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Publikationen

 

Bode U, Lörchner M, Pabst R, Wonigeit K, Overbeck S, Rink L, and Hundrieser J

The superantigen-induced polarization of T cells in rat peripheral lymph nodes is influenced by genetic polymorphisms in the IL-4 and IL-6 gene clusters

Int. Immunol. 2006 (accepted Okt 2006)

 

Hundrieser J, Düvel H, Trautewig B und Wonigeit K.

NKR-P1B Rezeptoren der Ratte sin dpolymorph und wirken als Alloantigen

Chirurgisches Forum 2005;34:11-13

 

Schwinzer R, Witte T, Hundrieser J, Ehlers S, Momot T, Hunzelmann N, Krieg T, Schmidt RE, Wonigeit K. <?xml:namespace prefix = o ns = "urn:schemas-microsoft-com:office:office" />

Enhanced frequency of a PTPRC (CD45) exon A mutation (77C-->G) in systemic sclerosis.

Genes Immun. 2003 Mar;4(2):168-9.

 

Bronsveld I, Mekus F, Bijman J, Ballmann M, Greipel J, Hundrieser J, Halley DJ, Laabs U, Busche R, De Jonge HR, Tummler B, Veeze HJ.

Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study Consortium.

Gastroenterology. 2000 Jul;119(1):32-40.

 

Parra E, Saha N, Soemantri AG, McGarvey ST, Hundrieser J, Shriver MD, Deka R.

Genetic variation at 9 autosomal microsatellite loci in Asian and Pacific populations.

Hum Biol. 1999 Oct;71(5):757-79.

 

Parra E, Shriver MD, Soemantri A, McGarvey ST, Hundrieser J, Saha N, Deka R.

Analysis of five Y-specific microsatellite loci in Asian and Pacific populations.

Am J Phys Anthropol. 1999 Sep;110(1):1-16.

 

Wonigeit K, Washington D, Hundrieser J.

Lessons from rat models on the genetic basis of interindividual differences in lymphocyte phenotype.

Transplant Proc. 1998 Aug;30(5):2341-3.

 

Ueda M, Hundrieser J, Hisanaga M, Tanaka K, Wonigeit K, Pichlmayr R, Schlitt HJ, Yamaoka Y.

Development of microchimerism in pediatric patients after living-related liver transplantation.

Clin Transplant. 1997 Jun;11(3):193-200.

 

Hisanaga M, Schlitt HJ, Hundrieser J, Wonigeit K, Nakajima Y, Kanehiro H, Nakano H, Pichlmayr R.

Frequency and clinical correlations of allogeneic microchimerism after heart, liver, and lung transplantation.

Transplant Proc. 1997 Feb-Mar;29(1-2):1215-7.

 

Hisanaga M, Schlitt HJ, Hundrieser J, Nakajima Y, Kanehiro H, Nakano H, Pichlmayr R.

Role of the graft as a source of donor-type microchimerism in liver transplant patients.

Transplant Proc. 1996 Apr;28(2):1073-5.

 

Hisanaga M, Schlitt HJ, Hundrieser J, Nakajima Y, Kanehiro H, Nakano H, Pichlmayr R.

Donor-derived microchimerism in heart transplant recipients: a parameter for immunological risk?

Transplant Proc. 1996 Apr;28(2):1036-8.

 

Deka R, Majumder PP, Shriver MD, Stivers DN, Zhong Y, Yu LM, Barrantes R, Yin SJ, Miki T, Hundrieser J, Bunker CH, McGarvey ST, Sakallah S, Ferrell RE, Chakraborty R.

Distribution and evolution of CTG repeats at the myotonin protein kinase gene in human populations.

Genome Res. 1996 Feb;6(2):142-54.

 

Hisanaga M, Hundrieser J, Boker K, Uthoff K, Raddatz G, Wahlers T, Wonigeit K, Pichlmayr R, Schlitt HJ.

Development, stability, and clinical correlations of allogeneic microchimerism after solid organ transplantation.

Transplantation. 1996 Jan 15;61(1):40-5.

 

Deka R, Miki T, Yin SJ, McGarvey ST, Shriver MD, Bunker CH, Raskin S, Hundrieser J, Ferrell RE, Chakraborty R.

Normal CAG repeat variation at the DRPLA locus in world populations.

Am J Hum Genet. 1995 Aug;57(2):508-11.

 

Thude H, Hundrieser J, Wonigeit K, Schwinzer R.

A point mutation in the human CD45 gene associated with defective splicing of exon A.

Eur J Immunol. 1995 Jul;25(7):2101-6.

 

Ringe B, Boker K, Schlitt HJ, Sproviero J, Hundrieser J, Tillmann HL, Chavan A, Flemming P, Galanski M, Pichlmayr R, et al.

Recurrence of hepatitis B virus cirrhosis and hepatocellular carcinoma: an indication for retransplantation?

Clin Transplant. 1995 Jun;9(3 Pt 1):190-6.

 

Hundrieser J, Hisanaga M, Boker K, Raddatz G, Brederlau A, Nashan B, Pichlmayr R, Schlitt HJ.

Long-term chimerism in liver transplantation: no evidence for immunological relevance but requirement for graft persistence.

Transplant Proc. 1995 Feb;27(1):216-8.

 

Hisanaga M, Hundrieser J, Uthoff K, Wahlers T, Pichlmayr R, Schlitt HJ.

Graft function and rejection patterns in heart-transplanted patients with and without systemic microchimerism.

Transplant Proc. 1995 Feb;27(1):202-4. No abstract available.

 

Schlitt HJ, Hundrieser J, Hisanaga M, Uthoff K, Karck M, Achtelik M, Wahlers T, Wonigeit K, Pichlmayr R.

Donor-type microchimerism after heart transplantation--a dynamic process.

Transplant Proc. 1995 Feb;27(1):155-7.

 

Deka R, Jin L, Shriver MD, Yu LM, DeCroo S, Hundrieser J, Bunker CH, Ferrell RE, Chakraborty R.

Population genetics of dinucleotide (dC-dA)n.(dG-dT)n polymorphisms in world populations.

Am J Hum Genet. 1995 Feb;56(2):461-74.

 

Schlitt HJ, Hundrieser J, Hisanaga M, Uthoff K, Karck M, Wahlers T, Wonigeit K, Pichlmayr R.

Patterns of donor-type microchimerism after heart transplantation.

Lancet. 1994 Jun 11;343(8911):1469-71.

 

Gomolka M, Hundrieser J, Nurnberg P, Roewer L, Epplen JT, Epplen C.

Selected di- and tetranucleotide microsatellites from chromosomes 7, 12, 14, and Y in various Eurasian populations.

Hum Genet. 1994 May;93(5):592-6.

 

Schlitt HJ, Hundrieser J, Ringe B, Pichlmayr R.

Donor-type microchimerism associated with graft rejection eight years after liver transplantation.

N Engl J Med. 1994 Mar 3;330(9):646-7.

 

Krawczak M, Bohm I, Nurnberg P, Hampe J, Hundrieser J, Poche H, Peters C, Slomski R, Kwiatkowska J, Nagy M, et al.

Paternity testing with oligonucleotide multilocus probe (CAC)5/(GTG)5: a multicenter study.

Forensic Sci Int. 1993 May;59(2):101-17.

 

Bohm I, Krawczak M, Nurnberg P, Hampe J, Hundrieser J, Poche H, Peters C, Slomski R, Kwiatkowska J, Nagy M, et al.

Oligonucleotide DNA fingerprinting: results of a multi-center study on reliability and validity.

EXS. 1993;67:257-60.

 

Epplen JT, Melmer G, Schmidt P, Roewer L, Hundrieser J, Epplen C, Buitkamp J.

On the potential of simple repetitive DNA for fingerprinting in clinical, forensic, and evolutionary dynamic studies.

Clin Investig. 1992 Nov;70(11):1043-51.

 

Hundrieser J, Nurnberg P, Czeizel AE, Metneki J, Rothganger S, Zischler H, Epplen JT.

Characterization of hypervariable locus-specific probes derived from a (CAC)5/(GTG)5 multilocus fingerprint in various Eurasian populations.

Hum Genet. 1992 Sep-Oct;90(1-2):27-33.

 

Reis A, Bremer S, Schlosser M, Dueck M, Bohm I, Hundrieser J, Macek M, Stuhrmann M, Wagner M, Dork T, et al.

Distribution patterns of the delta F508 mutation in the CFTR gene of CF-linked marker haplotypes in the German population.

Hum Genet. 1990 Sep;85(4):421-2.

 

Hundrieser J, Bremer S, Peinemann F, Stuhrmann M, Hoffknecht N, Wulf B, Schmidtke J, Reiss J, Maass G, Tummler B.

Frequency of the F508 deletion in the CFTR gene in Turkish cystic fibrosis patients.

Hum Genet. 1990 Sep;85(4):409-10.

 

Laig M, Pape M, Hundrieser J, Flatz G.

Mediterranean types of beta-thalassemia in the German population.

Hum Genet. 1990 Jun;85(1):135-7.

 

Tummler B, Aschendorff A, Darnedde T, Fryburg K, Maass G, Hundrieser J.

Marker haplotype association with growth in German cystic fibrosis patients.

Hum Genet. 1990 Feb;84(3):267-73.

 

Hundrieser J, Sanguansermsri T, Laig M, Pape M, Kuhnau W, Flatz G.

Direct demonstration of the HB Suan-Dok mutation in the alpha 2-globin gene by restriction analysis with Sma I.

Hemoglobin. 1990;14(1):69-77.

 

Hundrieser J, Laig M, Yongvanit P, Sriboonlue P, Sanguansermsri T, Kuhnau W, Pape M, Flatz G.

Study of alpha-thalassemia in northeastern Thailand at the DNA level.

Hum Hered. 1990;40(2):85-8.

 

Laig M, Pape M, Hundrieser J, Flatz G, Sanguansermsri T, Das BM, Deka R, Yongvanit P, Mularlee N.

The distribution of the Hb constant spring gene in Southeast Asian populations.

Hum Genet. 1990 Jan;84(2):188-90.

 

Sanguansermsri T, Pape M, Laig M, Hundrieser J, Flatz G.

Beta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin gene.

Hemoglobin. 1990;14(2):157-68.

 

Laig M, Sanguansermsri T, Wiangnon S, Hundrieser J, Pape M, Flatz G.

The spectrum of beta-thalassemia mutations in northern and northeastern Thailand.

Hum Genet. 1989 Dec;84(1):47-50.

 

Nurnberg P, Roewer L, Neitzel H, Sperling K, Popperl A, Hundrieser J, Poche H, Epplen C, Zischler H, Epplen JT.

DNA fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5: somatic stability and germline mutations.

Hum Genet. 1989 Dec;84(1):75-8.

 

Yongvanit P, Sriboonlue P, Mularlee N, Karnthong T, Areejitranusorn P, Hundrieser J, Limberg R, Schulze B, Laig M, Flatz SD, et al.

DNA haplotypes and frameworks linked to the beta-globin locus in an Austro-Asiatic population with a high prevalence of hemoglobin E.

Hum Genet. 1989 Sep;83(2):171-4.

 

Schulze B, Hundrieser J, Flatz G, Muller R, Stangel W.

Deletions and triplications of alpha globin genes in a German population.

Br J Haematol. 1989 May;72(1):114-5. No abstract available.

 

Hundrieser J, Sanguansermsri T, Papp T, Laig M, Flatz G.

Beta-globin gene linked DNA haplotypes and frameworks in three South-East Asian populations.

Hum Genet. 1988 Sep;80(1):90-4.