Dewald G - Search Results

1

Complement factor 7 gene mutations in relation to meningococcal infection and clinical recurrence of meningococcal disease.

Kuijpers TW, Nguyen M, Hopman CT, Nieuwenhuys E, Dewald G, Lankester AC, Roos A, van der Ende A, Fijen C, de Boer M. Kuijpers TW, et al. Among authors: dewald g. Mol Immunol. 2010 Jan;47(4):671-7. doi: 10.1016/j.molimm.2009.10.017. Epub 2009 Nov 22. Mol Immunol. 2010. PMID: 19931914

2

Polymorphism of the seventh component of complement (C7) in a healthy Caucasian population: an immunoblotting study with neuraminidase-treated samples.

Dewald G. Dewald G. Ann Inst Pasteur Immunol. 1988 Sep-Oct;139(5):507-15. doi: 10.1016/0769-2625(88)90096-7. Ann Inst Pasteur Immunol. 1988. PMID: 3207468

3

Human complement component C8. Molecular basis of the beta-chain polymorphism.

Dewald G, Hemmer S, Nöthen MM. Dewald G, et al. FEBS Lett. 1994 Mar 7;340(3):211-5. doi: 10.1016/0014-5793(94)80140-1. FEBS Lett. 1994. PMID: 8131848 Free article.

4

A common Ser/Thr polymorphism in the perforin-homologous region of human complement component C7.

Dewald G, Nöthen MM, Rüther K. Dewald G, et al. Hum Hered. 1994 Nov-Dec;44(6):301-4. doi: 10.1159/000154235. Hum Hered. 1994. PMID: 7860081

5

Polymorphism of human complement component C6: an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 B.

Dewald G, Nöthen MM, Cichon S. Dewald G, et al. Biochem Biophys Res Commun. 1993 Jul 15;194(1):458-64. doi: 10.1006/bbrc.1993.1841. Biochem Biophys Res Commun. 1993. PMID: 8101442

6

A common amino acid polymorphism in complement component C1R.

Nöthen MM, Dewald G. Nöthen MM, et al. Among authors: dewald g. Hum Mol Genet. 1994 Jan;3(1):217. doi: 10.1093/hmg/3.1.217-a. Hum Mol Genet. 1994. PMID: 8162045 No abstract available.

7

The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3.

Dewald G, Cichon S, Bryant SP, Hemmer S, Nöthen MM, Spurr NK. Dewald G, et al. Ann Hum Genet. 1996 Jul;60(4):281-91. doi: 10.1111/j.1469-1809.1996.tb01192.x. Ann Hum Genet. 1996. PMID: 8865989

8

Investigation of complement C4B deficiency in schizophrenia.

Schroers R, Nöthen MM, Rietschel M, Albus M, Maier W, Schwab S, Wildenauer D, Fimmers R, Propping P, Dewald G. Schroers R, et al. Among authors: dewald g. Hum Hered. 1997 Sep-Oct;47(5):279-82. doi: 10.1159/000154424. Hum Hered. 1997. PMID: 9358016

9

Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor.

Dewald G, Bork K. Dewald G, et al. Biochem Biophys Res Commun. 2006 May 19;343(4):1286-9. doi: 10.1016/j.bbrc.2006.03.092. Biochem Biophys Res Commun. 2006. PMID: 16638441

10

Dinucleotide repeat polymorphism at the human CD59 locus.

Nöthen MM, Dewald G. Nöthen MM, et al. Among authors: dewald g. Clin Genet. 1995 Mar;47(3):165-6. doi: 10.1111/j.1399-0004.1995.tb03952.x. Clin Genet. 1995. PMID: 7543386 No abstract available.

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