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Nomenclature for the description of human sequence variations

Human genetics, 2001-07, Vol.109 (1), p.121-124

2001

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Accessing the Transverse Dynamics and Polarization of Gluons inside the Proton at the LHC

Physical review letters, 2014-05, Vol.112 (21), Article 212001

2014

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Collembolan Transcriptomes Highlight Molecular Evolution of Hexapods and Provide Clues on the Adaptation to Terrestrial Life

PloS one, 2015-06, Vol.10 (6), p.e0130600-e0130600

2015

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Genome-wide assessment of differential roles for p300 and CBP in transcription regulation

Nucleic acids research, 2010-04, Vol.38 (16), p.5396-5408

2010

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Next generation sequencing technology: Advances and applications

Biochimica et biophysica acta. Molecular basis of disease, 2014-10, Vol.1842 (10), p.1932-1941

2014

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A full-body transcriptome and proteome resource for the European common carp

BMC genomics, 2016-09, Vol.17 (1), p.701-701, Article 701

2016

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Linearly polarized gluons and the Higgs transverse momentum distribution

Physical review letters, 2012-01, Vol.108 (3), p.032002-032002, Article 032002

2012

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Relative power and sample size analysis on gene expression profiling data

BMC genomics, 2009-09, Vol.10 (1), p.439-439, Article 439

2009

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FcγRIII stimulation breaks the tolerance of human nasal epithelial cells to bacteria through cross-talk with TLR4

Mucosal immunology, 2019-03, Vol.12 (2), p.425-433

2019

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Comparative analysis of antisense oligonucleotide analogs for targeted DMD exon 46 skipping in muscle cells

Gene therapy, 2004-09, Vol.11 (18), p.1391-1398

2004

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Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α- and β-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification

Journal of medical genetics, 2005-12, Vol.42 (12), p.922-931

2005

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Common pathological mechanisms in mouse models for muscular dystrophies

The FASEB journal, 2006-01, Vol.20 (1), p.127-129

2006

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TMD evolution and the Higgs transverse momentum distribution

Nuclear physics. B, 2014-09, Vol.886 (C), p.421-435

2014

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WHSC1, a 90 kb SET Domain-Containing Gene, Expressed in Early Development and Homologous to a Drosophila Dysmorphy Gene Maps in the Wolf-Hirschhorn Syndrome Critical Region and is Fused to IgH in t(1;14) Multiple Myeloma

Human molecular genetics, 1998-07, Vol.7 (7), p.1071-1082

1998

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Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD)

Neuromuscular disorders : NMD, 2011-08, Vol.21 (8), p.569-578

2011

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The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome

Familial cancer, 2013-06, Vol.12 (2), p.175-180

2013

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Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting

Clinical pharmacology and therapeutics, 2016-02, Vol.99 (2), p.172-185

2016

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Determining the Higgs spin and parity in the diphoton decay channel

Physical review letters, 2013-07, Vol.111 (3), p.032002-032002, Article 032002

2013

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Dysregulated Fcγ receptor IIa‐induced cytokine production in dendritic cells of lupus nephritis patients

Clinical and experimental immunology, 2020-01, Vol.199 (1), p.39-49

2020

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SAT0012 C-reactive protein: not only a marker, but also a cause of inflammation through metabolic reprogramming of human macrophages

Annals of the rheumatic diseases, 2018-06, Vol.77 (Suppl 2), p.874

2018

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Duplications in the DMD gene

Human mutation, 2006-09, Vol.27 (9), p.938-945

2006

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Bounding W-W' mixing with spin asymmetries at RHIC

Physical review letters, 2010-08, Vol.105 (7), p.071801, Article 071801

2010

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Variation of CNV distribution in five different ethnic populations

Cytogenetic and genome research, 2007-01, Vol.118 (1), p.19-30

2007

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Methods to detect CNVs in the human genome

Cytogenetic and genome research, 2008-01, Vol.123 (1-4), p.313-321

2008

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Becker muscular dystrophy patients with deletions around exon 51; a promising outlook for exon skipping therapy in Duchenne patients

Neuromuscular disorders : NMD, 2010-04, Vol.20 (4), p.251-254

2010

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Nomenclature for the description of human sequence variations

Accessing the Transverse Dynamics and Polarization of Gluons inside the Proton at the LHC

Collembolan Transcriptomes Highlight Molecular Evolution of Hexapods and Provide Clues on the Adaptation to Terrestrial Life

Genome-wide assessment of differential roles for p300 and CBP in transcription regulation

Next generation sequencing technology: Advances and applications

A full-body transcriptome and proteome resource for the European common carp

Linearly polarized gluons and the Higgs transverse momentum distribution

Relative power and sample size analysis on gene expression profiling data

FcγRIII stimulation breaks the tolerance of human nasal epithelial cells to bacteria through cross-talk with TLR4

Comparative analysis of antisense oligonucleotide analogs for targeted DMD exon 46 skipping in muscle cells

Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α- and β-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification

Common pathological mechanisms in mouse models for muscular dystrophies

TMD evolution and the Higgs transverse momentum distribution

WHSC1, a 90 kb SET Domain-Containing Gene, Expressed in Early Development and Homologous to a Drosophila Dysmorphy Gene Maps in the Wolf-Hirschhorn Syndrome Critical Region and is Fused to IgH in t(1;14) Multiple Myeloma

Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD)

The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome

Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting

Determining the Higgs spin and parity in the diphoton decay channel

Dysregulated Fcγ receptor IIa‐induced cytokine production in dendritic cells of lupus nephritis patients

SAT0012 C-reactive protein: not only a marker, but also a cause of inflammation through metabolic reprogramming of human macrophages

Duplications in the DMD gene

Bounding W-W' mixing with spin asymmetries at RHIC

Variation of CNV distribution in five different ethnic populations

Methods to detect CNVs in the human genome

Becker muscular dystrophy patients with deletions around exon 51; a promising outlook for exon skipping therapy in Duchenne patients

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