Homberger A - Search Results

1

Haplotyping of wild type and I278T alleles of the human cystathionine beta-synthase gene based on a cluster of novel SNPs in IVS12.

Linnebank M, Homberger A, Kraus JP, Harms E, Kozich V, Koch HG. Linnebank M, et al. Among authors: homberger a. Hum Mutat. 2001 Apr;17(4):350-1. doi: 10.1002/humu.36. Hum Mutat. 2001. PMID: 11295835

2

High prevalence of the I278T mutation of the human cystathionine beta-synthase detected by a novel screening application.

Linnebank M, Homberger A, Junker R, Nowak-Goettl U, Harms E, Koch HG. Linnebank M, et al. Among authors: homberger a. Thromb Haemost. 2001 Jun;85(6):986-8. Thromb Haemost. 2001. PMID: 11434706

3

A common haplotype for the 677T thermolabile variant of the 5,10-methylenetetrahydrofolate reductase gene in thrombophilic patients and controls.

Linnebank M, Homberger A, Nowak-Göttl U, Koch HG. Linnebank M, et al. Among authors: homberger a. Hum Mutat. 2002 Dec;20(6):478. doi: 10.1002/humu.9089. Hum Mutat. 2002. PMID: 12442281

4

Genomic structure and transcript variants of the human methylenetetrahydrofolate reductase gene.

Homberger A, Linnebank M, Winter C, Willenbring H, Marquardt T, Harms E, Koch HG. Homberger A, et al. Eur J Hum Genet. 2000 Sep;8(9):725-9. doi: 10.1038/sj.ejhg.5200522. Eur J Hum Genet. 2000. PMID: 10980581

5

Two novel mutations (E86A, R113W) in argininosuccinate lyase deficiency and evidence for highly variable splicing of the human argininosuccinate lyase gene.

Linnebank M, Homberger A, Rapp B, Winter C, Marquardt T, Harms E, Koch HG. Linnebank M, et al. Among authors: homberger a. J Inherit Metab Dis. 2000 Jun;23(4):308-12. doi: 10.1023/a:1005690005439. J Inherit Metab Dis. 2000. PMID: 10896281 No abstract available.

6

The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis.

Koch HG, Nabel P, Junker R, Auberger K, Schobess R, Homberger A, Linnebank M, Nowak-Göttl U. Koch HG, et al. Among authors: homberger a. Eur J Pediatr. 1999 Dec;158 Suppl 3:S113-6. doi: 10.1007/pl00014332. Eur J Pediatr. 1999. PMID: 10650848

7

Linkage disequilibrium of the common mutations 677C > T and 1298A > C of the human methylenetetrahydrofolate reductase gene as proven by the novel polymorphisms 129C > T, 1068C > T.

Linnebank M, Homberger A, Nowak-Göttl U, Marquardt T, Harms E, Koch HG. Linnebank M, et al. Among authors: homberger a. Eur J Pediatr. 2000 Jun;159(6):472-3. doi: 10.1007/s004310051311. Eur J Pediatr. 2000. PMID: 10867857 No abstract available.

8

Frequent polymorphism of the human methylenetetrahydrofolate reductase.

Linnebank M, Homberger A, Koch HG, Bova I, Sylantiev C, Bornstein NM, Chapman J, Korczyn AD. Linnebank M, et al. Among authors: homberger a. Stroke. 2000 Apr;31(4):990. doi: 10.1161/01.str.31.4.983-e. Stroke. 2000. PMID: 10754661 No abstract available.

9

[Contribution to the demonstration of collapse afferents in the pulmonary vagus of rabbits].

Homberger AC. Homberger AC. Helv Physiol Pharmacol Acta. 1968;26(1):97-118. Helv Physiol Pharmacol Acta. 1968. PMID: 5670383 German. No abstract available.

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