早稲田大学 武岡真司 研究室の博士論文のコピペ（盗用、剽窃）疑惑まとめ

早稲田大学の博士論文のコピペ発覚リスト
　　常田聡 研究室：　小保方晴子、松本慎也、古川和寛、寺原猛、岸田直裕、副島孝一　（計６名）
　　武岡真司 研究室：　藤枝俊宣、小幡洋輔、寺村裕治  （計３名）
　　西出宏之 研究室：　田中学  （計１名）

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調査１：藤枝俊宣氏（早稲田大学の武岡真司氏の研究室）の博士論文における文章のコピペ（盗用、剽窃）についてのまとめ

(丸ごとコピペや一部改変使用された文章や図の一部には、引用情報が示されていません。)

著者：　藤枝俊宣　（Toshinori FUJIE）
　　　　（現　早稲田大学 早稲田大学 先進理工学研究科 生命医科学専攻 武岡研究室 助教（東北大学より異動））
論文題目：　Construction of Biomacromolecular Nanosheets and Their Biomedical Application as a Wound Dressing Material
生体高分子からなるナノシートの構築と 創傷被覆材としての医用応用
http://dspace.wul.waseda.ac.jp/dspace/handle/2065/34612 （写し）
出版日：　2009年2月
審査員：　
  (主査) 早稲田大学 教授 工学博士 (早稲田大学) 
  （副査） 武岡真司 (副査) 早稲田大学 教授 医学博士 (慶応義塾大学) 
  （副査） 合田亘人 早稲田大学 教授 博士(工学) 東京大学 常田 聡
  （副査） Scuola Superire Sant' Anna, Assoc. Prof., Ph.D., Arianna Menciassi
博士論文概要（写し）
博士論文審査報告書（写し）
論文本文 （写し）

藤枝俊宣氏の博士論文のIntroductionにおける下記文章は、Stephan Forster氏らの論文からのコピペです（引用元情報は記載。しかし、丸ごとコピペ。）。

文章コピペ元の論文
From Self-Organizing Polymers to Nanohybrid and Biomaterials
Stephan Forster and Thomas Plantenberg
http://www.eng.buffalo.edu/Courses/ce435/Forster02.pdf （写し）

同一文章 

The ordered state is distinguished by the fact that individual molecules are located at restricted three-dimensional regions, for example, a lattice site in a crystal or the position in the three-dimensional structure of a protein. A localization is always accompanied by a decrease of the number of realizable states and hence a loss of entropy. Temperature plays always an important role in the case of phase transitions between different order states because of the contribution T'S to the free energy. Besides temperature, further external fields E may influence the degree of order and the phase transitions. The field strength and temperature at which the phase transitions take　place can be depicted schematically in phase diagrams (Fig. 1-4). The critical temperature Tc above which the system is disordered is indicated on the temperature axis. Phase transitions from the disordered phase (U) to different ordered phases (L, H) may take place below the critical temperature. These phase transitions are accompanied by a self-organization of the system. The stability range of the different phases can be taken from the phase diagram. Different ordered structures for one and the same material can be produced by varying the temperature and field strength. This variability has a favorable effect on the production and optimization of materials.

藤枝俊宣氏の博士論文の2-2. Principles of Self-Assemblyの6-7ページ目における下記文章は、Whitesides氏らのScience論文あるいはHeuer氏らのScience論文からのコピペです。Fig.1.3もWhitesides氏のScience論文からのコピペです。

文章コピペ元の論文
Molecular Self-Assembly and Nanochemistry: A Chemical Strategy for the Synthesis of Nanostructures
Whitesides, G.M., et al., Vol. 254, p. 1312 (1991)
http://www.cs.duke.edu/courses/cps296.5/spring06/papers/WMS91.pdf

Innovative Materials Processing Strategies: A Biomimetic Approach A.
H. Heuer, et al. Science, Vol. 255, p. 1098 (1992)
http://www.chemstone.net/Materials/Future.htm
（Heuer氏らも、Whitesides氏らの論文からコピペしています。）

同一文章１ （藤枝論文のpage5-6の文章（文章の途中に引用情報あり、しかし、丸ごとコピペ）、 Whitesides論文のpage1315左中央からの文章）

The single feature common to all of these biological structures is the reliance　upon non-covalent self-assembly of preformed and well-defined subassemblies to obtain the final structure, rather than the creation of a single, large, covalently linked　structure. Biological self-assembly can thus be described by a series of principles that　are often (but not always) obeyed 3:

1) Self-assembly involves association by many weak, reversible interactions to obtain a final structure that represents a thermodynamic minimum. Incorrect structural units are rejected in the dynamic, equilibrium assembly. This equilibration allows high fidelity in the process.
2) Self-assembly occurs by a modular process. The formation of stable subassemblies by sequential covalent processes precedes their assembly into the final structure. This mechanism allows for efficient assembly from the preformed units.
3) Only a small number of types of molecules are normally involved in modular
self-assembly. Consequently, a limited set of binding interactions is required to cause the final structure to form. This principle minimizes the amount of information required for a particular structure.
4) Self-assembly often displays positive co-operativity.
5) Complementarities in molecular shape provide the foundation for the association
between components. Shape-dependent association based on van der Waals and
hydrophobic interactions can be made more specific and stronger by hydrogen bonding and electrostatic interactions.

類似文章 （藤枝論文のpage6の文章（文章の後に引用情報なし） 、 Whitesides論文のpage1315の右中央の文章） 

Because self-assembled structures represent thermodynamic minima, because they are formed by reversible association of a number of individual molecules, an because the enthalpies of the interactions holding molecules together are relatively weak, the interplay of enthalpy and entropy ('H and 'S) in their formation is more important than in synthesis based on formation of covalent bonds (Fig. 1-3).

同一文章２ （藤枝論文のpage6-7の文章（文章の後に引用情報なし） 、 Whitesides論文のFig.3のレジェンドの文章） 

the values　of 'H vary widely depending on the type of molecular interactions that are involved.　The value for T'Stranslation is based exclusively on considerations of concentration and is provided only as an approximation. The value for T'Sconformation is of smaller magnitude than T'Stranslation but the sum of many contributions, resulting from freezing　conformations around many bonds in a large, flexible molecule, can make loss of　conformational entropy significant in the thermodynamics of self-assembly processes

同一文章３  （藤枝論文のpage7の文章（文章の後に引用情報なし）、Whitesides論文のpage1315の右中央の文章）

If there are a number of particles associating, and if a number of conformationally mobile sections of the participating molecules are frozen on aggregation, the sum of these unfavorable entropic terms can be significant. These considerations suggest that molecules designed for self-assembly should be as rigid as is consistent with achieving good intermolecular contact between the interacting surfaces and that the area of contacting molecular surface be made large. The criteria of rigidity and multipoint contact are also relatively easily met by using networks of hydrogen bonds in non-aqueous solvents, and these systems have, in consequence, been extensively examined as models for self-assembly.

類似画像

↓　　 藤枝論文のFig.1-3　（図の説明文に、引用情報はありません）

↓　　Whitesides論文のFig.3

藤枝俊宣氏の博士論文の3-4. Van der Waals Interactionsの14-15ページ目における文章やFig.1-7はIsraelachvili, J.氏の著作物 “Intermolecular and Surface Forces.” Academic Press, New York (1992) (Chapter 11.1, pages 176-179)からのコピペで、ほんの一部を改変したものです。文章中や図の説明文には引用情報は明記してありません。

類似画像 

↓　　 藤枝論文のFig.1-7　（図の説明文に、引用情報はありません）



↓　　Israelachvili, J.氏の著作物のFig.11.1

藤枝俊宣氏の博士論文のp.62-63の2-1. Structural Colors in Natureの文章は、下記のKinoshitaらの論文のAbstractを丸ごとコピペ（本文には引用無し；Fig3-1のlegendに引用があるのみ） しています。また、page63のFig.3-1とレジェンドの文章は、Kinoshita論文のFig.25を拝借したもので、文章もほぼ丸ごとコピペです。
Structural colors in nature: the role of regularity and irregularity in the structure. Kinoshita S, Yoshioka S. Chemphyschem. 2005 Aug 12;6(8):1442-59. http://www.ncbi.nlm.nih.gov/pubmed/16015669

同一文章１ （藤枝論文のpage62-63の文章（文章の後に引用情報なし） 、Kinoshita論文のAbstractの文章）
p.62-63Coloring in nature mostly comes from the inherent colors of materials, but it sometimes has a purely physical origin, such as diffraction or interference of light. The latter, called structural color or iridescence, has long been a problem of scientific interest. Recently, structural colors have attracted great interest because their applications have been rapidly progressing in many fields related to vision, such as the paint, automobile, cosmetics, and textile industries. As the research progresses, however, it has become clear that these colors are due to the presence of surprisingly minute microstructures, which are hardly attainable even by ultramodern nanotechnology. Fundamentally, most of the structural colors originate from basic optical processes represented by thin-film interference, multilayer interference, a diffraction grating effect, photonic crystals, light scattering, and so on (Fig. 3-1). However, to enhance the perception of the eyes, natural creatures have produced various designs, in the course of evolution, to fulfill simultaneously high reflectivity in a specific wavelength range and the generation of diffusive light in a wide angular range. At a glance, these two characteristics seem to contradict each other in the usual optical sense, but these seemingly conflicting requirements are realized by combining appropriate amounts of regularity and irregularity of the structure.

同一文章２ （藤枝論文のpage63のFig.3-1とレジェンドの文章（引用情報はあるが、ほぼ丸ごとコピペ） 、Kinoshita論文のFig.26のレジェンドの文章）Fig. 3-1 Hierarchy of the structure is contributing to structural colors1. The most
fundamental scale is that giving the interference of light around 0.2 μm. The regular
structures contributing to the light interference are retained within a range indicated as a gray zone. If this range is narrow, the diffraction of light plays an important role,
whereas if broad, the geometrical optics dominates. In either case, this range helps to produce diffusive light. The hierarchy in a larger scale indicates the irregularity at
various levels and possibly adds the macroscopic texture to the structural color.

同一文章３ （藤枝論文のpage63-64の文章（引用情報はあるが、丸ごとコピペ）やFig.3-2（引用なし） 、Kinoshita論文の2.1. Thin-Film Interferenceの文章やFig.1）
Thin-film interference is one of the simplest structural colors and is widely distributed in nature. Consider a plane wave of light that is incident on a thin layer of thickness d and refractive index nb at the angle of refraction θb (Fig. 3-2). Then, the reflected light beams from the two interfaces interfere with each other. In general, thecondition of interference differs whether the thin layer is or is not attached to a material having a higher refractive index. The former is the case for antireflective coatings on glass, while a typical example of the latter is a soap bubble. The condition of interference for light with wavelength λ, under which the reflection is enforced (constructive interference), becomes an equation (1)1:
　 mλ = 2(nbdcos θb) 　(1)
where m is an integer for antireflective coatings, while it is a half integer for the
soap-bubble case. Typical examples of the calculations for both cases are shown in Fig. 3-2. It is clear that the reflectivity is relatively low and changes smoothly with
wavelength. Thus, the thin-film interference shows only weak dependence on the
wavelength. It is easily understood from the eq. (1) that the wavelength showing a
maximum reflectivity changes continuously to a shorter wavelength as the incident
angle is increased. Thus, one of the characteristics of structural colors, that the color changes with viewing angle, is reproduced.

Fig. 3-2 Thin-film interference; (a) configuration, (b) and (c) reflectivity from a thin
film (n = 1.25) with a thickness of 100 nm (b) in air and (c) attached to a material with a higher refractive index (n = 1.5). Solid and dashed limes are the calculated curves.

藤枝俊宣氏の博士論文の第6章の2、Lorenz HPらの Wounds: Biology, Pathology, and Management http://recon.stanford.edu/Articles/LorenzWH.pdf のコピペ




藤枝俊宣氏の博士論文の第7章146ページにも引用表記の無いコピペ

「FT-IR imaging was performed on a Digilab Stingray imaging system consisting of a Digilab FTS 7000 spectrometer, a UMA 600 microscope, and 32 32 mercury cadmium telluride IR imaging focal plane array (MCT-FPA) image detector with an average spatial area of 176 m 176 m in a transmission mode. An 8 cm-1 nominal spectral resolution and an undersampling ratio (UDR) of 4 for the imaging were set up and spectral data was collected with 1240 scans.」 で検索すればわかります。

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調査２：小幡洋輔氏（早稲田大学の武岡真司氏の研究室）の博士論文における文章のコピペ（盗用、剽窃）についてのまとめ

著者：　小幡洋輔
論文題目：　Efficient intracellular delivery of biomacromolecules by liposomes containing amino-acid based lipids
アミノ酸型脂質を用いたリポソームによる生体高分子の高効率な細胞内運搬
http://dspace.wul.waseda.ac.jp/dspace/handle/2065/34612 （写し）
出版日：　2009年2月
審査員：　
  (主査) 早稲田大学 教授 工学博士(早稲田大学) 武岡 真司
  （副査） 早稲田大学 教授 工学博士(早稲田大学) 西出 宏之
  （副査） 早稲田大学 教授 工学博士(早稲田大学) 酒井 清孝
  （副査） Scuola Superire Sant’ Anna, Assoc. Prof., Ph.D. Arianna Menciassi
博士論文概要（写し）
博士論文審査報告書（写し）
論文本文 （写し）

コピペ文章１．小幡洋輔氏の博士論文のChapter 1の1. Introductionにおける下記文章は、アリゾナ州立大学のホームページの"Supramolecular Assemblies"の記事からのコピペです（引用元情報は記載されていません）。

同一文章   黄色でハイライトされている部分が同一文章

1. Introduction
The biological world is rich with ordered assemblies of molecules. Indeed, the assembly and function of supramolecular structures resulted from self-assembly or self-organization is central to modern biology. The forces holding together these assemblies are diverse: van der Waals, electrostatic, hydrophobic interactions, and hydrogen bonds, all contribute to specific recognition between members of the assembly. In this chapter, structures and techniques that can be used to fabricate supermolecules created from huge numbers of component molecules are introduced. Furthermore, programmed self-assemblies such as liposomes, micelles, and polymer-based particles are also explained for construction of efficient drug delivery.

コピペ文章２．小幡洋輔氏の博士論文のChapter 1の2-1 における下記文章は、Whitesides氏らのScience論文からのコピペです（引用元情報はコピペ文章の途中にだけ記載しているだけです。また、丸ごとコピペのため著作権違反です）。

文章コピペ元の論文
著者：　Whitesides, G.M., et al., Vol. 254, p. 1312 (1991)
論文題目：　Molecular Self-Assembly and Nanochemistry: A Chemical Strategy for the Synthesis of Nanostructures
http://www.cs.duke.edu/courses/cps296.5/spring06/papers/WMS91.pdf

同一文章   黄色でハイライトされている部分が同一文章

2. Molecular Self-Assembly Controlled by Intermolecular Interactions 2-1. Definition of Molecular Self-Assembly

　Nanostructures are assemblies of bonded atoms that have dimensions in the range of 1 to 102 nanometers1. Structures in this range of sizes can be considered as exceptionally large, unexceptional, or exceptionally small, depending on one's viewpoint, synthetic and analytical technologies, and interests (Fig. 1-1)2. To solid-state physicists, materials scientists, and electrical engineers, nanostructures are small. The techniques, such as microlithography and deposition from the vapor, that are used in these fields to fabricate microstructures and devices require increasingly substantial effort as they are extended to the range below 102 nm. To biologists, nanostructures are familiar objects. A range of biological structures-from proteins through viruses to cellular organelles-have dimensions of 1 to 102 nm. To chemists, nanostructures are large. Considered as molecules, nanostructures require the assembly of groups of atoms numbering from 103 to 109 and having molecular weights of 104 to 1010 Da. Synthetic techniques that generate well-defined structures at the lower ends of these ranges are only now being developed and the upper ends remain largely unexplored. Developing techniques for synthesizing and characterizing ultra large molecules and molecular assemblies-nanostructures-is one of the grand challenges now facing chemistry. Nanostructures provide major unsolved problems in complexity and require new strategies and technologies for their synthesis and characterization. The solutions to these problems would be both interesting in themselves and essential elements in extending chemistry toward problems in materials science and biology. 

コピペ文章３．小幡洋輔氏の博士論文のChapter 1の2-2 における下記文章は、Katsuhiko Ariga氏らの著作物からのコピペです（引用元情報は記載されておらず、著作権違反です）。

文章や図のコピペ元の論文
著者：　Katsuhiko Ariga、Toyoki Kunitak
著作物題目：　Supramolecular Chemistry - Fundamentals and Applications: Advanced Textbook

同一文章   黄色でハイライトされている部分が同一文章

2-2. Self-Assembly in Biological System
 The highly sophisticated functions seen in biological systems originate from their well-designed molecular arrangements, which are formed through self-assembly and self-organization (Fig.1-2). The characteristics of biological supermolecules mean that they provide good targets to aim for and good design rules to use when designing artificial functional systems.

(* ↑　Ariga氏著作物のPage 177よりコピペされた箇所)

 In this section, several examples of supermolecules in biology are introducded. The well constructed example of a biological supermolecule is a cellular membrane. Cellular membrane consists mainly of a fluidic lipid bilayer containing proteins (Fig. 1-2). The lipids are self-assembled into the bilayer structure and the proteins float within the lipid bilayer. The whole structure is formed through self-assembly processes. The membrane protein is stably buried in the lipid bilayer due to the amphiphilic nature of the membrane protein. The surfaces of some parts of the protein have mainly hydrophobic amino-acid residues, and hydrophilic residues are located on the other surfaces. The former parts are accommodated in the hydrophobic lipid bilayer and the latter protein regions are exposed to the surface of the water.

(* ↑　Ariga氏著作物のPage 178よりコピペされた箇所)

The major driving force for lipid bilayer formation is hydrophobic interaction. This interaction is much less specific and less directional than the hydrogen bonding and metal coordination interactions that are used in precisely programmed supramolecular assemblies. As shown in cellular membrane, the intermolecular interactions are existed to construct molecular assembly.

(* ↑　Ariga氏著作物のPage 89よりコピペされた箇所)

小幡洋輔氏の博士論文のChapter 1のFig.1-2は、Katsuhiko Ariga氏らの著作物のFig.6-2のコピペです（引用元情報さえも記載されておらず、著作権違反です）。

↓　小幡洋輔氏の博士論文のChapter 1のFig.1-2

↓　Katsuhiko Ariga氏らの著作物のFig.6-2

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調査３：寺村裕治氏（早稲田大学の武岡真司氏の研究室）の博士論文における文章のコピペ（盗用、剽窃）についてのまとめ

出版日：　2004年2月
著者：　寺村裕治　（現　東京大学大学院工学系研究科 バイオエンジニアリング専攻 特任准教授）
論文題目：　Other Titles: bunshi shugo ni yori kochikushita nano soshikitai no tokucho to sono kino seigyo Properties of nano-organizations constructed by molecular assembly and the control of their functions
機能性リポソームとナノシートを用いたナノ医療の展開
http://dspace.wul.waseda.ac.jp/dspace/handle/2065/473 （写し）
博士論文概要（写し）
博士論文審査報告書（写し）
論文本文 （写し）

コピペ指摘コメント：　http://ai.2ch.net/test/read.cgi/life/1395164308/209

文章や図のコピペ元の著作物
著者：　Peter R. Bergethon
著作物題目：　The Physical Basis of Biochemistry: The Foundations of Molecular Biophysics
http://www.amazon.co.jp/The-Physical-Basis-Biochemistry-Foundations/dp/0387982620/ref=sr_1_cc_1?s=aps&ie=UTF8&qid=1395193086&sr=1-1-catcorr&keywords=The+Physical+Basis+of+Biochemistry%3A+The+Foundations+of+Molecular+Biophysics

同一文章   黄色でハイライトされている部分が同一文章。Peter R. Bergethon氏の上記著作物の341ページからのコピペ。

3-2. Phase transition

　Lipids undergo changes in state just as other compounds do. A distinguishing characteristic of lipids in membranes is the ability to exhibit an intermediate or mesomorphic state called the liquid crystalline or gel state. A liquid crystalline state is intermediate in level of organization between the rigid crystal and the fluid liquid state (Fig. 1-6). The transition of state between the solid crystalline and the liquid crystalline form in lipid bilayer is sensitive to temperature (5).

　In pure lipid bilayer, there is a well-defined melting or transition temperature, Tm, below which the lipid will be in a solid crystalline phase and just above which the lipid will usually assume a less ordered liquid crystalline arrangement. In the pure lipid bilayer, there is significant cooperative in the melting process, which leads to the sharply defined transition temperature. Although we will confine our discussion in this section to the simpler cases of single-component membranes, the heterogeneous composition of real membranes does not give rise to a sharp transition points, and melting will occur over a several degree range of temperature. 

　At a temperature below the melting points, the solid crystalline phase exists in which the non-polar hydrocarbon tails are rigidly held in an all-trans configuration; there is little lateral mobility of each molecules. The all-trans arrangement of the nonpolar tails leads to occupation of a minimum volume by the hydrocarbon groups in the membrane. The cis configuration of that results from the presence of unsaturated bonds in the hydrocarbon are more limited, and the transition temperature is lower than that of chains with an all-trans configuration. Below the transition temperature, a saturated　

 　　　（↓　続き。　Peter R. Bergethon氏の上記著作物の342ページからのコピペ？ google booksでは見れない。情報求む。）

hydrocarbon chain will have a very low frequency of kink or cis-conformation formulation, about one kink per 10 acyl chains. As the temperature of the system is increased, there is increasing disturbance of the tightly packed crystalline structure until the transition temperature is reached, where there will be a kink frequency of about one per acyl chains. Above the melting point, the acyl chains will have two or more kinks per chains. The liquid crystalline phase is characterized by a fairly rigid structure near the polar head groups and considerably more disorganized and flexible region near the central hydrophobic portion of the bilayer. The loosened organization of the liquid crystal allows for lateral diffusion and a freedom of rotation along the long axis of the hydrocarbon chains. The transition from a stretched all-trans conformation to a kinked conformation is accompanied by an increase in membrane volume and a decrease in membrane thickness. The phase transition of the phispholipid membrane can be measured by differential scanning calorimetry (DSC) (6), spin probe method (7), and fluorescence probe method (8), etc.

　In artificial bilayers containing a mixture of phospholipids with varying degrees of saturation (different phase transition points), phase separation can occur with individual phospholipid molecules of the same type forming clusters of gel when their freezing points are reached. Since in biological membranes, both saturated and unsaturated fatty acid chains are usually found in the same lipid molecule, that is, one chain is unsaturated, while the other is not, they cannot separate in this way.　

　Cholesterol is another determinant of membrane fluidity (9). Eucaryotic plasma membranes contain relatively large amounts of cholesterol, as much as one molecule for every phospholipid molecule. In addition to regulating fluidity, cholesterol is thought to enhance the mechanical stability of the bilayer. Cholesterol molecules orient themselves in the bilayer with their hydroxyl groups close to the polar head groups of the phospholipid molecules; their platelike steroid rings interact with – and partly immobilize-those regions of the hydrocarbon chains closest to the polar head groups, leaving the rest of the chain flexible. Cholesterol inhibits temperature-induced phase transitions and therefore prevents the drastic decrease in fluidity that would otherwise occur at low temperature.

また、寺村裕治氏の博士論文のFig. 1-6 が、Bergethon氏著作物のFig 21.14からの盗用です。

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その他調査対象論文（武岡真司氏関連）：











著者：　武岡, 真司
論文題目：　機能性リポソームとナノシートを用いたナノ医療の展開
出版日：　2008
TECHNOFAIR2008_Takeoka.pdf

出版日：　Feb-2006

著者：　岡村, 陽介

Title: 分子集合を利用した血小板代替物の構築とin vitro,in vivo止血能評価

Other Titles: Construction of platelet substitutes using molecular assembly and evaluation of their hemostatic effects in vitro and in vivo
Gaiyo-4147.pdf

Shinsa-4147.pdf

Honbun-4147.pdf
コピペ指摘コメント：　http://ai.2ch.net/test/read.cgi/life/1395164308/312
2004年の寺村裕治氏の博士論文のコピペ文章が、2006年の岡村陽介氏の博士論文にも転載されています。ラボ内でのテンプレコピペ？

出版日：　Mar-2007

著者：　阿閉 友保

論文題目：　メトヘモグロビンのペルオキシターゼ活性を利用したヘモグロビン小胞体のメト化抑制系の構築 

Other Titles: Suppression of methemoglobin formation in hemoglobin vesicles using peroxidase activity of methemoglobin
（主査　武岡　真司教授）

http://dspace.wul.waseda.ac.jp/dspace/handle/2065/28485

Gaiyo-4481.pdf
Shinsa-4481.pdf
Honbun-4481.pdf

出版日： Feb-2007

著者：　新井 敏

論文題目：　水素結合部位を有するポルフィリン誘導体の合成と集合体形成挙動の解析

Other Titles: Synthesis of porphyrin derivatives bearing hydrogen-bonding units and the analysis of their self-assembling behaviors
（主査　武岡　真司教授）

http://dspace.wul.waseda.ac.jp/dspace/handle/2065/28505

Gaiyo-4380.pdf

Shinsa-4380.pdf

Honbun-4380.pdf

出版日： Feb-2008

著者：　石原 伸輔

論文題目：　カラム構造を有する超分子集合体の構築とその分子認識能の解析

Other Titles: Construction of columnar structured supramolecular assemblies and the analysis of their molecular recognition properties
（主査　武岡 真司教授）

http://dspace.wul.waseda.ac.jp/dspace/handle/2065/28653

Gaiyo-4753.pdf
Shinsa-4753.pdf
Honbun-4753.pdf

出版日：　Feb-2011

著者：　丹羽 大輔

論文題目：　表裏で異なる細胞親和性を持つナノシートの調製と癒着防止剤としての応用

Other Titles: Construction of Heterofunctional Nanosheets with Different Cytocompatibilities in Two Sides and Application as an Anti-Adhesion Barrier

http://dspace.wul.waseda.ac.jp/dspace/handle/2065/36339

Gaiyo-5629.pdf

Shinsa-5629.pdf

Honbun-5629.pdf

出版日：　Feb-2012

著者：　村田 篤

論文題目：　His-tagタンパク質のラベル化を目指した蛍光OFF/ON型低分子プローブの開発

Other Titles: Development of small molecular OFF/ON fluorescent probes for His-tagged protein labeling

http://dspace.wul.waseda.ac.jp/dspace/handle/2065/37576

Gaiyo-5917.pdf

Shinsa-5917.pdf

Honbun-5917.pdf