Schwarz K - Search Results

1

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. Among authors: schwarz k. 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.

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. 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. Among authors: schwarz k. Hum Genet. 1996 Dec;98(6):706-9. doi: 10.1007/s004390050290. Hum Genet. 1996. PMID: 8931706

4

DNA ligase IV is essential for V(D)J recombination and DNA double-strand break repair in human precursor lymphocytes.

Grawunder U, Zimmer D, Fugmann S, Schwarz K, Lieber MR. Grawunder U, et al. Among authors: schwarz k. Mol Cell. 1998 Oct;2(4):477-84. doi: 10.1016/s1097-2765(00)80147-1. Mol Cell. 1998. PMID: 9809069 Free article.

5

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: schwarz k. J Immunol. 2000 Jul 1;165(1):221-5. doi: 10.4049/jimmunol.165.1.221. J Immunol. 2000. PMID: 10861055

6

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: schwarz k. Cell. 2002 Mar 22;108(6):781-94. doi: 10.1016/s0092-8674(02)00671-2. Cell. 2002. PMID: 11955432 Free article.

7

The embryonic lethality in DNA ligase IV-deficient mice is rescued by deletion of Ku: implications for unifying the heterogeneous phenotypes of NHEJ mutants.

Karanjawala ZE, Adachi N, Irvine RA, Oh EK, Shibata D, Schwarz K, Hsieh CL, Lieber MR. Karanjawala ZE, et al. Among authors: schwarz k. DNA Repair (Amst). 2002 Dec 5;1(12):1017-26. doi: 10.1016/s1568-7864(02)00151-9. DNA Repair (Amst). 2002. PMID: 12531011

8

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: schwarz k. Immunol Cell Biol. 2003 Apr;81(2):130-6. doi: 10.1046/j.0818-9641.2002.01147.x. Immunol Cell Biol. 2003. PMID: 12631236

9

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

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

10

Human severe combined immune deficiency and DNA repair.

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

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