Weidinger S - Search Results

1

Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M allele.

Faber JP, Poller W, Weidinger S, Kirchgesser M, Schwaab R, Bidlingmaier F, Olek K. Faber JP, et al. Among authors: weidinger s. Am J Hum Genet. 1994 Dec;55(6):1113-21. Am J Hum Genet. 1994. PMID: 7977369 Free PMC article.

2

Mis-sense mutation of alpha 1-antichymotrypsin gene associated with chronic lung disease.

Poller W, Faber JP, Scholz S, Weidinger S, Bartholomé K, Olek K, Eriksson S. Poller W, et al. Among authors: weidinger s. Lancet. 1992 Jun 20;339(8808):1538. doi: 10.1016/0140-6736(92)91301-n. Lancet. 1992. PMID: 1351206 No abstract available.

3

Reliable phenotyping of alpha-1-antitrypsin by hybrid isoelectric focusing in an ultranarrow immobilized pH gradient.

Weidinger S. Weidinger S. Electrophoresis. 1992 Apr;13(4):234-9. doi: 10.1002/elps.1150130148. Electrophoresis. 1992. PMID: 1378388

4

Improved phenotyping of alpha 1-antichymotrypsin (ACT) by isoelectric focusing and immunoprinting: first demonstration of a deficient protein variant in the ACT system.

Weidinger S, Poller W, Faber JP, Schwarzfischer F. Weidinger S, et al. Electrophoresis. 1992 Sep-Oct;13(9-10):778-80. doi: 10.1002/elps.11501301169. Electrophoresis. 1992. PMID: 1459110

5

What is Pi (proteinase inhibitor) null or PiQO?: a problem highlighted by the alpha 1 antitrypsin Mheerlen mutation.

Kalsheker N, Hayes K, Weidinger S, Graham A. Kalsheker N, et al. Among authors: weidinger s. J Med Genet. 1992 Jan;29(1):27-9. doi: 10.1136/jmg.29.1.27. J Med Genet. 1992. PMID: 1552539 Free PMC article.

6

DNA polymorphisms associated with a new alpha 1-antitrypsin PIQ0 variant (PIQ0riedenburg).

Poller W, Faber JP, Weidinger S, Olek K. Poller W, et al. Among authors: weidinger s. Hum Genet. 1991 Mar;86(5):522-4. doi: 10.1007/BF00194647. Hum Genet. 1991. PMID: 1673114

7

New mutation versus exclusion at the alpha-1-antitrypsin locus: a multifaceted approach in a problematical paternity case.

Bender K, Kasulke D, Mayerovà A, Hummel K, Weidinger S, Epplen JT, Wienker TF. Bender K, et al. Among authors: weidinger s. Hum Hered. 1991;41(1):1-11. doi: 10.1159/000153966. Hum Hered. 1991. PMID: 2050377

8

Characterization of the normal alpha 1-antitrypsin allele Vmunich: a variant associated with a unique protein isoelectric focusing pattern.

Holmes MD, Brantly ML, Curiel DT, Weidinger S, Crystal RG. Holmes MD, et al. Among authors: weidinger s. Am J Hum Genet. 1990 Apr;46(4):810-6. Am J Hum Genet. 1990. PMID: 2316526 Free PMC article.

9

Sequence data of the rare deficient alpha 1-antitrypsin variant PI Zaugsburg.

Faber JP, Weidinger S, Olek K. Faber JP, et al. Among authors: weidinger s. Am J Hum Genet. 1990 Jun;46(6):1158-62. Am J Hum Genet. 1990. PMID: 2339709 Free PMC article.

10

Characterisation of the alpha-1-antitrypsin M3 gene, a normal variant.

Graham A, Hayes K, Weidinger S, Newton CR, Markham AF, Kalsheker NA. Graham A, et al. Among authors: weidinger s. Hum Genet. 1990 Aug;85(3):381-2. doi: 10.1007/BF00206766. Hum Genet. 1990. PMID: 2394452

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