Schwarz K - Search Results

1

Mutations in the gene for the common gamma chain (gammac) in X-linked severe combined immunodeficiency.

Fugmann SD, Müller S, Friedrich W, Bartram CR, Schwarz K. Fugmann SD, et al. Among authors: schwarz k. Hum Genet. 1998 Dec;103(6):730-1. doi: 10.1007/pl00008710. Hum Genet. 1998. PMID: 9921912

2

Human common acute lymphoblastic leukemia-derived cell lines are competent to recombine their T-cell receptor delta/alpha regions along a hierarchically ordered pathway.

Hansen-Hagge TE, Yokota S, Reuter HJ, Schwarz K, Bartram CR. Hansen-Hagge TE, et al. Among authors: schwarz k. Blood. 1992 Nov 1;80(9):2353-62. Blood. 1992. PMID: 1421406 Free article.

3

Severe combined immunodeficiency (SCID) in man: B cell-negative (B-) SCID patients exhibit an irregular recombination pattern at the JH locus.

Schwarz K, Hansen-Hagge TE, Knobloch C, Friedrich W, Kleihauer E, Bartram CR. Schwarz K, et al. J Exp Med. 1991 Nov 1;174(5):1039-48. doi: 10.1084/jem.174.5.1039. J Exp Med. 1991. PMID: 1940786 Free PMC article.

4

Improved yields of long PCR products using gene 32 protein.

Schwarz K, Hansen-Hagge T, Bartram C. Schwarz K, et al. Nucleic Acids Res. 1990 Feb 25;18(4):1079. doi: 10.1093/nar/18.4.1079. Nucleic Acids Res. 1990. PMID: 2107527 Free PMC article.

5

Alternative splicing restricts translation of rearrangements at the T-cell receptor delta/alpha locus.

Hansen-Hagge TE, Mahotka C, Panzer-Grümayer RE, Reuter HJ, Schwarz K, van Dongen JJ, Bartram CR. Hansen-Hagge TE, et al. Among authors: schwarz k. Blood. 1995 Apr 1;85(7):1888-96. Blood. 1995. PMID: 7535593 Free article.

6

Confirmation of the localization of the human recombination activating gene 1 (RAG1) to chromosome 11p13.

Schwarz K, Hameister H, Gessler M, Grzeschik KH, Hansen-Hagge TE, Bartram CR. Schwarz K, et al. Hum Genet. 1994 Feb;93(2):215-7. doi: 10.1007/BF00210617. Hum Genet. 1994. PMID: 8112753

7

Recombinase deficiency in mouse and man.

Schwarz K, Hansen-Hagge TE, Bartram CR. Schwarz K, et al. Immunodeficiency. 1993;4(1-4):249-52. Immunodeficiency. 1993. PMID: 8167711 No abstract available.

8

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

9

V(D)J recombination pathology.

Schwarz K, Bartram CR. Schwarz K, et al. Adv Immunol. 1996;61:285-326. doi: 10.1016/s0065-2776(08)60869-x. Adv Immunol. 1996. PMID: 8834498 Review. No abstract available.

10

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

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