Frei K - Search Results

1

Characterization of NKIP: a novel, Na+/K+-ATPase interacting protein mediates neural differentiation and apoptosis.

Pratscher B, Friedrich C, Goger W, Allen M, Fink D, Thallinger C, Wolschek M, Frei K, Schöfer C, Pehamberger H, Wacheck V, Sorensen PH, Müller M, Jansen B, Lucas T. Pratscher B, et al. Among authors: frei k. Exp Cell Res. 2008 Feb 1;314(3):463-77. doi: 10.1016/j.yexcr.2007.11.013. Epub 2007 Nov 24. Exp Cell Res. 2008. PMID: 18096156

2

Intranuclear anchoring of repetitive DNA sequences: centromeres, telomeres, and ribosomal DNA.

Weipoltshammer K, Schöfer C, Almeder M, Philimonenko VV, Frei K, Wachtler F, Hozák P. Weipoltshammer K, et al. Among authors: frei k. J Cell Biol. 1999 Dec 27;147(7):1409-18. doi: 10.1083/jcb.147.7.1409. J Cell Biol. 1999. PMID: 10613900 Free PMC article.

3

Expression and function of sialoadhesin in rat alveolar macrophages.

Frei K, Steger C, Samorapoompichit P, Lucas T, Förster O. Frei K, et al. Immunol Lett. 2000 Mar 1;71(3):167-70. doi: 10.1016/s0165-2478(99)00180-7. Immunol Lett. 2000. PMID: 10722868

4

The apical ectodermal ridge, fibroblast growth factors (FGF-2 and FGF-4) and insulin-like growth factor I (IGF-I) control the migration of epidermal melanoblasts in chicken wing buds.

Schöfer C, Frei K, Weipoltshammer K, Wachtler F. Schöfer C, et al. Among authors: frei k. Anat Embryol (Berl). 2001 Feb;203(2):137-46. doi: 10.1007/s004290000148. Anat Embryol (Berl). 2001. PMID: 11218060

5

Connexin 26 mutations in cases of sensorineural deafness in eastern Austria.

Frei K, Szuhai K, Lucas T, Weipoltshammer K, Schöfer C, Ramsebner R, Baumgartner WD, Raap AK, Bittner R, Wachtler FJ, Kirschhofer K. Frei K, et al. Eur J Hum Genet. 2002 Jul;10(7):427-32. doi: 10.1038/sj.ejhg.5200826. Eur J Hum Genet. 2002. PMID: 12107817

6

A novel connexin 26 mutation associated with autosomal recessive sensorineural deafness.

Frei K, Lucas T, Ramsebner R, Schöfer C, Baumgartner WD, Weipoltshammer K, Erginel-Unaltuna N, Wachtler FJ, Kirschhofer K. Frei K, et al. Audiol Neurootol. 2004 Jan-Feb;9(1):47-50. doi: 10.1159/000074186. Audiol Neurootol. 2004. PMID: 14676473

7

Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria.

Frei K, Ramsebner R, Lucas T, Baumgartner WD, Schoefer C, Wachtler FJ, Kirschhofer K. Frei K, et al. Hear Res. 2004 Oct;196(1-2):115-8. doi: 10.1016/j.heares.2004.07.001. Hear Res. 2004. PMID: 15464308

8

Alternative splicing of IL-24 in melanocytes by deletion of exons 3 and 5.

Allen M, Pratscher B, Krepler C, Frei K, Schöfer C, Pehamberger H, Müller M, Lucas T. Allen M, et al. Among authors: frei k. Int J Immunogenet. 2005 Dec;32(6):375-8. doi: 10.1111/j.1744-313X.2005.00540.x. Int J Immunogenet. 2005. PMID: 16313301

9

Vasoactive intestinal peptide gene alterations in patients with idiopathic pulmonary arterial hypertension.

Haberl I, Frei K, Ramsebner R, Doberer D, Petkov V, Albinni S, Lang I, Lucas T, Mosgoeller W. Haberl I, et al. Among authors: frei k. Eur J Hum Genet. 2007 Jan;15(1):18-22. doi: 10.1038/sj.ejhg.5201711. Epub 2006 Sep 27. Eur J Hum Genet. 2007. PMID: 17003842

10

High incidence of GJB2 mutations during screening of newborns for hearing loss in Austria.

Ramsebner R, Volker R, Lucas T, Hamader G, Weipoltshammer K, Baumgartner WD, Wachtler FJ, Kirschhofer K, Frei K. Ramsebner R, et al. Among authors: frei k. Ear Hear. 2007 Jun;28(3):298-301. doi: 10.1097/AUD.0b013e318047932d. Ear Hear. 2007. PMID: 17485979

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