Schwarz K - Search Results

1

MCM3AP and POMP Mutations Cause a DNA-Repair and DNA-Damage-Signaling Defect in an Immunodeficient Child.

Gatz SA, Salles D, Jacobsen EM, Dörk T, Rausch T, Aydin S, Surowy H, Volcic M, Vogel W, Debatin KM, Stütz AM, Schwarz K, Pannicke U, Hess T, Korbel JO, Schulz AS, Schumacher J, Wiesmüller L. Gatz SA, et al. Among authors: schwarz k. Hum Mutat. 2016 Mar;37(3):257-68. doi: 10.1002/humu.22939. Epub 2015 Dec 30. Hum Mutat. 2016. PMID: 26615982

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

Definition of a critical T cell threshold for prevention of GVHD after HLA non-identical PBPC transplantation in children.

Müller S, Schulz A, Reiss U, Schwarz K, Schreiner T, Wiesneth M, Debatin KM, Friedrich W. Müller S, et al. Among authors: schwarz k. Bone Marrow Transplant. 1999 Sep;24(6):575-81. doi: 10.1038/sj.bmt.1701970. Bone Marrow Transplant. 1999. PMID: 10490721

5

Transplacentally acquired maternal T lymphocytes in severe combined immunodeficiency: a study of 121 patients.

Müller SM, Ege M, Pottharst A, Schulz AS, Schwarz K, Friedrich W. Müller SM, et al. Among authors: schwarz k. Blood. 2001 Sep 15;98(6):1847-51. doi: 10.1182/blood.v98.6.1847. Blood. 2001. PMID: 11535520 Free article.

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

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.

8

Familial polycythemia vera with Budd-Chiari syndrome in childhood.

Cario H, Pahl HL, Schwarz K, Galm C, Hoffmann M, Burdelski M, Kohne E, Debatin KM. Cario H, et al. Among authors: schwarz k. Br J Haematol. 2003 Oct;123(2):346-52. doi: 10.1046/j.1365-2141.2003.04591.x. Br J Haematol. 2003. PMID: 14531919 Free article.

9

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.

10

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.

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