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Virology|April 20, 1995
Epstein-Barr virus replicative gene transcription during de novo infection of human thymocytes: simultaneous early expression of BZLF-1 and its repressor RAZC A Kelleher, R K Paterson, D H Dreyfus, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|December 27, 2011
Loss-of-function thrombospondin-1 mutations in familial pulmonary hypertensionJames P Maloney, Robert S Stearman, Todd M Bull, et al.
Nature Genetics|February 14, 1998
Mutations in PROP1 cause familial combined pituitary hormone deficiencyW Wu, J D Cogan, R W Pfäffle, et al.
American Journal of Medical Genetics. Part A|May 29, 2023
The contribution of mosaicism to genetic diseases and de novo pathogenic variantsRory J Tinker, Lisa Bastarache, Kimberly Ezell, et al.
Molecular Genetics and Metabolism Reports|October 22, 2024
Review and metabolomic profiling of unsolved case reveals newly reported autosomal dominant congenital disorder of glycosylation, type Iw formerly thought to only be an autosomal recessive conditionKimberly M Ezell, Yutaka Furuta, Devin Oglesbee, et al.
The New England Journal of Medicine|March 24, 1988
T-cell lymphomas containing Epstein-Barr viral DNA in patients with chronic Epstein-Barr virus infectionsJ F Jones, S Shurin, C Abramowsky, et al.
Chest|April 8, 2010
Identification of early interstitial lung disease in an individual with genetic variations in ABCA3 and SFTPCPeter F Crossno, Vasiliy V Polosukhin, Timothy S Blackwell, et al.
Nature Communications|April 16, 2015
Increased prevalence of EPAS1 variant in cattle with high-altitude pulmonary hypertensionJohn H Newman, Timothy N Holt, Joy D Cogan, et al.
Clinical Physiology (Oxford, England)|April 25, 2001
Circadian rhythm of core body temperature in subjects with chronic fatigue syndromeD L Hamilos, D Nutter, J Gershtenson, et al.
Pulmonary Circulation|December 6, 2011
Idiopathic and heritable PAH perturb common molecular pathways, correlated with increased MSX1 expressionEric D Austin, Swapna Menon, Anna R Hemnes, et al.
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