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leaf --- physiology --- pigments --- senescence
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Cell Aging --- Aging --- Cells --- Cellules --- physiology --- Periodicals. --- Vieillissement --- Périodiques --- physiology. --- Aging. --- Chemistry --- Health Sciences --- Life Sciences --- Biochemistry --- General and Others --- Biology --- Cellular Senescence --- Aging, Biological --- Biological Aging --- Senescence --- Cellular Aging --- Aging, Cell --- Cell Senescence --- Replicative Senescence --- Senescence, Cellular --- Senescence, Replicative --- Aging, Cellular --- Senescence, Cell --- ageing --- longevity --- lifespan --- apoptosis --- gerontology --- ageing --- Organisms --- Cytology --- Mutation Accumulation --- Cell Ageing --- Cellular Ageing --- Senescence-Associated Secretory Phenotype --- Ageing, Cell --- Ageing, Cellular --- Phenotype, Senescence-Associated Secretory --- Secretory Phenotype, Senescence-Associated --- Senescence Associated Secretory Phenotype --- Geriatrics --- gerontologie
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Human red blood cells are formed mainly in the bone marrow and are believed to have an average life span of approximately 120 days. However, is it true for all red blood cells? What are the changes associated with red cell maturation, adulthood and senescence? What are the determinants of red cell life span and clearance? What are the mechanisms in control of red cell mass in healthy humans and patients with various forms of anemia? What are the markers of circulating red cell senescence and in cells during storage and transfusion? Within the life span may properties of red cells change leading to age-mixed circulating cell populations. Although these cells appear to be genetically terminated by the time they are released into the blood stream, they undergo surprisingly versatile modifications depending on the life-style and health conditions of a “human host”. Numerous disorders are believed to be associated with facilitated ageing of red blood cells. “In vitro ageing” and damage of red blood cells during storage is yet one more important issue related to the risks and efficiency of blood transfusion. Many of the mechanisms behind such effects are far from being fully understood. In this context the Research Topic is set to include articles in the field of biochemical investigations, biophysical approaches, physiological and clinical studies related to red blood cell maturation and aging. This includes Original Research, Methods, Hypothesis and Theory, Reviews and Perspectives.
Erythropoiesis --- senescence --- neocytolysis --- blood storage --- Clearance --- Vesiculation --- erythrocyte --- Erythropoiesis --- senescence --- neocytolysis --- blood storage --- Clearance --- Vesiculation --- erythrocyte
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ECONOMIC PLANTS --- PLANTS --- CELLS --- ORGANS --- SENESCENCE --- MECHANISMS --- CONTROL --- plants --- Plant developmental stages --- Plant physiology --- Aging --- methodology --- genetic code --- Morphogenesis --- Senescence. --- Senescence
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Aging. --- Aging, Biological --- Biological Aging --- Senescence --- Mutation Accumulation --- Aging
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This volume summarizes recent progresses in the physiology, biochemistry, cell biology, molecular biology, genomics, proteomics, and biotechnology of plant senescence. Beginning with a chapter on senescence-related terminology and our current knowledge of mitotic senescence in plants (a less well-studied area), the book focuses on post-mitotic senescence, and includes chapters addressing the senescence of leaves, flowers and fruits. Later chapters examine the development of various new biotechnologies for manipulating the senescence processes of fruit and leaves, some of which are approaching commercialization. The book is directed at researchers and professionals in plant molecular genetics, physiology and biochemistry.
Plants --- Aging --- Plante --- plants --- Physiologie végétale --- Plant physiology --- Sénescence --- Senescence --- Aging. --- 57.016.67 --- 581.14 --- Ageing. Senescence --- Development --- 581.14 Development --- Aging in plants --- Plant aging --- Senescence. --- Plants - Aging
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Aging --- Aging. --- Aging, Biological --- Biological Aging --- Senescence --- Mutation Accumulation
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Human red blood cells are formed mainly in the bone marrow and are believed to have an average life span of approximately 120 days. However, is it true for all red blood cells? What are the changes associated with red cell maturation, adulthood and senescence? What are the determinants of red cell life span and clearance? What are the mechanisms in control of red cell mass in healthy humans and patients with various forms of anemia? What are the markers of circulating red cell senescence and in cells during storage and transfusion? Within the life span may properties of red cells change leading to age-mixed circulating cell populations. Although these cells appear to be genetically terminated by the time they are released into the blood stream, they undergo surprisingly versatile modifications depending on the life-style and health conditions of a “human host”. Numerous disorders are believed to be associated with facilitated ageing of red blood cells. “In vitro ageing” and damage of red blood cells during storage is yet one more important issue related to the risks and efficiency of blood transfusion. Many of the mechanisms behind such effects are far from being fully understood. In this context the Research Topic is set to include articles in the field of biochemical investigations, biophysical approaches, physiological and clinical studies related to red blood cell maturation and aging. This includes Original Research, Methods, Hypothesis and Theory, Reviews and Perspectives.
Erythropoiesis --- senescence --- neocytolysis --- blood storage --- Clearance --- Vesiculation --- erythrocyte
Choose an application
Human red blood cells are formed mainly in the bone marrow and are believed to have an average life span of approximately 120 days. However, is it true for all red blood cells? What are the changes associated with red cell maturation, adulthood and senescence? What are the determinants of red cell life span and clearance? What are the mechanisms in control of red cell mass in healthy humans and patients with various forms of anemia? What are the markers of circulating red cell senescence and in cells during storage and transfusion? Within the life span may properties of red cells change leading to age-mixed circulating cell populations. Although these cells appear to be genetically terminated by the time they are released into the blood stream, they undergo surprisingly versatile modifications depending on the life-style and health conditions of a “human host”. Numerous disorders are believed to be associated with facilitated ageing of red blood cells. “In vitro ageing” and damage of red blood cells during storage is yet one more important issue related to the risks and efficiency of blood transfusion. Many of the mechanisms behind such effects are far from being fully understood. In this context the Research Topic is set to include articles in the field of biochemical investigations, biophysical approaches, physiological and clinical studies related to red blood cell maturation and aging. This includes Original Research, Methods, Hypothesis and Theory, Reviews and Perspectives.
Erythropoiesis --- senescence --- neocytolysis --- blood storage --- Clearance --- Vesiculation --- erythrocyte
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