Hoth C - Search Results

1

Discovery of new piperidine amide triazolobenzodiazepinones as intestinal-selective CCK1 receptor agonists.

Cameron KO, Beretta EE, Chen Y, Chu-Moyer M, Fernando D, Gao H, Kohrt J, Lavergne S, Jardine Pda S, Guzman-Perez A, Hoth C, Perry DA, Hadcock JR, Gautreau D, Makowski M, Perez S, Polivkova J, Rogers L, Scott DO, Swick AG, Thiede L, Trebino CE, Trilles RV, Wilmowski J, Zhang Y. Cameron KO, et al. Among authors: hoth c. Bioorg Med Chem Lett. 2012 Apr 15;22(8):2943-7. doi: 10.1016/j.bmcl.2012.02.049. Epub 2012 Feb 23. Bioorg Med Chem Lett. 2012. PMID: 22424974

2

Expression of the rat adrenomedullin receptor or a putative human adrenomedullin receptor does not correlate with adrenomedullin binding or functional response.

Kennedy SP, Sun D, Oleynek JJ, Hoth CF, Kong J, Hill RJ. Kennedy SP, et al. Among authors: hoth cf. Biochem Biophys Res Commun. 1998 Mar 27;244(3):832-7. doi: 10.1006/bbrc.1998.8349. Biochem Biophys Res Commun. 1998. PMID: 9535752

3

Cloning, expression and pharmacological characterization of rabbit adenosine A1 and A3 receptors.

Hill RJ, Oleynek JJ, Hoth CF, Kiron MA, Weng W, Wester RT, Tracey WR, Knight DR, Buchholz RA, Kennedy SP. Hill RJ, et al. Among authors: hoth cf. J Pharmacol Exp Ther. 1997 Jan;280(1):122-8. J Pharmacol Exp Ther. 1997. PMID: 8996189

4

Printing highly efficient organic solar cells.

Hoth CN, Schilinsky P, Choulis SA, Brabec CJ. Hoth CN, et al. Nano Lett. 2008 Sep;8(9):2806-13. doi: 10.1021/nl801365k. Epub 2008 Aug 7. Nano Lett. 2008. PMID: 18683989

5

Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature.

Baldwin CT, Hoth CF, Macina RA, Milunsky A. Baldwin CT, et al. Among authors: hoth cf. Am J Med Genet. 1995 Aug 28;58(2):115-22. doi: 10.1002/ajmg.1320580205. Am J Med Genet. 1995. PMID: 8533800 Review.

6

Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.

Farrer LA, Arnos KS, Asher JH Jr, Baldwin CT, Diehl SR, Friedman TB, Greenberg J, Grundfast KM, Hoth C, Lalwani AK, et al. Farrer LA, et al. Among authors: hoth c. Am J Hum Genet. 1994 Oct;55(4):728-37. Am J Hum Genet. 1994. PMID: 7942851 Free PMC article.

7

Mutations in PAX3 associated with Waardenburg syndrome type I.

Baldwin CT, Lipsky NR, Hoth CF, Cohen T, Mamuya W, Milunsky A. Baldwin CT, et al. Among authors: hoth cf. Hum Mutat. 1994;3(3):205-11. doi: 10.1002/humu.1380030306. Hum Mutat. 1994. PMID: 8019556

8

Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I).

Hoth CF, Milunsky A, Lipsky N, Sheffer R, Clarren SK, Baldwin CT. Hoth CF, et al. Am J Hum Genet. 1993 Mar;52(3):455-62. Am J Hum Genet. 1993. PMID: 8447316 Free PMC article.

9

In situ hybridization applied to Waardenburg syndrome.

Wu BL, Milunsky A, Wyandt H, Hoth C, Baldwin C, Skare J. Wu BL, et al. Among authors: hoth c. Cytogenet Cell Genet. 1993;63(1):29-32. doi: 10.1159/000133495. Cytogenet Cell Genet. 1993. PMID: 8449034

10

An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome.

Baldwin CT, Hoth CF, Amos JA, da-Silva EO, Milunsky A. Baldwin CT, et al. Among authors: hoth cf. Nature. 1992 Feb 13;355(6361):637-8. doi: 10.1038/355637a0. Nature. 1992. PMID: 1347149

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