c-gassner.bio

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18 03 2020

Clonal hematopoiesis in donors and long-term survivors of related allogeneic HSCT

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12 01 2019

Validated Reference Panel from Renewable Source of Genomic DNA Available for Standardization of Blood Group Genotyping.

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24 07 2018

Optimized Antigen Matching - Chances and Challenges in Molecular Times.

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23 07 2018

Low-Frequency Blood Group Antigens in Switzerland.

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28 05 2017

Stepwise partitioning of Xp21: a profiling method for XK deletions causative of the McLeod syndrome.

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16 05 2017

Human platelet antigen antibody induction in uncomplicated pregnancy is associated with HLA sensitization.

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15 05 2017

Molekulare Blutgruppenbestimmung.

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15 03 2017

Genetic background of the rare Yus and Gerbich blood group phenotypes: homologous regions of the GYPC gene contribute to deletion alleles.

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15 09 2016

Impact of donor ABH-secretor status in ABO-mismatched living donor kidney transplantation.

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15 08 2016

MNSs genotyping by MALDI-TOF MS shows high concordance with serology, allows gene copy number testing and reveals new St(a) alleles.

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15 06 2015

RHD variants in Flanders, Belgium.

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14 06 2015

Neurodegeneration in the elderly - When the blood type matters: An overview of the McLeod syndrome with focus on hematological features.

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01 07 2014

Impact of recipient ABH secretor status on outcome in minor ABO-incompatible hematopoietic stem cell transplantation.

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15 06 2014

Responder individuality in red blood cell alloimmunization.

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01 06 2014

Physiology of iron metabolism.

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01 05 2014

High-throughput Kell, Kidd, and Duffy matrix-assisted laser desorption/ionization, time-of-flight mass spectrometry-based blood group genotyping of 4000 donors shows close to full concordance with serotyping and detects new alleles.

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02 04 2014

Molecular RHD screening of RhD negative donors can replace standard serological testing for RhD negative donors.

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01 04 2014

Implementation of a mandatory donor RHD screening in Switzerland.

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16 11 2013

Iron and transfusion medicine.

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15 11 2013

The liver graft as Trojan horse-multilineage donor-derived hematopoiesis after liver transplantation: case report.

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23 10 2013

High resolution mapping of Y haplogroup G in Tyrol (Austria).

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01 07 2013

Multiple recurrent mutations at four human Y-chromosomal single nucleotide polymorphism sites in a 37 bp sequence tract on the ARSDP1 pseudogene.

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01 05 2013

Novel RHD alleles with weak hemagglutination and genetic Exon 9 diversity: weak D Types 45.1, 75, and 76.

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01 10 2012

Aging and clearance of erythrocytes.

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21 08 2012

Frequency data for 17 Y-chromosomal STRs and 19 Y-chromosomal SNPs in the Tyrolean district of Reutte, Austria.

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21 08 2012

Pasture names with Romance and Slavic roots facilitate dissection of Y chromosome variation in an exclusively German-speaking alpine region.

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14 08 2011

Investigation of bacterial and viral agents and immune status in Behcet's disease patients from Iran.

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01 05 2011

Expression of blood group genes by mesenchymal stem cells.

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29 04 2010

Complement as an endogenous adjuvant for dendritic cell-mediated induction of retrovirus-specific CTLs.

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14 03 2010

Fine mapping of T-cell immunoglobulin mucin domain gene 1 failed to detect a significant association with multiple sclerosis.

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14 09 2009

Induction of complement-mediated lysis of HIV-1 by a combination of HIV-specific and HLA allotype-specific antibodies.

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01 06 2009

Molecular Blood Group Diagnostics.

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01 05 2009

Report of the third international workshop on molecular blood group genotyping.

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01 04 2009

A novel KEL*1,3 allele with weak Kell antigen expression confirming the cis-modifier effect of KEL3.

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14 11 2008

Age-related appearance of a CMV-specific high-avidity CD8+ T cell clonotype which does not occur in young adults.

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01 10 2008

Donors with a rare pheno (geno) type.

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14 08 2007

HIV-1 induced generation of C5a attracts immature dendriticcells and promotes infection of autologous T cells.

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14 06 2007

IgG opsonization of HIV impedes provirus formation in and infection of dendritic cells and subsequent long-term transfer to T cells.

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01 06 2007

Mosaicism due to myeloid lineage restricted loss of heterozygosity as cause of spontaneous Rh phenotype splitting.

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01 06 2007

Genetic diversity of KELnull and KELel: a nationwide Austrian survey.

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14 03 2007

Interleukin-4 promoter polymorphisms: a genetic prognostic factor for survival in metastatic renal cell carcinoma.

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01 08 2006

RHD DNA screening for weak D, DEL and D+/- 'chimeras'.

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14 07 2006

Dissection of mitochondrial superhaplogroup H using coding region SNPs.

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14 04 2005

Presence of RHD in serologically D-, C/E+ individuals: a European multicenter study.

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01 04 2004

Molecular and serologic characterization of DWI, a novel "high-grade" partial D.

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14 01 2004

Genetic variants in the tumor necrosis factor receptor II gene in patients with multiple sclerosis.

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01 04 2003

Expression of low-frequency Ala108Pro substitution in the platelet glycoprotein Ibbeta gene.

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14 01 2003

Mutations in the gene for toll-like receptor 4 and multiple sclerosis.

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01 01 2001

PCR screening for common weak D types shows different distributions in three Central European populations.

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01 01 2001

A new h allele detected in Europe has a missense mutationin alpha(1,2)-fucosyltransferase motif II.

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01 09 1999

Unusual association of the DRB4 null allele, DRB4*0103102N, with HLA DRB1*0402 in a sample of Austrian patients.

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01 06 1999

Mapping HLA for single nucleotide polymorphisms.

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14 04 1998

Escherichia coli bacteriophage T1 DNA methyltransferase appears to interact with Escherichia coli enolase.

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01 03 1998

Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features.

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01 10 1997

RHD/CE typing by polymerase chain reaction using sequence-specific primers.

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01 09 1996

ABO glycosyltransferase genotyping by polymerase chain reaction using sequence-specific primers.

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14 06 1996

Evidence for a graft-versus-tumor effect in a patient treated with marrow ablative chemotherapy and allogeneic bone marrow transplantation for breast cancer.