Monreal AW - Search Results

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Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia.

Monreal AW, Ferguson BM, Headon DJ, Street SL, Overbeek PA, Zonana J. Monreal AW, et al. Nat Genet. 1999 Aug;22(4):366-9. doi: 10.1038/11937. Nat Genet. 1999. PMID: 10431241

Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations.

Monreal AW, Zonana J, Ferguson B. Monreal AW, et al. Am J Hum Genet. 1998 Aug;63(2):380-9. doi: 10.1086/301984. Am J Hum Genet. 1998. PMID: 9683615 Free PMC article.

Integrating transcriptional and metabolite profiles to direct the engineering of lovastatin-producing fungal strains.

Askenazi M, Driggers EM, Holtzman DA, Norman TC, Iverson S, Zimmer DP, Boers ME, Blomquist PR, Martinez EJ, Monreal AW, Feibelman TP, Mayorga ME, Maxon ME, Sykes K, Tobin JV, Cordero E, Salama SR, Trueheart J, Royer JC, Madden KT. Askenazi M, et al. Among authors: monreal aw. Nat Biotechnol. 2003 Feb;21(2):150-6. doi: 10.1038/nbt781. Epub 2003 Jan 21. Nat Biotechnol. 2003. PMID: 12536215

Vasopressin-induced neurotrophism in cultured neurons of the cerebral cortex: dependency on calcium signaling and protein kinase C activity.

Chen Q, Patel R, Sales A, Oji G, Kim J, Monreal AW, Brinton RD. Chen Q, et al. Among authors: monreal aw. Neuroscience. 2000;101(1):19-26. doi: 10.1016/s0306-4522(00)00323-7. Neuroscience. 2000. PMID: 11068133

Vasopressin-induced neurotrophism in cultured hippocampal neurons via V1 receptor activation.

Brinton RD, Monreal AW, Fernandez JG. Brinton RD, et al. Among authors: monreal aw. J Neurobiol. 1994 Apr;25(4):380-94. doi: 10.1002/neu.480250404. J Neurobiol. 1994. PMID: 8077964

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