Gewies A - Search Results

1

Minor lesion mutational spectrum of the entire NF1 gene does not explain its high mutability but points to a functional domain upstream of the GAP-related domain.

Fahsold R, Hoffmeyer S, Mischung C, Gille C, Ehlers C, Kücükceylan N, Abdel-Nour M, Gewies A, Peters H, Kaufmann D, Buske A, Tinschert S, Nürnberg P. Fahsold R, et al. Among authors: gewies a. Am J Hum Genet. 2000 Mar;66(3):790-818. doi: 10.1086/302809. Am J Hum Genet. 2000. PMID: 10712197 Free PMC article.

2

Two novel mutations in exons 19a and 20 and a BsaBI [correction of BsaI] polymorphism in a newly characterized intron of the neurofibromatosis type 1 gene.

Klose A, Robinson N, Gewies A, Kluwe L, Kaufmann D, Buske A, Tinschert S, Peters H. Klose A, et al. Among authors: gewies a. Hum Genet. 1998 Mar;102(3):367-71. doi: 10.1007/s004390050706. Hum Genet. 1998. PMID: 9544853

3

Selective disactivation of neurofibromin GAP activity in neurofibromatosis type 1.

Klose A, Ahmadian MR, Schuelke M, Scheffzek K, Hoffmeyer S, Gewies A, Schmitz F, Kaufmann D, Peters H, Wittinghofer A, Nürnberg P. Klose A, et al. Among authors: gewies a. Hum Mol Genet. 1998 Aug;7(8):1261-8. doi: 10.1093/hmg/7.8.1261. Hum Mol Genet. 1998. PMID: 9668168

4

Recurrent NF1 gene mutation in a patient with oligosymptomatic neurofibromatosis type 1 (NF1).

Buske A, Gewies A, Lehmann R, Rüther K, Algermissen B, Nürnberg P, Tinschert S. Buske A, et al. Among authors: gewies a. Am J Med Genet. 1999 Oct 8;86(4):328-30. doi: 10.1002/(sici)1096-8628(19991008)86:4<328::aid-ajmg6>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10494088

5

Analysis of the NF1 gene by temperature gradient gel electrophoresis reveals a high incidence of mutations in exon 4b.

Toliat MR, Erdogan F, Gewies A, Fahsold R, Buske A, Tinschert S, Nürnberg P. Toliat MR, et al. Among authors: gewies a. Electrophoresis. 2000 Feb;21(3):541-4. doi: 10.1002/(SICI)1522-2683(20000201)21:3<541::AID-ELPS541>3.0.CO;2-L. Electrophoresis. 2000. PMID: 10726756

6

McCune-Albright syndrome: clinical and molecular evidence of mosaicism in an unusual giant patient.

Tinschert S, Gerl H, Gewies A, Jung HP, Nürnberg P. Tinschert S, et al. Among authors: gewies a. Am J Med Genet. 1999 Mar 12;83(2):100-8. Am J Med Genet. 1999. PMID: 10190480 Review.

7

ScCypB is a novel second cytosolic cyclophilin from Streptomyces chrysomallus which is phylogenetically distant from ScCypA.

Pahl A, Gewies A, Keller U. Pahl A, et al. Among authors: gewies a. Microbiology (Reading). 1997 Jan;143 ( Pt 1):117-126. doi: 10.1099/00221287-143-1-117. Microbiology (Reading). 1997. PMID: 9025285 Free article.

8

Uncoupling Malt1 threshold function from paracaspase activity results in destructive autoimmune inflammation.

Gewies A, Gorka O, Bergmann H, Pechloff K, Petermann F, Jeltsch KM, Rudelius M, Kriegsmann M, Weichert W, Horsch M, Beckers J, Wurst W, Heikenwalder M, Korn T, Heissmeyer V, Ruland J. Gewies A, et al. Cell Rep. 2014 Nov 20;9(4):1292-305. doi: 10.1016/j.celrep.2014.10.044. Epub 2014 Nov 13. Cell Rep. 2014. PMID: 25456129 Free article.

9

The CARD11-BCL10-MALT1 (CBM) signalosome complex: Stepping into the limelight of human primary immunodeficiency.

Turvey SE, Durandy A, Fischer A, Fung SY, Geha RS, Gewies A, Giese T, Greil J, Keller B, McKinnon ML, Neven B, Rozmus J, Ruland J, Snow AL, Stepensky P, Warnatz K. Turvey SE, et al. Among authors: gewies a. J Allergy Clin Immunol. 2014 Aug;134(2):276-84. doi: 10.1016/j.jaci.2014.06.015. J Allergy Clin Immunol. 2014. PMID: 25087226 Free PMC article. Review.

10

Bcl10-controlled Malt1 paracaspase activity is key for the immune suppressive function of regulatory T cells.

Rosenbaum M, Gewies A, Pechloff K, Heuser C, Engleitner T, Gehring T, Hartjes L, Krebs S, Krappmann D, Kriegsmann M, Weichert W, Rad R, Kurts C, Ruland J. Rosenbaum M, et al. Among authors: gewies a. Nat Commun. 2019 May 28;10(1):2352. doi: 10.1038/s41467-019-10203-2. Nat Commun. 2019. PMID: 31138793 Free PMC article.

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