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Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis

PloS one, 2010-12, Vol.5 (12), p.e15661-e15661

2010

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Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds

Genome Biology, 2015-01, Vol.16 (1), p.19, Article 19

2015

Volltextzugriff (PDF)

Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders

Journal of neurodevelopmental disorders, 2019-06, Vol.11 (1), p.11-11, Article 11

2019

Volltextzugriff (PDF)

Update on the Basic Helix-Loop-Helix Transcription Factor Gene Family in Arabidopsis thaliana

The Plant cell, 2003-11, Vol.15 (11), p.2497-2501

2003

Volltextzugriff (PDF)

The Saccharomyces cerevisiae W303-K6001 cross-platform genome sequence: insights into ancestry and physiology of a laboratory mutt

Open biology, 2012-08, Vol.2 (8), p.120093-120093

2012

Volltextzugriff (PDF)

The Tissue-Specific lncRNA Fendrr Is an Essential Regulator of Heart and Body Wall Development in the Mouse

Developmental cell, 2013-01, Vol.24 (2), p.206-214

2013

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The Tissue-Specific IncRNA Fendrr Is an Essential Regulator of Heart and Body Wall Development in the Mouse

Developmental cell, 2013-01, Vol.24 (2), p.206-214

2013

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The R2R3-MYB gene family in Arabidopsis thaliana

Current Opinion in Plant Biology, 2001-10, Vol.4 (5), p.447-456

2001

Volltextzugriff (PDF)

Clinical exome sequencing: results from 2819 samples reflecting 1000 families

European journal of human genetics : EJHG, 2017-02, Vol.25 (2), p.176-182

2017

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The tissue-specific transcriptomic landscape of the mid-gestational mouse embryo

Development (Cambridge), 2014-06, Vol.141 (11), p.2325-2330

2014

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The basic helix-loop-helix transcription factor family in plants: a genome-wide study of protein structure and functional diversity

Molecular biology and evolution, 2003-05, Vol.20 (5), p.735-747

2003

Volltextzugriff (PDF)

Novel NAXE variants as a cause for neurometabolic disorder: implications for treatment

Journal of neurology, 2020-03, Vol.267 (3), p.770-782

2020

Volltextzugriff (PDF)

De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders

American journal of human genetics, 2019-07, Vol.105 (1), p.213-220

2019

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Development of an evidence-based algorithm that optimizes sensitivity and specificity in ES-based diagnostics of a clinically heterogeneous patient population

Genetics in medicine, 2019-01, Vol.21 (1), p.53-61

2019

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Two long‐chain acyl‐CoA synthetases from Arabidopsis thaliana involved in peroxisomal fatty acid β‐oxidation

The Plant journal : for cell and molecular biology, 2002-10, Vol.32 (1), p.93-103

2002

Volltextzugriff (PDF)

A homozygous frameshift variant in an alternatively spliced exon of DLG5 causes hydrocephalus and renal dysplasia

Clinical genetics, 2019-05, Vol.95 (5), p.631-633

2019

Volltextzugriff (PDF)

Retention of gene products in syncytial spermatids promotes non-Mendelian inheritance as revealed by the t complex responder

Genes & development, 2009-12, Vol.23 (23), p.2705-2710

2009

Volltextzugriff (PDF)

Expression of Msgn1 in the presomitic mesoderm is controlled by synergism of WNT signalling and Tbx6

EMBO reports, 2007-08, Vol.8 (8), p.784-789

2007

Volltextzugriff (PDF)

High-throughput sequencing of microdissected chromosomal regions

European journal of human genetics : EJHG, 2010-04, Vol.18 (4), p.457-462

2010

Volltextzugriff (PDF)

Validation of a semiconductor next‐generation sequencing assay for the clinical genetic screening of CFTR

Molecular genetics & genomic medicine, 2015-09, Vol.3 (5), p.396-403

2015

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Isolation and linkage analysis of expressed disease-resistance gene analogues of sugar beet (Beta vulgaris L.)

Genome, 2003-02, Vol.46 (1), p.70

2003

Volltextzugriff (PDF)

Trace2PS and FSA2PS: two software toolkits for converting trace and fsa files to PostScript format

Source code for biology and medicine, 2009-07, Vol.4 (1), p.4-4, Article 4

2009

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SRF is essential for mesodermal cell migration during elongation of the embryonic body axis

Mechanisms of development, 2014-08, Vol.133, p.23-35

2014

Volltextzugriff (PDF)

The R2R3-MYB gene family in Arabidopsis thaliana: Cell signalling and gene regulation

Current opinion in plant biology, 2001, Vol.4 (5), p.447-456

2001

Volltextzugriff (PDF)

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Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis

Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds

Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders

Update on the Basic Helix-Loop-Helix Transcription Factor Gene Family in Arabidopsis thaliana

The Saccharomyces cerevisiae W303-K6001 cross-platform genome sequence: insights into ancestry and physiology of a laboratory mutt

The Tissue-Specific lncRNA Fendrr Is an Essential Regulator of Heart and Body Wall Development in the Mouse

The Tissue-Specific IncRNA Fendrr Is an Essential Regulator of Heart and Body Wall Development in the Mouse

The R2R3-MYB gene family in Arabidopsis thaliana

Clinical exome sequencing: results from 2819 samples reflecting 1000 families

The tissue-specific transcriptomic landscape of the mid-gestational mouse embryo

Successful application of genome sequencing in a diagnostic setting: 1007 index cases from a clinically heterogeneous cohort

The basic helix-loop-helix transcription factor family in plants: a genome-wide study of protein structure and functional diversity

Novel NAXE variants as a cause for neurometabolic disorder: implications for treatment

De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders

Development of an evidence-based algorithm that optimizes sensitivity and specificity in ES-based diagnostics of a clinically heterogeneous patient population

Two long‐chain acyl‐CoA synthetases from Arabidopsis thaliana involved in peroxisomal fatty acid β‐oxidation

A homozygous frameshift variant in an alternatively spliced exon of DLG5 causes hydrocephalus and renal dysplasia

Retention of gene products in syncytial spermatids promotes non-Mendelian inheritance as revealed by the t complex responder

Expression of Msgn1 in the presomitic mesoderm is controlled by synergism of WNT signalling and Tbx6

High-throughput sequencing of microdissected chromosomal regions

Validation of a semiconductor next‐generation sequencing assay for the clinical genetic screening of CFTR

Isolation and linkage analysis of expressed disease-resistance gene analogues of sugar beet (Beta vulgaris L.)

Trace2PS and FSA2PS: two software toolkits for converting trace and fsa files to PostScript format

SRF is essential for mesodermal cell migration during elongation of the embryonic body axis

The R2R3-MYB gene family in Arabidopsis thaliana: Cell signalling and gene regulation

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