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Lysosomes and Lysosomal Diseases

This new volume of Methods in Cell Biology looks at methods for lysosomes and lysosomal diseases. Chapters focus upon practical;

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Lysosomes: Biology, Diseases, and Therapeutics

biochemistry to illustrate the potential of lysosomes in drug discovery and development. Explores basic principles and properties of lysosomes that;

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Lysosomal Storage Disorders

our understanding of both the scientific and the clinical basis of these diseases. Lysosomal Storage Disorders: A Practical Guide is the fruit;

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Stem Cell Therapy in Lysosomal Storage Diseases

Stem Cell therapy for lysosomal diseases (LSDs) is developing rapidly. This volume discusses the history, current practice and future;

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Neurochemistry of Metabolic Diseases

abnormalities is useful to interpret possible targets in these diseases. This book reveals what factors contribute in lysosomal storage diseases;

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Glycobiology and Human Diseases

urinary glycans as a possible method for the diagnosis of lysosomal storage diseases, glycobiology of human milk (biological roles and diseases;

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Glycobiology and Human Diseases

urinary glycans as a possible method for the diagnosis of lysosomal storage diseases, glycobiology of human milk (biological roles and diseases;

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Clinical Neurogenetics, An Issue of Neurologic Clinics

; Autism/ASD; Fragile X Tremor Ataxia Syndrome (FXTAS); Lysosomal Storage Diseases; Psychiatric Disorders; Dominant Spinocerebellar Ataxias;

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Endocytosis

machinery can lead to diseases such as cancer.Written and edited by experts in the field, this collection from Cold Spring Harbor;

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Lysosomes

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Progranulin and Central Nervous System Disorders

neurodegenerative diseases. Following initial recognition of the importance of PGRN in sexual differentiation of the developing brain and adult neurogenesis;

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Progranulin and Central Nervous System Disorders

neurodegenerative diseases. Following initial recognition of the importance of PGRN in sexual differentiation of the developing brain and adult neurogenesis;

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Lysosomal Storage Diseases

description of the various pathophysiologic changes associated with the lysosomal storage disorders. Therapeutic considerations and aspects relating;

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Lysosomes

goal here, therefore, is simply to introduce the major features of lysosomes at a level I hope will be useful both to I;ldvanced students and;

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Plasma Membrane Repair

Lysosomes and Membrane Function, Volume 84 in the Current Topics in Membranes series, highlights new advances in the field, with this;

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Chemical Diagnostics

Screening: About Both Small Molecular Diseases and Lysosomal Storage Diseases, by W.-L. Hwu, Y.-H. Chien, N.-C. Lee, S.-F. Wang, S.-C. Chiang, L.-W;

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Autophagy: Cancer, Other Pathologies, Inflammation, Immunity, Infection, and Aging: Volume 9

Autophagy: Cancer, Other Pathologies, Inflammation, Immunity, Infection, and Aging: Volume 9: Human Diseases and Autophagosome offers a;

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Neurochemistry of Metabolic Diseases

. Several new developments on metabolic diseases research have been emerging. Gaucher disease is a lysosomal storage disorder caused by;

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Lysosomal Storage Diseases

The last fifteen years have witnessed the extraordinary evolution of basic and clinical research in the field of lysoso-mal storage;

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Rare Diseases

highlighted and we look at enzyme replacement therapy in lysosomal storage diseases. This work is part of a series, produced with the involvement;

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Charnolophagy in Health and Disease

, sarcopenia, cachexia, respiratory diseases, gastrointestinal diseases, hyperlipidemia, skin and hair diseases, pulmonary diseases, cardiovascular;

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Pharmaceutical Biocatalysis

treatment of thromboembolic diseases, and the molecular mechanisms for statin pleiotropy and its clinical relevance in cardiovascular diseases. The;

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Autophagy of the Nervous System

, ischemia/hypoxia and lysosomal storage diseases, will be discussed along with current drug development strategies targeting autophagy.;

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Recent Advances in iPSC Disease Modeling

diseases in vitro, and thus enabling us to study the cellular and molecular mechanisms involved in different pathologies. Further insights into;

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Biometals in Neurodegenerative Diseases

Biometals in Neurodegenerative Diseases: Mechanisms and Therapeutics is an authoritative and timely resource bringing together the;

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The Ubiquitin-proteasome System

to the discoverers of ubiquitin as a cofactor for intracellular non-lysosomal proteolysis. There is a voluminous literature showing that;

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Inborn Errors of Metabolism, An Issue of Pediatric Clinics of North America

storage diseases and gluconeogenesis defects; Inborn errors of metabolism with myopathy: defects of fatty acid oxidation and carnitine transport;

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