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The basic helix-loop-helix transcription factor, dHAND, is required for vascular development.
Transient cerebral ischemia. Association of apoptosis induction with hypoperfusion.
Altered representation of naive and memory CD8 T cell subsets in HIV-infected children.
Female germ line mosaicism as the origin of a unique IL-2 receptor gamma-chain mutation causing X-linked severe combined immunodeficiency.
Chronic nitric oxide inhibition in utero produces persistent pulmonary hypertension in newborn lambs.
Hypoxic and ischemic hypoxia exacerbate brain injury associated with metabolic encephalopathy in laboratory animals.
Normal genes for the cholesterol side chain cleavage enzyme, P450scc, in congenital lipoid adrenal hyperplasia.
Regulation of insulin-like growth factor (IGF) I receptor expression during muscle cell differentiation. Potential autocrine role of IGF-II.
X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings.
Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7.