Schneider PM - Search Results

1

The distribution of human C4 DNA variants in relation to major histocompatibility complex alleles and extended haplotypes.

Whitehead AS, Truedsson L, Schneider PM, Awdeh ZL, Fleischnick E, Blumenthal M, Costello W, Gerald PS, Yunis EJ, Alper CA. Whitehead AS, et al. Among authors: schneider pm. Hum Immunol. 1988 Jan;21(1):23-32. doi: 10.1016/0198-8859(88)90078-x. Hum Immunol. 1988. PMID: 3163333

2

Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codon.

Fredrikson GN, Gullstrand B, Schneider PM, Witzel-Schlömp K, Sjöholm AG, Alper CA, Awdeh Z, Truedsson L. Fredrikson GN, et al. Among authors: schneider pm. Hum Immunol. 1998 Nov;59(11):713-9. doi: 10.1016/s0198-8859(98)00068-8. Hum Immunol. 1998. PMID: 9796739

3

Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.

Schneider PM, Carroll MC, Alper CA, Rittner C, Whitehead AS, Yunis EJ, Colten HR. Schneider PM, et al. J Clin Invest. 1986 Sep;78(3):650-7. doi: 10.1172/JCI112623. J Clin Invest. 1986. PMID: 3018042 Free PMC article.

4

C4 nomenclature statement (1990).

Mauff G, Alper CA, Dawkins R, Doxiadis G, Giles CM, Hauptmann G, Rittner C, Schneider PM. Mauff G, et al. Among authors: schneider pm. Complement Inflamm. 1990;7(4-6):261-8. doi: 10.1159/000463159. Complement Inflamm. 1990. PMID: 2088664

5

Polymerase chain reaction analysis of the Xba I polymorphism of the human complement C4 genes provides evidence for strong haplotype conservation.

Witzel K, Chu X, Rittner C, Schneider PM. Witzel K, et al. Among authors: schneider pm. Hum Immunol. 1995 Jul;43(3):165-73. doi: 10.1016/0198-8859(94)00150-o. Hum Immunol. 1995. PMID: 7558933

6

Major histocompatibility complex haplotypes and complement C4 alleles in systemic lupus erythematosus. Results of a multicenter study.

Hartung K, Baur MP, Coldewey R, Fricke M, Kalden JR, Lakomek HJ, Peter HH, Schendel D, Schneider PM, Seuchter SA, et al. Hartung K, et al. Among authors: schneider pm. J Clin Invest. 1992 Oct;90(4):1346-51. doi: 10.1172/JCI116000. J Clin Invest. 1992. PMID: 1401069 Free PMC article.

7

The influence of major histocompatibility complex class II genes and T-cell Vbeta repertoire on response to immunization with HBsAg.

Höhler T, Meyer CU, Notghi A, Stradmann-Bellinghausen B, Schneider PM, Starke R, Zepp F, Sänger R, Clemens R, Meyer zum Büschenfelde KH, Rittner C. Höhler T, et al. Among authors: schneider pm. Hum Immunol. 1998 Apr;59(4):212-8. doi: 10.1016/s0198-8859(98)00014-7. Hum Immunol. 1998. PMID: 9568796

8

Bgl II restriction fragment length polymorphism of human complement C4A gene coincides with BF*F allele of factor B.

Schneider PM, Rittner C. Schneider PM, et al. Immunogenetics. 1988;27(3):225-8. doi: 10.1007/BF00346591. Immunogenetics. 1988. PMID: 2892787 No abstract available.

9

TAP-polymorphisms in juvenile onset psoriasis and psoriatic arthritis.

Höhler T, Weinmann A, Schneider PM, Rittner C, Schopf RE, Knop J, Hasenclever P, Meyer zum Büschenfelde KH, Märker-Hermann E. Höhler T, et al. Among authors: schneider pm. Hum Immunol. 1996 Nov;51(1):49-54. doi: 10.1016/s0198-8859(96)00156-5. Hum Immunol. 1996. PMID: 8911997

10

Major histocompatibility complex (MHC) class III genetics in two Amerindian tribes from southern Brazil: the Kaingang and the Guarani.

Weg-Remers S, Brenden M, Schwarz E, Witzel K, Schneider PM, Guerra LK, Rehfeldt IR, Lima MT, Hartmann D, Petzl-Erler ML, de Messias IJ, Mauff G. Weg-Remers S, et al. Among authors: schneider pm. Hum Genet. 1997 Oct;100(5-6):548-56. doi: 10.1007/s004390050550. Hum Genet. 1997. PMID: 9341869

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