Malignancy in Noonan syndrome and related disorders von Smpokou, P., Zand, D.J., Rosenbaum, K.N., Summar, M.L.

Volltext

Assessing the Functional Characteristics of Synonymous and Nonsynonymous Mutation Candidates by Use of Large DNA Constructs von Eeds, A.M., Mortlock, D., Wade-Martins, R., Summar, M.L.

Volltext

The frequent observation of evidence for nonsense-mediated decay in RNA from patients with carbamyl phosphate synthetase I deficiency von Eeds, A.M., Hall, L.D., Yadav, M., Willis, A., Summar, S., Putnam, A., Barr, F., Summar, M.L.

Volltext

Characterization of genomic structure and polymorphisms in the human carbamyl phosphate synthetase I gene von Summar, M.L., Hall, L.D., Eeds, A.M., Hutcheson, H.B., Kuo, A.N., Willis, A.S., Rubio, V., Arvin, M.K., Schofield, J.P., Dawson, E.P.

Volltext

Induction of Glutathione Synthesis by Indomethacin is Regulated by Nrf2/Inrf2 redox Interactions and MEK-1 activity von Freeman, M, Sekhar, K.R, Spitz, D.R, Meredith, M.J, Holt, J.T, Guis, D, Summar, M.L

Volltext

Linkage Mapping of the Gene for Type III Collagen (COL3A1) to Human Chromosome 2q Using a VNTR Polymorphism von Tiller, George E., Polumbo, Paula A., Summar, Marshall L.

Volltext

Genes regulating glutathione concentrations in X-ray-transformed rat embryo fibroblasts: changes in γ-glutamylcysteine synthetase and γ-glutamyltranspeptidase expression von Sierra-Rivera, E., Meredith, M.J., Summar, M.L., Smith, M.D., Voorhees, G.J., Stoffel, C.M., Freeman, M.L.

Volltext

Linkage analysis of the human dopamine β-hydroxylase gene von Perry, S.E., Summar, M.L., Phillips, J.A., Robertson, D.

Volltext

Genetic Mapping of the Human Growth Hormone-Releasing Factor Gene (GHRF) Using Two Intragenic Polymorphisms Detected by PCR Amplification von Jurado, L.A.Pérez, Phillips, J.A., Summar, M.L., Mao, J., Weber, J.L., Schaefer, F.V., Hazan, J., Argente, J.

Volltext

Protein kinase C: A new linkage marker for growth hormone and for COL1A1 von Summar, M.L., Phillips, J.A., Krishnamani, M.R.S., Keefer, J., Trofatter, J., Schwartz, R.C., Tsipouras, P., Willard, H., Ullrich, A.

Volltext

Interstitial deletion of chromosome 2q32‐34 associated with multiple congenital anomalies and a urea cycle defect (CPS I deficiency) von Loscalzo, M.L., Galczynski, R.L., Hamosh, A., Summar, M., Chinsky, J.M., Thomas, G.H.

Volltext

Interstitial deletion of chromosome 2q32-34 associated with multiple congenital anomalies and a urea cycle defect (CPS I deficiency) von Loscalzo, M.L., Galczynski, R.L., Hamosh, A., Summar, M., Chinsky, J.M., Thomas, G.H.

Volltext