is localized via SNAP-tag labeling.

Mako Kamiya, Y. Urano, T. Nagano, 2014, Analytical chemistry.

Knock-In Mouse Model of Dilated Cardiomyopathy Caused by Troponin Mutation

Yuan-yuan Wang, F. Takahashi‐Yanaga, T. Sasaguri, 2007, Circulation research.

Molecular cloning and the functional expression of two isoforms of human metabotropic glutamate receptor subtype 5.

H. Sugiyama, K. Nakamura, T. Yamamoto, 1994, Biochemical and biophysical research communications.

Phagocytosis-Coupled Activation of the Superoxide-Producing Phagocyte Oxidase, a Member of the NADPH Oxidase (Nox) Family

H. Sumimoto, R. Minakami, 2006, International journal of hematology.

Targeted disruption of the cardiac troponin T gene causes sarcomere disassembly and defects in heartbeat within the early mouse embryo.

K. Nishii, Y. Shibata, Q. Lu, 2008, Developmental biology.

Membrane phospholipid metabolism during phagocytosis in human neutrophils

H. Sumimoto, R. Minakami, K. Miyano, 2010, Genes to cells : devoted to molecular & cellular mechanisms.

The Nox Family of NADPH Oxidases that Deliberately Produce Reactive Oxygen Species

H. Sumimoto, R. Minakami, K. Miyano, 2010 .

Ca2+-sensitizing effects of the mutations at Ile-79 and Arg-92 of troponin T in hypertrophic cardiomyopathy.

I. Ohtsuki, R. Minakami, S. Morimoto, 1998, The American journal of physiology.

Selective cloning and sequence analysis of the human L1 (LINE-1) sequences which transposed in the relatively recent past.

Y. Sakaki, H. Hohjoh, R. Minakami, 1990, Nucleic acids research.

A region N-terminal to the tandem SH3 domain of p47phox plays a crucial role in the activation of the phagocyte NADPH oxidase.

H. Sumimoto, R. Minakami, K. Miyano, 2009, The Biochemical journal.

A novel protein specifically interacting with Homer2 regulates ubiquitin-proteasome systems.

H. Sugiyama, Akihiko Kato, Yasuko Hashiguchi, 2005, Journal of biochemistry.

Interaction of Vesl-1L/Homer 1c with syntaxin 13.

H. Sugiyama, Akihiko Kato, R. Minakami, 2000, Biochemical and biophysical research communications.

Soluble Regulatory Proteins for Activation of NOX Family NADPH Oxidases.

H. Sumimoto, R. Minakami, K. Miyano, 2019, Methods in molecular biology.

The Expression of Two Splice Variants of Metabotropic Glutamate Receptor Subtype 5 in the Rat Brain and Neuronal Cells During Development

H. Sugiyama, R. Minakami, Ken‐ichiro Iida, 1995, Journal of neurochemistry.

Phosphorylation and Calmodulin Binding of the Metabotropic Glutamate Receptor Subtype 5 (mGluR5) Are Antagonistic in Vitro *

H. Sugiyama, N. Jinnai, R. Minakami, 1997, The Journal of Biological Chemistry.

Full‐length p40phox structure suggests a basis for regulation mechanism of its membrane binding

F. Inagaki, S. Yuzawa, H. Sumimoto, 2007, The EMBO journal.

Functional Consequences of the Deletion Mutation ΔlGlul6O in Human Cardiac Troponin T

F. Takahashi‐Yanaga, I. Ohtsuki, K. Harada, 2000 .

Cardiac Troponin Tl

F. Takahashi‐Yanaga, I. Ohtsuki, K. Harada, 2000 .

Ca2+-desensitizing effect of a deletion mutation ΔK210 in cardiac troponin T that causes familial dilated cardiomyopathy

F. Takahashi‐Yanaga, I. Ohtsuki, Q. Lu, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Identification of an internal cis-element essential for the human L1 transcription and a nuclear factor(s) binding to the element.

M. Hattori, Y. Sakaki, R. Minakami, 1992, Nucleic acids research.

Functional consequences of the mutations in human cardiac troponin I gene found in familial hypertrophic cardiomyopathy.

F. Takahashi‐Yanaga, T. Sasaguri, I. Ohtsuki, 2001, Journal of molecular and cellular cardiology.

Ca2+-sensitizing effects of the mutations at Ile-79 and Arg-92 of troponin T in hypertrophic cardiomyopathy.

I. Ohtsuki, R. Minakami, S. Morimoto, 1998, American journal of physiology. Cell physiology.

Postnatal development of mRNA specific for a metabotropic glutamate receptor in the rat brain

H. Sugiyama, M. Tohyama, H. Kiyama, 1992, Neuroscience Research.

Functional consequences of the deletion mutation deltaGlu160 in human cardiac troponin T.

F. Takahashi‐Yanaga, I. Ohtsuki, K. Harada, 2000, Journal of Biochemistry (Tokyo).

Homer1c interacts with Hippi and protects striatal neurons from apoptosis.

H. Sugiyama, R. Minakami, H. Udo, 2007, Biochemical and biophysical research communications.