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Accelerated evolution of nervous system genes in the origin of Homo sapiens.
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Dental microwear texture analysis of Homo sapiens sapiens: Foragers, farmers, and pastoralists.
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Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens.
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Characterization and localization to human chromosome 1 of human fast-twitch skeletal muscle calsequestrin gene.
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Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.
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Modulation of human intestinal epithelial cell IL-8 secretion by human milk factors.
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An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells.
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Analysis of tumor suppressor gene on human chromosome 9 in mouse x human somatic cell hybrids.
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Human somatostatin receptor genes: localization of SSTR5 to human chromosome 20p11.2.
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DNA methylation profiling of human chromosomes 6, 20 and 22.
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Contraction of human bronchial smooth muscle caused by activated human eosinophils.
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Editorial overview: Genetics of human origin: New horizons in human population genetics.
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Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia.
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An immunocytochemical method for demonstrating estrogen receptor in human uterus using monoclonal antibodies to human estrophilin.
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Effect of human lymphoblastoid interferon on insulin synthesis and secretion in isolated human pancreatic islets.
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