Results 241 to 250 of about 1,357,403 (269)
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Genetics of Sarcoidosis

Seminars in Respiratory and Critical Care Medicine, 2014
Sarcoidosis is a multifactorial and polygenic disorder. Recently, several novel predisposing genes have been identified by genome-wide association studies, and fast progress in molecular technologies such as systematic and large-scale resequencing will aid the discovery of further risk loci and variants.
Fischer, Annegret   +5 more
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Genetics of Apoptosis

1997
Publisher Summary The genetic analysis of apoptosis, or programmed cell death, provides important information on the biology of naturally occurring cell death. Identification of genes regulating apoptosis has confirmed that this process follows a similar paradigm in all multicellular organisms.
Desnoyers, S, Hengartner, M O
openaire   +2 more sources

Genetic Analysis

1998
The Mendelian analysis of genetic variation, available as induced mutants or as natural variation, requires a number of steps that are described in this chapter. These include the determination of the number of genes involved in the observed trait's variation, the determination of dominance relationships between alleles of the same locus, and epistatic
Koornneef, M.   +2 more
openaire   +5 more sources

Genetic and Non-Genetic Operators in ALECSYS

Evolutionary Computation, 1993
It is well known that standard learning classifier systems, when applied to many different domains, exhibit a number of problems: payoff oscillation, difficulty in regulating interplay between the reward system and the background genetic algorithm (GA), rule chains' instability, default hierarchies' instability, among others.
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Genetics of Autism

Child and Adolescent Psychiatric Clinics of North America, 1998
In summary, autism genetics has moved from a time of identification of heritability and determination of risk of "lesser variants" or the "broader phenotype" in relatives to a phase where some cases of autism have a definite basis such as maternally inherited duplications of 15q11-q13, identification of mutations causing AS, Rett syndrome, and FRAXA ...
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Genetics

Clinical Journal of Oncology Nursing, 2003
Suzanne M. Mahon, William P. Hogle
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GENETICS

Medical Journal of Australia, 1939
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Genetics

JAMA: The Journal of the American Medical Association, 1978
openaire   +4 more sources

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