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Rifaximin preserves intestinal microbiota balance in patients undergoing allogeneic stem cell transplantation

Bone marrow transplantation (Basingstoke), 2016-08, Vol.51 (8), p.1087-1092

2016

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Nuclear magnetic resonance and mass spectrometry-based milk metabolomics in dairy cows during early and late lactation

Journal of dairy science, 2010-04, Vol.93 (4), p.1539-1550

2010

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The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations

Annals of human genetics, 2001-01, Vol.65 (1), p.43-62

2001

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Increased incidence of chronic GvHD and CMV disease in patients with vitamin D deficiency before allogeneic stem cell transplantation

Bone marrow transplantation (Basingstoke), 2015-09, Vol.50 (9), p.1217-1223

2015

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The Genetic Legacy of Paleolithic Homo sapiens sapiens in Extant Europeans: A Y Chromosome Perspective

Science (American Association for the Advancement of Science), 2000-11, Vol.290 (5494), p.1155-1159

2000

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High-Resolution Analysis of Human Y-Chromosome Variation Shows a Sharp Discontinuity and Limited Gene Flow between Northwestern Africa and the Iberian Peninsula

American journal of human genetics, 2001-04, Vol.68 (4), p.1019-1029

2001

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Comparison of next-generation sequencing systems

BioMed research international, 2012-01, Vol.2012, p.251364

2012

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Optimal Temperature Selection for Mutation Detection by Denaturing HPLC and Comparison to Single-Stranded Conformation Polymorphism and Heteroduplex Analysis

Clinical chemistry (Baltimore, Md.), 1999-08, Vol.45 (8), p.1133-1140

1999

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BITES: balanced individual treatment effect for survival data

Bioinformatics, 2022-06, Vol.38 (Supplement_1), p.i60-i67

2022

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Origins and Divergence of the Roma (Gypsies)

American journal of human genetics, 2001-12, Vol.69 (6), p.1314-1331

2001

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Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography

Genome research, 1997-10, Vol.7 (10), p.996

1997

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A Simple Procedure for the Analysis of Single Nucleotide Polymorphisms Facilitates Map-Based Cloning in Arabidopsis

Plant physiology (Bethesda), 2000-12, Vol.124 (4), p.1483-1492

2000

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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

Cell, 1996-11, Vol.87 (3), p.543-552

1996

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Genome-wide mapping with biallelic markers in Arabidopsis thaliana

Nature genetics, 1999-10, Vol.23 (2), p.203-207

1999

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Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection

Genomics (San Diego, Calif.), 1998-08, Vol.52 (1), p.44-49

1998

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Reference point insensitive molecular data analysis

Bioinformatics (Oxford, England), 2017-01, Vol.33 (2), p.219-226

2017

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A Pre-Columbian Y Chromosome-Specific Transition and its Implications for Human Evolutionary History

Proceedings of the National Academy of Sciences - PNAS, 1996-01, Vol.93 (1), p.196-200

1996

Volltextzugriff (PDF)

Molecular signatures that can be transferred across different omics platforms

Bioinformatics (Oxford, England), 2017-07, Vol.33 (14), p.i333-i340

2017

Volltextzugriff (PDF)

Y chromosome sequence variation and the history of human populations

Nature genetics, 2000-11, Vol.26 (3), p.358-361

2000

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Molecular signatures that can be transferred across different omics platforms

Bioinformatics (Oxford, England), 2017-09, Vol.33 (17), p.2790-2790

2017

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Dissecting the architecture of a quantitative trait locus in yeast

Nature (London), 2002-03, Vol.416 (6878), p.326-330

2002

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Systematic screen for human disease genes in yeast

Nature genetics, 2002-08, Vol.31 (4), p.400-404

2002

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Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene

Journal of medical genetics, 2002-11, Vol.39 (11), p.812-816

2002

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High-Accuracy DNA Sequence Variation Screening by DHPLC

BioTechniques, 2000-11, Vol.29 (5), p.1084-1092

2000

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The extent of linkage disequilibrium in Arabidopsis thaliana

Nature genetics, 2002-02, Vol.30 (2), p.190-193

2002

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Rifaximin preserves intestinal microbiota balance in patients undergoing allogeneic stem cell transplantation

Nuclear magnetic resonance and mass spectrometry-based milk metabolomics in dairy cows during early and late lactation

The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations

Increased incidence of chronic GvHD and CMV disease in patients with vitamin D deficiency before allogeneic stem cell transplantation

The Genetic Legacy of Paleolithic Homo sapiens sapiens in Extant Europeans: A Y Chromosome Perspective

High-Resolution Analysis of Human Y-Chromosome Variation Shows a Sharp Discontinuity and Limited Gene Flow between Northwestern Africa and the Iberian Peninsula

Comparison of next-generation sequencing systems

Optimal Temperature Selection for Mutation Detection by Denaturing HPLC and Comparison to Single-Stranded Conformation Polymorphism and Heteroduplex Analysis

BITES: balanced individual treatment effect for survival data

Origins and Divergence of the Roma (Gypsies)

Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography

A Simple Procedure for the Analysis of Single Nucleotide Polymorphisms Facilitates Map-Based Cloning in Arabidopsis

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

Genome-wide mapping with biallelic markers in Arabidopsis thaliana

Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection

Reference point insensitive molecular data analysis

A Pre-Columbian Y Chromosome-Specific Transition and its Implications for Human Evolutionary History

Molecular signatures that can be transferred across different omics platforms

Y chromosome sequence variation and the history of human populations

Molecular signatures that can be transferred across different omics platforms

Dissecting the architecture of a quantitative trait locus in yeast

Systematic screen for human disease genes in yeast

Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene

High-Accuracy DNA Sequence Variation Screening by DHPLC

The extent of linkage disequilibrium in Arabidopsis thaliana

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