Pannicke U - Search Results

1

Lethal hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type II.

Enders A, Zieger B, Schwarz K, Yoshimi A, Speckmann C, Knoepfle EM, Kontny U, Müller C, Nurden A, Rohr J, Henschen M, Pannicke U, Niemeyer C, Nurden P, Ehl S. Enders A, et al. Among authors: pannicke u. Blood. 2006 Jul 1;108(1):81-7. doi: 10.1182/blood-2005-11-4413. Epub 2006 Mar 21. Blood. 2006. PMID: 16551969 Free article.

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

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

4

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.

5

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.

6

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

7

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.

8

A variant of SCID with specific immune responses and predominance of gamma delta T cells.

Ehl S, Schwarz K, Enders A, Duffner U, Pannicke U, Kühr J, Mascart F, Schmitt-Graeff A, Niemeyer C, Fisch P. Ehl S, et al. Among authors: pannicke u. J Clin Invest. 2005 Nov;115(11):3140-8. doi: 10.1172/JCI25221. Epub 2005 Oct 6. J Clin Invest. 2005. PMID: 16211094 Free PMC 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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