Karolyi IJ - Search Results

1

Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia.

Karolyi IJ, Probst FJ, Beyer L, Odeh H, Dootz G, Cha KB, Martin DM, Avraham KB, Kohrman D, Dolan DF, Raphael Y, Camper SA. Karolyi IJ, et al. Hum Mol Genet. 2003 Nov 1;12(21):2797-805. doi: 10.1093/hmg/ddg308. Epub 2003 Sep 9. Hum Mol Genet. 2003. PMID: 12966030

2

Transgene correction maintains normal cochlear structure and function in 6-month-old Myo15a mutant mice.

Kanzaki S, Beyer L, Karolyi IJ, Dolan DF, Fang Q, Probst FJ, Camper SA, Raphael Y. Kanzaki S, et al. Among authors: karolyi ij. Hear Res. 2006 Apr;214(1-2):37-44. doi: 10.1016/j.heares.2006.01.017. Epub 2006 Apr 3. Hear Res. 2006. PMID: 16580798

3

Age-related changes in cochlear gene expression in normal and shaker 2 mice.

Gong TW, Karolyi IJ, Macdonald J, Beyer L, Raphael Y, Kohrman DC, Camper SA, Lomax MI. Gong TW, et al. Among authors: karolyi ij. J Assoc Res Otolaryngol. 2006 Sep;7(3):317-28. doi: 10.1007/s10162-006-0046-7. Epub 2006 Jun 23. J Assoc Res Otolaryngol. 2006. PMID: 16794912 Free PMC article.

4

Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice.

Karolyi IJ, Dootz GA, Halsey K, Beyer L, Probst FJ, Johnson KR, Parlow AF, Raphael Y, Dolan DF, Camper SA. Karolyi IJ, et al. Mamm Genome. 2007 Aug;18(8):596-608. doi: 10.1007/s00335-007-9038-0. Epub 2007 Sep 22. Mamm Genome. 2007. PMID: 17899304

5

A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type.

Geister KA, Brinkmeier ML, Hsieh M, Faust SM, Karolyi IJ, Perosky JE, Kozloff KM, Conti M, Camper SA. Geister KA, et al. Among authors: karolyi ij. Hum Mol Genet. 2013 Jan 15;22(2):345-57. doi: 10.1093/hmg/dds432. Epub 2012 Oct 12. Hum Mol Genet. 2013. PMID: 23065701 Free PMC article.

6

Skeletal dysplasia and male infertility locus on mouse chromosome 9.

Cha KB, Karolyi IJ, Hunt A, Wenglikowski AM, Wilkinson JE, Dolan DF, Dootz G, Finnegan AA, Seasholtz AF, Hankenson KD, Siracusa LD, Camper SA. Cha KB, et al. Among authors: karolyi ij. Genomics. 2004 Jun;83(6):951-60. doi: 10.1016/j.ygeno.2003.12.020. Genomics. 2004. PMID: 15177549

7

The gene coding for variant hepatic nuclear factor 1 (Tcf-2), maps between the Edp-1 and Erba genes on mouse chromosome 11.

Karolyi IJ, Guénet JL, Rey-Campos J, Camper SA. Karolyi IJ, et al. Mamm Genome. 1992;3(3):184-5. doi: 10.1007/BF00352466. Mamm Genome. 1992. PMID: 1352161 Free article. No abstract available.

8

Expression of corticotropin-releasing hormone transgenes in neurons of adult and developing mice.

Keegan CE, Karolyi IJ, Knapp LT, Bourbonais FJ, Camper SA, Seasholtz AF. Keegan CE, et al. Among authors: karolyi ij. Mol Cell Neurosci. 1994 Dec;5(6):505-14. doi: 10.1006/mcne.1994.1062. Mol Cell Neurosci. 1994. PMID: 7704423 Free article.

9

Mouse models of altered CRH-binding protein expression.

Seasholtz AF, Burrows HL, Karolyi IJ, Camper SA. Seasholtz AF, et al. Among authors: karolyi ij. Peptides. 2001 May;22(5):743-51. doi: 10.1016/s0196-9781(01)00387-4. Peptides. 2001. PMID: 11337087 Review.

10

Implementing transgenic and embryonic stem cell technology to study gene expression, cell-cell interactions and gene function.

Camper SA, Saunders TL, Kendall SK, Keri RA, Seasholtz AF, Gordon DF, Birkmeier TS, Keegan CE, Karolyi IJ, Roller ML, et al. Camper SA, et al. Among authors: karolyi ij. Biol Reprod. 1995 Feb;52(2):246-57. doi: 10.1095/biolreprod52.2.246. Biol Reprod. 1995. PMID: 7711194 Review.

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