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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.
Physiologic regulation of the serum concentration of 1,25-dihydroxyvitamin D by phosphorus in normal men.
Regulation of messenger RNAs for the hydrophobic surfactant proteins in human lung.
Effect of fetal adrenalectomy on catecholamine release and physiologic adaptation at birth in sheep.