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      Transdifferentiation : flexibility in cell differentiation

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      https://www.riss.kr/link?id=M371617

      • 저자
      • 발행사항

        Oxford : Clarendon Press ; Oxford ; New York : Oxford University Press, 1991

      • 발행연도

        1991

      • 작성언어

        영어

      • 주제어
      • DDC

        599/.087612 판사항(20)

      • ISBN

        019854281X :

      • 자료형태

        일반단행본

      • 발행국(도시)

        England

      • 서명/저자사항

        Transdifferentiation : flexibility in cell differentiation / T.S. Okada.

      • 형태사항

        x, 238 p. : ill. ; 24 cm.

      • 일반주기명

        Includes bibliographical references (p. [193]-229) and index.

      • 소장기관
        • 경북대학교 중앙도서관 소장기관정보
        • 국립중앙도서관 국립중앙도서관 우편복사 서비스
        • 대진대학교 도서관 소장기관정보
        • 서울대학교 의학도서관 소장기관정보 Deep Link
        • 서울대학교 중앙도서관 소장기관정보 Deep Link
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      부가정보

      목차 (Table of Contents)

      • CONTENTS
      • 1. Introduction = 1
      • 1.1. the scope of the monograph = 1
      • 1.2. Historical survey = 3
      • 1.3. Terminology = 9
      • CONTENTS
      • 1. Introduction = 1
      • 1.1. the scope of the monograph = 1
      • 1.2. Historical survey = 3
      • 1.3. Terminology = 9
      • 1.3.1. Metaplasia and related terminology = 9
      • 1.3.2. Transdifferentiation = 9
      • 1.3.3. Transdetermination = 11
      • 1.3.4. Some other terms = 12
      • 2. Are dormant genes in differentiated cells activated? = 13
      • 2.1. Nuclear transplantation = 13
      • 2.2. Heterokaryons = 16
      • 2.3. Possble re-activation of dormant genes by hypomethylation = 18
      • 2.4. Does transdifferentiation occur in differentiated plant cells? = 19
      • 2.5. Transdetermination in Drosophila imaginal discs = 21
      • 3. Does change in differentiated cell phenotypes occur in normal development? = 25
      • 3.1. Examples from invertebrate development = 25
      • 3.2. Developmental shift of molecular markers = 29
      • 4. Examples of transdifferentiation among single or related cell classes = 32
      • 4.1. Flexibility of differentiation phenotypes of neurons = 32
      • 4.2. Transdifferentiation among different subclasses of chromatophores = 42
      • 4.3. Transdifferentiation of endocrine cells to neurons = 47
      • 4.3.1. Chromaffin cells can change to neuronal cells = 49
      • 4.3.2. Factors influencing transdifferentiation of chromaffin cells into neuronal cells = 53
      • 5. Re-evaluation of classical examples of metaplasia and some relatedsystems = 56
      • 5.1. Epithelial metaplasia = 56
      • 5.1.1. Skin metaplasia = 57
      • 5.1.2. Endodermal derivatives = 58
      • 5.1.3. Corneal epithelium = 64
      • 5.2. Pancreatic hepatocytes = 66
      • 5.3. Bone metaplasia : myocytes transdifferentiate into cartilage cells = 72
      • 5.4. Other systems = 78
      • 6. Does transdifferentiation occur in regeneration? = 80
      • 6.1. Regeneration in representative invertebrates = 80
      • 6.1.1. Regeneration in planarians = 80
      • 6.1.2. Other invertebrates systems = 85
      • 6.2. Regeneration of amphibian limbs = 88
      • 6.2.1. Nuclear transplantation and cell culture = 89
      • 6.2.2. Cell differentiation of blastema cells in situ = 91
      • 6.2.3. Regeneration from putative 'reserve' cells = 95
      • 6.2.4. Summary of studies on limb regeneration = 96
      • 6.3. Lens regeneration by transdifferentiation = 99
      • 6.3.1. A short historical note = 99
      • 6.3.2. Regenerated lens is derived from iris pigmented epithelium (IPE) by transdifferentiation = 100
      • 6.3.3. Retinal pigmented epithelium transdifferentiates into lens = 105
      • 6.3.4. Lens regeneration from cornea = 105
      • 6.3.5. Possible lens transdifferentiation from neural retina in vivo = 107
      • 6.4. Regeneration of neural retina by transdifferentiation = 111
      • 6.5. Summary of studies on regeneration of eyes = 116
      • 7. Transdifferentiation in cell culture conditions = 119
      • 7.1. Transdifferentiation from pigmented cells of eyes = 119
      • 7.1.1. Retinal pigmented epithelial cells transdifferentiate into lens = 119
      • 7.1.2. Retinal pigmented epithelial cells transdifferentiate into neural retina = 125
      • 7.1.3. Iris pigmented epithelial cells transdifferentiate into lengs = 127
      • 7.1.4. Other pigment cells = 129
      • 7.2. Transdifferentiation from neural retina = 130
      • 7.2.1. General features of transdifferentiating cultures of neural retina = 132
      • 7.2.2. Molecular events = 134
      • 7.2.3. Progenitor cell type in transdifferentiated lens = 138
      • 7.2.4. Extrinsic factors affecting transdifferentiation of neural retina = 140
      • 7.3. the pineal body as a multipotential system in cell differentiation = 143
      • 7.4. the unusually wide differentiation repertoire of isolated strated muscle of medusa = 146
      • 7.4.1. Birth of new cell types from isolated striated muscle = 147
      • 7.4.2. Organ regeneration from isolated striated muscle = 150
      • 8. Factors influencing transdifferentiation = 155
      • 8.1. Are preceding mitotic sycles obligatory for transdifferentiation? = 155
      • 8.2. Is a loss of the pre-existing phenotype a necessary condition for transdifferentiation? = 161
      • 8.3. A possible cue to trigger the process of transdifferentiation = 163
      • 8.4. Does disruption of contact-mediated cell interaction control phenotypic modification? = 165
      • 8.5. Do speific molecules induce new pathways in transdifferentiation systems? = 170
      • 8.6. Is 'molecular memory' a possible prerequisite for transdifferentiation? = 173
      • 9. Characteristics of the transdifferentiation process = 178
      • 9.1. Transdifferentiation is basically a unidirectional process = 178
      • 9.2. Can the dichotomy of transdifferentiation (metaplasia) versus differentiation of stem cells be reconciled? = 182
      • 9.3. Speculation on the mechanisms of transdifferentiation = 186
      • References = 193
      • Index = 230
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