The pigmentary system : physiology and pathophysiology
著者
書誌事項
The pigmentary system : physiology and pathophysiology
Blackwell Pub., 2006
2nd ed
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注記
Includes bibliographical references and index
HTTP:URL=http://www.loc.gov/catdir/toc/ecip062/2005030369.html Information=Table of contents
収録内容
- A history of the science of pigmentation
- Comparative anatomy and physiology of pigment cells in nonmammalian tissues
- General biology of mammalian pigmentation
- Extracutaneous melanocytes
- Regulation of melanoblast migration and differentiation
- Melanoblast development and associated disorders
- Biogenesis of melanosomes
- Melanosome trafficking and transfer
- Melanosome processing in keratinocytes
- The regulation of melanin formation
- The tyrosinase gene family
- Molecular regulation of melanin formation: melanosome transporter proteins
- Transcriptional regulation of melanocyte function
- Enzymology of melanin formation
- Chemistry of melanins
- The physical properties of melanins
- Photobiology of melanins
- Toxicological aspects of melanin and melanogenesis
- Regulation of pigment type switching by agouti, melanocortin signaling, attractin, and mahoganoid
- Human pigmentation: its regulation by ultraviolet light and by endocrine, paracrine and autocrine factors
- Paracrine interactions of melanocytes in pigmentary disorders
- Growth factor receptors and signal transduction regulating the proliferation and differentiation of melanocytes
- Aging and senescence of melanocytes
- The genetics of melanoma
- The transformed phenotype of melanocytes
- A more precise lexicon for pigmentation, pigmentary disorders and chromatic abnormalities
- The normal color of human skin
- Mechanisms that cause abnormal skin color
- Genetic hypomelanoses: disorders characterized by congenital white spotting-piebaldism, Waardenburg syndrome, and related genetic disorders of melanocyte development-clinical aspects
- Genetic hypomelanoses: acquired depigmentation
- Genetic hypomelanoses: generalized hypopigmentation
- Genetic hypomelanoses: localised hypopigmentation
- Genetic hypomelanoses: disorders characterized by hypopigmentation of hair
- Metabolic, nutritional and endocrine disorders
- Chemical, pharmacologic and physical agents causing hypomelanoses
- Infectious hypomelanoses
- Inflammatory hypomelanoses
- Hypomelanoses associated with melanocytic neoplasia
- Miscellaneous hypomelanoses: depigmentation
- Miscellaneous hypomelanoses: hypopigmentation
- Miscellaneous hypomelanoses: extracutaneous loss of pigmentation
- Hypopigmentation without hypomelanosis
- Genetic epidermal syndromes: disorders characterized by generalized hyperpigmentation
- Genetic epidermal syndromes: disorders characterized by reticulated hyperpigmentation
- Genetic epidermal syndromes with Café-au-Lait macules
- Genetic epidermal pigmentation with lentigines
- Genetic epidermal syndromes: localized hyperpigmentation
- Genetic epidermal syndromes: disorders of aging
- Congenital epidermal hypermelanoses
- Acquired epidermal hypermelanoses
- Hypermelanosis associated with gastrointestinal disorders
- Acquired and congenital dermal hypermelanosis
- Mixed epidermal and dermal hypermelanoses and hyperchromias
- Drug-induced or -related pigmentation
- The melanocyte system of the nails and its disorders
- Pigmentary abnormalities and discolorations of the mucous membranes
- Common benign neoplasms of melanocytes
- Rare benign neoplasms of melanocytes
- Topical treatment of pigmentary disorders
- Chemophototherapy of pigmentary disorders
- UVB therapy for pigmentary disorders
- Sunscreens and cosmetics
- Surgical treatment of pigmentary disorders
- Laser treatment of pigmentary disorders
