Molecular Biology of Hematopoiesis 6 by E. Donnall Thomas (auth.), Nader G. Abraham, Antonio

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By E. Donnall Thomas (auth.), Nader G. Abraham, Antonio Tabilio, Massimo Martelli, Shigetaka Asano, Alberto Donfrancesco (eds.)

This quantity of Molecular Biology of Hematopoiesis is devoted to many inter­ nationwide scientists and clinicians for his or her contribution to the sphere of Hematology/ Oncology provided on the eleventh overseas Symposium on Molecular Biology of Hematopoiesis, which was once held in Bormio, Italy, June 25-29, 1998. the continual help of the Presidents of the assembly, Professor F. Takaku, President of Jichi collage, and E. D. Thomas, Nobel Laureate, was once drastically said, specifically Professor Takaku, for his imaginative and prescient and help for improvement of gene remedy in Japan. New info on BMT for autoimmune affliction and organ transplantation was once provided on the symposium and is released during this quantity. numerous new findings on gene therapy/transfer into HSC have been provided by means of E. F. Vanin and A. Nienhuis, okay. Humphries, 1. A. Nolta, H. E. Heslop, and M. ok. Brenner. Professors S. Asano and okay. Tani awarded new reviews on gene move into primates. one of the highlights have been the recent papers on gene move provided via G. salary maker, N. G. Abraham, and M. Onoderea from R. M. BJaese's staff. using BMT for organ transplant and autoim­ mune disorder used to be up to date and a consultant paper is gifted during this volume.

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14 FLT3 transcript has been detected in murine and human cell populations enriched for hematopoietic stem cells and progenitors and is absent in more mature cells. 2o,21 FLT3 receptor is frequently expressed on the surface of acute myelogenous leukemia blasts and FL, as a single factor or in combination with other growth factors, induces significant proliferation and colony formation by clonogenic progenitors from AML samples in primary leukemias,zz In addition, targeted disruption of the FLT3 gene led to deficiencies in primitive hematopoietic progenitors.

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