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In this work, author Frank B. Livingstone has collected and interpreted data on abnormal hemoglobins and G6PD deficiency in humans around the globe. He reports on blood abnormalities by continent and ethnicity and relates these findings to the historic and prehistoric movements of populations.
Research on abnormal human hemoglobins (protein in blood that carries oxygen), has taught us about the inheritance, biochemistry, and distribution of these traits. Th is knowledge, coupled with mathematical research using computer models of population genetics, has enabled researchers to marry biological fact and genetic theory. This volume places medical understanding in an evolutionary framework. Using published data on the frequencies of abnormal hemoglobins in the world's populations, Livingston analyzes and interprets these frequencies in the light of world distribution of diff erent forms of diseases such as malaria. He further develops the genetic theory of the evolutionary homeostasis. Livingston discusses the relation of abnormal hemoglobins to endemic malaria and, shows how natural selection pressures explain the known distribution of these traits. Where non-coinciding distributions arise, the book presents other genetic, anthropological, evolutionary, and epidemiological evidence to explain these discrepancies. This classic work remains a useful sourcebook for professors and graduate students of anthropology, genetics, epidemiology, and hematology. Frank B. Livingstone was professor emeritus of biological anthropology at the University of Michigan. He recieved the Martin Luther King Award from the Southern Christian Leadership Conference for his groundbreaking research on sickle cell anemia and is the author of Data on the Abnormal Hemoglobin's and Glucose-Six-Phosphate Deficiency in Human Populations. Jonathan Marks is a professor of anthropology, at the University of North Carolina, Charlotte.
Glucose-6-Phosphate Dehydrogenase covers the proceedings of an international symposium on G6PD, held in November 1985 under the auspices of the National Institutes of Health and the City of Hope National Medical Center. The said conference is a response to the need for a comprehensive conference on the diverse subjects related to the enzyme G6PD. The book is divided into four parts. Part I includes topics related to G6PD deficiency and hemolytic anemia such as drug-induced and non-spherocytic hemolytic anemia; favism; and G6PD-related neonatal jaundice. Part II discusses G6PD variations; the o ...
Research on abnormal human hemoglobins (protein in blood that carries oxygen), has taught us about the inheritance, biochemistry, and distribution of these traits. This knowledge, coupled with mathematical research using computer models of population genetics, has enabled researchers to marry biological fact and genetic theory. This volume places medical understanding in an evolutionary framework. Using published data on the frequencies of abnormal hemoglobins in the world's populations, Livingston analyzes and interprets these frequencies in the light of world distribution of different forms of diseases such as malaria. He further develops the genetic theory of the evolutionary homeostasis. Livingston discusses the relation of abnormal hemoglobins to endemic malaria and, shows how natural selection pressures explain the known distribution of these traits. Where non-coinciding distributions arise, the book presents other genetic, anthropological, evolutionary, and epidemiological evidence to explain these discrepancies. This classic work remains a useful sourcebook for professors and graduate students of anthropology, genetics, epidemiology, and hematology.
The aim of this volume is to promote a bio-behavioral focus for indigenous plant research.
Blood Cells has been written with both the practisinghaematologist and the trainee in mind. It aims to provide a guidefor use in the diagnostic haematology laboratory, covering methodsof collection of blood specimens, blood film preparation andstaining, the principles of manual and automated blood counts andthe assessment of the morphological features of blood cells. Thepractising haematologist should find this book sufficientlycomprehensive to be a reference source while, at the same time, thetrainee haematologist and biomedical scientist should find it astraightforward and practical bench manual. Enables both the haematologist and laboratory scientist toidentify blood cell features, from the most common to the moreobscure Provides essential information on methods of collection, bloodfilm preparation and staining, together with the principles ofmanual and automated blood counts Completely revised and updated, incorporating much newlypublished information: now includes advice on further tests when aspecific diagnosis is suspected Four hundred high quality photographs to aid with blood cellidentification Highlights the purpose and clinical relevance of haematologylaboratory tests throughout
The first two editions of this book, published in 1979 and in 1986, were well re ceived by the scientific community. Translations into Italian, Japanese, and Rus sian suggest that this book was regarded useful in many parts of the world. Mean while, human genetics has seen dramatic developments, and the "molecular revo lution" has attracted thousands of scientists, including many molecular biologists, to this field. About 3700 human genes have already been mapped to chromosomal sites. Many such genes have been cloned, and the various mutations causing dis ease have been identified. Novel mutational mechanisms such as expanded trinu cleotide repeats have been discovered in conditions such as Huntington's disease and the fragile X syndrome of mental retardation. Gene action now can often be elucidated by studying the pathway from gene to phenotype following positional cloning rather than working in the opposite direction, as was customarily done be fore the tools of "new genetics" were available. In an increasing number of genetic diseases, the pathogenic mechanisms have been elucidated with positive conse quences for prevention and treatment. It therefore became necessary to rewrite al most completely major portions of this book. These developments are now making genetics arguably the leading basic science for medicine, as well as a recognized medical speciality. But all these changes do not mean that the entire framework of human genetics had to be reconstructed.
This monograph presents data from a systematic regional archaeological survey carried out over an area of ca. 600 square kilometers during May through December 1973 by the University of Michigan Museum of Anthropology.
This study examines plants associated with ritual purity, fertility, prosperity and life, and plants associated with ritual impurity, sickness, ill fate and death. It provides detail from history, ethnography, religious studies, classics, folklore, ethnobotany and medicine.