5 results for author:"Dishop M.K." in Literature citations
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| Extending the phenotypes associated with DICER1 mutations. Foulkes W.D., Bahubeshi A., Hamel N., Pasini B., Asioli S., Baynam G., Choong C.S., Charles A., Frieder R.P., Dishop M.K. et al. |
| Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA. Suzuki T., Sakagami T., Rubin B.K., Nogee L.M., Wood R.E., Zimmerman S.L., Smolarek T., Dishop M.K., Wert S.E., Whitsett J.A. et al. J. Exp. Med. 205:2703-2710(2008) · UniProtKB (1) |
| Promotion of lung carcinogenesis by chronic obstructive pulmonary disease-like airway inflammation in a K-ras-induced mouse model. Moghaddam S.J., Li H., Cho S.N., Dishop M.K., Wistuba I.I., Ji L., Kurie J.M., Dickey B.F., Demayo F.J. Am. J. Respir. Cell Mol. Biol. 40:443-453(2009) · Mapped (8) |
| Self-healing collodion membrane and mild nonbullous congenital ichthyosiform erythroderma due to 2 novel mutations in the ALOX12B gene. Harting M., Brunetti-Pierri N., Chan C.S., Kirby J., Dishop M.K., Richard G., Scaglia F., Yan A.C., Levy M.L. Arch Dermatol 144:351-356(2008) · Mapped (1) |
| Clinical, radiological and pathological features of ABCA3 mutations in children. Doan M.L., Guillerman R.P., Dishop M.K., Nogee L.M., Langston C., Mallory G.B., Sockrider M.M., Fan L.L. Thorax 63:366-373(2008) · Mapped (4) |