All individuals in MeSH

Label Id Description
General Practitioners D058005 [Physicians whose practice is not restricted to a specific field of MEDICINE. ]
General Surgery D013502 [A specialty in which manual or operative procedures are used in the treatment of disease, injuries, or deformities. ]
Generalization, Psychological D005793 [The phenomenon of an organism's responding to all situations similar to one in which it has been conditioned. ]
Generalization, Response D005794 [The principle that after an organism learns to respond in a particular manner to a stimulus, that stimulus is effective in eliciting similar responses. ]
Generalization, Stimulus D005795 [The tendency to react to stimuli that are different from, but somewhat similar to, the stimulus used as a conditioned stimulus. ]
Genes D005796 [A category of nucleic acid sequences that function as units of heredity and which code for the basic instructions for the development, reproduction, and maintenance of organisms. ]
Genes, APC D017491 [Tumor suppressor genes located in the 5q21 region on the long arm of human chromosome 5. The mutation of these genes is associated with familial adenomatous polyposis (ADENOMATOUS POLYPOSIS COLI) and GARDNER SYNDROME, as well as some sporadic colorectal cancers. ]
Genes, Archaeal D019766 [The functional genetic units of ARCHAEA. ]
Genes, BRCA1 D019398 [A tumor suppressor gene (GENES, TUMOR SUPPRESSOR) located on human CHROMOSOME 17 at locus 17q21. Mutations of this gene are associated with the formation of HEREDITARY BREAST AND OVARIAN CANCER SYNDROME. It encodes a large nuclear protein that is a component of DNA repair pathways. ]
Genes, BRCA2 D024522 [A tumor suppressor gene (GENES, TUMOR SUPPRESSOR) located on human chromosome 13 at locus 13q12.3. Mutations in this gene predispose humans to breast and ovarian cancer. It encodes a large, nuclear protein that is an essential component of DNA repair pathways, suppressing the formation of gross chromosomal rearrangements. (from Genes Dev 2000;14(11):1400-6) ]
Genes, Bacterial D005798 [The functional hereditary units of BACTERIA. ]
Genes, Chloroplast D061125 [Those nucleic acid sequences that function as units of heredity which are located within the CHLOROPLAST DNA. ]
Genes, DCC D016163 [Tumor suppressor genes located in the 18q21-qter region of human chromosome 18. The absence of these genes is associated with the formation of colorectal cancer (DCC stands for deleted in colorectal cancer). The products of these genes show significant homology to neural cell adhesion molecules and other related cell surface glycoproteins. ]
Genes, Developmental D050437 [Genes that determine the fate of a cell or CELLS in a region of the embryo during EMBRYONIC DEVELOPMENT. ]
Genes, Dominant D005799 [Genes that influence the PHENOTYPE both in the homozygous and the heterozygous state. ]
Genes, Duplicate D020131 [Two identical genes showing the same phenotypic action but localized in different regions of a chromosome or on different chromosomes. (From Rieger et al., Glossary of Genetics: Classical and Molecular, 5th ed) ]
Genes, Essential D020043 [Those genes found in an organism which are necessary for its viability and normal function. , Constitutively and evenly expressed genes involved in routine cellular metabolisms. ]
Genes, Fungal D005800 [The functional hereditary units of FUNGI. ]
Genes, Helminth D017238 [The functional hereditary units of HELMINTHS. ]
Genes, Homeobox D005801 [Genes that encode highly conserved TRANSCRIPTION FACTORS that control positional identity of cells (BODY PATTERNING) and MORPHOGENESIS throughout development. Their sequences contain a 180 nucleotide sequence designated the homeobox, so called because mutations of these genes often results in homeotic transformations, in which one body structure replaces another. The proteins encoded by homeobox genes are called HOMEODOMAIN PROTEINS. ]