Terutoshi Kimura

K. Sakaguchi, T. Fujita, M. Fukase, 1987, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Total synthesis of marinostatin, a serine protease inhibitor isolated from the marine bacterium Pseudoallteromonas sagamiensis

T. Yamazaki, Y. Nishiuchi, Misako Taichi, 2009 .

Total Synthesis of Marinostatin, a Serine Protease Inhibitor Isolated from the Marine Bacterium Pseudoallteromonas sagamiensis.

T. Yamazaki, Y. Nishiuchi, Misako Taichi, 2009 .

3-Pentyl (Pen) group as a new base-resistant side chain protecting group for tyrosine

Y. Nishiuchi, H. Nishio, T. Inui, 1998 .

Stability of the O-octanoyl group of rat ghrelin during chemical synthesis: Counter-ion-dependent alteration of an ester bond breakage

K. Kangawa, N. Chino, Terutoshi Kimura, 2004, Letters in Peptide Science.

Protective effects of Aβ-derived tripeptide, Aβ32–34, on Aβ1–42-induced phosphatidylinositol 4-kinase inhibition and neurotoxicity

C. Inagaki, K. Kitagawa, Y. Nishiuchi, 2007, Neuroscience Letters.

Acetyl-Ile-Gly-Leu protects neurons from Abeta(1-42) induced toxicity in vitro and in V337M human tau-expressing mice.

C. Inagaki, K. Kitagawa, Y. Nishiuchi, 2009, Life sciences.

Synthesis of γ-carboxyglutamic acid-containing peptides by the Boc strategy

S. Sakakibara, Y. Nishiuchi, Terutoshi Kimura, 2009 .

AGELENIN, A SPIDER NEUROTOXIN: DETERMINATION OF THE C-TERMINUS AS AMIDE FORM, AND INVESTIGATION OF THE DISULFIDE BOND ARRANGEMENT

C. Kitada, M. Fujino, T. Nakajima, 1991 .

Combined solid‐phase and solution approach for the synthesis of large peptides or proteins

Y. Nishiuchi, H. Nishio, T. Inui, 2000, Journal of peptide science : an official publication of the European Peptide Society.

Total synthesis of human parathyroid hormone (1–84)

S. Sakakibara, Terutoshi Kimura, T. Morikawa, 1982 .

Three‐dimensional structure of monoanionic methionine‐enkephalin: X‐ray structure of tert‐butyloxycarbonyl‐Tyr‐Gly‐Gly‐(4‐bromo)Phe‐Met‐OH

T. Ishida, T. Fujiwara, K. Tomita, 1984 .

Solution-phase synthesis of the K+ channel blocker, charybdotoxin

H. Kuroda, S. Sakakibara, N. Chino, 1991 .

Crystal Structures of [Met5] and [(4-Bromo)Phe4, Met5]: Formation of a Dimeric Antiparallel β-Structure

G. Sheldrick, T. Ishida, T. Fujiwara, 1987 .

Solution structure of charybdotoxin determined by NMR and distance geometry calculations

Y. Kyōgoku, Yuji Kobayashi, H. Kuroda, 1991 .

Nin-cyclohexyloxycarbonyl group as a new protecting group for tryptophan

S. Sakakibara, Y. Nishiuchi, H. Nishio, 1996 .

Solution synthesis of human midkine, a novel heparin‐binding neurotrophic factor consisting of 121 amino acid residues with five disulphide bonds

S. Kojima, T. Muramatsu, S. Sakakibara, 1996, Journal of peptide science : an official publication of the European Peptide Society.

Synthesis of amyloid β-peptides: Segment condensation of sparingly soluble protected peptides in chloroform-phenol mixed solvent

Y. Nishiuchi, H. Nishio, T. Inui, 2002 .

Suppression of Side Reactions Associated with Use of the Benzyloxymethyl Group on Histidine

Y. Nishiuchi, Terutoshi Kimura, T. Ishizu, 2006 .

Synthesis and disulfide structure determination of conotoxin GS, a γ-carboxyglutamic acid-containing neurotoxic peptide

S. Sakakibara, Y. Nishiuchi, Terutoshi Kimura, 1995, Letters in Peptide Science.

Combined solid-phase and solution approach to protein synthesis

S. Sakakibara, Y. Nishiuchi, H. Nishio, 1999 .

Solution syntheses of α-conotoxin SI and its biological activity

S. Sakakibara, T. Watanabe, Terutoshi Kimura, 1993 .

Bipolar undifferentiated CG‐4 oligodendroglial line cells adhere, extend processes and disperse on midkine, a heparin‐binding growth factor: orthovanadate and chondroitin sulphate E inhibit cell attachment

Maria I F Scott, T. Muramatsu, M. Rumsby, 2001 .

Anti‐nociceptive responses produced by human putative counterpart of nocistatin

E. Okuda‐Ashitaka, Y. Nishiuchi, T. Minami, 1998, British journal of pharmacology.

Midkine binds to 37-kDa laminin binding protein precursor, leading to nuclear transport of the complex.

K. Zou, T. Muramatsu, T. Kimura, 2001, Experimental cell research.

Midkine binds specifically to sulfatide the role of sulfatide in cell attachment to midkine-coated surfaces.

T. Muramatsu, T. Kimura, S. Ikematsu, 2000, European journal of biochemistry.

A receptor-like protein-tyrosine phosphatase PTPzeta/RPTPbeta binds a heparin-binding growth factor midkine. Involvement of arginine 78 of midkine in the high affinity binding to PTPzeta.

M. Noda, T. Muramatsu, T. Kimura, 1999, The Journal of biological chemistry.

Powerful solvent systems useful for synthesis of sparingly-soluble peptides in solution.

H. Kuroda, T. Kimura, S. Sakakibara, 2009, International journal of peptide and protein research.

Strategy for the synthesis of large peptides: An application to the total synthesis of human parathyroid hormone [hPTH(1–84)]

T. Kimura, S. Sakakibara, Y. Masui, 1981, Biopolymers.

Highly sensitive peptide-4-methylcoumaryl-7-amide substrates for blood-clotting proteases and trypsin.

K Fujikawa, K. Fujikawa, S. Kawabata, 1988, European journal of biochemistry.

Synthesis and disulfide structure determination of porcine endothelin: an endothelium-derived vasoconstricting peptide.

T. Masaki, H. Kuroda, T. Kimura, 2009, International journal of peptide and protein research.

Synthetic peptides derived from midkine enhance plasminogen activator activity in bovine aortic endothelial cells.

S. Kojima, H. Amanuma, T. Muramatsu, 1995, Biochemical and biophysical research communications.

Localization of heparin-binding, neurite outgrowth and antigenic regions in midkine molecule.

T. Muramatsu, T. Kimura, S. Sakakibara, 1994, Biochemical and biophysical research communications.

Topological isomers of human uroguanylin: interconversion between biologically active and inactive isomers

M. Nakazato, K. Kangawa, Yuji Kobayashi, 1998, FEBS letters.

A NOVEL ENZYME IN RAT BRAIN CONVERTING β‐ENDORPHIN INTO METHIONINE ENKEPHALIN: AFFINITY CHROMATOGRAPHY AND SPECIFICITY

T. Yoshimoto, M. Koida, S. Sakakibara, 1979, Journal of neurochemistry.

The 69-84 amino acid region of the parathyroid hormone molecule is essential for the interaction of the hormone with the binding sites with carboxyl-terminal specificity.

K. Chihara, T. Fujita, T. Kimura, 1996, Endocrinology.

Synthesis of Endothelin‐1 Analogues, Endothelin‐3, and Sarafotoxin S6b: Structure‐Activity Relationships

Yuji Kobayashi, H. Kuroda, T. Kimura, 1989, Journal of cardiovascular pharmacology.

Chemical Synthesis of Human β-Defensin (hBD)-1, -2, -3 and -4: Optimization of the Oxidative Folding Reaction

M. Nakazato, Y. Nishiuchi, N. Chino, 2006, International Journal of Peptide Research and Therapeutics.

Protective effects of Abeta-derived tripeptide, Abeta(32-34), on Abeta(1-42)-induced phosphatidylinositol 4-kinase inhibition and neurotoxicity.

C. Inagaki, K. Kitagawa, Y. Nishiuchi, 2007, Neuroscience Letters.

Solution synthesis and biological activity of human pleiotrophin, a novel heparin-binding neurotrophic factor consisting of 136 amino acid residues with five disulfide bonds.

S. Kojima, T. Muramatsu, T. Kimura, 2000, The journal of peptide research : official journal of the American Peptide Society.

Strategy for the chemical synthesis of large peptides; synthesis of angiogenin as an example.

H. Kuroda, S. Sakakibara, N. Chino, 1990, Biochemical Society transactions.

Solution synthesis of charybdotoxin (ChTX), a K+ channel blocker.

H. Kuroda, T. Kimura, S. Sakakibara, 1990, Biochemical and biophysical research communications.

Clusters of basic amino acids in midkine: roles in neurite-promoting activity and plasminogen activator-enhancing activity.

F. Inagaki, S. Kojima, T. Muramatsu, 1998, Journal of biochemistry.

Optimization of the Oxidative Folding Reaction and Disulfide Structure Determination of Human α-Defensin 1, 2, 3 and 5

Y. Nishiuchi, N. Chino, H. Nishio, 2008, International Journal of Peptide Research and Therapeutics.

Chemical synthesis of dendrotoxin-I: Revision of the reported structure

T. Yamazaki, E. Katoh, A. Harvey, 2009 .

Nocistatin and its derivatives antagonize the impairment of short-term acquisition induced by nociceptin

Tat-Leang Lee, Y. Nishiuchi, Terutoshi Kimura, 2007, Neuroscience Letters.

Midkine is a heat and acid stable polypeptide capable of enhancing plasminogen activator activity and neurite outgrowth extension.

S. Kojima, T. Muramatsu, T. Kimura, 1995, Biochemical and biophysical research communications.