Bauer JW - Search Results

1

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: bauer jw. 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

2

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: bauer jw. J Invest Dermatol. 1997 Apr;108(4):463-8. doi: 10.1111/1523-1747.ep12289718. J Invest Dermatol. 1997. PMID: 9077475 Free article.

3

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: bauer jw. 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.

4

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: bauer jw. 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.

5

Generalized atrophic benign epidermolysis bullosa.

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

6

Novel and de novo glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: implications for genetic counseling.

Rouan F, Pulkkinen L, Jonkman MF, Bauer JW, Cserhalmi-Friedman PB, Christiano AM, Uitto J. Rouan F, et al. Among authors: bauer jw. J Invest Dermatol. 1998 Dec;111(6):1210-3. doi: 10.1046/j.1523-1747.1998.00422.x. J Invest Dermatol. 1998. PMID: 9856843 Free article.

7

[Prenatal diagnosis of recessive hereditary dystrophic epidermolysis bullosa with haplotype analysis of the type VII collagen gene].

Bauer JW, Ortiz S, Hengstschläger M, Pulkkinen L, Uitto J, Hintner H, Rappersberger K. Bauer JW, et al. Hautarzt. 1999 Feb;50(2):121-6. doi: 10.1007/s001050050875. Hautarzt. 1999. PMID: 10097955 German.

8

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: bauer jw. J Clin Invest. 1999 May 15;103(10):1371-7. doi: 10.1172/JCI4338. J Clin Invest. 1999. PMID: 10330419 Free PMC article.

9

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. Br J Dermatol. 1999 Nov;141(5):887-92. doi: 10.1046/j.1365-2133.1999.03163.x. Br J Dermatol. 1999. PMID: 10583173

10

A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiency.

Bauer JW, Rouan F, Kofler B, Rezniczek GA, Kornacker I, Muss W, Hametner R, Klausegger A, Huber A, Pohla-Gubo G, Wiche G, Uitto J, Hintner H. Bauer JW, et al. Am J Pathol. 2001 Feb;158(2):617-25. doi: 10.1016/S0002-9440(10)64003-5. Am J Pathol. 2001. PMID: 11159198 Free PMC article.

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