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Prothrombotic genetic markers.
Italian heart journal : official journal of the Italian Federation of Cardiology, 2002The last decade has been characterized by an explosion of research studies on genetic epidemiology. In particular, as far as ischemic heart disease is concerned, a lot of research was focused on prothrombotic genetic risk factors. Unfortunately, the success of this approach in the field of venous thrombosis has not been replicated in the field of ...
Rossi M L, Merlini P A, Ardissino D
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JAMA: The Journal of the American Medical Association, 1973
To the Editor.— In the article by Gelpi and Perrine (224:605, 1973), part of the speculation on the origin of the sickle cell gene is based on an error in fact. The authors state "... it is clear that the R o (cDe) blood group gene complex, considered to be a reliable genetic marker for African Negro populations, occurs at high frequency among the ...
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To the Editor.— In the article by Gelpi and Perrine (224:605, 1973), part of the speculation on the origin of the sickle cell gene is based on an error in fact. The authors state "... it is clear that the R o (cDe) blood group gene complex, considered to be a reliable genetic marker for African Negro populations, occurs at high frequency among the ...
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Translocations as Genetic Markers
1994If two nonhomologous chromosomes interchange ends following chromosome breakage, the products of this event are termed a reciprocal interchange or reciprocal translocation. The two rearranged chromosomes that result are fully stable and, when transmitted together, contain all the chromosomal material that was present in the two normally arranged ...
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Constitutional genetic markers of aging
Experimental Gerontology, 1988Constitutional genetic markers of aging can be defined as members of that subset of genes that modulate the times of onset and/or the rates of progression of one or more of the processes of aging, or the response of the target cells, tissues and organisms to a particular process. These genetic factors are classified into: (1) those that control changes
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Linkage and Association to Genetic Markers
2015Genetic markers that are sufficiently polymorphic (as measured by their heterozygosities) can be used in linkage and association analyses to detect Mendelian segregation underlying disease phenotypes. Each type of analysis can either be based on a specific genetic model or not make any assumptions about the mode of inheritance of the disease ...
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Genetic Markers for Schizophrenic Subgroups
Psychopathology, 1982By the study of hereditary serum protein markers in psychotic patients and normal controls, a surplus of Gc 1-1 (p < 0.01) and transferrin B variants (p < 0.0027) has been established in schizophrenias. Affective psychoses are characterized by an excess of the haptoglobin (Hp) serum type 2-2 (p < 0.001).
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Dermatoglyphics as Genetic Markers
1990Populations composed of mixed descendants from two different racial groups provide a means for detecting whether or not a particular variation may have a genetic basis. Dermatoglyphics provide an excellent tool for such investigations. They have high heritabilities and are not altered by postnatal factors.
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Genetic Markers in Human Hypertension
American Journal of Hypertension, 1991A rapidly increasing abundance of genetic markers which can be characterized on a large scale makes an application of the genetic linkage strategy, so successful with Mendelian diseases, ever more attractive for genetic investigations of common diseases such as essential hypertension.
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