3 results for author:"Stricker H.M." in Literature citations
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| Biochemical analysis of phenotypic diversity associated with mutations in codon 244 of the retinal degeneration slow gene. Conley S.M., Stricker H.M., Naash M.I. Biochemistry 49:905-911(2010) · Mapped (3) |
| Annexin A2 interactions with Rab14 in alveolar type II cells. Gou D., Mishra A., Weng T., Su L., Chintagari N.R., Wang Z., Zhang H., Gao L., Wang P., Stricker H.M. et al. J. Biol. Chem. 283:13156-13164(2008) · Mapped (8) |
| The Cys214-->Ser mutation in peripherin/rds causes a loss-of-function phenotype in transgenic mice. Stricker H.M., Ding X.Q., Quiambao A., Fliesler S.J., Naash M.I. Biochem. J. 388:605-613(2005) · Mapped (3) |