20 research outputs found
Koszul incidence algebras, affine semigroups, and Stanley-Reisner ideals
We prove a theorem unifying three results from combinatorial homological and
commutative algebra, characterizing the Koszul property for incidence algebras
of posets and affine semigroup rings, and characterizing linear resolutions of
squarefree monomial ideals. The characterization in the graded setting is via
the Cohen-Macaulay property of certain posets or simplicial complexes, and in
the more general nongraded setting, via the sequential Cohen-Macaulay property.Comment: 31 pages, 1 figure. Minor changes from previous version. To appear in
Advances in Mathematic
Migration of Erythropoietic and Prebursal Stem Cells from the Early Chicken Embryo to the Yolk Sac
The chromosomal localization of human β-galactosidase revisited: a locus for β-galactosidase on human chromosome 3 and for its protective protein on human chromosome 22
Transferrin endocytosis and iron uptake by developing erythroid cells in the chicken (Gallus domesticus)
The use of polymorphic Alu insertions in human DNA fingerprinting
We have characterized several Human Specific (HS) Alu insertions as either dimorphic (TPA25, PV92, APO), slightly dimorphic (C2N4 and C4N4) or monomorphic (C3N1, C4N6, C4N2, C4N5, C4N8) based on studies of Caucasian, Asian, American Black and African Black populations. Our approach is based upon: 1) PCR amplification using primers complementary to the unique DNA sequences that flank the site of insertion of the different Alu elements studied; 2) gel electrophoresis and scoring according to the presence or absence of an Alu insertion in one or both homologous chromosomes; 3) allele frequencies determined by gene counting and compared to Hardy-Weinberg expectations. Our DNA fingerprinting procedure using PCR amplification of diallelic polymorphic (dimorphic) Human Specific Alu insertions, may be used as a tool for genetic mapping, to characterize populations, study human migrational patterns, and track the inheritance of human genetic disorders
