Hintner H - Search Results

1

Premature termination codons are present on both alleles of the bullous pemphigoid antigen 2/type XVII collagen gene in five Austrian families with generalized atrophic benign epidermolysis bullosa.

Darling TN, McGrath JA, Yee C, Gatalica B, Hametner R, Bauer JW, Pohla-Gubo G, Christiano AM, Uitto J, Hintner H, Yancey KB. Darling TN, et al. Among authors: hintner h. J Invest Dermatol. 1997 Apr;108(4):463-8. doi: 10.1111/1523-1747.ep12289718. J Invest Dermatol. 1997. PMID: 9077475 Free article.

2

Diminished expression of the extracellular domain of bullous pemphigoid antigen 2 (BPAG2) in the epidermal basement membrane of patients with generalized atrophic benign epidermolysis bullosa.

Pohla-Gubo G, Lazarova Z, Giudice GJ, Liebert M, Grassegger A, Hintner H, Yancey KB. Pohla-Gubo G, et al. Among authors: hintner h. Exp Dermatol. 1995 Aug;4(4 Pt 1):199-206. doi: 10.1111/j.1600-0625.1995.tb00245.x. Exp Dermatol. 1995. PMID: 8535614

3

A homozygous deletion mutation in the gene encoding the 180-kDa bullous pemphigoid antigen (BPAG2) in a family with generalized atrophic benign epidermolysis bullosa.

McGrath JA, Darling T, Gatalica B, Pohla-Gubo G, Hintner H, Christiano AM, Yancey K, Uitto J. McGrath JA, et al. Among authors: hintner h. J Invest Dermatol. 1996 Apr;106(4):771-4. doi: 10.1111/1523-1747.ep12345821. J Invest Dermatol. 1996. PMID: 8618019 Free article.

4

Cycloheximide facilitates the identification of aberrant transcripts resulting from a novel splice-site mutation in COL17A1 in a patient with generalized atrophic benign epidermolysis bullosa.

Darling TN, Yee C, Koh B, McGrath JA, Bauer JW, Uitto J, Hintner H, Yancey KB. Darling TN, et al. Among authors: hintner h. J Invest Dermatol. 1998 Feb;110(2):165-9. doi: 10.1046/j.1523-1747.1998.00103.x. J Invest Dermatol. 1998. PMID: 9457913 Free article.

5

A deletion mutation in COL17A1 in five Austrian families with generalized atrophic benign epidermolysis bullosa represents propagation of an ancestral allele.

Darling TN, Koh BB, Bale SJ, Compton JG, Bauer JW, Hintner H, Yancey KB. Darling TN, et al. Among authors: hintner h. J Invest Dermatol. 1998 Feb;110(2):170-3. doi: 10.1046/j.1523-1747.1998.00101.x. J Invest Dermatol. 1998. PMID: 9457914 Free article.

6

Generalized atrophic benign epidermolysis bullosa.

Darling TN, Bauer JW, Hintner H, Yancey KB. Darling TN, et al. Among authors: hintner h. Adv Dermatol. 1997;13:87-119; discussion 120. Adv Dermatol. 1997. PMID: 9551142 Review.

7

Revertant mosaicism: partial correction of a germ-line mutation in COL17A1 by a frame-restoring mutation.

Darling TN, Yee C, Bauer JW, Hintner H, Yancey KB. Darling TN, et al. Among authors: hintner h. J Clin Invest. 1999 May 15;103(10):1371-7. doi: 10.1172/JCI4338. J Clin Invest. 1999. PMID: 10330419 Free PMC article.

8

Ocular involvement in IgA-epidermolysis bullosa acquisita.

Bauer JW, Schaeppi H, Metze D, Muss W, Pohla-Gubo G, Hametner R, Ruckhofer J, Grabner G, Hintner H. Bauer JW, et al. Among authors: hintner h. Br J Dermatol. 1999 Nov;141(5):887-92. doi: 10.1046/j.1365-2133.1999.03163.x. Br J Dermatol. 1999. PMID: 10583173

9

A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type Köbner.

Lanschuetzer CM, Klausegger A, Pohla-Gubo G, Hametner R, Richard G, Uitto J, Hintner H, Bauer JW. Lanschuetzer CM, et al. Among authors: hintner h. Clin Exp Dermatol. 2003 Jan;28(1):77-9. doi: 10.1046/j.1365-2230.2003.01218.x. Clin Exp Dermatol. 2003. PMID: 12558637

10

Gene expression analysis of an epidermolysis bullosa simplex Dowling-Meara cell line by subtractive hybridization: recapitulation of cellular differentiation, migration and wound healing.

Wagner M, Hintner H, Bauer JW, Onder K. Wagner M, et al. Among authors: hintner h. Exp Dermatol. 2012 Feb;21(2):111-7. doi: 10.1111/j.1600-0625.2011.01420.x. Epub 2011 Dec 14. Exp Dermatol. 2012. PMID: 22168818

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