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Titlebook: Molecular Basis of Chronic Myeloproliferative Disorders; Petro E. Petrides,Heike L. Pahl Conference proceedings 2004 Springer-Verlag Berli

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发表于 2025-3-21 16:29:21 | 显示全部楼层 |阅读模式
书目名称Molecular Basis of Chronic Myeloproliferative Disorders
编辑Petro E. Petrides,Heike L. Pahl
视频video
图书封面Titlebook: Molecular Basis of Chronic Myeloproliferative Disorders;  Petro E. Petrides,Heike L. Pahl Conference proceedings 2004 Springer-Verlag Berli
描述.Since the first description of Philadelphia chromosome-negative chronic myeloproliferative disorders more than 100 years ago, the diagnosis and therapy of these conditions have been based primarily on clinical experience and judgement. Until recently very little was known about the molecular basis of these diseases. In order to spark research in this area basic scientists and clinicians from various parts of the world have contributed to this volume, the first of its kind to put together the current knowledge. The book deals with the new WHO classification of these disorders, novel aspects of diagnostic pathology, the search for disease-relevant genes utilizing molecular biology and proteomic techniques, the description of the roles of PVR-1 and VHL genes for polycythemias and the discovery of the gene mutation responsible for the idiopathic hypereosinophilic syndrome. A chapter on anagrelide, an important novel drug for the treatment of primary thrombocythemia, is included. .
出版日期Conference proceedings 2004
关键词classification; growth factor; idiopathic hypereosinophilic syndrome; idiopathic myelofibrosis; mastocyt
版次1
doihttps://doi.org/10.1007/978-3-642-18738-4
isbn_softcover978-3-642-62271-7
isbn_ebook978-3-642-18738-4
copyrightSpringer-Verlag Berlin Heidelberg 2004
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https://doi.org/10.1007/978-3-642-18738-4classification; growth factor; idiopathic hypereosinophilic syndrome; idiopathic myelofibrosis; mastocyt
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Molecular Basis of Chronic Myeloproliferative Disorders978-3-642-18738-4
发表于 2025-3-22 14:53:38 | 显示全部楼层
Conference proceedings 2004-1 and VHL genes for polycythemias and the discovery of the gene mutation responsible for the idiopathic hypereosinophilic syndrome. A chapter on anagrelide, an important novel drug for the treatment of primary thrombocythemia, is included. .
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发表于 2025-3-22 21:47:39 | 显示全部楼层
and therapy of these conditions have been based primarily on clinical experience and judgement. Until recently very little was known about the molecular basis of these diseases. In order to spark research in this area basic scientists and clinicians from various parts of the world have contributed
发表于 2025-3-23 03:18:05 | 显示全部楼层
Conference proceedings 2004py of these conditions have been based primarily on clinical experience and judgement. Until recently very little was known about the molecular basis of these diseases. In order to spark research in this area basic scientists and clinicians from various parts of the world have contributed to this vo
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