Pannicke U - Search Results

1

The polarization defect of Wiskott-Aldrich syndrome macrophages is linked to dislocalization of the Arp2/3 complex.

Linder S, Higgs H, Hüfner K, Schwarz K, Pannicke U, Aepfelbacher M. Linder S, et al. Among authors: pannicke u. J Immunol. 2000 Jul 1;165(1):221-5. doi: 10.4049/jimmunol.165.1.221. J Immunol. 2000. PMID: 10861055

2

Two novel missense and frameshift mutations in exons 5 and 6 of the purine nucleoside phosphorylase (PNP) gene in a severe combined immunodeficiency (SCID) patient.

Pannicke U, Tuchschmid P, Friedrich W, Bartram CR, Schwarz K. Pannicke U, et al. Hum Genet. 1996 Dec;98(6):706-9. doi: 10.1007/s004390050290. Hum Genet. 1996. PMID: 8931706

3

Hairpin opening and overhang processing by an Artemis/DNA-dependent protein kinase complex in nonhomologous end joining and V(D)J recombination.

Ma Y, Pannicke U, Schwarz K, Lieber MR. Ma Y, et al. Among authors: pannicke u. Cell. 2002 Mar 22;108(6):781-94. doi: 10.1016/s0092-8674(02)00671-2. Cell. 2002. PMID: 11955432 Free article.

4

Macrophages of patients with X-linked thrombocytopenia display an attenuated Wiskott-Aldrich syndrome phenotype.

Linder S, Wintergerst U, Bender-Götze C, Schwarz K, Pannicke U, Aepfelbacher M. Linder S, et al. Among authors: pannicke u. Immunol Cell Biol. 2003 Apr;81(2):130-6. doi: 10.1046/j.0818-9641.2002.01147.x. Immunol Cell Biol. 2003. PMID: 12631236

5

Mechanism and regulation of human non-homologous DNA end-joining.

Lieber MR, Ma Y, Pannicke U, Schwarz K. Lieber MR, et al. Among authors: pannicke u. Nat Rev Mol Cell Biol. 2003 Sep;4(9):712-20. doi: 10.1038/nrm1202. Nat Rev Mol Cell Biol. 2003. PMID: 14506474 Review.

6

Human severe combined immune deficiency and DNA repair.

Schwarz K, Ma Y, Pannicke U, Lieber MR. Schwarz K, et al. Among authors: pannicke u. Bioessays. 2003 Nov;25(11):1061-70. doi: 10.1002/bies.10344. Bioessays. 2003. PMID: 14579247 Review.

7

Functional and biochemical dissection of the structure-specific nuclease ARTEMIS.

Pannicke U, Ma Y, Hopfner KP, Niewolik D, Lieber MR, Schwarz K. Pannicke U, et al. EMBO J. 2004 May 5;23(9):1987-97. doi: 10.1038/sj.emboj.7600206. Epub 2004 Apr 8. EMBO J. 2004. PMID: 15071507 Free PMC article.

8

Omenn syndrome due to ARTEMIS mutations.

Ege M, Ma Y, Manfras B, Kalwak K, Lu H, Lieber MR, Schwarz K, Pannicke U. Ege M, et al. Among authors: pannicke u. Blood. 2005 Jun 1;105(11):4179-86. doi: 10.1182/blood-2004-12-4861. Epub 2005 Feb 24. Blood. 2005. PMID: 15731174 Free article.

9

A severe form of human combined immunodeficiency due to mutations in DNA ligase IV.

Enders A, Fisch P, Schwarz K, Duffner U, Pannicke U, Nikolopoulos E, Peters A, Orlowska-Volk M, Schindler D, Friedrich W, Selle B, Niemeyer C, Ehl S. Enders A, et al. Among authors: pannicke u. J Immunol. 2006 Apr 15;176(8):5060-8. doi: 10.4049/jimmunol.176.8.5060. J Immunol. 2006. PMID: 16585603

10

Disulfide bridge disruption in the alpha2 domain of the HLA class I molecule leads to low expression of the corresponding antigen.

Hirv K, Pannicke U, Mytilineos J, Schwarz K. Hirv K, et al. Among authors: pannicke u. Hum Immunol. 2006 Aug;67(8):589-96. doi: 10.1016/j.humimm.2006.04.010. Epub 2006 May 24. Hum Immunol. 2006. PMID: 16916654

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