Nucleotide polymorphisms in the alpha2 gene define multiple alleles that are associated with differences in platelet alpha2 beta1 density. Blood. 1998; 92 (7):2382–2388.Kritzik M, Savage B, Nugent DJ, Santoso S, Ruggeri ZM, Kunicki TJ. Nucleotide polymorphisms in the alpha2 gene define ...
respectively, which passed this threshold (TableS6). One of the strongest associations in our suggestive results was between the distribution in size of RNA particles in the cytoplasm (Cytoplasm_Granularity_3_RNA) and rare
Resolving the heterogeneity of cell types in rheumatic disorders with unbiased single-cell technologies is critical to understanding the genetics of disease. J. Autoimmun.33, 197–207 (2009). ArticlePubMedPubMed CentralGoogle Scholar Bogdanos, D. P. et al. Twin studies in autoimmune disease: gen...
Just as average expression of PAM50 genes in tumor cells from snRNA-seq could discriminate tumor subtype, chromatin accessibility in the promoters of PAM50 genes from snATAC-seq showed good segregation of tumors by subtype in the 21 samples (from 21 cases) with both data types available (Fig....
Especially when combined with tightly controlled genetics of both insect and host plant, multi-omics approaches are powerful tools for revealing and filtering candidate lists down to plausible genes for further functional analysis as putative aphid effectors. ...
HLA/MHC class II molecules show high degree of polymorphism in the human population. The individual polymorphic motifs have been suggested to be propagated and mixed by transfer of genetic material (recombination, gene conversion) between alleles, but no clear molecular basis for this has been ident...
More de novo rare mutations in genes of major effect have been associated with simplex autism [108], while an interactive effect of multiple common susceptibility alleles have long been hypothesized as risk factors of familial autistic syndromes [123, 124]. Whether some clinical variables may help...
Step-by-Step Text Solution:1. Definition of Dominant: Dominant refers to a genetic trait that is expressed or appears in the phenotype of an organism when at least one dominant allele is present. 2.
MS Meyn,JM Lu-Kuo,LBK Herzing - 《American Journal of Human Genetics》 被引量: 121发表: 1993年 Assessing the genetic diversity of Centaurea parlatoris group (sect. Dissectae, Compositae) in Sicily using isozymes The Centaurea parlatoris group belongs to sect. Dissectae and is one of the ...
More de novo rare mutations in genes of major effect have been associated with simplex autism [108], while an interactive effect of multiple common susceptibility alleles have long been hypothesized as risk factors of familial autistic syndromes [123, 124]. Whether some clinical variables may help...