Pannicke U - Search Results

1

Lesson from hypomorphic recombination-activating gene (RAG) mutations: Why asymptomatic siblings should also be tested.

Schuetz C, Pannicke U, Jacobsen EM, Burggraf S, Albert MH, Hönig M, Niehues T, Feyen O, Ehl S, Debatin KM, Friedrich W, Schulz AS, Schwarz K. Schuetz C, et al. Among authors: pannicke u. J Allergy Clin Immunol. 2014 Apr;133(4):1211-5. doi: 10.1016/j.jaci.2013.10.021. Epub 2013 Dec 10. J Allergy Clin Immunol. 2014. PMID: 24331380 No abstract available.

2

RAG mutations in human B cell-negative SCID.

Schwarz K, Gauss GH, Ludwig L, Pannicke U, Li Z, Lindner D, Friedrich W, Seger RA, Hansen-Hagge TE, Desiderio S, Lieber MR, Bartram CR. Schwarz K, et al. Among authors: pannicke u. Science. 1996 Oct 4;274(5284):97-9. doi: 10.1126/science.274.5284.97. Science. 1996. PMID: 8810255

3

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

4

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.

5

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

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

The mechanism of vertebrate nonhomologous DNA end joining and its role in V(D)J recombination.

Lieber MR, Ma Y, Pannicke U, Schwarz K. Lieber MR, et al. Among authors: pannicke u. DNA Repair (Amst). 2004 Aug-Sep;3(8-9):817-26. doi: 10.1016/j.dnarep.2004.03.015. DNA Repair (Amst). 2004. PMID: 15279766 Review.

9

Two siblings with lethal pneumococcal meningitis in a family with a mutation in Interleukin-1 receptor-associated kinase 4.

Enders A, Pannicke U, Berner R, Henneke P, Radlinger K, Schwarz K, Ehl S. Enders A, et al. Among authors: pannicke u. J Pediatr. 2004 Nov;145(5):698-700. doi: 10.1016/j.jpeds.2004.06.065. J Pediatr. 2004. PMID: 15520784

10

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.

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